A species of parasitic nematode causing Malayan filariasis and having a distribution centering roughly on the Malay peninsula. The life cycle of B. malayi is similar to that of WUCHERERIA BANCROFTI, except that in most areas the principal mosquito vectors belong to the genus Mansonia.
A filarial worm of Southeast Asia, producing filariasis and elephantiasis in various mammals including man. It was formerly included in the genus WUCHERERIA.
A species of parasitic nematode found in man and other mammals. It has been reported from Malaya and East Pakistan and may produce symptoms of tropical eosinophilia.
Infections with nematodes of the superfamily FILARIOIDEA. The presence of living worms in the body is mainly asymptomatic but the death of adult worms leads to granulomatous inflammation and permanent fibrosis. Organisms of the genus Elaeophora infect wild elk and domestic sheep causing ischemic necrosis of the brain, blindness, and dermatosis of the face.
The prelarval stage of Filarioidea in the blood and other tissues of mammals and birds. They are removed from these hosts by blood-sucking insects in which they metamorphose into mature larvae.
Parasitic infestation of the human lymphatic system by WUCHERERIA BANCROFTI or BRUGIA MALAYI. It is also called lymphatic filariasis.
A superfamily of nematodes of the suborder SPIRURINA. Its organisms possess a filiform body and a mouth surrounded by papillae.
A genus of bacteria comprised of a heterogenous group of gram-negative small rods and coccoid forms associated with arthropods. (From Bergey's Manual of Systematic Bacteriology, vol 1, 1984)
Proteins found in any species of helminth.
Any part or derivative of a helminth that elicits an immune reaction. The most commonly seen helminth antigens are those of the schistosomes.
A subfamily of the Muridae consisting of several genera including Gerbillus, Rhombomys, Tatera, Meriones, and Psammomys.
A white threadlike worm which causes elephantiasis, lymphangitis, and chyluria by interfering with the lymphatic circulation. The microfilaria are found in the circulating blood and are carried by mosquitoes.
Immunoglobulins produced in a response to HELMINTH ANTIGENS.
A filarial parasite primarily of dogs but occurring also in foxes, wolves, and humans. The parasite is transmitted by mosquitoes.
A filarial nematode parasite of mammalian blood with the vector being a tick or small fly.
Deoxyribonucleic acid that makes up the genetic material of helminths.
An anthelmintic used primarily as the citrate in the treatment of filariasis, particularly infestations with Wucheria bancrofti or Loa loa.
A subfamily in the family MURIDAE, comprising the Old World MICE and RATS.
Pharmacological agents destructive to nematodes in the superfamily Filarioidea.
Ribonucleic acid in helminths having regulatory and catalytic roles as well as involvement in protein synthesis.
An enzyme that activates aspartic acid with its specific transfer RNA. EC 6.1.1.12.
A genus of parasitic nematodes whose organisms live and breed in skin and subcutaneous tissues. Onchocercal microfilariae may also be found in the urine, blood, or sputum.
The genetic complement of a helminth (HELMINTHS) as represented in its DNA.
A family of the order DIPTERA that comprises the mosquitoes. The larval stages are aquatic, and the adults can be recognized by the characteristic WINGS, ANIMAL venation, the scales along the wing veins, and the long proboscis. Many species are of particular medical importance.
The joining of RNA from two different genes. One type of trans-splicing is the "spliced leader" type (primarily found in protozoans such as trypanosomes and in lower invertebrates such as nematodes) which results in the addition of a capped, noncoding, spliced leader sequence to the 5' end of mRNAs. Another type of trans-splicing is the "discontinuous group II introns" type (found in plant/algal chloroplasts and plant mitochondria) which results in the joining of two independently transcribed coding sequences. Both are mechanistically similar to conventional nuclear pre-mRNA cis-splicing. Mammalian cells are also capable of trans-splicing.
The functional hereditary units of HELMINTHS.
The small RNAs which provide spliced leader sequences, SL1, SL2, SL3, SL4 and SL5 (short sequences which are joined to the 5' ends of pre-mRNAs by TRANS-SPLICING). They are found primarily in primitive eukaryotes (protozoans and nematodes).
A class of unsegmented helminths with fundamental bilateral symmetry and secondary triradiate symmetry of the oral and esophageal structures. Many species are parasites.
The relationship between an invertebrate and another organism (the host), one of which lives at the expense of the other. Traditionally excluded from definition of parasites are pathogenic BACTERIA; FUNGI; VIRUSES; and PLANTS; though they may live parasitically.
The relationship between two different species of organisms that are interdependent; each gains benefits from the other or a relationship between different species where both of the organisms in question benefit from the presence of the other.
A genus of small free-living nematodes. Two species, CAENORHABDITIS ELEGANS and C. briggsae are much used in studies of genetics, development, aging, muscle chemistry, and neuroanatomy.
Wormlike or grublike stage, following the egg in the life cycle of insects, worms, and other metamorphosing animals.
Organs and other anatomical structures of non-human vertebrate and invertebrate animals.
Inflammation of the renal glomeruli (KIDNEY GLOMERULUS) that can be classified by the type of glomerular injuries including antibody deposition, complement activation, cellular proliferation, and glomerulosclerosis. These structural and functional abnormalities usually lead to HEMATURIA; PROTEINURIA; HYPERTENSION; and RENAL INSUFFICIENCY.
Inflammation of the throat (PHARYNX).
Infections with bacteria of the genus STREPTOCOCCUS.
A species of gram-positive, coccoid bacteria isolated from skin lesions, blood, inflammatory exudates, and the upper respiratory tract of humans. It is a group A hemolytic Streptococcus that can cause SCARLET FEVER and RHEUMATIC FEVER.
A febrile disease occurring as a delayed sequela of infections with STREPTOCOCCUS PYOGENES. It is characterized by multiple focal inflammatory lesions of the connective tissue structures, such as the heart, blood vessels, and joints (POLYARTHRITIS) and brain, and by the presence of ASCHOFF BODIES in the myocardium and skin.
Chronic glomerulonephritis characterized histologically by proliferation of MESANGIAL CELLS, increase in the MESANGIAL EXTRACELLULAR MATRIX, and a thickening of the glomerular capillary walls. This may appear as a primary disorder or secondary to other diseases including infections and autoimmune disease SYSTEMIC LUPUS ERYTHEMATOSUS. Various subtypes are classified by their abnormal ultrastructures and immune deposits. Hypocomplementemia is a characteristic feature of all types of MPGN.
A broad-spectrum penicillin antibiotic used orally in the treatment of mild to moderate infections by susceptible gram-positive organisms.

Efficacy of five annual single doses of diethylcarbamazine for treatment of lymphatic filariasis in Fiji. (1/222)

Annual single-dose treatments with diethylcarbamazine citrate (DEC) at a dose of 6 mg/kg have been reported effective in reducing microfilariae (mf) rate and density and applicable to large-scale filariasis control campaigns. However, the efficacy of such treatments has not been studied quantitatively in relation to different pretreatment levels of endemicity. This study of 32 villages in Fiji revealed that five treatments repeated annually steadily reduced village mf rate, and that the degree of reduction was not influenced by pretreatment levels of mf density or rate. This indicates that an annual dosage scheme is applicable to high-endemicity areas. The results also suggest that such treatment affected juvenile forms of Wuchereria bancrofti and may prevent them from reproducing.  (+info)

Anti-filarial IgG4 in men and women living in Brugia malayi-endemic areas. (2/222)

To assess whether antifilarial IgG4 can be used to study various epidemiological facets of filarial infections, we studied this isotype in 238 individuals resident in areas endemic for brugian filariasis, focusing on the differences between men and women. In the study area, the prevalence of microfilariae was 6.7% and the prevalence of antifilarial IgG4 was 49.2%. All microfilariae carriers were positive for antifilarial IgG4, whereas a proportion of the endemic normals (94/208) and clephantiasis patients (7/14) had IgG4 antibodies to filarial antigens. Data were analysed as a function of gender in distinct clinical groups and stratified for age. The prevalence of microfilariae was higher in males in all age groups, as reflected in significantly higher antifilarial IgG4 antibody levels compared to females. The prevalence of IgG4 increased to reach a plateau at the age of 30 years in both males and females. These results indicate that antifilarial IgG4 antibodies can reflect the differences in the extent of infection in males and females as measured by microfilarial counts, and that this parameter can be used for epidemiological assessments of filarial infection.  (+info)

Immunity in experimental murine filariasis: roles of T and B cells revisited. (3/222)

We have reevaluated the contributions of T and B cells in Brugia malayi infection by utilizing knockout mice on a uniform background (C57BL/6J). We find that B-cell-deficient mice are more permissive to infection than T-cell-deficient mice.  (+info)

Homologs of the Caenorhabditis elegans masculinizing gene her-1 in C. briggsae and the filarial parasite Brugia malayi. (4/222)

The masculinizing gene her-1 in Caenorhabditis elegans (Ce-her-1) encodes a novel protein, HER-1A, which is required for male development. To identify conserved elements in her-1 we have cloned and characterized two homologous nematode genes: one by synteny from the closely related free-living species C. briggsae (Cb-her-1) and the other, starting with a fortuitously identified expressed sequence tag, from the distantly related parasite Brugia malayi (Bm-her-1). The overall sequence identities of the predicted gene products with Ce-HER-1A are only 57% for Cb-HER-1, which is considerably lower than has been found for most homologous briggsae genes, and 35% for Bm-HER-1. However, conserved residues are found throughout both proteins, and like Ce-HER-1A, both have putative N-terminal signal sequences. Ce-her-1 produces a larger masculinizing transcript (her-1a) and a smaller transcript of unknown function (her-1b); both are present essentially only in males. By contrast, Cb-her-1 appears to produce only one transcript, corresponding to her-1a; it is enriched in males but present also in hermaphrodites. Injection of dsRNA transcribed from Cb-her-1 into C. briggsae hermaphrodites (RNA interference) caused XO animals to develop into partially fertile hermaphrodites. Introducing a Cb-her-1 construct as a transgene under control of the C. elegans unc-54 myosin heavy chain promoter caused strong masculinization of both C. briggsae and C. elegans hermaphrodites. Introduction of a similar Bm-her-1 construct into C. elegans caused only very weak, if any, masculinization. We conclude that in spite of considerable divergence the Cb gene is likely to be a functional ortholog of Ce-her-1, while the function of the distantly related Bm gene remains uncertain.  (+info)

A novel serpin expressed by blood-borne microfilariae of the parasitic nematode Brugia malayi inhibits human neutrophil serine proteinases. (5/222)

Serine proteinase inhibitors (serpins) play a vital regulatory role in a wide range of biological processes, and serpins from viruses have been implicated in pathogen evasion of the host defence system. For the first time, we report a functional serpin gene from nematodes that may function in this manner. This gene, named Bm-spn-2, has been isolated from the filarial nematode Brugia malayi, a causative agent of human lymphatic filariasis. Polymerase chain reaction (PCR) and Western blot experiments indicate that Bm-spn-2 is expressed only by microfilariae (Mf), which are the long-lived blood-dwelling larval stage. A survey of the greater than 14,000 expressed sequence tags (ESTs) from B malayi deposited in dbEST shows that greater than 2% of the ESTs sequenced from Mf cDNA libraries correspond to Bm-spn-2. Despite its abundance in the microfilarial stage, Bm-spn-2 has not been found in any other point in the life cycle. The predicted protein encoded by Bm-spn-2 contains 428 amino acids with a putative signal peptide. Antibodies to recombinant Bm-SPN-2 protein react specifically with a 47.5-kD native protein in Mf extract. Bm-SPN-2 is one of the largest of the 93 known serpins, due to a 22 amino acid carboxy-terminal extension, and contains the conserved serpin signature sequence. Outside these regions, levels of homology are low, and only a distant relationship can been seen to a Caenorhabditis elegans serpin. The Bm-spn-2 gene contains 6 introns, 2 of which appear to be shared by both nematode species. The B malayi introns have an extended and conserved 3' splice site and are relatively large compared with C elegans. A panel of mammalian serine proteinases were screened and Bm-SPN-2 protein was found to specifically inhibit enzymatic activity of human neutrophil cathepsin G and human neutrophil elastase, but not a range of other serine proteinases. It is possible that Bm-SPN-2 could function as a stage-specific serpin in the blood environment of the microfilarial parasite in protection from human immunity and thus may be a good candidate for protective vaccine.  (+info)

Comparative analysis of glycosylated and nonglycosylated filarial homologues of the 20-kilodalton retinol binding protein from Onchocerca volvulus (Ov20). (6/222)

Ov20 is a structurally novel 20-kDa retinol binding protein secreted by Onchocerca volvulus. Immunological and biological investigation of this protein has been hampered by the inability to maintain O. volvulus in a laboratory setting. In an effort to find a system more amenable to laboratory investigation, we have cloned, sequenced, and expressed cDNA encoding homologues of Ov20 from two closely related filarial species, Brugia malayi (Bm20) and Acanthocheilonema viteae (Av20). Sequence comparisons have highlighted differences in glycosylation of the homologues. We present here an analysis of mouse immune responses to Ov20, Bm20, and Av20. The results suggest a strong genetic restriction in response to native Bm20 that is overcome when recombinant, nonnative material is used. Reactivity of human filarial sera to the three recombinant proteins confirmed previous specificity studies with Ov20 but highlighted important differences in the reactivity patterns of the O. volvulus and B. malayi homologues that may be due to differences in glycosylation patterns. Ov20 is a dominant antigen in infected individuals, while Bm20 is not. The availability of the B. malayi homologue enabled us to use defined murine reagents and inbred strains for genetic analysis of responsiveness in a way that is not possible for Ov20. However, the close sequence similarity between Ov20 and Av20 suggests that the A. viteae model may be more suited to the investigation of the biological functions of Ov20.  (+info)

Calgranulin C has filariacidal and filariastatic activity. (7/222)

The calgranulins are a family of calcium- and zinc-binding proteins produced by neutrophils, monocytes, and other cells. Calgranulins are released during inflammatory responses and have antimicrobial activity. Recently, one of the calgranulins, human calgranulin C (CaGC), has been implicated as an important component of the host responses that limit the parasite burden during filarial nematode infections. The goal of this work was to test the hypothesis that human CaGC has biologic activity against filarial parasites. Brugia malayi microfilariae and adults were exposed in vitro to 0.75 to 100 nM recombinant human CaGC. Recombinant CaGC affected adult and larval parasites in a dose-dependent fashion. Microfilariae were more sensitive to the action of CaGC than were adult parasites. At high levels, CaGC was both macrofilariacidal and microfilariacidal. At lower levels, the percentage of parasites killed was dependent on the level of CaGC in the culture system. The larvae not killed had limited motility. The filariastatic effect of low-level CaGC was reversed when the CaGC was removed from the culture system. Immunohistochemical analysis demonstrated that human CaGC accumulated in the cells of the hypodermis-lateral chord of adult and larval parasites. The antifilarial activity of CaGC was not due to the sequestration of zinc. Thus, the cellular and molecular mechanisms that result in the production and release of CaGC in humans may play a key role in the regulation of filarial parasite numbers.  (+info)

B1 B lymphocytes play a critical role in host protection against lymphatic filarial parasites. (8/222)

Host defense against multicellular, extracellular pathogens such as nematode parasites is believed to be mediated largely, if not exclusively, by T lymphocytes. During our investigations into the course of Brugia malayi and Brugia pahangi infections in immunodeficient mouse models, we found that mice lacking B lymphocytes were permissive for Brugian infections, whereas immunocompetent mice were uniformly resistant. Mice bearing the Btk(xid) mutation were as permissive as those lacking all B cells, suggesting that the B1 subset may be responsible for host protection. Reconstitution of immunodeficient recombination activating gene (Rag)-1(-/)- mice with B1 B cells conferred resistance, even in the absence of conventional B2 lymphocytes and most T cells. These results suggest that B1 B cells are necessary to mediate host resistance to Brugian infection. Our data are consistent with a model wherein early resistance to B. malayi is mediated by humoral immune response, with a significant attrition of the incoming infectious larval load. Sterile clearance of the remaining parasite burden appears to require cell-mediated immunity. These data raise the possibility that the identification of molecule(s) recognized by humoral immune mechanisms might help generate prophylactic vaccines.  (+info)

'Brugia malayi' is a species of parasitic nematode (roundworm) that can infect humans and cause the tropical disease known as lymphatic filariasis. The adult worms typically reside in the lymphatic vessels, where they can cause inflammation, obstruction, and damage to the lymphatic system.

The life cycle of 'Brugia malayi' involves several stages, including microfilariae (immature worms) that are transmitted to a human host through the bite of an infected mosquito vector. Once inside the human body, the microfilariae migrate to the lymphatic vessels and mature into adult worms over a period of several months.

The symptoms of lymphatic filariasis can range from mild to severe, depending on the extent of the infection and the individual's immune response. In some cases, the disease can lead to chronic swelling and deformity of the affected limbs or genitalia, a condition known as elephantiasis.

Preventive measures for lymphatic filariasis include avoiding mosquito bites through the use of insect repellent, long-sleeved clothing, and bed nets, as well as mass drug administration programs to eliminate the parasite from affected communities.

'Brugia' is a genus of parasitic nematode worms that are known to cause lymphatic filariasis, a tropical disease affecting the lymphatic system. There are three main species of Brugia that infect humans: Brugia malayi, Brugia timori, and Brugia garinii. These parasites are transmitted to humans through the bite of infected mosquitoes.

Brugia malayi is found primarily in Southeast Asia, while Brugia timori is restricted to the island of Timor in Indonesia. Brugia garinii, on the other hand, is more widely distributed and can be found in parts of Africa and Asia.

The infection caused by these parasites can lead to a range of symptoms, including fever, swelling of the lymph nodes, and elephantiasis, a condition characterized by severe swelling of the limbs or genitals. Preventive measures such as avoiding mosquito bites and mass drug administration programs are in place to control the spread of lymphatic filariasis caused by Brugia species.

'Brugia pahangi' is a species of parasitic nematode (roundworm) that can cause lymphatic filariasis in humans. It is primarily found in Southeast Asia and is transmitted through the bite of infected mosquitoes. The adult worms reside in the lymphatic system, where they can cause inflammation, swelling, and damage to the lymph vessels and nodes. This can lead to a range of symptoms, including fever, chills, headache, and lymphadenopathy (swollen lymph nodes). In advanced cases, it can result in elephantiasis, a severe and disfiguring condition characterized by the thickening and hardening of the skin and underlying tissues.

It's important to note that 'Brugia pahangi' is primarily a veterinary parasite, infecting animals such as cats and dogs, but it can also cause human infections under certain circumstances. Preventive measures include avoiding mosquito bites through the use of insect repellent, wearing long sleeves and pants, and staying indoors during peak mosquito hours. In areas where the parasite is common, public health programs may provide mass drug administration to control the spread of the infection.

Filariasis is a parasitic disease caused by infection with roundworms of the Filarioidea type. The infection is spread through the bite of infected mosquitoes and can lead to various symptoms depending on the type of filarial worm, including lymphatic dysfunction (elephantiasis), eye damage (onchocerciasis or river blindness), and tropical pulmonary eosinophilia. The disease is prevalent in tropical areas with poor sanitation and lack of access to clean water. Preventive measures include wearing protective clothing, using insect repellents, and sleeping under mosquito nets. Treatment typically involves the use of antiparasitic drugs such as diethylcarbamazine or ivermectin.

Microfilaria is the larval form of certain parasitic roundworms (nematodes) belonging to the family Onchocercidae. These worms include species that cause filariasis, which are diseases transmitted through the bite of infected mosquitoes or blackflies. The microfilariae are found in the blood or tissue fluids of the host and can measure from 200 to 300 microns in length. They have a distinct sheath and a characteristic tail taper, which helps in their identification under a microscope. Different filarial species have specific microfilariae characteristics, such as size, shape, and lifestyle patterns (nocturnal or diurnal periodicity). The presence of microfilariae in the host's blood or tissue fluids is indicative of an ongoing infection with the respective filarial parasite.

Elephantiasis, filarial is a medical condition characterized by the severe swelling of limbs or other parts of the body due to the blockage of lymphatic vessels by parasitic worms. It is caused by infection with threadlike nematode filarial worms, such as Wuchereria bancrofti and Brugia timori. These worms are transmitted to humans through mosquito bites.

The blockage of lymphatic vessels leads to the accumulation of lymph fluid in the affected area, causing progressive swelling, thickening, and hardening of the skin and underlying tissues. In advanced cases, the skin may become rough, nodular, and fissured, resembling the hide of an elephant, hence the name "elephantiasis."

The condition is usually chronic and can cause significant disability and social stigma. While there is no cure for filarial elephantiasis, various treatments are available to alleviate symptoms, prevent transmission, and halt the progression of the disease. These include antibiotics to kill the worms, surgery to remove the lymphatic obstruction, and various supportive measures to manage the swelling and prevent secondary infections.

Filarioidea is a superfamily of parasitic nematode (roundworm) worms, many of which are important pathogens in humans and animals. They are transmitted to their hosts through the bite of insect vectors, such as mosquitoes or flies. The filarioid worms can cause a range of diseases known as filariases. Some examples include Wuchereria bancrofti, Brugia malayi, and Onchocerca volvulus, which cause lymphatic filariasis (elephantiasis) and river blindness, respectively. The adult worms live in the lymphatic system or subcutaneous tissues of their hosts, where they produce microfilariae, the infective stage for the insect vector.

The medical definition of Filarioidea is: A superfamily of parasitic nematode worms that includes several important human pathogens and causes various filariases. The adult worms live in the lymphatic system or subcutaneous tissues, while the microfilariae are taken up by insect vectors during a blood meal and develop into infective larvae inside the vector. These larvae are then transmitted to a new host through the bite of the infected vector.

Wolbachia is a genus of intracellular bacteria that naturally infects a wide variety of arthropods (insects, spiders, mites) and filarial nematodes (roundworms). These bacteria are transmitted vertically from mother to offspring, often through the cytoplasm of eggs. Wolbachia can manipulate the reproductive biology of their hosts in various ways, such as feminization, parthenogenesis, male killing, and cytoplasmic incompatibility, which favor the spread and maintenance of the bacteria within host populations. The interactions between Wolbachia and their hosts have implications for insect pest management, disease transmission, and evolutionary biology.

Helminth proteins refer to the proteins that are produced and expressed by helminths, which are parasitic worms that cause diseases in humans and animals. These proteins can be found on the surface or inside the helminths and play various roles in their biology, such as in development, reproduction, and immune evasion. Some helminth proteins have been identified as potential targets for vaccines or drug development, as blocking their function may help to control or eliminate helminth infections. Examples of helminth proteins that have been studied include the antigen Bm86 from the cattle tick Boophilus microplus, and the tetraspanin protein Sm22.6 from the blood fluke Schistosoma mansoni.

Helminth antigens refer to the proteins or other molecules found on the surface or within helminth parasites that can stimulate an immune response in a host organism. Helminths are large, multicellular parasitic worms that can infect various tissues and organs in humans and animals, causing diseases such as schistosomiasis, lymphatic filariasis, and soil-transmitted helminthiases.

Helminth antigens can be recognized by the host's immune system as foreign invaders, leading to the activation of various immune cells and the production of antibodies. However, many helminths have evolved mechanisms to evade or suppress the host's immune response, allowing them to establish long-term infections.

Studying helminth antigens is important for understanding the immunology of helminth infections and developing new strategies for diagnosis, treatment, and prevention. Some researchers have also explored the potential therapeutic use of helminth antigens or whole helminths as a way to modulate the immune system and treat autoimmune diseases or allergies. However, more research is needed to determine the safety and efficacy of these approaches.

Gerbillinae is a subfamily of rodents that includes gerbils, jirds, and sand rats. These small mammals are primarily found in arid regions of Africa and Asia. They are characterized by their long hind legs, which they use for hopping, and their long, thin tails. Some species have adapted to desert environments by developing specialized kidneys that allow them to survive on minimal water intake.

Wuchereria bancrofti is a parasitic roundworm that causes lymphatic filariasis, also known as elephantiasis. It is transmitted to humans through the bite of infected mosquitoes. The worms infect the lymphatic system and can lead to chronic swelling of body parts such as the limbs, breasts, and genitals, as well as other symptoms including fever, chills, and skin rashes. Wuchereria bancrofti is a significant public health problem in many tropical and subtropical regions around the world.

Antibodies are proteins produced by the immune system in response to the presence of a foreign substance, known as an antigen. They are capable of recognizing and binding to specific antigens, neutralizing or marking them for destruction by other immune cells.

Helminths are parasitic worms that can infect humans and animals. They include roundworms, tapeworms, and flukes, among others. Helminth infections can cause a range of symptoms, depending on the type of worm and the location of the infection.

Antibodies to helminths are produced by the immune system in response to an infection with one of these parasitic worms. These antibodies can be detected in the blood and serve as evidence of a current or past infection. They may also play a role in protecting against future infections with the same type of worm.

There are several different classes of antibodies, including IgA, IgD, IgE, IgG, and IgM. Antibodies to helminths are typically of the IgE class, which are associated with allergic reactions and the defense against parasites. IgE antibodies can bind to mast cells and basophils, triggering the release of histamine and other inflammatory mediators that help to protect against the worm.

In addition to IgE, other classes of antibodies may also be produced in response to a helminth infection. For example, IgG antibodies may be produced later in the course of the infection and can provide long-term immunity to reinfection. IgA antibodies may also be produced and can help to prevent the attachment and entry of the worm into the body.

Overall, the production of antibodies to helminths is an important part of the immune response to these parasitic worms. However, in some cases, the presence of these antibodies may also be associated with allergic reactions or other immunological disorders.

"Dirofilaria immitis" is a species of parasitic roundworm that can infect dogs, cats, and other animals, including humans. It is the causative agent of heartworm disease in these animals. The adult worms typically reside in the pulmonary arteries and hearts of infected animals, where they can cause serious damage to the cardiovascular system.

The life cycle of Dirofilaria immitis involves mosquitoes as intermediate hosts. Infected animals produce microfilariae, which are taken up by mosquitoes during blood meals. These larvae then develop into infective stages within the mosquito and can be transmitted to other animals through the mosquito's bite.

In dogs, heartworm disease is often asymptomatic in the early stages but can progress to cause coughing, exercise intolerance, heart failure, and even death if left untreated. In cats, heartworm disease is more difficult to diagnose and often causes respiratory symptoms such as coughing and wheezing.

Preventive measures, such as regular administration of heartworm preventatives, are essential for protecting animals from this parasitic infection.

Dipetalonema is a genus of parasitic nematodes (roundworms) that can infect various mammals, including humans. Two species within this genus, Dipetalonema perstans and Dipetalonema streptocerca, are known to cause human filariasis, a group of tropical diseases characterized by the presence of parasitic worms in the lymphatic system.

Dipetalonema perstans is also known as "persistent strongyloides" and can cause a condition called "tropical pulmonary eosinophilia." This species has a complex life cycle involving mosquitoes as intermediate hosts. The adult worms reside in the abdominal cavity of the human host, where they produce microfilariae that circulate in the bloodstream. When an infected mosquito takes a blood meal, it ingests the microfilariae, which then develop into infective larvae inside the mosquito. Upon subsequent bites by the mosquito, these infective larvae enter the human host and migrate to the abdominal cavity, where they mature into adults and continue the life cycle.

Dipetalonema streptocerca is primarily found in West Africa and causes a condition known as "cutaneous filariasis" or "subcutaneous filariasis." This species has a similar life cycle to D. perstans, but it involves biting midges (culicoides) instead of mosquitoes as intermediate hosts. The adult worms reside in the subcutaneous tissue, where they produce microfilariae that circulate in the skin. Infective larvae develop inside the biting midge and are transmitted to humans during blood feeding.

The symptoms of Dipetalonema infections can vary widely depending on the species and the severity of the infection. Some people may not experience any symptoms, while others may have fever, cough, wheezing, skin rashes, or lymphatic swelling (lymphedema). Treatment typically involves administration of anti-parasitic drugs such as diethylcarbamazine or ivermectin.

Helminth DNA refers to the genetic material found in parasitic worms that belong to the phylum Platyhelminthes (flatworms) and Nematoda (roundworms). These parasites can infect various organs and tissues of humans and animals, causing a range of diseases.

Helminths have complex life cycles involving multiple developmental stages and hosts. The study of their DNA has provided valuable insights into their evolutionary history, genetic diversity, and mechanisms of pathogenesis. It has also facilitated the development of molecular diagnostic tools for identifying and monitoring helminth infections.

Understanding the genetic makeup of these parasites is crucial for developing effective control strategies, including drug discovery, vaccine development, and disease management.

Diethylcarbamazine (DECT or DEC) is an anti-parasitic medication used to treat infections caused by roundworms, including lymphatic filariasis (elephantiasis) and river blindness (onchocerciasis). It works by killing the parasitic worms, thus helping to prevent the progression of these diseases.

Diethylcarbamazine is typically available as a prescription oral medication in the form of tablets or capsules. The dosage and duration of treatment will depend on the type and severity of the infection being treated. It's important to note that DEC should only be taken under the supervision of a healthcare professional, as it may have side effects and potential drug interactions.

Medical Citation:
"Diethylcarbamazine." National Center for Biotechnology Information. PubChem Compound Database. U.S. National Library of Medicine. . Accessed on April 18, 2023.

'Murinae' is not a medical term. It is a taxonomic classification used in biology, specifically for a subfamily of rodents that includes mice, rats, and several related species. The term 'Murinae' comes from the family Muridae, which is the largest family of mammals, containing over 700 species.

The misconception might arise because medical professionals sometimes use common names for various animals or organisms in their diagnoses, treatments, or research. However, it is essential to clarify that 'Murinae' is a scientific classification and not a medical term.

Filaricides are a type of medication used to treat infections caused by filarial worms, which are parasitic roundworms that can infect humans and animals. These medications work by killing or inhibiting the development of the larval stages of the worms, thereby helping to eliminate the infection and prevent further transmission.

Filaricides are often used to treat diseases such as onchocerciasis (river blindness), lymphatic filariasis (elephantiasis), and loiasis (African eye worm). Examples of filaricides include ivermectin, diethylcarbamazine, and albendazole. It is important to note that these medications should only be used under the guidance of a healthcare professional, as they can have serious side effects if not used properly.

RNA (Ribonucleic acid) is a single-stranded molecule that plays a crucial role in the process of gene expression. It acts as a messenger carrying genetic information copied from DNA to the ribosomes, where proteins are synthesized. RNA is also involved in catalyzing chemical reactions and regulating gene expression.

Helminths, on the other hand, refer to parasitic worms that infect humans and animals. They belong to various phyla, including Nematoda (roundworms), Platyhelminthes (flatworms), and Acanthocephala (spiny-headed worms). Helminth infections can cause a range of diseases and conditions, such as intestinal inflammation, anemia, stunted growth, and cognitive impairment.

There is no medical definition for "RNA, Helminth" since RNA is a type of molecule found in all living organisms, including helminths. However, researchers have studied the genetic material of various helminth species to better understand their biology, evolution, and pathogenesis. This includes sequencing and analyzing the RNA transcriptome of these parasites, which can provide insights into their gene expression patterns and help identify potential drug targets for developing new treatments.

Aspartate-tRNA ligase is an enzyme that plays a crucial role in protein synthesis. Its specific function is to join the amino acid aspartic acid to its corresponding transfer RNA (tRNA) molecule, forming an aspartyl-tRNA complex. This complex is essential for the accurate translation of genetic information encoded in messenger RNA (mRNA) into a polypeptide chain during protein synthesis.

The systematic name for this enzyme is L-aspartate:tRNA(Asn) ligase (AMP-forming), which reflects its role in catalyzing the reaction between aspartic acid and tRNA(Asn). The enzyme can also activate aspartic acid by forming an aspartyl-AMP intermediate before transferring the activated aspartate to the appropriate tRNA molecule.

Deficiencies or mutations in aspartate-tRNA ligase can lead to various genetic disorders and impairments in protein synthesis, which may have severe consequences for cellular function and overall health.

Onchocerca is a genus of filarial nematode worms that are the causative agents of onchocerciasis, also known as river blindness. The most common species to infect humans is Onchocerca volvulus. These parasites are transmitted through the bite of infected blackflies (Simulium spp.) that breed in fast-flowing rivers and streams.

The adult female worms live in nodules beneath the skin, while the microfilariae, which are released by the females, migrate throughout various tissues, including the eyes, where they can cause inflammation and scarring, potentially leading to blindness if left untreated. The infection is primarily found in Africa, with some foci in Central and South America. Onchocerciasis is considered a neglected tropical disease by the World Health Organization (WHO).

A helminth genome refers to the complete set of genetic information present in the DNA of a helminth organism. Helminths are parasitic worms that include nematodes (roundworms), cestodes (tapeworms), and trematodes (flukes). The genome of a helminth includes all of the genes that code for proteins, as well as non-coding DNA sequences that regulate gene expression and other functions.

The study of helminth genomics has provided important insights into the biology and evolution of these parasites, as well as their interactions with their hosts. For example, genomic studies have identified potential drug targets and vaccine candidates, and have helped to elucidate the mechanisms of host-parasite coevolution.

It's worth noting that the size and complexity of helminth genomes can vary widely depending on the species. Some helminth genomes are relatively small and compact, while others are large and complex, with a high degree of genetic diversity. The human whipworm (Trichuris trichiura), for example, has a genome size of approximately 120 megabases, while the tapeworm Schistosoma mansoni has a genome size of over 360 megabases.

Overall, the study of helminth genomics is an important area of research that has the potential to inform the development of new strategies for preventing and treating helminth infections, which affect millions of people worldwide.

'Culicidae' is the biological family that includes all species of mosquitoes. It consists of three subfamilies: Anophelinae, Culicinae, and Toxorhynchitinae. Mosquitoes are small, midge-like flies that are known for their ability to transmit various diseases to humans and other animals, such as malaria, yellow fever, dengue fever, and Zika virus. The medical importance of Culicidae comes from the fact that only female mosquitoes require blood meals to lay eggs, and during this process, they can transmit pathogens between hosts.

Trans-splicing is a process in which two different RNA molecules are spliced together to form a single, chimeric RNA molecule. This process involves the removal of introns (non-coding sequences) from both RNA molecules and the ligation of the remaining exons (coding sequences) to create a new RNA molecule that contains genetic information from both original RNAs.

In cis-splicing, which is the more common form of splicing, introns are removed and exons are ligated within the same RNA molecule. However, in trans-splicing, the exons to be ligated come from two separate RNA molecules that have been transcribed from different genes or different regions of the same gene.

Trans-splicing is found in a variety of organisms, including some higher eukaryotes such as humans, where it plays a role in generating genetic diversity and regulating gene expression. It can also occur in certain viruses, where it is used to generate new mRNA molecules that encode for essential viral proteins.

Genes are the fundamental units of heredity in living organisms. They are made up of DNA (deoxyribonucleic acid) and are located on chromosomes. Genes carry the instructions for the development and function of an organism, including its physical and behavioral traits.

Helminths, also known as parasitic worms, are a type of parasite that can infect various organs and tissues in humans and animals. They have complex life cycles that involve multiple hosts and stages of development. Examples of helminths include roundworms, tapeworms, and flukes.

In the context of genetics, genes from helminths are studied to understand their role in the biology and evolution of these parasites, as well as to identify potential targets for the development of new drugs or vaccines to control or eliminate helminth infections. This involves studying the genetic makeup of helminths, including their DNA, RNA, and proteins, and how they interact with their hosts and the environment.

"Spliced leader RNA (SL-RNA)" is a type of RNA molecule that is present in some single-celled eukaryotic organisms, such as trypanosomes and nematodes. In these organisms, spliced leader RNAs play a critical role in the process of gene expression by providing a "leader" sequence that is added to the beginning of messenger RNA (mRNA) molecules during the process of RNA splicing.

SL-RNAs are typically composed of two regions: a conserved 5' " leader" sequence, which is added to the beginning of mRNAs, and a variable 3' " trailer" sequence, which contains the sequences required for recognition and cleavage by the splicing machinery. During RNA splicing, the spliced leader RNA is joined to the target mRNA through a process called trans-splicing, in which the leader sequence of the SL-RNA is ligated to the 5' end of the target mRNA, replacing the original 5' exon.

The addition of the spliced leader sequence to mRNAs can have several important consequences for gene expression. For example, it can help ensure that all mRNAs produced from a given gene contain the same 5' end, even if the gene is transcribed from multiple promoters or undergoes alternative splicing. Additionally, the presence of the conserved leader sequence can serve as a recognition site for RNA-binding proteins, which can regulate mRNA stability, localization, and translation.

Overall, spliced leader RNAs are an important component of the gene expression machinery in many eukaryotic organisms, and their study has provided valuable insights into the mechanisms of RNA processing and regulation.

Nematoda is a phylum of pseudocoelomate, unsegmented worms with a round or filiform body shape. They are commonly known as roundworms or threadworms. Nematodes are among the most diverse and numerous animals on earth, with estimates of over 1 million species, of which only about 25,000 have been described.

Nematodes are found in a wide range of habitats, including marine, freshwater, and terrestrial environments. Some nematode species are free-living, while others are parasitic, infecting a variety of hosts, including plants, animals, and humans. Parasitic nematodes can cause significant disease and economic losses in agriculture, livestock production, and human health.

The medical importance of nematodes lies primarily in their role as parasites that infect humans and animals. Some common examples of medically important nematodes include:

* Ascaris lumbricoides (human roundworm)
* Trichuris trichiura (whipworm)
* Ancylostoma duodenale and Necator americanus (hookworms)
* Enterobius vermicularis (pinworm or threadworm)
* Wuchereria bancrofti, Brugia malayi, and Loa loa (filarial nematodes that cause lymphatic filariasis, onchocerciasis, and loiasis, respectively)

Nematode infections can cause a range of clinical symptoms, depending on the species and the location of the parasite in the body. Common symptoms include gastrointestinal disturbances, anemia, skin rashes, and lymphatic swelling. In some cases, nematode infections can lead to serious complications or even death if left untreated.

Medical management of nematode infections typically involves the use of anthelmintic drugs, which are medications that kill or expel parasitic worms from the body. The choice of drug depends on the species of nematode and the severity of the infection. In some cases, preventive measures such as improved sanitation and hygiene can help reduce the risk of nematode infections.

Host-parasite interactions refer to the relationship between a parasitic organism (the parasite) and its host, which can be an animal, plant, or human body. The parasite lives on or inside the host and derives nutrients from it, often causing harm in the process. This interaction can range from relatively benign to severe, depending on various factors such as the species of the parasite, the immune response of the host, and the duration of infection.

The host-parasite relationship is often categorized based on the degree of harm caused to the host. Parasites that cause little to no harm are called commensals, while those that cause significant damage or disease are called parasitic pathogens. Some parasites can even manipulate their hosts' behavior and physiology to enhance their own survival and reproduction, leading to complex interactions between the two organisms.

Understanding host-parasite interactions is crucial for developing effective strategies to prevent and treat parasitic infections, as well as for understanding the ecological relationships between different species in natural ecosystems.

In the context of medicine and biology, symbiosis is a type of close and long-term biological interaction between two different biological organisms. Generally, one organism, called the symbiont, lives inside or on another organism, called the host. This interaction can be mutually beneficial (mutualistic), harmful to the host organism (parasitic), or have no effect on either organism (commensal).

Examples of mutualistic symbiotic relationships in humans include the bacteria that live in our gut and help us digest food, as well as the algae that live inside corals and provide them with nutrients. Parasitic symbioses, on the other hand, involve organisms like viruses or parasitic worms that live inside a host and cause harm to it.

It's worth noting that while the term "symbiosis" is often used in popular culture to refer to any close relationship between two organisms, in scientific contexts it has a more specific meaning related to long-term biological interactions.

"Caenorhabditis" is a genus of nematode (roundworm) animals, which are commonly used as model organisms in scientific research. The most widely studied species within this genus is "Caenorhabditis elegans," which has been extensively researched due to its simple anatomy, short lifespan, and fully sequenced genome. These nematodes are found in various environments, including soil and decaying organic matter, and play a crucial role in the decomposition process. The term "Caenorhabditis" itself is derived from Greek roots, with "caeno" meaning "recent" or "new," and "rhabditis" referring to the shape of their tails.

A larva is a distinct stage in the life cycle of various insects, mites, and other arthropods during which they undergo significant metamorphosis before becoming adults. In a medical context, larvae are known for their role in certain parasitic infections. Specifically, some helminth (parasitic worm) species use larval forms to infect human hosts. These invasions may lead to conditions such as cutaneous larva migrans, visceral larva migrans, or gnathostomiasis, depending on the specific parasite involved and the location of the infection within the body.

The larval stage is characterized by its markedly different morphology and behavior compared to the adult form. Larvae often have a distinct appearance, featuring unsegmented bodies, simple sense organs, and undeveloped digestive systems. They are typically adapted for a specific mode of life, such as free-living or parasitic existence, and rely on external sources of nutrition for their development.

In the context of helminth infections, larvae may be transmitted to humans through various routes, including ingestion of contaminated food or water, direct skin contact with infective stages, or transmission via an intermediate host (such as a vector). Once inside the human body, these parasitic larvae can cause tissue damage and provoke immune responses, leading to the clinical manifestations of disease.

It is essential to distinguish between the medical definition of 'larva' and its broader usage in biology and zoology. In those fields, 'larva' refers to any juvenile form that undergoes metamorphosis before reaching adulthood, regardless of whether it is parasitic or not.

'Animal structures' is a broad term that refers to the various physical parts and organs that make up animals. These structures can include everything from the external features, such as skin, hair, and scales, to the internal organs and systems, such as the heart, lungs, brain, and digestive system.

Animal structures are designed to perform specific functions that enable the animal to survive, grow, and reproduce. For example, the heart pumps blood throughout the body, delivering oxygen and nutrients to the cells, while the lungs facilitate gas exchange between the animal and its environment. The brain serves as the control center of the nervous system, processing sensory information and coordinating motor responses.

Animal structures can be categorized into different systems based on their function, such as the circulatory system, respiratory system, nervous system, digestive system, and reproductive system. Each system is made up of various structures that work together to perform a specific function.

Understanding animal structures and how they function is essential for understanding animal biology and behavior. It also has important implications for human health, as many animals serve as models for studying human disease and developing new treatments.

Glomerulonephritis is a medical condition that involves inflammation of the glomeruli, which are the tiny blood vessel clusters in the kidneys that filter waste and excess fluids from the blood. This inflammation can impair the kidney's ability to filter blood properly, leading to symptoms such as proteinuria (protein in the urine), hematuria (blood in the urine), edema (swelling), hypertension (high blood pressure), and eventually kidney failure.

Glomerulonephritis can be acute or chronic, and it may occur as a primary kidney disease or secondary to other medical conditions such as infections, autoimmune disorders, or vasculitis. The diagnosis of glomerulonephritis typically involves a combination of medical history, physical examination, urinalysis, blood tests, and imaging studies, with confirmation often requiring a kidney biopsy. Treatment depends on the underlying cause and severity of the disease but may include medications to suppress inflammation, control blood pressure, and manage symptoms.

Pharyngitis is the medical term for inflammation of the pharynx, which is the back portion of the throat. This condition is often characterized by symptoms such as sore throat, difficulty swallowing, and scratchiness in the throat. Pharyngitis can be caused by a variety of factors, including viral infections (such as the common cold), bacterial infections (such as strep throat), and irritants (such as smoke or chemical fumes). Treatment for pharyngitis depends on the underlying cause of the condition, but may include medications to relieve symptoms or antibiotics to treat a bacterial infection.

Streptococcal infections are a type of infection caused by group A Streptococcus bacteria (Streptococcus pyogenes). These bacteria can cause a variety of illnesses, ranging from mild skin infections to serious and potentially life-threatening conditions such as sepsis, pneumonia, and necrotizing fasciitis (flesh-eating disease).

Some common types of streptococcal infections include:

* Streptococcal pharyngitis (strep throat) - an infection of the throat and tonsils that can cause sore throat, fever, and swollen lymph nodes.
* Impetigo - a highly contagious skin infection that causes sores or blisters on the skin.
* Cellulitis - a bacterial infection of the deeper layers of the skin and underlying tissue that can cause redness, swelling, pain, and warmth in the affected area.
* Scarlet fever - a streptococcal infection that causes a bright red rash on the body, high fever, and sore throat.
* Necrotizing fasciitis - a rare but serious bacterial infection that can cause tissue death and destruction of the muscles and fascia (the tissue that covers the muscles).

Treatment for streptococcal infections typically involves antibiotics to kill the bacteria causing the infection. It is important to seek medical attention if you suspect a streptococcal infection, as prompt treatment can help prevent serious complications.

Streptococcus pyogenes is a Gram-positive, beta-hemolytic streptococcus bacterium that causes various suppurative (pus-forming) and nonsuppurative infections in humans. It is also known as group A Streptococcus (GAS) due to its ability to produce the M protein, which confers type-specific antigenicity and allows for serological classification into more than 200 distinct Lancefield groups.

S. pyogenes is responsible for a wide range of clinical manifestations, including pharyngitis (strep throat), impetigo, cellulitis, erysipelas, scarlet fever, rheumatic fever, and acute poststreptococcal glomerulonephritis. In rare cases, it can lead to invasive diseases such as necrotizing fasciitis (flesh-eating disease) and streptococcal toxic shock syndrome (STSS).

The bacterium is typically transmitted through respiratory droplets or direct contact with infected skin lesions. Effective prevention strategies include good hygiene practices, such as frequent handwashing and avoiding sharing personal items, as well as prompt recognition and treatment of infections to prevent spread.

Rheumatic fever is a systemic inflammatory disease that may occur following an untreated Group A streptococcal infection, such as strep throat. It primarily affects children between the ages of 5 and 15, but it can occur at any age. The condition is characterized by inflammation in various parts of the body, including the heart (carditis), joints (arthritis), skin (erythema marginatum, subcutaneous nodules), and brain (Sydenham's chorea).

The onset of rheumatic fever usually occurs 2-4 weeks after a streptococcal infection. The exact cause of the immune system's overreaction leading to rheumatic fever is not fully understood, but it involves molecular mimicry between streptococcal antigens and host tissues.

The Jones Criteria are used to diagnose rheumatic fever, which include:

1. Evidence of a preceding streptococcal infection (e.g., positive throat culture or rapid strep test, elevated or rising anti-streptolysin O titer)
2. Carditis (heart inflammation), including new murmurs or changes in existing murmurs, electrocardiogram abnormalities, or evidence of heart failure
3. Polyarthritis (inflammation of multiple joints) – typically large joints like the knees and ankles, migratory, and may be associated with warmth, swelling, and pain
4. Erythema marginatum (a skin rash characterized by pink or red, irregularly shaped macules or rings that blanch in the center and spread outward)
5. Subcutaneous nodules (firm, round, mobile lumps under the skin, usually over bony prominences)
6. Sydenham's chorea (involuntary, rapid, irregular movements, often affecting the face, hands, and feet)

Treatment of rheumatic fever typically involves antibiotics to eliminate any residual streptococcal infection, anti-inflammatory medications like corticosteroids or nonsteroidal anti-inflammatory drugs (NSAIDs) to manage symptoms and prevent long-term heart complications, and secondary prophylaxis with regular antibiotic administration to prevent recurrent streptococcal infections.

Membranoproliferative Glomerulonephritis (MPGN) is a type of glomerulonephritis, which is a group of kidney disorders characterized by inflammation and damage to the glomeruli, the tiny blood vessels in the kidneys responsible for filtering waste and excess fluids from the blood.

MPGN is specifically characterized by thickening of the glomerular basement membrane and proliferation (increased number) of cells in the mesangium, a region within the glomerulus. This condition can be primary or secondary to other diseases such as infections, autoimmune disorders, or monoclonal gammopathies.

MPGN is typically classified into three types based on the pattern of injury seen on electron microscopy: Type I, Type II (Dense Deposit Disease), and Type III. Each type has distinct clinical features, laboratory findings, and treatment approaches. Symptoms of MPGN may include hematuria (blood in urine), proteinuria (protein in urine), hypertension (high blood pressure), edema (swelling), and eventually progress to chronic kidney disease or end-stage renal disease if left untreated.

Penicillin V, also known as Penicillin V Potassium, is an antibiotic medication used to treat various bacterial infections. It belongs to the class of medications called penicillins, which work by interfering with the bacteria's ability to form a protective covering (cell wall), causing the bacteria to become more susceptible to destruction by the body's immune system.

Penicillin V is specifically used to treat infections of the respiratory tract, skin, and ear. It is also used to prevent recurrent rheumatic fever and chorea (Sydenham's chorea), a neurological disorder associated with rheumatic fever.

The medication is available as oral tablets or liquid solutions and is typically taken by mouth every 6 to 12 hours, depending on the severity and type of infection being treated. As with any antibiotic, it is important to take Penicillin V exactly as directed by a healthcare professional and for the full duration of treatment, even if symptoms improve before all doses have been taken.

Penicillin V is generally well-tolerated, but like other penicillins, it can cause allergic reactions in some people. It may also interact with certain medications, so it is important to inform a healthcare provider of any other medications being taken before starting Penicillin V therapy.

... ". Edeson, J. F. B. & Wilson, T. (1964), "The epidemiology of filariasis due to Wuchereria Bancrofti and Brugia ... "Brugia malayi". Web Atlas of Medical Parasitology. "Bench aids for the diagnosis of filarial infections. Plate 2 - Brugia ... "Brugia malayi". American Association of Veterinary Parasitologists. 2010-01-01. Retrieved 2022-01-16. "Life cycle of Brugia ... the Brugia malayi MIF gene is expressed in all life-cycle stages of the parasite, and results suggest that B. malayi MIF may ...
... malayi and Brugia timori cause lymphatic filariasis in humans; and Brugia pahangi and Brugia patei infect domestic cats ... Vincent, Albert L.; Frommes, Stephen P.; Ash, Lawrence R. (1976). "Brugia malayi, Brugia pahangi, and Brugia patei: Pulmonary ... Buckley, J. J. C. (1960). "On Brugia Gen. Nov. For Wuchereria Spp. of the Malayi Group i.e., W. Malayi (Brug, 1927), W. Pahangi ... He created a new genus Brugia in honour of the original discoverer, thus renaming B. malayi, B. pahangi, and B. patei. In 1977 ...
Brugia malayi causes most of the remainder of the cases, while Brugia timori is a rare cause. W. bancrofti largely affects ... Three types of worms are known to cause the disease: Wuchereria bancrofti, Brugia malayi, and Brugia timori, with Wuchereria ... Brugia malayi, and Brugia timori. The filarial roundworms are transmitted by the bite of an infected mosquito of genera Aedes, ... On 20 September 2007, geneticists published the first draft of the complete genome (genetic content) of Brugia malayi, one of ...
September 2007). "Draft genome of the filarial nematode parasite Brugia malayi". Science. 317 (5845): 1756-60. Bibcode:2007Sci ... Brugia malayi (Strain:TRS), human-infecting filarial parasite (2007) Bursaphelenchus xylophilus, infects pine trees (2011) ...
It is a vector of nocturnally subperiodic Brugia malayi. Females are known to be strongly anthropophilic (human biters). Larvae ... to nocturnally subperiodic Brugia malayi (Spirurida: Filariodea)". J Med Entomol. 39: 215-7. PMID 11931259. "Bionomics". ENVIS ...
"Mining predicted essential genes of Brugia malayi for nematode drug targets". PLOS ONE. 2 (11): e1189. Bibcode:2007PLoSO... ...
The second Wolbachia genome to be determined was of strain wBm, which infects Brugia malayi nematodes. Genome sequencing ... April 2005). "The Wolbachia genome of Brugia malayi: endosymbiont evolution within a human pathogenic nematode". PLOS Biology. ... April 2005). "The Wolbachia genome of Brugia malayi: endosymbiont evolution within a human pathogenic nematode". PLOS Biology. ... In the parasitic filarial nematode species responsible for elephantiasis, such as Brugia malayi and Wuchereria bancrofti, ...
2005). "The Wolbachia genome of Brugia malayi: endosymbiont evolution within a human pathogenic nematode". PLOS Biol. 3 (4): ...
Brugia malayi: Proteomic profile of adult excretory-secretory products". Molecular and Biochemical Parasitology. 160 (1): 8-21 ...
The microfilariae of Brugia timori are longer and morphologically distinct from those of Brugia malayi and Wuchereria bancrofti ... The life cycle of Brugia timori is very similar to that of Wuchereria bancrofti and Brugia malayi, leading to nocturnal ... B. timori microfilariae are slightly larger than B. malayi microfilariae. Aside from vectoring Brugia species, mosquitoes also ... 1977 = Timor microfilaria, David and Edeson, 1964): morphologic description with comparison to Brugia malayi of Indonesia". J. ...
While posted in Hanoi, he made major advances in the study of Brugia malayi and strongyloidiasis. He also noted how ...
A 2019 report identified dogs in Kerala who have another worm which can cause filariasis, Brugia malayi. This worm is not known ... Sadarama, PV; Chirayath, D; Pillai, UN; Unny, NM; Lakshmanan, B; Sunanda, C (December 2019). "Canine Brugia malayi ...
"Field and laboratory observations on Coquillettidia crassipes in relation to transmission of Brugia malayi in Peninsular ...
His current research focuses on enteric fever and on a rapid antigen detection test for brugia malayi. Honorary Member of ...
Brugia malayi, and Brugia timori. Tropical pulmonary eosinophilia is a rare syndrome characterised by pulmonary interstitial ... The syndrome is caused by a distinct hypersensitive immunological reaction to microfilariae of W. bancrofti and Brugia malayi. ...
Compared to infections with other filarial parasites such as Wuchereria bancrofti, Brugia malayi, and Loa loa, Mansonella ... and Brugia malayi. The dependence of these parasites on their endosymbionts has led to the use of antibiotics directed against ... Such lateral gene transfer has occurred in various geographic isolates of B. malayi, in which a fraction of the Wolbachia ...
... other species are secondary or suspected vectors of Brugia malayi the cause of lymphatic filariasis, and Rift Valley fever. ...
There is evidence it is a vector for Japanese encephalitis, as well as the roundworm Brugia malayi in Thailand. Norbert Becker ...
"Immunization of Mastomys coucha with Brugia malayi Recombinant Trehalose-6-Phosphate Phosphatase Results in Significant ... Similarly, unlike the common murine research model, M. coucha can support the complete lifecycle of B. malayi, a parasite that ...
It shows a high affinity for human biting and is a potent vector of Brugia malayi to cause Malayan filariasis. In 1980, The ... Natural Mortality of Mansonia annulifera with Special Reference to Mortality due to Brugia malayi Infection and Distribution of ...
Since Brugia malayi relies on symbiotic Wolbachia, this would mean that albendazole is targeting both the worm and its ... In cases of lymphatic filariasis (elephantiasis) caused by Wuchereria bancrofti or Brugia malayi, albendazole is sometimes ...
It is one of the three parasitic worms, together with Brugia malayi and B. timori, that infect the lymphatic system to cause ...
Brugia malayi, and other worms and parasites. Another important disadvantage of the existence of tolerance may be ...
Brugia malayi, or Brugia timori; loiasis and tropical pulmonary eosinophilia.The WHO recommends prescribing diethylcarbamazine ...
Brugia pahangi and Brugia malayi, and, as in other nematodes, code for components of the cuticle". Molecular and Biochemical ...
Brugia malayi, and Brugia timori. These worms occupy the lymphatic system, including the lymph nodes; in chronic cases, these ... while Brugia timori rarely affects the genitals.[citation needed] Those who develop the chronic stages of elephantiasis are ...
... brugia MeSH B01.500.500.294.700.750.700.300.088.500 - brugia malayi MeSH B01.500.500.294.700.750.700.300.088.550 - brugia ...
... chronic infection of Wuchereria bancrofti or Brugia malayi, two mosquito-borne parasites of Africa and Southeast Asia, ...
... the C-terminal domain of a metalloprotease from filarial worm Brugia malayi, adopt helical structures closely resembling ShK. ...
Brugia malayi Brugia timori Wuchereria bancrofti Three other medically important parasitic species are: Loa loa causes Loa loa ...
Brugia Malayi". Edeson, J. F. B. & Wilson, T. (1964), "The epidemiology of filariasis due to Wuchereria Bancrofti and Brugia ... "Brugia malayi". Web Atlas of Medical Parasitology. "Bench aids for the diagnosis of filarial infections. Plate 2 - Brugia ... "Brugia malayi". American Association of Veterinary Parasitologists. 2010-01-01. Retrieved 2022-01-16. "Life cycle of Brugia ... the Brugia malayi MIF gene is expressed in all life-cycle stages of the parasite, and results suggest that B. malayi MIF may ...
The Wolbachia genome of Brugia malayi: Endosymbiont evolution within a human pathogenic nematode. PLoS Biology. 2005 Apr;3(4): ... The Wolbachia genome of Brugia malayi : Endosymbiont evolution within a human pathogenic nematode. In: PLoS Biology. 2005 ; Vol ... Dive into the research topics of The Wolbachia genome of Brugia malayi: Endosymbiont evolution within a human pathogenic ... The Wolbachia genome of Brugia malayi: Endosymbiont evolution within a human pathogenic nematode. / Foster, Jeremy; Ganatra, ...
Brugia malayi is known to have a cuticle composed of a polysaccharide, chitin. Our research, therefore, is investigating the ... Brugia malayi is the mosquito vector parasite responsible for causing lymphatic system edema, which most often causes life-long ... Brugia malayi is known to have a cuticle composed of a polysaccharide, chitin. Our research, therefore, is investigating the ... Brugia malayi is known to have a cuticle composed of a polysaccharide, chitin. Our research, therefore, is investigating the ...
... for Bm7253 from Brugia malayi WS250. Plus protein sequence and external database links. ... pep supercontig:B_malayi-3.1:Bmal_v3_scaffold12:595257:600985:1 gene:WBGene00227514 transcript:Bm7253 gene_biotype:protein_ ...
There is a pressing need for new drugs against filarial parasites, such as B. malayi. As wBm is required for B. malayi ... However, the lifecycle of neither B. malayi nor wBm can be maintained in vitro. To facilitate selection of potential drug ... is an obligate endosymbiotic bacterium of Brugia malayi, a parasitic filarial nematode of humans and one of the causative ... the Wolbachia endosymbiont of Brugia malayi, (wBm).. B. malayi is a parasitic filarial nematode of humans which, along with ...
... in Brugia malayi WS250. Domain architectures illustrate each occurrence of 57184,_gap_. ... Domain combinations for 57184,_gap_ superfamilies in Brugia malayi WS250. The selected domain combination is the occurrence of ... 2 sequences contain the 57184,_gap_ domain architecture in Brugia malayi WS250. . ...
... is genetically variable for its capacity to harbor the filarial nematode Brugia malayi. The genome of Ae. aegypti is large and ... We found evidence for Toll, IMD, and JAK-STAT pathway activity in response to early stages of B. malayi infection when the ... Exome and transcriptome sequencing of Aedes aegypti identifies a locus that confers resistance to Brugia malayi and alters the ... Exome and transcriptome sequencing of Aedes aegypti identifies a locus that confers resistance to Brugia malayi and alters the ...
The genome of Brugia malayi - All worms are not created equal. / Scott, Alan L.; Ghedin, Elodie. In: Parasitology International ... The genome of Brugia malayi - All worms are not created equal. In: Parasitology International. 2009 ; Vol. 58, No. 1. pp. 6-11. ... Scott AL, Ghedin E. The genome of Brugia malayi - All worms are not created equal. Parasitology International. 2009 Mar;58(1):6 ... Scott, A. L., & Ghedin, E. (2009). The genome of Brugia malayi - All worms are not created equal. Parasitology International, ...
Wuchereria bancrofti and Brugia malayi EIA. Serum or plasma separated from cells. ...
Brugia malayi. Listeria monocytogenes. Dengue. Loa loa. Parvovirus. Onchocerca volvulus. Syphilis. Trichinella spiralis. ...
Brugia malayi. Filariasis. Nematodes (clade IVa). Phylum (clade). Strongyloides stercoralis. Strongyloidiasis. Nematodes (clade ...
... malayi microfilariae. The remaining 47 (38%) transcripts in B. pahangi and 46 (43%) transcripts in B. malayi microfilariae were ... A cross-species microarray analysis employing the B. malayi V2 array was carried out to determine the transcriptional ... malayi microfilariae. The data obtained from real-time PCR analysis of ten genes selected from the microarray list of ... malayi microfilariae. In B. pahangi, there were 76 (62%) up-regulated transcripts that coded for known proteins that mapped ...
Release of Prostaglandin E2 by Microfilariae of Wuchereria bancrofti and Brugia malayi ...
This gene, named Bm-spn-2, has been isolated from the filarial nematode Brugia malayi, a causative agent of human lymphatic ... This gene, named Bm-spn-2, has been isolated from the filarial nematode Brugia malayi, a causative agent of human lymphatic ... This gene, named Bm-spn-2, has been isolated from the filarial nematode Brugia malayi, a causative agent of human lymphatic ... This gene, named Bm-spn-2, has been isolated from the filarial nematode Brugia malayi, a causative agent of human lymphatic ...
... and Brugia malayi (B.malayi). In silico virtual screening, approach was used to screen the selected natural compounds against ... GST from W.bancrofti and B.malayi. On the basis of our results, here we are reporting some of the natural compounds which were ... and Brugia malayi (B.malayi). In silico virtual screening, approach was used to screen the selected natural compounds against ... Virtual screening of natural anti-filarial compounds against glutathione-S-transferase of Brugia malayi and Wuchereria ...
Exome and Transcriptome Sequencing of Aedes aegypti Identifies a Locus That Confers Resistance to Brugia malayi and Alters the ... Exome and Transcriptome Sequencing of Aedes aegypti Identifies a Locus That Confers Resistance to Brugia malayi and Alters the ... Exome and Transcriptome Sequencing of Aedes aegypti Identifies a Locus That Confers Resistance to Brugia malayi and Alters the ... Exome and Transcriptome Sequencing of Aedes aegypti Identifies a Locus That Confers Resistance to Brugia malayi and Alters the ...
The Drug Development and Therapeutics (DDT) is an open access peer-reviewed journal committed to publishing high-quality articles in the field of Drug synthesis and development and Therapeutics from industry, Clinicians and Academia.
Draft genome of the filarial nematode parasite Brugia malayi. Science 317, 1756-1760 (2007). ...
Brugia pahangi: A0A0N4TLS2; Brugia malayi: A0A4E9FFK1, A0A0K0JD75; Acanthocheilonema viteae: A0A498SFA0; Toxocara canis: ... Brugia timori: A0A0R3Q8V2; Phocoena sinus: A0A8C9B3Q4; Sakesphorus luctuosus: A0A7K8Y9J1; Camelus ferus: T0MJ22; Tropilaelaps ...
Surveillance and Selective Treatment of Brugia malayi Filariasis Eleven Years after Stopping Mass Drug Administration in ...
... in Brugia malayi infections (42). Interestingly, microfilariae of Wuchereria bancrofti have also been shown to infect ...
Categories: Brugia malayi Image Types: Photo, Illustrations, Video, Color, Black&White, PublicDomain, CopyrightRestricted 24 ...
Insights into the structure-function relationship of Brugia Malayi Thymidylate Kinase (Bmtmk). Int. J. Biol. Macromol. 88, 565- ...
Brugia malayi. Taxonomy ID:. 6279. Select appropriate tab below to view additional metadata details:. ...
Human Parasitic Nematodes Ancylostoma ceylanicum Ancylostoma duodenale Ascaris lumbricoides Brugia malayi Loa loa Necator ...
Filariasis: An estimated 120 million people are infected with Wuchereria bancrofti, Brugia malayi, and Brugia timori. ...
Regulation of development in filarial parasites, such as D. immitis and B. malayi. The expression and function of parasitic ... Dirofilaria immitis and Brugia malayi. Development of molecular markers for albendazole and mebendazole (benzimidazoles) in ... Dirofilaria immitis and Brugia malayi.. *Development of molecular markers for albendazole and mebendazole (benzimidazoles) in ... Regulation of development in filarial parasites, such as D. immitis and B. malayi. ...
  • The two other filarial causes of lymphatic filariasis are Wuchereria bancrofti and Brugia timori, which both differ from B. malayi morphologically, symptomatically, and in geographical extent. (wikipedia.org)
  • Brugia timori is restricted to the Lesser Sunda Islands of Indonesia. (cdc.gov)
  • Wuchereria bancrofti, Brugia malayi , and Brugia timori transmitted by several mosquito species cause the majority of human LF infections ( 2 ). (frontiersin.org)
  • Wuchereria subjects, they ingest MF along with their bancrofti , Brugia malayi and B. timori . (who.int)
  • This syndrome is felt to be due to immune hyperresponsiveness in patients infected with the filarial parasites Wuchereria bancrofti , Brugia malayi , or Brugia timori . (logicalimages.com)
  • Brugia timori, which also causes the disease. (crackittoday.com)
  • The parasites which can cause this disease are the following: Wuchereria Bancrofti, Brugia Malayi and Brugya Timori. (aarogya.com)
  • Persons between 3 and 100 years of age diagnosed with or suspected of infection with Wuchereria bancrofti, Bugia malayi, Onchocerca volvulus, Loa loa, or other parasitic worms may be eligible for this study. (nih.gov)
  • If, in a patient, filarial infection is suspected, the optimum collection time for Brugia or Wuchereria is at night after 10, while for Loa loa, it is midday between 10AM to 2 pm). (yashodahospitals.com)
  • The life cycle of B. malayi is similar to that of WUCHERERIA BANCROFTI , except that in most areas the principal mosquito vectors belong to the genus Mansonia. (nih.gov)
  • Brugia malayi is a filarial (arthropod-borne) nematode (roundworm), one of the three causative agents of lymphatic filariasis in humans. (wikipedia.org)
  • B. malayi is one of the causative agents of lymphatic filariasis, a condition marked by infection and swelling of the lymphatic system. (wikipedia.org)
  • In this article, we first reported the lipid profile of adult Brugia malayi using ultra-performance liquid chromatography electrospray ionization mass spectrometry (UPLC-ESI-MS) to provide a promising drug target for lymphatic filariasis (LF). (tropmedres.ac)
  • Of the three nematodes responsible for lymphatic filariasis in humans, only Brugia malayi is actively maintained in research settings owing to its viability in small animal hosts, principal among which is the domestic cat. (uga.edu)
  • To better understand the transcriptomic interplay of organisms associated with lymphatic filariasis, we conducted multispecies transcriptome sequencing (RNA-Seq) on the filarial nematode Brugia malayi , its Wolbachia endosymbiont w Bm, and its laboratory vector Aedes aegypti across the entire B. malayi life cycle. (nih.gov)
  • In an effort to identify new drug candidates for lymphatic filariasis, we conducted a three-way transcriptomics/systems biology study of one of the causative agents of lymphatic filariasis, Brugia malayi , its Wolbachia endosymbiont w Bm, and its vector host Aedes aegypti at 16 distinct B. malayi life stages. (nih.gov)
  • In an effort to better understand the transcriptomic interplay of organisms associated with lymphatic filariasis, a research team from the University of Maryland School of Medicine (UMSOM) Institute for Genome Sciences conducted multispecies transcriptome sequencing (RNA-Seq) on Brugia malayi ( one of the three filarial nematodes ) , its bacterial Wolbachia endosymbiont, and the mosquito vector Aedes aegypti across the entire B. malayi life cycle. (genengnews.com)
  • Immune Response to Brugia malayi Asparaginyl-tRNA Synthetase in Balb/c Mice and Human Clinical Samples of Lymphatic Filariasis. (mcw.edu)
  • Brugia malayi causes the human tropical disease, lymphatic filariasis. (worktribe.com)
  • S, Padma, G. Dhananjayan (2009) Antifilarial drugs, in the doses employed in mass drug administrations by the Global Programme to Eliminate Lymphatic Filariasis, reverse lymphatic pathology in children with Brugia malayi infection. (tdmcalappuzha.org)
  • Lymphoscintigraphic evidence of lymphatic dilation in the limbs of children with Brugia malayi infection. (tdmcalappuzha.org)
  • Adults produce microfilariae, measuring 177 to 230 μm in length and 5 to 7 μm in width, which are sheathed and have nocturnal periodicity (in some regions B. malayi may be sub-periodic, and note that microfilariae are usually not produced in B. pahangi infections). (cdc.gov)
  • 7. In vitro killing of microfilariae of Brugia pahangi and Brugia malayi by eosinophil granule proteins. (nih.gov)
  • Richard Martin, a Distinguished Professor of biomedical sciences , has developed a means of determining the function of individual genes in Brugia malayi, a parasitic nematode that threatens populations in tropical regions of Africa, South America and Asia. (iastate.edu)
  • Brugia malayi, the parasitic nematode shown here, infects around 2 million people in tropical regions of Africa, South America and Asia. (iastate.edu)
  • Several types of parasitic roundworms have iPGM, including Brugia malayi and Onchocerca volvulus , which infect roughly 150 million people living mostly in tropical regions. (nih.gov)
  • It is an early manifestation of filariasis, usually occurs in the inguinal area during B. malayi infection and can occur before the worms mature. (wikipedia.org)
  • Abscess formation and ulceration of the affected lymph node occasionally occurs during B. malayi infection, more often than in Bancroftian filariasis. (wikipedia.org)
  • The results of this study demonstrate the competence of the dog as a host for B. malayi and its potential to serve in the laboratory role currently provided by the cat, while also clarifying the potential for zoonosis in filariasis-endemic regions. (uga.edu)
  • Detection of filariasis requires the examination of blood smear presence of larval roundworm B.malayi and W.bancrofti. (yashodahospitals.com)
  • Consequently, the lipid profile of adult B. malayi is significant and not only provides a promising drug target for LF but also assists in a better understanding of the biological process and mechanism by which parasites interfere with LF disease in the future.Supplementary informationThe online version contains supplementary material available at 10.1007/s13205-022-03296-y. (tropmedres.ac)
  • However, members of this mosquito complex do not act as natural vectors for Brugian LF caused by Brugia malayi, or for the cat parasite B. pahangi, despite their presence in South Asia where these parasites are endemic. (unicamp.br)
  • 4875 inhibiting Brugia malayi asparaginyl-tRNA synthetase and killing adult Brugia malayi parasites. (mcw.edu)
  • Elephantiasis resulting from B. malayi infection typically affects the distal portions of the extremities. (wikipedia.org)
  • For A. aegypti , the transcriptional response reflects the stress that B. malayi infection exerts on the mosquito with indicators of increased energy demand. (nih.gov)
  • 90% of worldwide infections, with 9% quitoes transmit the infection from person caused by B. malayi in southeast and east- to person. (who.int)
  • p. pipiens vector in the Nile Delta, however it is refractory to infection with Brugia spp. (unicamp.br)
  • Following per os Brugia exposures, the prevalence of infection is significantly lower in Cx. (unicamp.br)
  • Relevance of anti-BmR1 IgG4 antibodies in children from an area endemic for Brugia malayi infection. (tdmcalappuzha.org)
  • Ultrasonographic findings in children with Brugia malayi infection, in an endemic area. (tdmcalappuzha.org)
  • 2007) Preliminary findings of a cross sectional study of children to define the clinical and pathological changes caused by Brugia malayi infection, in an endemic area. (tdmcalappuzha.org)
  • P-TUFT-ALT-2 showed 55% to 80% with an average of 65% cytotoxicity in B. malayi L3 larvae in in vitro ADCC assay. (elsevierpure.com)
  • We recently developed an in vitro assay for monitoring the attachment to and killing of B. malayi Mf by human neutrophils (PMNs) and monocytes (PBMCs), however, the levels of both cell to worm attachment and leukocyte mediated Mf killing varied greatly between individual experiments. (uga.edu)
  • In vitro , we find that the existing cancer therapeutic JQ1(+), which is a bromodomain and extraterminal protein inhibitor, has adulticidal activity in B. malayi . (nih.gov)
  • We performed binding assays with Brugia malayi antigen extracts and human IL-10R1. (nih.gov)
  • Lipid biomarker profiling of adult Brugia malayi using mass spectrometry detection. (tropmedres.ac)
  • In B. malayi , expression modules associated with adult female samples consistently contained an overrepresentation of genes involved in chromatin remodeling, such as the bromodomain-containing proteins. (nih.gov)
  • All bromodomain-containing proteins encoded by B. malayi were observed to be upregulated in the adult female, embryo, and microfilaria life stages, including 2 members of the bromodomain and extraterminal (BET) protein family. (nih.gov)
  • B. malayi upregulates the expression of bromodomain-containing proteins in the adult female, embryo, and microfilaria stages. (nih.gov)
  • Apparent failure of ultrasonography to detect adult worms of Brugia malayi. (tdmcalappuzha.org)
  • B. malayi is transmitted by Mansonia mosquitoes and is restricted to South and Southeast Asia. (wikipedia.org)
  • Stable integrative transfection of Brugia malayi is here! (filariasiscenter.org)
  • We want to announce that after over 20 years of trying, we have finally developed a method for efficient stable integrative transfection for Brugia malayi ! (filariasiscenter.org)
  • There she led her own group on the Brugia malayi and Influenza Virus genome projects. (nih.gov)
  • The method is based on the piggyBac transposase/transposon system that results in semi-random integration of sequences into the B. malayi genome at TTAA sites. (filariasiscenter.org)
  • Development and replication of B. malayi occurs in two discrete phases: in the mosquito vector and in the human. (wikipedia.org)
  • citation needed] Mosquito: The mosquito serves as a biological vector and intermediate host - it is required for the developmental cycle and transmission of B. malayi. (wikipedia.org)
  • The typical vector for Brugia spp. (cdc.gov)
  • Hosts of B. malayi include Southeast Asian cats. (wikipedia.org)
  • For this reason, we investigated the capacity in which dogs may serve as competent laboratory hosts for B. malayi . (uga.edu)
  • Effects of diethylcarbamazine and ivermectin treatment on Brugia malayi gene expression in infected gerbils (Meriones unguiculatus). (nih.gov)
  • Evaluation of the angiogenic properties of Brugia malayi asparaginyl-tRNA synthetase and its mutants: A study on the molecular target for antifilarial drug development. (mcw.edu)