Proteins encoded by a VIRAL GENOME that are produced in the organisms they infect, but not packaged into the VIRUS PARTICLES. Some of these proteins may play roles within the infected cell during VIRUS REPLICATION or act in regulation of virus replication or VIRUS ASSEMBLY.
The type species of PARVOVIRUS prevalent in mouse colonies and found as a contaminant of many transplanted tumors or leukemias.
The process of intracellular viral multiplication, consisting of the synthesis of PROTEINS; NUCLEIC ACIDS; and sometimes LIPIDS, and their assembly into a new infectious particle.
Ribonucleic acid that makes up the genetic material of viruses.
Established cell cultures that have the potential to propagate indefinitely.
Proteins found in any species of virus.
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.
Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories.
A genus of FLAVIVIRIDAE causing parenterally-transmitted HEPATITIS C which is associated with transfusions and drug abuse. Hepatitis C virus is the type species.
A species of the genus FLAVIVIRUS which causes an acute febrile and sometimes hemorrhagic disease in man. Dengue is mosquito-borne and four serotypes are known.
The type species of ALPHAVIRUS normally transmitted to birds by CULEX mosquitoes in Egypt, South Africa, India, Malaya, the Philippines, and Australia. It may be associated with fever in humans. Serotypes (differing by less than 17% in nucleotide sequence) include Babanki, Kyzylagach, and Ockelbo viruses.
Proteins which are synthesized as a single polymer and then cleaved into several distinct proteins.
A family of proteins that promote unwinding of RNA during splicing and translation.
A genus of the family PARVOVIRIDAE, subfamily PARVOVIRINAE, infecting a variety of vertebrates including humans. Parvoviruses are responsible for a number of important diseases but also can be non-pathogenic in certain hosts. The type species is MINUTE VIRUS OF MICE.
Any DNA sequence capable of independent replication or a molecule that possesses a REPLICATION ORIGIN and which is therefore potentially capable of being replicated in a suitable cell. (Singleton & Sainsbury, Dictionary of Microbiology and Molecular Biology, 2d ed)
The complete genetic complement contained in a DNA or RNA molecule in a virus.
An enzyme that catalyses RNA-template-directed extension of the 3'- end of an RNA strand by one nucleotide at a time, and can initiate a chain de novo. (Enzyme Nomenclature, 1992, p293)
A CELL LINE derived from the kidney of the African green (vervet) monkey, (CERCOPITHECUS AETHIOPS) used primarily in virus replication studies and plaque assays.
The order of amino acids as they occur in a polypeptide chain. This is referred to as the primary structure of proteins. It is of fundamental importance in determining PROTEIN CONFORMATION.
The type species of APHTHOVIRUS, causing FOOT-AND-MOUTH DISEASE in cloven-hoofed animals. Several different serotypes exist.
A species of CERCOPITHECUS containing three subspecies: C. tantalus, C. pygerythrus, and C. sabeus. They are found in the forests and savannah of Africa. The African green monkey (C. pygerythrus) is the natural host of SIMIAN IMMUNODEFICIENCY VIRUS and is used in AIDS research.
A species of ALPHAVIRUS isolated in central, eastern, and southern Africa.
Proteins found mainly in icosahedral DNA and RNA viruses. They consist of proteins directly associated with the nucleic acid inside the NUCLEOCAPSID.
A genus of REOVIRIDAE, causing acute gastroenteritis in BIRDS and MAMMALS, including humans. Transmission is horizontal and by environmental contamination. Seven species (Rotaviruses A thru G) are recognized.
A genus of PARVOVIRIDAE, subfamily DENSOVIRINAE, comprising helper-independent viruses containing only two species. Junonia coenia densovirus is the type species.
A species of FLAVIVIRUS, one of the Japanese encephalitis virus group (ENCEPHALITIS VIRUSES, JAPANESE), which is the etiological agent of Japanese encephalitis found in Asia, southeast Asia, and the Indian subcontinent.
A species of ORTHOREOVIRUS infecting birds, with outcomes ranging from inapparent to lethal depending on the virus strain and age of the host bird. This species does not infect mammals.
A genus of TOGAVIRIDAE, also known as Group A arboviruses, serologically related to each other but not to other Togaviridae. The viruses are transmitted by mosquitoes. The type species is the SINDBIS VIRUS.
Viral proteins that are components of the mature assembled VIRUS PARTICLES. They may include nucleocapsid core proteins (gag proteins), enzymes packaged within the virus particle (pol proteins), and membrane components (env proteins). These do not include the proteins encoded in the VIRAL GENOME that are produced in infected cells but which are not packaged in the mature virus particle,i.e. the so called non-structural proteins (VIRAL NONSTRUCTURAL PROTEINS).
Foot-and-Mouth Disease (FMD) is a highly contagious and severe viral disease in cloven-hoofed animals, characterized by fever, formation of vesicles and erosions in the mouth, on the tongue, lips, teats, and feet, causing significant economic losses in agriculture and livestock farming.
The type species of ORBIVIRUS causing a serious disease in sheep, especially lambs. It may also infect wild ruminants and other domestic animals.
The type (and only) species of RUBIVIRUS causing acute infection in humans, primarily children and young adults. Humans are the only natural host. A live, attenuated vaccine is available for prophylaxis.
The type species of ERYTHROVIRUS and the etiological agent of ERYTHEMA INFECTIOSUM, a disease most commonly seen in school-age children.
Specific, characterizable, poisonous chemicals, often PROTEINS, with specific biological properties, including immunogenicity, produced by microbes, higher plants (PLANTS, TOXIC), or ANIMALS.
A family of unenveloped RNA viruses with cubic symmetry. The twelve genera include ORTHOREOVIRUS; ORBIVIRUS; COLTIVIRUS; ROTAVIRUS; Aquareovirus, Cypovirus, Phytoreovirus, Fijivirus, Seadornavirus, Idnoreovirus, Mycoreovirus, and Oryzavirus.
The sequence of PURINES and PYRIMIDINES in nucleic acids and polynucleotides. It is also called nucleotide sequence.
An enzyme which catalyzes the hydrolysis of nucleoside triphosphates to nucleoside diphosphates. It may also catalyze the hydrolysis of nucleotide triphosphates, diphosphates, thiamine diphosphates and FAD. The nucleoside triphosphate phosphohydrolases I and II are subtypes of the enzyme which are found mostly in viruses.
A genus of the family CORONAVIRIDAE which causes respiratory or gastrointestinal disease in a variety of vertebrates.
A country spanning from central Asia to the Pacific Ocean.
Aspects of health and disease related to travel.
Sudden increase in the incidence of a disease. The concept includes EPIDEMICS and PANDEMICS.
Virus diseases caused by the CORONAVIRUS genus. Some specifics include transmissible enteritis of turkeys (ENTERITIS, TRANSMISSIBLE, OF TURKEYS); FELINE INFECTIOUS PERITONITIS; and transmissible gastroenteritis of swine (GASTROENTERITIS, TRANSMISSIBLE, OF SWINE).
A species of CORONAVIRUS causing atypical respiratory disease (SEVERE ACUTE RESPIRATORY SYNDROME) in humans. The organism is believed to have first emerged in Guangdong Province, China, in 2002. The natural host is the Chinese horseshoe bat, RHINOLOPHUS sinicus.
A viral disorder characterized by high FEVER, dry COUGH, shortness of breath (DYSPNEA) or breathing difficulties, and atypical PNEUMONIA. A virus in the genus CORONAVIRUS is the suspected agent.

A premature termination codon interferes with the nuclear function of an exon splicing enhancer in an open reading frame-dependent manner. (1/3998)

Premature translation termination codon (PTC)-mediated effects on nuclear RNA processing have been shown to be associated with a number of human genetic diseases; however, how these PTCs mediate such effects in the nucleus is unclear. A PTC at nucleotide (nt) 2018 that lies adjacent to the 5' element of a bipartite exon splicing enhancer within the NS2-specific exon of minute virus of mice P4 promoter-generated pre-mRNA caused a decrease in the accumulated levels of P4-generated R2 mRNA relative to P4-generated R1 mRNA, although the total accumulated levels of P4 product remained the same. This effect was seen in nuclear RNA and was independent of RNA stability. The 5' and 3' elements of the bipartite NS2-specific exon enhancer are redundant in function, and when the 2018 PTC was combined with a deletion of the 3' enhancer element, the exon was skipped in the majority of the viral P4-generated product. Such exon skipping in response to a PTC, but not a missense mutation at nt 2018, could be suppressed by frame shift mutations in either exon of NS2 which reopened the NS2 open reading frame, as well as by improvement of the upstream intron 3' splice site. These results suggest that a PTC can interfere with the function of an exon splicing enhancer in an open reading frame-dependent manner and that the PTC is recognized in the nucleus.  (+info)

A human sequence homologue of Staufen is an RNA-binding protein that is associated with polysomes and localizes to the rough endoplasmic reticulum. (2/3998)

In the course of a two-hybrid screen with the NS1 protein of influenza virus, a human clone capable of coding for a protein with high homology to the Staufen protein from Drosophila melanogaster (dmStaufen) was identified. With these sequences used as a probe, cDNAs were isolated from a lambda cDNA library. The encoded protein (hStaufen-like) contained four double-stranded RNA (dsRNA)-binding domains with 55% similarity and 38% identity to those of dmStaufen, including identity at all residues involved in RNA binding. A recombinant protein containing all dsRNA-binding domains was expressed in Escherichia coli as a His-tagged polypeptide. It showed dsRNA binding activity in vitro, with an apparent Kd of 10(-9) M. Using a specific antibody, we detected in human cells a major form of the hStaufen-like protein with an apparent molecular mass of 60 to 65 kDa. The intracellular localization of hStaufen-like protein was investigated by immunofluorescence using a series of markers for the cell compartments. Colocalization was observed with the rough endoplasmic reticulum but not with endosomes, cytoskeleton, or Golgi apparatus. Furthermore, sedimentation analyses indicated that hStaufen-like protein associates with polysomes. These results are discussed in relation to the possible functions of the protein.  (+info)

RNA binding by the novel helical domain of the influenza virus NS1 protein requires its dimer structure and a small number of specific basic amino acids. (3/3998)

The RNA-binding/dimerization domain of the NS1 protein of influenza A virus (73 amino acids in length) exhibits a novel dimeric six-helical fold. It is not known how this domain binds to its specific RNA targets, one of which is double-stranded RNA. To elucidate the mode of RNA binding, we introduced single alanine replacements into the NS1 RNA-binding domain at specific positions in the three-dimensional structure. Our results indicate that the dimer structure is essential for RNA binding, because any alanine replacement that causes disruption of the dimer also leads to the loss of RNA-binding activity. Surprisingly, the arginine side chain at position 38, which is in the second helix of each monomer, is the only amino-acid side chain that is absolutely required only for RNA binding and not for dimerization, indicating that this side chain probably interacts directly with the RNA target. This interaction is primarily electrostatic, because replacement of this arginine with lysine had no effect on RNA binding. A second basic amino acid, the lysine at position 41, which is also in helix 2, makes a strong contribution to the affinity of binding. We conclude that helix 2 and helix 2', which are antiparallel and next to each other in the dimer conformation, constitute the interaction face between the NS1 RNA-binding domain and its RNA targets, and that the arginine side chain at position 38 and possibly the lysine side chain at position 41 in each of these antiparallel helices contact the phosphate backbone of the RNA target.  (+info)

Dengue virus NS3 serine protease. Crystal structure and insights into interaction of the active site with substrates by molecular modeling and structural analysis of mutational effects. (4/3998)

The mosquito-borne dengue viruses are widespread human pathogens causing dengue fever, dengue hemorrhagic fever, and dengue shock syndrome, placing 40% of the world's population at risk with no effective treatment. The viral genome is a positive strand RNA that encodes a single polyprotein precursor. Processing of the polyprotein precursor into mature proteins is carried out by the host signal peptidase and by NS3 serine protease, which requires NS2B as a cofactor. We report here the crystal structure of the NS3 serine protease domain at 2.1 A resolution. This structure of the protease combined with modeling of peptide substrates into the active site suggests identities of residues involved in substrate recognition as well as providing a structural basis for several mutational effects on enzyme activity. This structure will be useful for development of specific inhibitors as therapeutics against dengue and other flaviviral proteases.  (+info)

Restricted isotypic antibody reactivity to hepatitis C virus synthetic peptides in immunocompromised patients. (5/3998)

An enzyme immunoassay based on three synthetic peptides from the core, NS4, and NS5 regions of hepatitis C virus allowed the detection of antibodies in 100% of immunocompetent infected patients and in 91% of immunocompromised patients (hemodialysis and hemophiliac patients). Immune impairment seemed to restrict the spectrum of antibody isotypes reacting to the core peptide.  (+info)

Characterization of the nucleoside triphosphatase activity of poliovirus protein 2C reveals a mechanism by which guanidine inhibits poliovirus replication. (6/3998)

The highly conserved non-structural protein 2C of picornaviruses is involved in viral genome replication and encapsidation and in the rearrangement of intracellular structures. 2C binds RNA, has nucleoside triphosphatase activity, and shares three motifs with superfamily III helicases. Motifs "A" and "B" are involved in nucleotide triphosphate (NTP) binding and hydrolysis, whereas a function for motif "C" has not yet been demonstrated. Poliovirus RNA replication is inhibited by millimolar concentrations of guanidine hydrochloride (GdnHCl). Resistance and dependence to GdnHCl map to 2C. To characterize the nucleoside triphosphatase activity of 2C, we purified poliovirus recombinant 2C fused to glutathione S-transferase (GST-2C) from Escherichia coli. GST-2C hydrolyzed ATP with a Km of 0.7 mM. Other NTPs, including GTP, competed with ATP for binding to 2C but were poor substrates for hydrolysis. Mutation of conserved residues in motif A and B abolished ATPase activity, as did mutation of the conserved asparagine residue in motif C, an observation indicating the involvement of this motif in ATP hydrolysis. GdnHCl at millimolar concentrations inhibited ATP hydrolysis. Mutations in 2C that confer poliovirus resistant to or dependent on GdnHCl increased the tolerance to GdnHCl up to 100-fold.  (+info)

Sequence heterogeneity within three different regions of the hepatitis G virus genome. (7/3998)

Two sets of primers derived from the 5'-terminal region and the NS5 region of the hepatitis G virus (HGV) genome were used to amplify PCR fragments from serum specimens obtained from different parts of the world. All PCR fragments from the 5'-terminal region (5'-PCR, n = 56) and from the NS5 region (NS5-PCR, n = 85) were sequenced and compared to corresponding published HGV sequences. The range of nucleotide sequence similarity varied from 74 and 78% to 100% for 5'-PCR and NS5-PCR fragments, respectively. Additionally, five overlapping PCR fragments comprising an approximately 2.0-kb structural region of the HGV genome were sequenced from each of five sera obtained from three United States residents. These sequences were compared to 20 published sequences comprising the same region of the HGV genome. Nucleotide and deduced amino acid sequences obtained from different individuals were homologous from 82.9 to 93. 6% and from 90.4 to 99.0%, respectively. Sequences obtained from follow-up specimens were almost identical. Comparative analysis of deduced amino acid sequences of the HGV structural proteins and hepatitis C virus (HCV) structural proteins combined with an analysis of predicted secondary structures and hydrophobic profiles allowed prediction of processing sites within the HGV structural proteins. A phylogenetic sequence analysis performed on the 2.0-kb structural region supports the existence of three previously identified HGV genetic groups. However, phylogenetic analysis performed on only small DNA fragments yielded inconsistent genetic grouping and failed to confirm the existence of genetic groups. Thus, in contrast to HCV where almost any region can be used for genotyping, only large or carefully selected genome fragments can be used to identify consistent HGV genetic groups.  (+info)

North American and European porcine reproductive and respiratory syndrome viruses differ in non-structural protein coding regions. (8/3998)

Although North American and European serotypes of porcine reproductive and respiratory syndrome virus (PRRSV) are recognized, only the genome of the European Lelystad strain (LV) has been sequenced completely. Here, the genome of the pathogenic North American PRRSV isolate 16244B has been sequenced and compared with LV. The genomic organization of 16244B was the same as LV but with only 63.4% nucleotide identity. The 189 nucleotide 5' non-coding region (NCR) of 16244B was distinct from the LV NCR, with good conservation (83%) only over a 43 base region immediately upstream of open reading frame (ORF) 1a. Major differences were found in the region encoding the non-structural part of the ORF1a polyprotein, which shared only 47% amino acid identity over 2503 residues of the six non-structural proteins (Nsps) encoded. Nsp2, thought to have a species-specific function, showed the greatest divergence, sharing only 32% amino acid identity with LV and containing 120 additional amino acids in the central region. Nsps encoded by the 5'-proximal and central regions of ORF1b had from 66 to 75% amino acid identity; however, the carboxy-terminal protein CP4 was distinct (42% identity). The ORF 1a-1b frameshift region of 16244B had 98% nucleotide identity with LV. Consistent with previous reports for North American isolates, the six structural proteins encoded were 58 to 79% identical to LV proteins. The 3' NCR (150 nucleotides) was 76% identical between isolates. These genomic differences confirm the presence of distinct North American and European PRRSV genotypes.  (+info)

Viral nonstructural proteins (NS) are viral proteins that are not part of the virion structure. They play various roles in the viral life cycle, such as replication of the viral genome, transcription, translation regulation, and modulation of the host cell environment to favor virus replication. These proteins are often produced in large quantities during infection and can manipulate or disrupt various cellular pathways to benefit the virus. They may also be involved in evasion of the host's immune response. The specific functions of viral nonstructural proteins vary depending on the type of virus.

The Minute Virus of Mice (MVM) is a small, single-stranded DNA parvovirus that primarily infects laboratory mice. It was so named because of its extremely small size and the minimal cytopathic effect it causes in infected cells. MVM is not known to cause disease in humans or other animals. However, it has been used as a model system for studying parvovirus biology and pathogenesis due to its ability to efficiently infect and replicate in many types of mammalian cells. There are three strains of MVM (MVMp, MVMi, and MVMc) that vary in their host range and tissue tropism.

Virus replication is the process by which a virus produces copies or reproduces itself inside a host cell. This involves several steps:

1. Attachment: The virus attaches to a specific receptor on the surface of the host cell.
2. Penetration: The viral genetic material enters the host cell, either by invagination of the cell membrane or endocytosis.
3. Uncoating: The viral genetic material is released from its protective coat (capsid) inside the host cell.
4. Replication: The viral genetic material uses the host cell's machinery to produce new viral components, such as proteins and nucleic acids.
5. Assembly: The newly synthesized viral components are assembled into new virus particles.
6. Release: The newly formed viruses are released from the host cell, often through lysis (breaking) of the cell membrane or by budding off the cell membrane.

The specific mechanisms and details of virus replication can vary depending on the type of virus. Some viruses, such as DNA viruses, use the host cell's DNA polymerase to replicate their genetic material, while others, such as RNA viruses, use their own RNA-dependent RNA polymerase or reverse transcriptase enzymes. Understanding the process of virus replication is important for developing antiviral therapies and vaccines.

A viral RNA (ribonucleic acid) is the genetic material found in certain types of viruses, as opposed to viruses that contain DNA (deoxyribonucleic acid). These viruses are known as RNA viruses. The RNA can be single-stranded or double-stranded and can exist as several different forms, such as positive-sense, negative-sense, or ambisense RNA. Upon infecting a host cell, the viral RNA uses the host's cellular machinery to translate the genetic information into proteins, leading to the production of new virus particles and the continuation of the viral life cycle. Examples of human diseases caused by RNA viruses include influenza, COVID-19 (SARS-CoV-2), hepatitis C, and polio.

A cell line is a culture of cells that are grown in a laboratory for use in research. These cells are usually taken from a single cell or group of cells, and they are able to divide and grow continuously in the lab. Cell lines can come from many different sources, including animals, plants, and humans. They are often used in scientific research to study cellular processes, disease mechanisms, and to test new drugs or treatments. Some common types of human cell lines include HeLa cells (which come from a cancer patient named Henrietta Lacks), HEK293 cells (which come from embryonic kidney cells), and HUVEC cells (which come from umbilical vein endothelial cells). It is important to note that cell lines are not the same as primary cells, which are cells that are taken directly from a living organism and have not been grown in the lab.

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.

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.

Molecular sequence data refers to the specific arrangement of molecules, most commonly nucleotides in DNA or RNA, or amino acids in proteins, that make up a biological macromolecule. This data is generated through laboratory techniques such as sequencing, and provides information about the exact order of the constituent molecules. This data is crucial in various fields of biology, including genetics, evolution, and molecular biology, allowing for comparisons between different organisms, identification of genetic variations, and studies of gene function and regulation.

Hepacivirus is a genus of viruses in the family Flaviviridae. The most well-known member of this genus is Hepatitis C virus (HCV), which is a major cause of liver disease worldwide. HCV infection can lead to chronic hepatitis, cirrhosis, and liver cancer.

Hepaciviruses are enveloped viruses with a single-stranded, positive-sense RNA genome. They have a small icosahedral capsid and infect a variety of hosts, including humans, non-human primates, horses, and birds. The virus enters the host cell by binding to specific receptors on the cell surface and is then internalized through endocytosis.

HCV has a high degree of genetic diversity and is classified into seven major genotypes and numerous subtypes based on differences in its RNA sequence. This genetic variability can affect the virus's ability to evade the host immune response, making treatment more challenging.

In addition to HCV, other hepaciviruses have been identified in various animal species, including equine hepacivirus (EHCV), rodent hepacivirus (RHV), and bat hepacivirus (BtHepCV). These viruses are being studied to better understand the biology of hepaciviruses and their potential impact on human health.

Dengue virus (DENV) is a single-stranded, positive-sense RNA virus that belongs to the genus Flavivirus in the family Flaviviridae. It is primarily transmitted to humans through the bites of infected female mosquitoes, mainly Aedes aegypti and Aedes albopictus.

The DENV genome contains approximately 11,000 nucleotides and encodes three structural proteins (capsid, pre-membrane/membrane, and envelope) and seven non-structural proteins (NS1, NS2A, NS2B, NS3, NS4A, NS4B, and NS5). There are four distinct serotypes of DENV (DENV-1, DENV-2, DENV-3, and DENV-4), each of which can cause dengue fever, a mosquito-borne viral disease.

Infection with one serotype provides lifelong immunity against that particular serotype but only temporary and partial protection against the other three serotypes. Subsequent infections with different serotypes can increase the risk of developing severe dengue, such as dengue hemorrhagic fever or dengue shock syndrome, due to antibody-dependent enhancement (ADE) and original antigenic sin phenomena.

DENV is a significant public health concern in tropical and subtropical regions worldwide, with an estimated 390 million annual infections and approximately 100-400 million clinical cases. Preventive measures include vector control strategies to reduce mosquito populations and the development of effective vaccines against all four serotypes.

Sindbis virus is an alphavirus that belongs to the Togaviridae family. It's named after the location where it was first isolated, in Sindbis, Egypt, in 1952. This virus is primarily transmitted by mosquitoes and can infect a wide range of animals, including birds and humans. In humans, Sindbis virus infection often causes a mild flu-like illness characterized by fever, rash, and joint pain. However, some people may develop more severe symptoms, such as neurological disorders, although this is relatively rare. There is no specific treatment for Sindbis virus infection, and management typically involves supportive care to alleviate symptoms.

A polyprotein is a long, continuous chain of amino acids that are produced through the translation of a single mRNA (messenger RNA) molecule. This occurs in some viruses, including retroviruses like HIV, where the viral genome contains instructions for the production of one or more polyproteins.

After the polyprotein is synthesized, it is cleaved into smaller, functional proteins by virus-encoded proteases. These individual proteins then assemble to form new virus particles. The concept of polyproteins is important in understanding viral replication and may provide targets for antiviral therapy.

RNA helicases are a class of enzymes that are capable of unwinding RNA secondary structures using the energy derived from ATP hydrolysis. They play crucial roles in various cellular processes involving RNA, such as transcription, splicing, translation, ribosome biogenesis, and RNA degradation. RNA helicases can be divided into several superfamilies based on their sequence and structural similarities, with the two largest being superfamily 1 (SF1) and superfamily 2 (SF2). These enzymes typically contain conserved motifs that are involved in ATP binding and hydrolysis, as well as RNA binding. By unwinding RNA structures, RNA helicases facilitate the access of other proteins to their target RNAs, thereby enabling the coordinated regulation of RNA metabolism.

Parvovirus is a type of virus that is known to cause diseases in various animals, including dogs and humans. The most common strain that infects humans is called Parvovirus B19. This particular strain is responsible for the illness known as Fifth disease, which primarily affects young children and causes symptoms such as fever, rash, and joint pain.

Parvovirus B19 spreads through respiratory droplets, such as when an infected person coughs or sneezes. It can also be transmitted through blood or contaminated objects. Once the virus enters the body, it typically targets and infects rapidly dividing cells, particularly those found in the bone marrow and the fetal heart.

In dogs, a different strain of parvovirus called Canine Parvovirus (CPV) is responsible for a highly contagious and often fatal gastrointestinal illness. CPV primarily affects puppies between 6 weeks and 6 months old, but older dogs can also be infected if they haven't been vaccinated.

It is essential to maintain good hygiene practices and ensure proper vaccination to prevent parvovirus infections in both humans and animals.

I'm sorry for any confusion, but "replicon" is not a term that has a widely accepted or specific medical definition. It is a term that is used in the field of molecular biology, where it refers to a segment of DNA that contains an origin of replication. The origin of replication is the site on the DNA molecule where the process of DNA replication is initiated. This concept is important in the fields of genetics and virology, but it is not a term that is commonly used in clinical medicine.

If you have any questions related to the medical field, I would be happy to try to help answer them for you!

A viral genome is the genetic material (DNA or RNA) that is present in a virus. It contains all the genetic information that a virus needs to replicate itself and infect its host. The size and complexity of viral genomes can vary greatly, ranging from a few thousand bases to hundreds of thousands of bases. Some viruses have linear genomes, while others have circular genomes. The genome of a virus also contains the information necessary for the virus to hijack the host cell's machinery and use it to produce new copies of the virus. Understanding the genetic makeup of viruses is important for developing vaccines and antiviral treatments.

RNA-dependent RNA polymerase, also known as RNA replicase, is an enzyme that catalyzes the production of RNA from an RNA template. It plays a crucial role in the replication of certain viruses, such as positive-strand RNA viruses and retroviruses, which use RNA as their genetic material. The enzyme uses the existing RNA strand as a template to create a new complementary RNA strand, effectively replicating the viral genome. This process is essential for the propagation of these viruses within host cells and is a target for antiviral therapies.

Vero cells are a line of cultured kidney epithelial cells that were isolated from an African green monkey (Cercopithecus aethiops) in the 1960s. They are named after the location where they were initially developed, the Vervet Research Institute in Japan.

Vero cells have the ability to divide indefinitely under certain laboratory conditions and are often used in scientific research, including virology, as a host cell for viruses to replicate. This allows researchers to study the characteristics of various viruses, such as their growth patterns and interactions with host cells. Vero cells are also used in the production of some vaccines, including those for rabies, polio, and Japanese encephalitis.

It is important to note that while Vero cells have been widely used in research and vaccine production, they can still have variations between different cell lines due to factors like passage number or culture conditions. Therefore, it's essential to specify the exact source and condition of Vero cells when reporting experimental results.

An amino acid sequence is the specific order of amino acids in a protein or peptide molecule, formed by the linking of the amino group (-NH2) of one amino acid to the carboxyl group (-COOH) of another amino acid through a peptide bond. The sequence is determined by the genetic code and is unique to each type of protein or peptide. It plays a crucial role in determining the three-dimensional structure and function of proteins.

Foot-and-Mouth Disease Virus (FMDV) is a single-stranded, positive-sense RNA virus belonging to the family Picornaviridae and the genus Aphthovirus. It is the causative agent of Foot-and-Mouth Disease (FMD), a highly contagious and severe viral disease that affects cloven-hoofed animals, including cattle, swine, sheep, goats, and buffalo. The virus can be transmitted through direct contact with infected animals or their bodily fluids, as well as through aerosolized particles in the air. FMDV has seven distinct serotypes (O, A, C, Asia 1, and South African Territories [SAT] 1, 2, and 3), and infection with one serotype does not provide cross-protection against other serotypes. The virus primarily targets the animal's epithelial tissues, causing lesions and blisters in and around the mouth, feet, and mammary glands. FMD is not a direct threat to human health but poses significant economic consequences for the global livestock industry due to its high infectivity and morbidity rates.

'Cercopithecus aethiops' is the scientific name for the monkey species more commonly known as the green monkey. It belongs to the family Cercopithecidae and is native to western Africa. The green monkey is omnivorous, with a diet that includes fruits, nuts, seeds, insects, and small vertebrates. They are known for their distinctive greenish-brown fur and long tail. Green monkeys are also important animal models in biomedical research due to their susceptibility to certain diseases, such as SIV (simian immunodeficiency virus), which is closely related to HIV.

Semliki Forest Virus (SFV) is an alphavirus in the Togaviridae family, which is primarily transmitted to vertebrates through mosquito vectors. The virus was initially isolated from mosquitoes in the Semliki Forest of Uganda and has since been found in various parts of Africa and Asia. SFV infection in humans can cause a mild febrile illness characterized by fever, headache, muscle pain, and rash. However, it is more commonly known for causing severe disease in animals, particularly non-human primates and cattle, where it can lead to encephalitis or hemorrhagic fever. SFV has also been used as a model organism in laboratory studies of virus replication and pathogenesis.

Viral core proteins are the structural proteins that make up the viral capsid or protein shell, enclosing and protecting the viral genome. These proteins play a crucial role in the assembly of the virion, assist in the infection process by helping to deliver the viral genome into the host cell, and may also have functions in regulating viral replication. The specific composition and structure of viral core proteins vary among different types of viruses.

Rotavirus is a genus of double-stranded RNA virus in the Reoviridae family, which is a leading cause of severe diarrhea and gastroenteritis in young children and infants worldwide. The virus infects and damages the cells lining the small intestine, resulting in symptoms such as vomiting, watery diarrhea, abdominal cramps, and fever.

Rotavirus is highly contagious and can be spread through contact with infected individuals or contaminated surfaces, food, or water. The virus is typically transmitted via the fecal-oral route, meaning that it enters the body through the mouth after coming into contact with contaminated hands, objects, or food.

Rotavirus infections are often self-limiting and resolve within a few days to a week, but severe cases can lead to dehydration, hospitalization, and even death, particularly in developing countries where access to medical care and rehydration therapy may be limited. Fortunately, there are effective vaccines available that can prevent rotavirus infection and reduce the severity of symptoms in those who do become infected.

A densovirus is a type of single-stranded DNA virus that belongs to the family Parvoviridae and the subfamily Densovirinae. These viruses are known to infect insects, including crustaceans and arthropods, and are often associated with diseases in these hosts. They have a small, icosahedral capsid and a linear, ssDNA genome that is around 5-6 kilobases in length. Densoviruses are non-enveloped viruses, meaning they do not have a lipid membrane surrounding their capsid.

It's important to note that densoviruses are not known to infect humans or other mammals, and therefore are not considered a threat to human health.

Japanese Encephalitis Virus (JEV) is a type of flavivirus that is the causative agent of Japanese encephalitis, a mosquito-borne viral infection of the brain. The virus is primarily transmitted to humans through the bite of infected Culex species mosquitoes, particularly Culex tritaeniorhynchus and Culex gelidus.

JEV is endemic in many parts of Asia, including China, Japan, Korea, India, Nepal, Thailand, and Vietnam. It is estimated to cause around 68,000 clinical cases and 13,000-20,000 deaths each year. The virus is maintained in a transmission cycle between mosquitoes and vertebrate hosts, primarily pigs and wading birds.

Most JEV infections are asymptomatic or result in mild symptoms such as fever, headache, and muscle aches. However, in some cases, the infection can progress to severe encephalitis, which is characterized by inflammation of the brain, leading to neurological symptoms such as seizures, tremors, paralysis, and coma. The case fatality rate for Japanese encephalitis is estimated to be 20-30%, and around half of those who survive have significant long-term neurological sequelae.

Prevention of JEV infection includes the use of insect repellent, wearing protective clothing, and avoiding outdoor activities during peak mosquito feeding times. Vaccination is also an effective means of preventing Japanese encephalitis, and vaccines are available for travelers to endemic areas as well as for residents of those areas.

Orthoreovirus, avian refers to a type of orthoreovirus that primarily infects birds. Orthoreoviruses are non-enveloped, double-stranded RNA viruses belonging to the family Reoviridae. The avian orthoreoviruses are divided into three groups based on their host range and serological properties: orthoreovirus group 1 (avian reovirus), orthoreovirus group 2 (fiscal reovirus), and orthoreovirus group 3 (ptarmigan reovirus). Avian reoviruses are the most well-known and studied among these, causing various diseases in poultry, such as viral arthritis/tenosynovitis, runting-stunting syndrome, and enteric disease. They have a segmented genome consisting of 10 separate RNA segments that encode for several structural and non-structural proteins involved in virus replication, assembly, and pathogenesis.

Alphaviruses are a genus of single-stranded, positive-sense RNA viruses that belong to the family Togaviridae. They are enveloped viruses and have a icosahedral symmetry with a diameter of approximately 70 nanometers. Alphaviruses are transmitted to vertebrates by mosquitoes and other arthropods, and can cause a range of diseases in humans and animals, including arthritis, encephalitis, and rash.

Some examples of alphaviruses that can infect humans include Chikungunya virus, Eastern equine encephalitis virus, Western equine encephalitis virus, Sindbis virus, and Venezuelan equine encephalitis virus. These viruses are usually found in tropical and subtropical regions around the world, and can cause outbreaks of disease in humans and animals.

Alphaviruses have a wide host range, including mammals, birds, reptiles, and insects. They replicate in the cytoplasm of infected cells and have a genome that encodes four non-structural proteins (nsP1 to nsP4) involved in viral replication, and five structural proteins (C, E3, E2, 6K, and E1) that form the virion.

Prevention and control of alphavirus infections rely on avoiding mosquito bites, using insect repellents, wearing protective clothing, and reducing mosquito breeding sites. There are no specific antiviral treatments available for alphavirus infections, but supportive care can help manage symptoms. Vaccines are available for some alphaviruses, such as Eastern equine encephalitis virus and Western equine encephalitis virus, but not for others, such as Chikungunya virus.

Viral structural proteins are the protein components that make up the viral particle or capsid, providing structure and stability to the virus. These proteins are encoded by the viral genome and are involved in the assembly of new virus particles during the replication cycle. They can be classified into different types based on their location and function, such as capsid proteins, matrix proteins, and envelope proteins. Capsid proteins form the protein shell that encapsulates the viral genome, while matrix proteins are located between the capsid and the envelope, and envelope proteins are embedded in the lipid bilayer membrane that surrounds some viruses.

Foot-and-mouth disease (FMD) is a highly contagious viral disease that affects cloven-hoofed animals, including cattle, sheep, goats, pigs, and buffalo. The virus can also infect wild animals like deer and antelope. FMD is not a direct threat to human health but may have significant economic impacts due to restrictions on trade and movement of infected animals.

The disease is characterized by fever, blister-like sores (vesicles) in the mouth, on the tongue, lips, gums, teats, and between the hooves. The vesicles can rupture, causing painful erosions that make it difficult for affected animals to eat, drink, or walk. In severe cases, FMD can lead to death, particularly among young animals.

The causative agent of foot-and-mouth disease is the foot-and-mouth disease virus (FMDV), which belongs to the Picornaviridae family and Aphthovirus genus. There are seven serotypes of FMDV: O, A, C, Asia 1, and South African Territories (SAT) 1, SAT 2, and SAT 3. Infection with one serotype does not provide cross-protection against other serotypes.

Prevention and control measures for foot-and-mouth disease include vaccination, quarantine, movement restrictions, disinfection, and culling of infected animals in severe outbreaks. Rapid detection and response are crucial to prevent the spread of FMD within and between countries.

Bluetongue virus (BTV) is an infectious agent that causes Bluetongue disease, a non-contagious viral disease affecting sheep and other ruminants. It is a member of the Orbivirus genus within the Reoviridae family. The virus is transmitted by biting midges of the Culicoides species and can infect various animals such as sheep, cattle, goats, and wild ruminants.

The virus has a double-stranded RNA genome and consists of ten segments that encode seven structural and four non-structural proteins. The clinical signs of Bluetongue disease in sheep include fever, salivation, swelling of the head and neck, nasal discharge, and respiratory distress, which can be severe or fatal. In contrast, cattle usually show milder symptoms or are asymptomatic, although they can serve as reservoirs for the virus.

Bluetongue virus is an important veterinary pathogen that has a significant economic impact on the global sheep industry. The disease is prevalent in many parts of the world, particularly in tropical and subtropical regions, but has also spread to temperate areas due to climate change and the movement of infected animals. Prevention and control measures include vaccination, insect control, and restricting the movement of infected animals.

Rubella virus is the sole member of the genus Rubivirus, within the family Togaviridae. It is a positive-sense single-stranded RNA virus that causes the disease rubella (German measles) in humans. The virus is typically transmitted through respiratory droplets and has an incubation period of 12-23 days.

Rubella virus infection during pregnancy, particularly during the first trimester, can lead to serious birth defects known as congenital rubella syndrome (CRS) in the developing fetus. The symptoms of CRS may include hearing impairment, eye abnormalities, heart defects, and developmental delays.

The virus was eradicated from the Americas in 2015 due to widespread vaccination programs. However, it still circulates in other parts of the world, and travelers can bring the virus back to regions where it has been eliminated. Therefore, maintaining high vaccination rates is crucial for preventing the spread of rubella and protecting vulnerable populations from CRS.

Parvovirus B19, Human is a single-stranded DNA virus that primarily infects humans. It belongs to the Parvoviridae family and Erbovirus genus. This virus is the causative agent of erythema infectiosum, also known as fifth disease, a mild, self-limiting illness characterized by a facial rash and occasionally joint pain or inflammation.

Parvovirus B19 has a strong tropism for erythroid progenitor cells in the bone marrow, where it replicates and causes temporary suppression of red blood cell production (aplastic crisis) in individuals with underlying hemolytic disorders such as sickle cell disease or spherocytosis.

Additionally, Parvovirus B19 can cause more severe complications in immunocompromised individuals, pregnant women, and fetuses. Infection during pregnancy may lead to hydrops fetalis, anemia, or even fetal death, particularly in the first and second trimesters. Transmission of the virus occurs primarily through respiratory droplets and occasionally via blood transfusions or vertical transmission from mother to fetus.

Biological toxins are poisonous substances that are produced by living organisms such as bacteria, plants, and animals. They can cause harm to humans, animals, or the environment. Biological toxins can be classified into different categories based on their mode of action, such as neurotoxins (affecting the nervous system), cytotoxins (damaging cells), and enterotoxins (causing intestinal damage).

Examples of biological toxins include botulinum toxin produced by Clostridium botulinum bacteria, tetanus toxin produced by Clostridium tetani bacteria, ricin toxin from the castor bean plant, and saxitoxin produced by certain types of marine algae.

Biological toxins can cause a range of symptoms depending on the type and amount of toxin ingested or exposed to, as well as the route of exposure (e.g., inhalation, ingestion, skin contact). They can cause illnesses ranging from mild to severe, and some can be fatal if not treated promptly and effectively.

Prevention and control measures for biological toxins include good hygiene practices, vaccination against certain toxin-producing bacteria, avoidance of contaminated food or water sources, and personal protective equipment (PPE) when handling or working with potential sources of toxins.

Reoviridae is a family of double-stranded RNA viruses that are non-enveloped and have a segmented genome. The name "Reoviridae" is derived from Respiratory Enteric Orphan virus, as these viruses were initially discovered in respiratory and enteric (gastrointestinal) samples but did not appear to cause any specific diseases.

The family Reoviridae includes several important human pathogens such as rotaviruses, which are a major cause of severe diarrhea in young children worldwide, and orthoreoviruses, which can cause respiratory and systemic infections in humans. Additionally, many Reoviridae viruses infect animals, including birds, mammals, fish, and insects, and can cause a variety of diseases.

Reoviridae virions are typically composed of multiple protein layers that encase the genomic RNA segments. The family is divided into two subfamilies, Sedoreovirinae and Spinareovirinae, based on structural features and genome organization. Reoviruses have a complex replication cycle that involves multiple steps, including attachment to host cells, uncoating of the viral particle, transcription of the genomic RNA, translation of viral proteins, packaging of new virions, and release from infected cells.

A base sequence in the context of molecular biology refers to the specific order of nucleotides in a DNA or RNA molecule. In DNA, these nucleotides are adenine (A), guanine (G), cytosine (C), and thymine (T). In RNA, uracil (U) takes the place of thymine. The base sequence contains genetic information that is transcribed into RNA and ultimately translated into proteins. It is the exact order of these bases that determines the genetic code and thus the function of the DNA or RNA molecule.

Nucleoside-triphosphatase (NTPase) is not a medical term per se, but rather a biochemical term. However, it is often used in the context of molecular biology and genetics, which are essential components of medical research and practice. Therefore, I will provide a definition related to these fields.

Nucleoside-triphosphatase (NTPase) refers to an enzyme that catalyzes the hydrolysis of nucleoside triphosphates (NTPs) into nucleoside diphosphates (NDPs) and inorganic phosphate (Pi). NTPs, such as adenosine triphosphate (ATP), guanosine triphosphate (GTP), cytidine triphosphate (CTP), and uridine triphosphate (UTP), are crucial for energy transfer in cells.

In the context of molecular biology, NTPases play essential roles in various cellular processes, including DNA replication, transcription, translation, and degradation. For example, DNA polymerase, an enzyme involved in DNA replication, is a type of NTPase that utilizes dNTPs (deoxynucleoside triphosphates) to synthesize new DNA strands. Similarly, RNA polymerase, which catalyzes the transcription of DNA into RNA, uses NTPs as substrates and has NTPase activity.

In summary, Nucleoside-triphosphatase (NTPase) is an enzyme that hydrolyzes nucleoside triphosphates (NTPs), releasing energy and playing a critical role in various cellular processes, including DNA replication, transcription, translation, and degradation.

A coronavirus is a type of virus that causes respiratory illnesses, such as the common cold, and more severe diseases including Severe Acute Respiratory Syndrome (SARS) and Middle East Respiratory Syndrome (MERS). These viruses are typically spread through close contact with an infected person when they cough or sneeze. They can also spread by touching a surface or object that has the virus on it and then touching your own mouth, nose, or eyes.

Coronaviruses are named for the crown-like spikes on their surface. They are zoonotic, meaning they can be transmitted between animals and people. Common signs of infection include fever, cough, and shortness of breath. In more severe cases, infection can cause pneumonia, severe acute respiratory syndrome, kidney failure, and even death.

One of the most recently discovered coronaviruses is SARS-CoV-2, which causes the disease COVID-19. This virus was first identified in Wuhan, China in late 2019 and has since spread to become a global pandemic.

I am not aware of a specific medical definition for the term "China." Generally, it is used to refer to:

1. The People's Republic of China (PRC), which is a country in East Asia. It is the most populous country in the world and the fourth largest by geographical area. Its capital city is Beijing.
2. In a historical context, "China" was used to refer to various dynasties and empires that existed in East Asia over thousands of years. The term "Middle Kingdom" or "Zhongguo" (中国) has been used by the Chinese people to refer to their country for centuries.
3. In a more general sense, "China" can also be used to describe products or goods that originate from or are associated with the People's Republic of China.

If you have a specific context in which you encountered the term "China" related to medicine, please provide it so I can give a more accurate response.

I'm sorry for any confusion, but "travel" is not a term that has a specific medical definition. In general, travel refers to the act of moving or journeying from one place to another, often over long distances. However, in a medical context, it might refer to the recommendation that individuals with certain medical conditions or those who are immunocompromised avoid traveling to areas where they may be at increased risk of exposure to infectious diseases. It's always best to check with a healthcare professional for advice related to specific medical situations and travel.

A disease outbreak is defined as the occurrence of cases of a disease in excess of what would normally be expected in a given time and place. It may affect a small and localized group or a large number of people spread over a wide area, even internationally. An outbreak may be caused by a new agent, a change in the agent's virulence or host susceptibility, or an increase in the size or density of the host population.

Outbreaks can have significant public health and economic impacts, and require prompt investigation and control measures to prevent further spread of the disease. The investigation typically involves identifying the source of the outbreak, determining the mode of transmission, and implementing measures to interrupt the chain of infection. This may include vaccination, isolation or quarantine, and education of the public about the risks and prevention strategies.

Examples of disease outbreaks include foodborne illnesses linked to contaminated food or water, respiratory infections spread through coughing and sneezing, and mosquito-borne diseases such as Zika virus and West Nile virus. Outbreaks can also occur in healthcare settings, such as hospitals and nursing homes, where vulnerable populations may be at increased risk of infection.

Coronaviruses are a large family of viruses that can cause illnesses ranging from the common cold to more severe diseases such as pneumonia. The name "coronavirus" comes from the Latin word "corona," which means crown or halo, reflecting the distinctive appearance of the virus particles under electron microscopy, which have a crown-like structure due to the presence of spike proteins on their surface.

Coronaviruses are zoonotic, meaning they can be transmitted between animals and humans. Some coronaviruses are endemic in certain animal populations and occasionally jump to humans, causing outbreaks of new diseases. This is what happened with Severe Acute Respiratory Syndrome (SARS) in 2002-2003, Middle East Respiratory Syndrome (MERS) in 2012, and the most recent Coronavirus Disease 2019 (COVID-19), caused by SARS-CoV-2.

Coronavirus infections typically cause respiratory symptoms such as cough, shortness of breath, and fever. In severe cases, they can lead to pneumonia, acute respiratory distress syndrome (ARDS), and even death, especially in older adults or people with underlying medical conditions. Other symptoms may include fatigue, muscle aches, headache, sore throat, and gastrointestinal issues such as nausea, vomiting, and diarrhea.

Preventive measures for coronavirus infections include frequent hand washing, wearing face masks, practicing social distancing, avoiding close contact with sick individuals, and covering the mouth and nose when coughing or sneezing. There are currently vaccines available to prevent COVID-19, which have been shown to be highly effective in preventing severe illness, hospitalization, and death from the disease.

Severe Acute Respiratory Syndrome (SARS) is a viral respiratory illness caused by the SARS coronavirus (SARS-CoV). This virus is a member of the Coronaviridae family and is thought to be transmitted most readily through close person-to-person contact via respiratory droplets produced when an infected person coughs or sneezes.

The SARS outbreak began in southern China in 2002 and spread to several other countries before it was contained. The illness causes symptoms such as fever, chills, and body aches, which progress to a dry cough and sometimes pneumonia. Some people also report diarrhea. In severe cases, the illness can cause respiratory failure or death.

It's important to note that SARS is not currently a global health concern, as there have been no known cases since 2004. However, it remains a significant example of how quickly and widely a new infectious disease can spread in today's interconnected world.

Severe Acute Respiratory Syndrome (SARS) is a viral respiratory illness characterized by fever, cough, shortness of breath, and sometimes severe pneumonia. It is caused by the SARS coronavirus (SARS-CoV).

The syndrome is considered severe due to its potential to cause rapid spread in communities and healthcare settings, and for its high case fatality rate. In the global outbreak of 2002-2003, approximately 8,000 people were infected and nearly 800 died. Since then, no large outbreaks have been reported, although there have been isolated cases linked to laboratory accidents or animal exposures.

SARS is transmitted through close contact with an infected person's respiratory droplets, such as when they cough or sneeze. It can also be spread by touching a surface contaminated with the virus and then touching the mouth, nose, or eyes. Healthcare workers and others in close contact with infected individuals are at higher risk of infection.

Preventive measures include good personal hygiene, such as frequent handwashing, wearing masks and other protective equipment when in close contact with infected individuals, and practicing respiratory etiquette (covering the mouth and nose when coughing or sneezing). Infected individuals should be isolated and receive appropriate medical care to help manage their symptoms and prevent transmission to others.

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... on UniProt (Simplexviruses, Viral nonstructural proteins). ... is one of seven proteins encoded in the viral genome of HSV-1 ... Zhou, C; Knipe, DM (2002). "Association of herpes simplex virus type 1 ICP8 and ICP27 proteins with cellular RNA polymerase II ... ICP8, the herpes simplex virus type-1 single-strand DNA-binding protein, ...
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Three non-structural proteins have been found (1). "Viral Zone". ExPASy. Retrieved 15 June 2015. "Virus Taxonomy: 2020 Release ... The genome also codes for non-structural proteins as well as structural proteins (1). ... Viral replication is cytoplasmic. Entry into the host cell is achieved by penetration into the host cell. Replication follows ... The virus exits the host cell by tubule-guided viral movement. Plants serve as the natural host. Transmission routes are ...
Protein pages needing a picture, Rotaviruses, Viral nonstructural proteins). ... Putative transmembrane domain more commonly known as Non-structural Protein 6 (NSP6) is one of the two non-structural proteins ... how mutation of Non-Structural Protein 6 (NSP6) could affect viral autophagy". Journal of Infection. 81 (1): e24-e27. doi: ... "Reverse Genetics System Demonstrates that Rotavirus Nonstructural Protein NSP6 Is Not Essential for Viral Replication in Cell ...
The early region encodes nonstructural proteins E1 to E7. There are three viral oncoproteins, E5, E6 and E7; BPVs of the ... L1 protein or (for BPV-4) L2 protein confers long-lasting protection against challenge with the same BPV type, but is generally ... The capsid is formed of the L1 and L2 structural proteins, with the L1 C-terminus exposed. All BPVs have a circular double- ... The late region encodes structural proteins L1 and L2. There is also a non-coding long control region (LCR). Six types of BPV ...
ORF1 encodes a nonstructural protein (NS1) that is involved in viral genome replication. ORF2 encodes the two capsid proteins- ... Sukhu, L; Fasina, O; Burger, L; Rai, A; Qiu, J; Pintel, D. J (2012). "Characterization of the Nonstructural Proteins of the ... This gene encodes a highly phosphorylated nonstructural protein (NP1). ... In Canine minute virus NP1 has been shown to be essential for an early step in viral replication and is also required for the ...
Nonstructural protein 4B (NS4B) is a viral protein found in the hepatitis C virus. It has mass of 27 kDa and probably involved ... v t e (Viral nonstructural proteins, Hepatitis C virus, All stub articles, Virus stubs). ...
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v t e v t e (CS1: long volume value, Protein pages needing a picture, Rotaviruses, Viral nonstructural proteins, All stub ... The rotavirus nonstructural protein NSP4 was the first viral enterotoxin discovered. It is a viroporin and induces diarrhea and ... Hu L, Crawford SE, Hyser JM, Estes MK, Prasad BV (August 2012). "Rotavirus non-structural proteins: structure and function". ... Gebert JT, Hyser J (May 2022). "Using Forward and Reverse Genetics to Understand Calcium Dysregulation in Enteric Viral ...
... and groups of viral proteins include structural proteins, nonstructural proteins, regulatory proteins, and accessory proteins. ... and transactivation of viral structural protein encoding genes. Viral nonstructural proteins interact with host cell proteins ... The viral envelope is made up of a lipid bilayer embedded with viral proteins, including viral glycoproteins. These viral ... Many copies of a single viral protein or a number of different viral proteins make up the capsid, and each of these viral ...
... these genes encode seven nonstructural proteins and three structural proteins. The RNA strand is held within a nucleocapsid ... the capsid is contained within a host-derived membrane altered by two viral membrane proteins. West Nile virus has been seen to ... Arthropod-borne viral fevers and viral haemorrhagic fevers, Zoonoses, Tropical diseases, Insect-borne diseases, Animal vaccines ... Vertical transmission, the transmission of a viral or bacterial disease from the female of the species to her offspring, has ...
v t e (Simplexviruses, Viral nonstructural proteins, All stub articles, Virus stubs). ... Stynen, B.; Tournu, H.; Tavernier, J.; Van Dijck, P. (11 June 2012). "Diversity in Genetic In Vivo Methods for Protein-Protein ... Vmw65, also known as VP16 or α-TIF (Trans Inducing Factor) is a trans-acting protein that forms a complex with the host ... "Crystal structure of the conserved core of the herpes simplex virus transcriptional regulatory protein VP16". Genes Dev. 13 (13 ...
Protein pages needing a picture, Rotaviruses, RNA-binding proteins, Viral nonstructural proteins). ... Rotavirus protein NSP3 (NS34) is bound to the 3' end consensus sequence of viral mRNAs in infected cells. Four nucleotides are ... Poncet D, Aponte C, Cohen J (June 1993). "Rotavirus protein NSP3 (NS34) is bound to the 3' end consensus sequence of viral ... Rotavirus RNA-binding protein NSP3 interacts with eIF4GI and evicts the poly(A)-binding protein from eIF4F. And NSP3A, by ...
This viral genome codes for seven structural proteins and one non-structural protein. The gene order is 3′ - leader - NP - VP35 ... the mRNA is translated into individual viral proteins. These viral proteins are processed: a glycoprotein precursor (GP0) is ... Viral proteins VP40 and VP24 are located between the envelope and the nucleocapsid (see following), in the matrix space. At the ... Animal viral diseases, Arthropod-borne viral fevers and viral haemorrhagic fevers, Hemorrhagic fevers, Virus-related cutaneous ...
This is accomplished through the action of the viral Nonstructural Protein NSP3 which specifically binds the 3' consensus ... This protein also interacts with the rotavirus non-structural protein NSP3. Rotavirus mRNAs are capped but not polyadenylated, ... associated non-structural protein) also known as ZC3H7B (zinc finger CCCH-type containing 7B), is a protein that in humans is ... cellular protein that contains a minimum of three regions predicted to be involved in protein-protein or nucleic acid-protein ...
... are synthesized by viral DNA/RNA and do not play a role in the replication or the viral protein coating. The nonstructural S ... Viral+Nonstructural+Proteins at the U.S. National Library of Medicine Medical Subject Headings (MeSH) ZHANG, S.; ZHENG, B.; ... Simons, J F; Persson, R; Pettersson, R F (1992-07-01). "Association of the nonstructural protein NSs of Uukuniemi virus with ... The NSs protein in different viruses have been shown to differ in amino acid sequence by up to 85%. NSs protein is distributed ...
... which are denoted as non-structural proteins. The non-structural proteins function in viral replication and assembly. These ... The other non-structural proteins function in RNA replication, viral assembly and release, processing the viral polyprotein and ... The envelope protein then helps the viral envelope fuse to the host cell membrane in order to release the viral capsid into the ... Entry of Sepik virus into the cell is mediated by the envelope protein (E), which is the viral entry protein. The envelope ...
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Cytotoxic Nonstructural Protein S2-σ2 - Core Clamp Protein S3-σNS - unknown function, nonstructural. S4-σ1 - Viral Attachment ... "The non-structural protein μNS of piscine orthoreovirus (PRV) forms viral factory-like structures". Veterinary Research. 47 (1 ... Outer Clamp Protein). Additionally, the outer layer has fiber proteins (σ1) that mediate viral attachment and entry into the ... posited to aid in viral factory formation. S1-σ3 - Outer Clamp Protein (Capsid protein) & p13 - ...
... as well as a non-structural protein Nsm. The Gc and Gn proteins start as one precursor protein and are then cleaved ... Bunyamwera virus NSs protein is a nonessential gene that contributes to viral pathogenesis. It has been shown that in mammalian ... Depending on the initiation site, it can either code for the protein that makes up the nucleocapsid, N, or a non-structural ... Bunyamwera virus (BUNV) codes for two non-structural proteins: NSm on the medium RNA segment and NSs on the smallest RNA ...
... the viral structural proteins assemble the virus particle at the plasma membrane and form a complex with the viral RNA as the ... It also contains at least five non-structural accessory gene open reading frames (ORF). These are in the region between the pol ... Other accessory genes include vif (viral infectivity factor), tat (transcription activator), and rev (protein expression ... The virus matures after proteolytic processing by the viral protease (PR). The virus is then ready to infect another cell and ...
The genome also encodes several nonstructural proteins (NS1, NS2a, NS2b, NS3, N4a, NS4b, NS5). NS1 is produced as a secretory ... and rapidly accumulates substantial amounts of viral proteins. Based on the envelope gene, there are five genotypes (I-V). The ... and modulating cellular levels of stress-related proteins. It has also been shown that the production of infective viral ... The outer envelope is formed by envelope protein and is the protective antigen. It aids in entry of the virus into the cell. ...
v t e (Viral nonstructural proteins, Enzymes, DNA replication, All stub articles, Virus stubs). ... A helicase-primase associated factor protein may also be present. The complex is used by herpesviruses, in which it is ... Weller SK, Kuchta RD (October 2013). "The DNA helicase-primase complex as a target for herpes viral infection". Expert Opinion ... EBV: helicase:BBLF4 primase: BSLF1 accessory protein:BBLF2/3 Amenamevir (ASP2151) Pritelivir (BAY 57-1293, AIC316) BILS 22 BS ...
... core antigen of hepatitis B Bunyaviridae nonstructural S proteins Viral structural protein Viral+Nonstructural+Proteins at the ... In virology, a nonstructural protein is a protein encoded by a virus but that is not part of the viral particle. They typically ... Viral nonstructural proteins, All stub articles, Protein stubs). ... Influenza non-structural protein NS1 influenza protein HBcAg, ... include the various enzymes and transcription factors the virus uses to replicate itself, such as a viral protease (3CL/nsp5, ...
"Viral Nonstructural Proteins" by people in this website by year, and whether "Viral Nonstructural Proteins" was a major or ... Viral Nonstructural Proteins NS2*Viral Nonstructural Proteins NS2. Viral Nonstructural Proteins NS1*Viral Nonstructural ... "Viral Nonstructural Proteins" by people in Profiles.. * SIRT5 is a proviral factor that interacts with SARS-CoV-2 Nsp14 protein ... "Viral Nonstructural Proteins" is a descriptor in the National Library of Medicines controlled vocabulary thesaurus, MeSH ( ...
Host cyclophilins (Cyps) have been implicated in viral evasion of host antiviral responses, although the mechanisms are still ... Here, we show that hepatitis C virus (HCV) co-opts the host protein CypA to aid evasion … ... Counteracting innate immunity is essential for successful viral replication. ... Viral Nonstructural Proteins * EIF2AK2 protein, human * eIF-2 Kinase * NS-5 protein, hepatitis C virus ...
VP2, viral protein 2; NS, nonstructural. †Samples originally sent to HUSLAB (Helsinki, Finland) for bacterial diagnosis were ... Viral. 3.2 × 104. 89/F. Norovirus. Norovirus. 2013 Apr 23. VP2, 2786-4495, 1.36. ... Viral. 3.6 × 103. 89/F. Norovirus. 0. 2013 Apr 20. Partial NS, 16-1080, 1.13. ... Samples collected for bacterial and viral testing that were subsequently positive for bufavirus DNA* ...
Viral Nonstructural Proteins ...
... and six nonstructural proteins (NSP1 to NSP6). Although specific functions have been ascribed to each of the 12 viral proteins ... Reverse Genetics System Demonstrates that Rotavirus Nonstructural Protein NSP6 Is Not Essential for Viral Replication in Cell ... In this study, we demonstrated that the NSP6 protein is not essential for viral replication in cell culture by using a recently ... Segment 11 of the rotavirus genome encodes two nonstructural proteins, NSP5 and NSP6. The NSP6 ORF is present in the vast ...
Role of viral core and NS5A proteins. Gut. 53:1665-1672. 2004. View Article : Google Scholar : PubMed/NCBI ... HCV nonstructural 5A (NS5A) encodes a 447 amino acid phosphoprotein (2). This protein serves as a transcriptional activator of ... Quan M, Liu S, Zhou L, Feng S, Zhang Y and Cheng J: Hepatitis C virus nonstructural 5A protein inhibits the starvation‑induced ... NS5A, nonstructural protein 5A; EBSS, Earles Balanced Salt Solution; 7-AAD, 7-aminoactinomycin D; CQ, chloroquine; 3-MA, 3- ...
Viral Nonstructural Proteins. *Transcription. *Gene Regulatory Networks. *DNA Methylation. *Promoter Regions. Tag cloud ... protein binding - protein complex - protein complex binding - protein domain specific binding - protein homodimerization ... RING finger protein 38 induces gastric cancer cell growth by decreasing the stability of the protein tyrosine phosphatase SHP-1 ... proteins. Conversely, crocin increased the pro-apoptotic (BAX) protein, which was correlated with the induction of apoptosis ...
Reovirus Nonstructural Protein σNS Recruits Viral RNA to Replication Organelles. mBio. 2021 Aug 31;12(4):e0140821. ... Parvovirus nonstructural protein 2 interacts with chromatin-regulating cellular proteins. PLoS Pathog. 2022 Apr 8;18(4): ... 2021). The multi-functional reovirus σ3 protein is a virulence factor that suppresses stress granule formation and is ... E-Protein Inhibition in ILC2 Development Shapes the Function of Mature ILC2s during Allergic Airway Inflammation. J Immunol. ...
... a nonstructural protein encoded by HCV. Daclatasvir binds to the N-terminus of NS5A and inhibits both viral RNA replication and ... DAKLINZA (daclatasvir) is an inhibitor of HCV nonstructural protein 5A (NS5A). The chemical name for drug substance daclatasvir ... Daclatasvir is highly protein bound to plasma proteins and is unlikely to be removed by dialysis. ... With multiple dosing, protein binding of daclatasvir in HCV-infected subjects was approximately 99% and independent of dose at ...
NP1 is also nonstructural and is a highly conserved protein of unknown function. The capsid proteins are viral protein 1 (VP1) ... NP1 is also nonstructural and is a highly conserved protein of unknown function. The capsid proteins are viral protein 1 (VP1) ... Nonstructural protein 1 (NS1) is a DNA-binding protein involved in gene transcription. ... Nonstructural protein 1 (NS1) is a DNA-binding protein involved in gene transcription. ...
... codes for the nonstructural proteins responsible for viral replication. ORF-2 contains genes encoding the capsid. The function ... An early viral response predicts the virological response to ribavirin in hepatitis E virus organ transplant patients. ... Ribavirin therapy inhibits viral replication on patients with chronic hepatitis e virus infection. Gastroenterology. 2010 Nov. ...
This inhibitory effect has been associated with two viral non-structural proteins, NS3A and N^pro. For instance, the dsRNA- ... thus inhibiting the production of IFN-alpha and decreasing the anti-viral cellular response (Fiebach et al., 2011). Also, N^pro ... and post-translational processing of the polyprotein by cellular and viral proteases (Rice, 1996). Prophylactic vaccination ...
Choi et al. SFTSV nonstructural protein activates TPL2 signalling pathway for viral immunopathogenesis. 2019 Nature ... Herpesviral protein targets a cellular WD repeat endosomal protein to downregulate T lymphocyte receptor expression. 2002 ... Researchers use viral strategies to improve level, duration of protection provided by COVID-19 mRNA vaccine The improved mRNA ... Rubicon autophagic protein is a feedback inhibitor of CARD9-mediated host innate immunity. 2012 Cell Host & Microbe 11:277. ...
In addition, these animals did not develop an antibody response against viral nonstructural proteins indicating sterile ... and did not develop antibodies against viral nonstructural (NS) proteins, suggesting that complete protection from infection ... Citation: CHINSANGARAM, J., MORAES, M.P., KOSTER, M.J., GRUBMAN, M.J. A NOVEL STRATEGY TO CONTROL INFECTIOUS VIRAL DISEASES: ... Title: A NOVEL STRATEGY TO CONTROL INFECTIOUS VIRAL DISEASES: ADENOVIRUS CONTAINING INTERFERON ALPHA PROTECTS SWINE FROM FOOT- ...
... matrix proteins 1 and 2; NS1: non-structural protein 1; NEP: nuclear export protein; vRNA: viral ribonucleic acid (genome). See ... matrix proteins 1 and 2; NS1: non-structural protein 1; NEP: nuclear export protein; vRNA: viral ribonucleic acid (genome). See ... The viral polymerase (made up of viral proteins PB2, PB1, and PA), is an enzyme complex which makes new copies of viral RNA ( ... but there is also room for it to take up other viral proteins such as the nuclear export protein (NEP) and non-structural ...
Conserved Protein Domain Family Novirhabdo_Nv, This family consists of several viral hemorrhagic septicemia virus non-virion ( ... This family consists of several viral hemorrhagic septicemia virus non-virion (Nv) proteins. The NV protein is a nonstructural ... Q1AES6 1 MATQPALSTTSFSPLVLREMITHRLKFDPSNYLNCDLDRSDISPVDFFETTLPRILDDLRASTRLPHLHVLDMRISLLER 80 Viral hemorrhagic sep... Q1AEQ5 1 ... Q1AES6 81 THYMFRNVPSSPATTGRLTDPELVIISHAEVGLLTRGSGLTS 122 Viral hemorrhagic septicemia virus Q1AEQ5 81 THYMFRNIPSSPAITGRRSDPELII ...
These encoded sequences for the non-structural protein NSP3 and some parts of the viral spike. ... These encoded sequences for the non-structural protein NSP3 and some parts of the viral spike. ... Spike Protein, Structural Protein, T-Cell, Transcription, Translation, Vaccine, Viral Vector, Virus ... A set of viral vectors was thus generated, all of which contained SARS-CoV-2 coding sequences for the spike S1 subunit, the NTD ...
... non-structureal protein;NSP),但市售不活化疫苗為純化的病毒,不含或只含極微量的某些NSP,因此,自然感染 ... Non-structural proteins (NSP) are produced during viral replication. The inactivated vaccines consist of purified viral ... Expression of poliovirus nonstructural proteins in escherichia coli cells. Iss. Aug., 5:15932-15937.. Lama, J., Guinea, R., ... Immunogenicity of non-structural proteins of food-and-mouth
Non-human primates (NHPs) can sustain viral replication in relevant cell types and develop a robust immune response, but they ... A potential role for the nonstructural viral protein NS1 and complement. J. Infect. Dis. 2006, 193, 1078-1088. [Google Scholar ... Tropism of dengue virus in mice and humans defined by viral nonstructural protein 3-specific immunostaining. Am. J. Trop. Med. ... A single amino acid in nonstructural protein NS4B confers virulence to dengue virus in AG129 mice through enhancement of viral ...
FHV-1-infected cells and decreased expression of the protein within infected cells, compared with control samples. Treatment ... The knockdown of glycoprotein D mRNA resulted in reduced glycoprotein D protein production, as evidenced by 27% and 43% ... Rotavirus nonstructural protein NSP3 is not required for viral protein synthesis. J Virol 2006;80:9031-9038. ... Rotavirus nonstructural protein NSP3 is not required for viral protein synthesis. J Virol 2006;80:9031-9038. ...
... viral replication, platelet formation and a role in mitosis. The molecular basis of these activities of PI3KC2α is poorly ... Kaposis sarcoma-associated herpesvirus nonstructural membrane protein pK15 recruits the class II phosphatidylinositol 3-kinase ... viral infection21,22, diabetes29 or cancer1,14. Finally, we provide a structural basis for the scaffolding function of PI3KC2α ... The identified homologs share functional features by serving as scaffolds for protein-protein interactions. c, The HBD targets ...
... which are cleaved to the main protease Mpro and nonstructural proteins (nsps). Mpro is involved in the producing of nsps. Nsps ... Due to lacking Boc group, 14b could not cross the cellular membrane to inhibit viral replication ... Further the binding of 13a with plasma proteins was reported to decrease to 97% as compared to 11r which showed 99% binding ... To increase solubility of the inhibitor and reduce its binding to plasma proteins, the authors replaced the hydrophobic ...
... and ASTRAL compendium for protein structure and sequence analysis ... Class: viral protein. Keywords: rotavirus enterotoxin, non ... structural protein, nsp4, pentameric coiled coil, virulence, viral protein. Deposited on 2010-04-12, released 2011-05-25. The ... Compound: Non-structural glycoprotein 4. Species: Human rotavirus G4 [TaxId:10960]. Gene: G10. Database cross-references and ... Compound: Non-structural glycoprotein 4. Species: Human rotavirus G4 [TaxId:10960]. Gene: G10. Database cross-references and ...
Finally, a summary of the immune biomarkers that have been reported for dengue and Zika viral infections are discussed which ... As the pathogenesis of viral illnesses is affected by host immune responses, various immune modulators have been proposed as ... As the pathogenesis of viral illnesses is affected by host immune responses, various immune modulators have been proposed as ... may be useful indicators for future anti-viral targets or predictors for disease severity. Together, this information appraises ...
The 5 cap open reading frame encodes a variety of non-structural proteins. Non-structural proteins are involved in the ... 32 For viral infectivity, host cell proteases affect the S protein cleavage is crucial. TMPRSS2 can activate the spike protein ... proteins. Structural proteins are all encoded by the 3 terminus of the viral genome. They are essential for virus-cell ... which is mainly associated with the inhibition of viral replication, viral protein synthesis, gene expression, and nucleic acid ...
During influenza A virus infection, this function is performed by viral non-structural protein 1 (NS1). The aim of this study ... Its activation leads to the production of interferons: a group of cytokines important in overcoming viral infection. In order ...
... nonstructural protein 3A plays important roles in virus replication, virulence, and host range. In other picornaviruses, ... The viral genome encodes four structural capsid proteins (VP1 to VP4) and seven nonstructural (NS) proteins, the leader Lb/ab ... Specific interaction between human parechovirus nonstructural 2A protein and viral RNA. J. Biol. Chem. 279:37822-37831. ... A protein linkage map of the P2 nonstructural proteins of poliovirus. J. Virol. 72:1297-1307. ...
... of Texas MD Anderson Cancer Center in Houston identified 437 human proteins as the high-confidence interacting proteins - with ... including 16 non-structural proteins, 4 structural proteins and 9 accessory factors. Furthermore, stable viral gene expression ... Our systemic study of the SARS-CoV-2 protein-protein interaction network provides useful data on viral gene/protein functions ... High-confidence interacting proteins. In short, from a total of 437 high-confidence interacting proteins that bind to one or ...

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