A species of ORTHOPOXVIRUS infecting mice and causing a disease that involves internal organs and produces characteristic skin lesions.
A viral infection of mice, causing edema and necrosis followed by limb loss.
Virus diseases caused by the POXVIRIDAE.
A genus of the family POXVIRIDAE, subfamily CHORDOPOXVIRINAE, comprising many species infecting mammals. Viruses of this genus cause generalized infections and a rash in some hosts. The type species is VACCINIA VIRUS.
A species of ORTHOPOXVIRUS that is the etiologic agent of COWPOX. It is closely related to but antigenically different from VACCINIA VIRUS.
A family of double-stranded DNA viruses infecting mammals (including humans), birds and insects. There are two subfamilies: CHORDOPOXVIRINAE, poxviruses of vertebrates, and ENTOMOPOXVIRINAE, poxviruses of insects.
A species of ORTHOPOXVIRUS causing infections in humans. No infections have been reported since 1977 and the virus is now believed to be virtually extinct.
Gross hypo- or aplasia of one or more long bones of one or more limbs. The concept includes amelia, hemimelia, phocomelia, and sirenomelia.
The type species of ORTHOPOXVIRUS, related to COWPOX VIRUS, but whose true origin is unknown. It has been used as a live vaccine against SMALLPOX. It is also used as a vector for inserting foreign DNA into animals. Rabbitpox virus is a subspecies of VACCINIA VIRUS.
Compounds that negatively regulate the cascade process of COMPLEMENT ACTIVATION. Uncontrolled complement activation and resulting cell lysis is potentially dangerous for the host.
The cutaneous and occasional systemic reactions associated with vaccination using smallpox (variola) vaccine.
An area showing altered staining behavior in the nucleus or cytoplasm of a virus-infected cell. Some inclusion bodies represent "virus factories" in which viral nucleic acid or protein is being synthesized; others are merely artifacts of fixation and staining. One example, Negri bodies, are found in the cytoplasm or processes of nerve cells in animals that have died from rabies.
Proteins found in any species of virus.
An encapsulated lymphatic organ through which venous blood filters.

Granzymes are the essential downstream effector molecules for the control of primary virus infections by cytolytic leukocytes. (1/85)

Analysis of perforin-deficient mice has identified the cytolytic pathway and perforin as the preeminent effector molecule in T cell-mediated control of virus infections. In this paper, we show that mice lacking both granzyme A (gzmA) and granzyme B (gzmB), which are, beside perforin, key constituents of cytolytic vesicles, are as incapable as are perforin-deficient mice of controlling primary infections by the natural mouse pathogen ectromelia, a poxvirus. Death of gzmAxgzmB double knockout mice occurred in a dose-dependent manner, despite the expression of functionally active perforin and the absence of an intrinsic defect to generate splenic cytolytic T cells. These results establish that both gzmA and gzmB are indispensable effector molecules acting in concert with perforin in granule exocytosis-mediated host defense against natural viral pathogens.  (+info)

Expression of mouse interleukin-4 by a recombinant ectromelia virus suppresses cytolytic lymphocyte responses and overcomes genetic resistance to mousepox. (2/85)

Genetic resistance to clinical mousepox (ectromelia virus) varies among inbred laboratory mice and is characterized by an effective natural killer (NK) response and the early onset of a strong CD8(+) cytotoxic T-lymphocyte (CTL) response in resistant mice. We have investigated the influence of virus-expressed mouse interleukin-4 (IL-4) on the cell-mediated response during infection. It was observed that expression of IL-4 by a thymidine kinase-positive ectromelia virus suppressed cytolytic responses of NK and CTL and the expression of gamma interferon by the latter. Genetically resistant mice infected with the IL-4-expressing virus developed symptoms of acute mousepox accompanied by high mortality, similar to the disease seen when genetically sensitive mice are infected with the virulent Moscow strain. Strikingly, infection of recently immunized genetically resistant mice with the virus expressing IL-4 also resulted in significant mortality due to fulminant mousepox. These data therefore suggest that virus-encoded IL-4 not only suppresses primary antiviral cell-mediated immune responses but also can inhibit the expression of immune memory responses.  (+info)

Enhanced resistance in STAT6-deficient mice to infection with ectromelia virus. (3/85)

We inoculated BALB/c mice deficient in STAT6 (STAT6(-/-)) and their wild-type (wt) littermates (STAT6(+/+)) with the natural mouse pathogen, ectromelia virus (EV). STAT6(-/-) mice exhibited increased resistance to generalized infection with EV when compared with STAT6(+/+) mice. In the spleens and lymph nodes of STAT6(-/-) mice, T helper 1 (Th1) cytokines were induced at earlier time points and at higher levels postinfection when compared with those in STAT6(+/+) mice. Elevated levels of NO were evident in plasma and splenocyte cultures of EV-infected STAT6(-/-) mice in comparison with STAT6(+/+) mice. The induction of high levels of Th1 cytokines in the mutant mice correlated with a strong natural killer cell response. We demonstrate in genetically susceptible BALB/c mice that the STAT6 locus is critical for progression of EV infection. Furthermore, in the absence of this transcription factor, the immune system defaults toward a protective Th1-like response, conferring pronounced resistance to EV infection and disease progression.  (+info)

Serial backcross analysis of genetic resistance to mousepox, using marker loci for Rmp-2 and Rmp-3. (4/85)

At least three genes from C57BL/6 mice that mediate dominant resistance to lethal mousepox were isolated and transferred onto a susceptible DBA/2 background. Three [(C57BL/6 x DBA/2)F1 x DBA/2] male mice that survived infection were selected as founders on the basis of different complements of marker loci for two resistance genes, Rmp-2r (Hc1) and Rmp-3r (H-2Db). They were crossed with DBA/2 mice, male progeny were infected with ectromelia virus, and the cycle was repeated with surviving male progeny through seven backcross generations. Two founders carried a marker locus for Rmp-2r or Rmp-3r, and the third carried neither marker locus. Resistance pedigrees were analyzed for passage of marker loci. From the three founders, resistance was passaged through multiple generations, producing backcross lines with intermediate-male-resistance phenotypes (20% resistant). Females of backcross lines with intermediate male resistance had high resistance (> 50%). High-resistance backcross lines (40% male resistance) also developed from the founders that carried marker loci for Rmp-2r and Rmp-3r, and marker loci were passaged through all generations of high resistance but not intermediate-resistance lines. About one-third of all resistant mice in high-resistance lines sired by mice that carried marker loci for Rmp-2r and Rmp-3r did not carry the respective marker locus. In lines that carried Rmp-2r, this was apparently not the result of recombination between Rmp-2r and Hc1, because Rmp-2 was not in the predicted location on chromosome 2 and because mice that did not inherit Hc1 transmitted significantly less male resistance than Hc1-positive mice, although female resistance remained high. These results confirmed that C57BL/6 mice have redundant resistance mechanisms, two of which are controlled at least in part by Rmp-2r and Rmp-3r, and provided evidence for a fourth resistance gene, herein presumptively named Rmp-4, which protects females more than males and which may be epistatic to Rmp-2.  (+info)

The genomic sequence of ectromelia virus, the causative agent of mousepox. (5/85)

Ectromelia virus is the causative agent of mousepox, an acute exanthematous disease of mouse colonies in Europe, Japan, China, and the U.S. The Moscow, Hampstead, and NIH79 strains are the most thoroughly studied with the Moscow strain being the most infectious and virulent for the mouse. In the late 1940s mousepox was proposed as a model for the study of the pathogenesis of smallpox and generalized vaccinia in humans. Studies in the last five decades from a succession of investigators have resulted in a detailed description of the virologic and pathologic disease course in genetically susceptible and resistant inbred and out-bred mice. We report the DNA sequence of the left-hand end, the predicted right-hand terminal repeat, and central regions of the genome of the Moscow strain of ectromelia virus (approximately 177,500 bp), which together with the previously sequenced right-hand end, yields a genome of 209,771 bp. We identified 175 potential genes specifying proteins of between 53 and 1924 amino acids, and 29 regions containing sequences related to genes predicted in other poxviruses, but unlikely to encode for functional proteins in ectromelia virus. The translated protein sequences were compared with the protein database for structure/function relationships, and these analyses were used to investigate poxvirus evolution and to attempt to explain at the cellular and molecular level the well-characterized features of the ectromelia virus natural life cycle.  (+info)

Efficacy of oral active ether lipid analogs of cidofovir in a lethal mousepox model. (6/85)

Cidofovir (CDV) is a highly effective inhibitor of orthopoxvirus replication and may be used intravenously to treat smallpox or complications arising from the smallpox vaccine under an investigational new drug application (IND). However, CDV is absorbed poorly following oral administration and is inactive orally. To improve the bioavailability of CDV, others synthesized alkoxyalkanol esters of CDV and observed >100-fold more activity than unmodified CDV against cowpox, vaccinia, and variola virus (VARV) replication. These ether lipid analogs of CDV have high oral bioavailability in mice. In this study, we compared the oral activity of CDV with the hexadecyloxypropyl (HDP)-, octadecyloxyethyl-, oleyloxypropyl-, and oleyloxyethyl-esters of CDV in a lethal, aerosol ectromelia virus (ECTV) challenge model in A/NCR mice. Octadecyloxyethyl-CDV appeared to be the most potent CDV analog as a dose regimen of 5 mg/kg started 4 h following challenge completely blocked virus replication in spleen and liver, and protected 100% of A/NCR mice, although oral, unmodified CDV was inactive. These results suggest that this family of compounds deserves further evaluation as poxvirus antiviral.  (+info)

Protective effect of exogenous recombinant mouse interferon-gamma and tumour necrosis factor-alpha on ectromelia virus infection in susceptible BALB/c mice. (7/85)

The resistance to mousepox is correlated with the production of type I cytokines: interleukin (IL)-2, IL-12, interferon (IFN)-gamma and tumour necrosis factor (TNF)-alpha. We intend to describe the modulation of generalized ectromelia virus (EV) infection with exogenous administration of mrIFN-gamma and mrTNF-alpha separately and in combination using susceptible BALB/c mice. The treatment schemes presented resulted in the localization of the generalized EV infection and its development into non-fatal sloughing of the infected limb. This was accompanied by low virus titres in the treated mice due to control of systemic virus replication and virus clearance. The balance of type I versus type II cytokines was dominated by a type I response in the treated groups. The group treated with the combination of IFN-gamma and TNF-alpha exhibited the best survival with Th1-dominant (IFN-gamma and IL-12) cytokine profiles, whereas the TNF-alpha-treated group of mice was less successful in clearance of virus and demonstrated the lowest survival rate. The successful cytokine treatment schemes in this orthopoxvirus model system may have important implications in the treatment of viral diseases in humans and, in particular, of variola virus infection.  (+info)

Polarized type 1 cytokine response and cell-mediated immunity determine genetic resistance to mousepox. (8/85)

Ectromelia virus (ECTV), a natural mouse pathogen and an orthopoxvirus, has been used to investigate the correlation between polarized type 1 or type 2 immune responses and resistance to disease in poxvirus infections by using well defined resistant and susceptible mouse strains. Our data show that distinct differences exist in the cytokine profiles expressed in resistant and susceptible mice infected with ECTV. Resistant C57BL/6 mice generate a type 1 cytokine response [IFN-gamma, IL-2, and tumor necrosis factor (TNF)], within the first few days of infection, which is associated with strong cytotoxic T lymphocyte response (CTL) and recovery from ECTV infection. Susceptible strains of mice (BALB/c and A/J) on the other hand generate a type 2 cytokine response (IL-4 but little or no IFN-gamma and IL-2), which is associated with a weak or an absent CTL response, resulting in uncontrolled virus replication and death. Although deletion of IL-4 function alone did not change the outcome of infection in susceptible mice, the loss of IFN-gamma function in resistant mice abrogated natural killer (NK) cell and CTL effector functions resulting in fulminant disease and 100% mortality. Therefore, a clear link exists between the early production of specific type 1 cytokines, in particular, IFN-gamma, the nature of the cellular immune response, and disease outcome in this virus model. This finding in the mousepox model raises the possibility that inappropriate cytokine responses may result in increased susceptibility to smallpox in humans.  (+info)

Ectromelia virus, also known as mousepox virus, is a species of Poxviridae family that specifically infects mice. It is the causative agent of a disease called ectromelia or mousepox, which is similar to smallpox in humans. The virus primarily affects the spleen, liver, and lungs of the host, leading to symptoms such as rash, fever, weight loss, and hind limb paralysis. Ectromelia virus has been used as a model organism to study poxvirus immunology and pathogenesis.

Ectromelia, infectious, also known as mousepox, is a viral disease that primarily affects mice. It is caused by the ectromelia virus, which belongs to the Poxviridae family. The infection results in various symptoms such as skin lesions, rash, weight loss, and in severe cases, death.

The infection spreads through direct contact with infected mice or their excretions. It can also be transmitted through contaminated bedding, food, and water. In the lab setting, the virus can be transmitted through aerosolized particles, making it highly contagious in populations of mice.

The incubation period for ectromelia, infectious ranges from 5 to 10 days. The initial symptoms include a loss of appetite, lethargy, and hunched posture. As the infection progresses, a rash may develop on the ears, nose, and tail, which eventually spreads to the rest of the body. In severe cases, the rash can ulcerate and become necrotic, leading to the loss of limbs or digits.

There is no specific treatment for ectromelia, infectious. However, supportive care such as fluid therapy, nutritional support, and pain management can help manage the symptoms and improve outcomes. Prevention measures include maintaining good hygiene practices, quarantine of infected animals, and vaccination of susceptible populations.

While ectromelia, infectious is primarily a disease of mice, it has been used as a model for studying poxviruses and developing vaccines. The virus shares many similarities with variola virus, the causative agent of smallpox, making it a valuable tool for research.

Poxviridae infections refer to diseases caused by the Poxviridae family of viruses, which are large, complex viruses with a double-stranded DNA genome. This family includes several pathogens that can infect humans, such as Variola virus (which causes smallpox), Vaccinia virus (used in the smallpox vaccine and can rarely cause infection), Monkeypox virus, and Cowpox virus.

These viruses typically cause skin lesions or pocks, hence the name "Poxviridae." The severity of the disease can vary depending on the specific virus and the immune status of the host. Smallpox, once a major global health threat, was declared eradicated by the World Health Organization in 1980 thanks to a successful vaccination campaign. However, other Poxviridae infections continue to pose public health concerns, particularly in regions with lower vaccination rates and where animal reservoirs exist.

Orthopoxvirus is a genus of large, complex, enveloped DNA viruses in the family Poxviridae. It includes several species that are significant human pathogens, such as Variola virus (which causes smallpox), Vaccinia virus (used in the smallpox vaccine and also known to cause cowpox and buffalopox), Monkeypox virus, and Camelpox virus. These viruses can cause a range of symptoms in humans, from mild rashes to severe disease and death, depending on the specific species and the immune status of the infected individual. Historically, smallpox was one of the most devastating infectious diseases known to humanity, but it was declared eradicated by the World Health Organization in 1980 due to a successful global vaccination campaign. However, other Orthopoxviruses continue to pose public health concerns and require ongoing surveillance and research.

Cowpox virus is a species of the Orthopoxvirus genus, which belongs to the Poxviridae family. It is a double-stranded DNA virus that primarily infects cows and occasionally other animals such as cats, dogs, and humans. The virus causes a mild disease in its natural host, cattle, characterized by the development of pustular lesions on the udder or teats.

In humans, cowpox virus infection can cause a localized skin infection, typically following contact with an infected animal or contaminated fomites. The infection is usually self-limiting and resolves within 1-2 weeks without specific treatment. However, in rare cases, the virus may spread to other parts of the body and cause more severe symptoms.

Historically, cowpox virus has played a significant role in medical research as it was used by Edward Jenner in 1796 to develop the first successful vaccine against smallpox. The similarity between the two viruses allowed for cross-protection, providing immunity to smallpox without exposing individuals to the more deadly disease. Smallpox has since been eradicated globally, and vaccination with cowpox virus is no longer necessary. However, understanding the biology of cowpox virus remains important due to its potential use as a model organism for studying poxvirus infections and developing countermeasures against related viruses.

Poxviridae is a family of large, complex, double-stranded DNA viruses that includes many significant pathogens affecting humans and animals. The most well-known member of this family is the Variola virus, which causes smallpox in humans, a highly contagious and deadly disease that has been eradicated through global vaccination efforts. Other important human pathogens in this family include the Monkeypox virus, which can cause a smallpox-like illness, and the Molluscum contagiosum virus, which causes benign skin tumors.

Poxviruses have a unique ability to replicate in the cytoplasm of host cells, rather than in the nucleus like many other DNA viruses. They also have a complex structure, with a large, brick-shaped virion that contains a lateral body, a core, and an outer envelope. The genome of poxviruses is relatively large, ranging from 130 to 375 kilobases in length, and encodes many genes involved in viral replication, host immune evasion, and modulation of host cell processes.

Poxviridae is further divided into two subfamilies: Chordopoxvirinae, which includes viruses that infect vertebrates, and Entomopoxvirinae, which includes viruses that infect insects. The Chordopoxvirinae subfamily is divided into several genera, including Orthopoxvirus (which includes Variola, Monkeypox, and Vaccinia viruses), Parapoxvirus (which includes Orf virus and Bovine papular stomatitis virus), and Yatapoxvirus (which includes Yaba monkey tumor virus and Tanapox virus).

Overall, Poxviridae is a diverse family of viruses that pose significant public health and agricultural threats, and continue to be the subject of ongoing research and development efforts aimed at understanding their biology and developing new vaccines and therapies.

Variola virus is the causative agent of smallpox, a highly contagious and deadly disease that was eradicated in 1980 due to a successful global vaccination campaign led by the World Health Organization (WHO). The virus belongs to the family Poxviridae and genus Orthopoxvirus. It is a large, enveloped, double-stranded DNA virus with a complex structure that includes a lipoprotein membrane and an outer protein layer called the lateral body.

The Variola virus has two main clinical forms: variola major and variola minor. Variola major is more severe and deadly, with a mortality rate of up to 30%, while variola minor is less severe and has a lower mortality rate. The virus is transmitted through direct contact with infected individuals or contaminated objects, such as clothing or bedding.

Smallpox was once a major public health threat worldwide, causing millions of deaths and severe illnesses. However, since its eradication, Variola virus has been kept in secure laboratories for research purposes only. The virus is considered a potential bioterrorism agent, and efforts are being made to develop new vaccines and antiviral treatments to protect against possible future outbreaks.

Ectromelia is a medical term that refers to the congenital absence or malformation of a limb or extremity. It is also known as "congenital amputation" or "limb reduction defect." This condition can affect any extremity, including arms, legs, hands, or feet, and can range from mild, such as a missing finger or toe, to severe, such as the absence of an entire limb.

Ectromelia can be caused by various factors, including genetic mutations, environmental factors, or a combination of both. In some cases, the cause may be unknown. Treatment options for ectromelia depend on the severity and location of the malformation and may include prosthetics, physical therapy, or surgery.

Vaccinia virus is a large, complex DNA virus that belongs to the Poxviridae family. It is the virus used in the production of the smallpox vaccine. The vaccinia virus is not identical to the variola virus, which causes smallpox, but it is closely related and provides cross-protection against smallpox infection.

The vaccinia virus has a unique replication cycle that occurs entirely in the cytoplasm of infected cells, rather than in the nucleus like many other DNA viruses. This allows the virus to evade host cell defenses and efficiently produce new virions. The virus causes the formation of pocks or lesions on the skin, which contain large numbers of virus particles that can be transmitted to others through close contact.

Vaccinia virus has also been used as a vector for the delivery of genes encoding therapeutic proteins, vaccines against other infectious diseases, and cancer therapies. However, the use of vaccinia virus as a vector is limited by its potential to cause adverse reactions in some individuals, particularly those with weakened immune systems or certain skin conditions.

Complement inactivating agents are substances or drugs that inhibit the complement system, which is a part of the immune system responsible for the recognition and elimination of foreign substances and microorganisms. The complement system consists of a group of proteins that work together to help eliminate pathogens from the body.

Complement inactivating agents are used in medical settings to prevent or treat various conditions associated with excessive or unwanted activation of the complement system, such as inflammation, autoimmune diseases, and transplant rejection. These agents can inhibit different components of the complement pathway, including C1 esterase inhibitors, C3 convertase inhibitors, and C5a receptor antagonists.

Examples of complement inactivating agents include eculizumab, ravulizumab, and Alexion's Ultomiris, which are monoclonal antibodies that target C5, a protein involved in the final steps of the complement pathway. These drugs have been approved for the treatment of paroxysmal nocturnal hemoglobinuria (PNH), atypical hemolytic uremic syndrome (aHUS), and other complement-mediated diseases.

Other complement inactivating agents include C1 esterase inhibitors, such as Berinert and Ruconest, which are used to treat hereditary angioedema (HAE). These drugs work by inhibiting the activation of the classical pathway of the complement system, thereby preventing the release of inflammatory mediators that can cause swelling and pain.

Overall, complement inactivating agents play an important role in the treatment of various complement-mediated diseases, helping to reduce inflammation, prevent tissue damage, and improve patient outcomes.

Vaccinia is actually not a medical term with a specific definition, but it refers to the virus used in the smallpox vaccine. The vaccinia virus is related to, but less harmful than, the variola virus that causes smallpox. When vaccinia virus is introduced into the skin, it leads to an immune response that protects against smallpox.

The term "vaccinia" also refers to the characteristic pockmark-like lesion that forms on the skin as part of the body's reaction to the vaccine. This lesion is a result of the infection and replication of the vaccinia virus in the skin cells, which triggers an immune response that helps protect against smallpox.

It's worth noting that while the smallpox vaccine is no longer routinely administered due to the eradication of smallpox, it may still be used in certain circumstances, such as in laboratory workers who handle the virus or in the event of a bioterrorism threat involving smallpox.

Inclusion bodies, viral are typically described as intracellular inclusions that appear as a result of viral infections. These inclusion bodies consist of aggregates of virus-specific proteins, viral particles, or both, which accumulate inside the host cell's cytoplasm or nucleus during the replication cycle of certain viruses.

The presence of inclusion bodies can sometimes be observed through histological or cytological examination using various staining techniques. Different types of viruses may exhibit distinct morphologies and locations of these inclusion bodies, which can aid in the identification and diagnosis of specific viral infections. However, it is important to note that not all viral infections result in the formation of inclusion bodies, and their presence does not necessarily indicate active viral replication or infection.

Viral proteins are the proteins that are encoded by the viral genome and are essential for the viral life cycle. These proteins can be structural or non-structural and play various roles in the virus's replication, infection, and assembly process. Structural proteins make up the physical structure of the virus, including the capsid (the protein shell that surrounds the viral genome) and any envelope proteins (that may be present on enveloped viruses). Non-structural proteins are involved in the replication of the viral genome and modulation of the host cell environment to favor viral replication. Overall, a thorough understanding of viral proteins is crucial for developing antiviral therapies and vaccines.

The spleen is an organ in the upper left side of the abdomen, next to the stomach and behind the ribs. It plays multiple supporting roles in the body:

1. It fights infection by acting as a filter for the blood. Old red blood cells are recycled in the spleen, and platelets and white blood cells are stored there.
2. The spleen also helps to control the amount of blood in the body by removing excess red blood cells and storing platelets.
3. It has an important role in immune function, producing antibodies and removing microorganisms and damaged red blood cells from the bloodstream.

The spleen can be removed without causing any significant problems, as other organs take over its functions. This is known as a splenectomy and may be necessary if the spleen is damaged or diseased.

Marchal, J. (1930). "Infectious ectromelia. A hitherto undescribed virus disease of mice". The Journal of Pathology and ... Ectromelia virus belongs to the genus Orthopoxvirus of the family Poxviridae. It is a large virus with a complex structure. It ... Ectromelia virus (ECTV) is a virus of the family Poxviridae and the genus Orthopoxvirus that causes mousepox, a disease of mice ... Ectromelia virus can survive for 11 days at room temperature in blood. All other animal house materials should be discarded as ...
Fremont is also a principal investigator in the Center for Structural Genomics of Infectious Disease and his laboratory has ... "Structural determinants of chemokine binding by an Ectromelia virus-encoded decoy receptor.", Journal of Virology, 2006 ... "Center for Structural Genomics of Infectious Diseases - Investigators". Csgid.org. Retrieved 2013-09-28. Phoebe L. Arnold, et ...
... ectromelia, infectious MeSH C22.795.600 - monkeypox MeSH C22.795.650 - murine acquired immunodeficiency syndrome MeSH C22.836. ... infectious canine MeSH C22.467.435.812 - rift valley fever MeSH C22.488.088 - african horse sickness MeSH C22.488.304 - equine ... infectious canine MeSH C22.268.485 - hip dysplasia, canine MeSH C22.331.693 - swine erysipelas MeSH C22.362.224 - furunculosis ... infectious bovine rhinotracheitis MeSH C22.196.497 - lumpy skin disease MeSH C22.196.540 - malignant catarrh MeSH C22.196.581 ...
... ectromelia, infectious MeSH C02.256.743.366 - fowlpox MeSH C02.256.743.494 - lumpy skin disease MeSH C02.256.743.611 - ... infectious canine MeSH C02.256.430.400 - hepatitis b MeSH C02.256.430.400.100 - hepatitis b, chronic MeSH C02.256.466.087 - ... infectious bovine rhinotracheitis MeSH C02.256.466.606 - malignant catarrh MeSH C02.256.466.650 - marek disease MeSH C02.256. ... equine infectious anemia MeSH C02.782.815.616.350 - feline acquired immunodeficiency syndrome MeSH C02.782.815.616.400 - hiv ...
National Center for Infectious Diseases, Centers for Disease Control and Prevention, 1600 Clifton Rd., Atlanta, GA 30333, USA ... Within the Othopoxvirus genus Cowpox virus strain Brighton Red, Ectromelia virus and Monkeypox virus do not group closely with ... is also infectious. They vary in their shape depending upon the species but are generally shaped like a brick or as an oval ... Emerging Infectious Diseases. 27 (4): 1177-1180. doi:10.3201/eid2704.203818. PMC 8007330. PMID 33754985. Smithson C, Meyer H, ...
... infectious pancreatic necrosis virus MeSH B04.820.075.060 - avibirnavirus MeSH B04.820.075.060.400 - infectious bursal disease ... ectromelia virus MeSH B04.280.650.160.650.500 - monkeypox virus MeSH B04.280.650.160.650.900 - vaccinia virus MeSH B04.280. ... infectious pancreatic necrosis virus MeSH B04.909.777.123.060 - avibirnavirus MeSH B04.909.777.123.060.400 - infectious bursal ... infectious bronchitis virus MeSH B04.820.504.540.150.580 - murine hepatitis virus MeSH B04.820.504.540.150.750 - sars virus ...
Tomato golden leaf spot virus Tomato golden mosaic virus Tomato golden mottle virus Tomato golden vein virus Tomato infectious ... virus Eclunavirus EcL1 Ectocarpus fasciculatus virus a Ectocarpus siliculosus virus 1 Ectocarpus siliculosus virus a Ectromelia ... virus Lessievirus bcep22 Lessievirus bcepil02 Lessievirus bcepmigl Lessievirus DC1 Lettuce chlorosis virus Lettuce infectious ... Epsilontectivirus toil Epsilontorquevirus calli1 Eptesipox virus Equine encephalosis virus Equine foamy virus Equine infectious ...
Others, such as ectromelia and camelpox viruses, are highly host-specific. Vaccinia virus, maintained in vaccine institutes and ... Emerging Infectious Diseases. 14 (4): 670-671. doi:10.3201/eid1404.070817. PMC 2570944. PMID 18394293. Martinez, Mark; Michael ... Emerging Infectious Diseases. 13 (7): 965-972. doi:10.3201/eid1307.061404. ISSN 1080-6040. PMC 2878226. PMID 18214166. Gigante ... Abatino macacapox virus Akhmeta virus Alaskapox virus Camelpox virus Cowpox virus Ectromelia virus Monkeypox virus Raccoonpox ...
Interferon has since become prominent in the treatment of a variety of cancers and infectious diseases. In 2007, an outbreak of ... DALLDORF G, GIFFORD R (February 1955). "Recognition of mouse ectromelia". Proc. Soc. Exp. Biol. Med. 88 (2): 290-2. doi:10.3181 ...
... infectious MeSH C05.550.114.099.500 - arthritis, reactive MeSH C05.550.114.145 - arthritis, psoriatic MeSH C05.550.114.154 - ... ectromelia MeSH C05.660.585.512 - lower extremity deformities, congenital MeSH C05.660.585.512.380 - foot deformities, ...
Cross-hybridizations suggest that the HA of RCN, VPX, and SKP are separately diverged and that the HA of VV, ECT (ectromelia ... Uses in veterinary medicine: have potential use for this treatment technique in infectious disease, ex vivo therapies, and ... and Infectious Diseases, 26, 343-355. Alexander, A. D.; Flyger, V.; Herman, Y. F.; Mcconnell, S. J.; Rothstein, N.; Yager, R. H ...
National Center for Infectious Diseases. Lymphocytic Choriomeningitis Virus from Pet Rodents. CDC, n.d. Web. 22 Sept. 2009 ... In addition, infection will increase the sensitivity of the mouse to ectromelia virus and to bacterial endotoxins. Reported ... The National Center for Infectious Disease suggests the following precautions to reduce the risk of LCMV infection: Wash hands ... The virus seems to be relatively resistant to drying and therefore humans can become infected by inhaling infectious ...
Jackson, RJ; DJ Maguire; LA Hinds; IA Ramshaw (1998). "Infertility in mice induced by a recombinant ectromelia virus expressing ... Naz, RK; R Changanamkandath (2004). "Passive immunization for immunocontraception: lessons learned from infectious diseases". ... in Australia by engineering murine zona pellucida antigens into a recombinant ectromelia virus and a recombinant ...
André JB, Hochberg ME (July 2005). "Virulence evolution in emerging infectious diseases". Evolution. 59 (7): 1406-12. doi: ... "Expression of Mouse Interleukin-4 by a Recombinant Ectromelia Virus Suppresses Cytolytic Lymphocyte Responses and Overcomes ... increased spread of known infectious diseases such as malaria, and rapid mutation of microorganisms. A common belief is that ... particularly from air pollution which was linked to deaths by increasing susceptibility to non-infectious diseases, such as ...
Marchal, J. (1930). "Infectious ectromelia. A hitherto undescribed virus disease of mice". The Journal of Pathology and ... Ectromelia virus belongs to the genus Orthopoxvirus of the family Poxviridae. It is a large virus with a complex structure. It ... Ectromelia virus (ECTV) is a virus of the family Poxviridae and the genus Orthopoxvirus that causes mousepox, a disease of mice ... Ectromelia virus can survive for 11 days at room temperature in blood. All other animal house materials should be discarded as ...
Ectromelia virus. Moscow (ECTV-MOS). AF012825. Camelpox virus. CMS (CMLV-CMS). AY009089. ...
infectious ectromelia DOID:3296 * breast fibroadenoma DOID:1618 * ethmoid sinus inverted papilloma ...
Infectious Ectromelia; dsDNA Virus; Poxviridae; C57BL/6 Strain. References. *Andrewes CH and Elford WJ. "Infectious ectromelia ... Infectious ectromelia (ECTV) is an infectious viral disease caused by dsDNA virus of poxviridae family. It is an acute, ... Short Communication on Infectious Ectromelia Sheikh Uzma Farooq1, Aditya Sharma2* and Varun Khajuria3 ... Citation: Aditya Sharma., et al. "Short Communication on Infectious Ectromelia". Acta Scientific Veterinary Sciences 4.12 (2022 ...
Mousepox (infectious ectromelia): past, present, and future. Lab Anim Sci. 1981;31:553-9.PubMed ... Ectromelia virus: the causative agent of mousepox. J Gen Virol. 2005;86:2645-59. DOIPubMed ... Gruber is a member of the bioinformatics unit of the Laboratory of Virology at the National Institute for Infectious Diseases ... Her research interests are controlling animal infectious diseases and zoonoses, including those involving reptiles, bees, and ...
BALB/c mice infected with ectromelia virus). In the pivotal studies in each model, brincidofovir resulted in statistically ... Other infectious disease approvals Apretude (cabotegravir) - Every 2 month IM administration for preexposure prophylaxis (PrEP ...
Ectromelia, Infectious. *Fowlpox. *Lumpy Skin Disease. *Molluscum Contagiosum. *Monkeypox. *Myxomatosis, Infectious. *Smallpox ...
... of ectromelia virus. Infectious virus titers at day 8 postinfection in liver, spleen, and lung from ST-246-treated animals were ... Vírus da Ectromelia/isolamento & purificação , Ectromelia Infecciosa/prevenção & controle , Feminino , Indóis/efeitos adversos ... Half of the group I animals were infected with a recombinant infectious clone SARS-CoV derived from the SARS-CoV Urbani strain ... This infectious clone produced disease indistinguishable from wild-type Urbani strain. CONCLUSIONS: SARS-CoV infection of ...
However, researches on infectious diseases and microbiology always have a potential risk related to scientific ambiguity, i.e ... "Expression of mouse interleukin-4 by a recombinant ectromelia virus suppresses cytolytic lymphocyte responses and overcomes ... Microbiology researches and infectious disease researches have to contribute to the progress of science and contribute to ... Department of Virology 1, National Institute of Infectious Diseases, Toyama 1-23-1, Shinjuku-ku, Tokyo 162-8640, Japan ...
Infectious ectromelia, Infantile diarrhea, murine hepatitis virus, Lymphocytic choriomeningitis); Pathology of important ... UNIT-4 (PATHOLOGY OF INFECTIOUS AND NON-INFECTIOUS DISEASES OF DOMESTIC ANIMALS). Pathology of viral infections: Pathogenesis, ... UNIT-4 (PATHOLOGY OF INFECTIOUS AND NON-INFECTIOUS DISEASES OF DOMESTIC ANIMALS). Post mortem examination and its ... infectious bronchitis, infectious laryngotracheitis, fowl pox, avian influenza, Mareks disease, leukosisorsarcoma group of ...
Roberts J. A. 1964; Growth of virulent and attenuated ectromelia virus in cultured macrophages from normal and ectromelia- ... Journal of Infectious Diseases 137:587-591. [Google Scholar] * Osborn J. E., Walker D. L. 1970; Virulence and attenuation of ...
... infectious diarrhea of infant rats) Rat theilovirus (Theilers-like virus of rats) Reovirus Rabbit picobirnavirus Sendai virus ... of Terms Agent Aleutian disease virus Cilia-associated respiratory bacillus Clostridium piliforme Distemper virus Ectromelia ...
"Chemical Synthesis of Poliovirus cDNA: Generation of Infectious Virus in the Absence of Natural Template." Science 297:1016-18. ... "Expression of Mouse Interleukin-4 by a Recombinant Ectromelia Virus Suppresses Cytolytic Lymphocyte Responses and Overcomes ...
EquineInfectious bronchitis virusTorque teno virusInfluenza A Virus, H5N2 SubtypeAKR murine leukemia virusEctromelia virusAvian ... Infectious bronchitis virus. A species of CORONAVIRUS causing infections in chickens and possibly pheasants. Chicks up to four ... Ectromelia virus. A species of ORTHOPOXVIRUS infecting mice and causing a disease that involves internal organs and produces ... Infectious Anemia Virus, Equine. A species of LENTIVIRUS, subgenus equine lentiviruses (LENTIVIRUSES, EQUINE), causing acute ...
Ectromelia virus Ectromelia viruses use Ectromelia virus Ectromelia, Infectious Ectropion Ectropions use Ectropion ...
Ectromelia virus Ectromelia viruses use Ectromelia virus Ectromelia, Infectious Ectropion Ectropions use Ectropion ...
Ectromelia virus Ectromelia viruses use Ectromelia virus Ectromelia, Infectious Ectropion Ectropions use Ectropion ...
Ectromelia virus Ectromelia viruses use Ectromelia virus Ectromelia, Infectious Ectropion Ectropions use Ectropion ...
Ectromelia virus Ectromelia viruses use Ectromelia virus Ectromelia, Infectious Ectropion Ectropions use Ectropion ...
OBJECTIVES: Foodborne disease is a pervasive problem caused by consuming food or drink contaminated by infectious or ... Genomic analysis revealed evidence suggestive of recombination with Ectromelia virus in two putative regions that contain seven ... including infectious diseases. However, the laboratories adopting NGS methods face significant challenges due to the complex ...
6. Pritchett-Corning KR, Cosentino J, Clifford, CB: Contemporary prevalence of infectious agents in laboratory mice and rats. ... c) mouse pox caused by ectromelia virus, an orthopoxvirus characterized by splenic necrosis (tiger striping) and skin lesions ...
Nair A., Daniel O., Gopalan S. V., George S., Kumar K. S., Merilä J., and Teacher A. G. F. (2011), «Infectious disease ... Ouellet M., Bonin J., Rodrigue J., DesGranges J.-L., and Lair S. (1997), «Hindlimb deformities (ectromelia, ectrodactyly) in ... Daszak P., Berger L, Cunningham A. A., Hyatt A. D., Green D. E., and Speare R. (1999), «Emerging infectious diseases and ...
Induction of cell-cell fusion by ectromelia virus is not inhibited by its fusion inhibitory complex.. 2009 Sep 29 ... A sensitive cell-based assay for the detection of residual infectious West Nile virus.. 2007 Sep 28 ... Validation of betapropiolactone (BPL) as an inactivant for infectious bovine rhinotracheitis (IBR) virus.. 2008 Dec ... Serological response in cattle immunized with inactivated oil and Algel adjuvant vaccines against infectious bovine ...
Identification of nitric oxide synthase 2 as an innate resistance locus against ectromelia virus infection.. J. Virol. 72(9): ... Infectious Disease. *Inflammation. *Metabolic Disease. *Microbiome and Germ-Free. *Model Generation Solutions ...
Armed Forces Infectious Diseases Society, Association of Military Surgeons of the US, Infectious Diseases Society of America, ... including ectromelia, cowpox, monkeypox, vaccinia, and camelpox. Unlike other DNA viruses, the variola virus multiplies in the ... John L Brusch, MD, FACP is a member of the following medical societies: American College of Physicians and Infectious Diseases ... John L Brusch, MD, FACP is a member of the following medical societies: American College of Physicians, Infectious Diseases ...

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