An enterovirus infection of swine clinically indistinguishable from FOOT-AND-MOUTH DISEASE, vesicular stomatitis, and VESICULAR EXANTHEMA OF SWINE. It is caused by a strain of HUMAN ENTEROVIRUS B.
Species of ENTEROVIRUS causing mild to severe neurological diseases among pigs especially in Eastern Europe. Mild strains are also present in Canada, U.S., and Australia. Specific species include Porcine enterovirus A and Porcine enterovirus B.
A species of ENTEROVIRUS infecting humans and containing 36 serotypes. It is comprised of all the echoviruses and a few coxsackieviruses, including all of those previously named coxsackievirus B.
A calicivirus infection of swine characterized by hydropic degeneration of the oral and cutaneous epithelia.
Enterovirus Infections are acute viral illnesses caused by various Enterovirus serotypes, primarily transmitted through the fecal-oral route, manifesting as a wide range of clinical symptoms, from asymptomatic or mild self-limiting fever to severe and potentially life-threatening conditions, such as meningitis, encephalitis, myocarditis, and neonatal sepsis-like illness, depending on the age, immune status, and serotype of the infected individual.
Any of various animals that constitute the family Suidae and comprise stout-bodied, short-legged omnivorous mammals with thick skin, usually covered with coarse bristles, a rather long mobile snout, and small tail. Included are the genera Babyrousa, Phacochoerus (wart hogs), and Sus, the latter containing the domestic pig (see SUS SCROFA).
A genus of the family PICORNAVIRIDAE whose members preferentially inhabit the intestinal tract of a variety of hosts. The genus contains many species. Newly described members of human enteroviruses are assigned continuous numbers with the species designated "human enterovirus".
The type species of the genus VESIVIRUS infecting pigs. The resulting infection is an acute febrile disease which is clinically indistinguishable from FOOT AND MOUTH DISEASE. Transmission is by contaminated food.
A family of small RNA viruses comprising some important pathogens of humans and animals. Transmission usually occurs mechanically. There are nine genera: APHTHOVIRUS; CARDIOVIRUS; ENTEROVIRUS; ERBOVIRUS; HEPATOVIRUS; KOBUVIRUS; PARECHOVIRUS; RHINOVIRUS; and TESCHOVIRUS.
The type species of APHTHOVIRUS, causing FOOT-AND-MOUTH DISEASE in cloven-hoofed animals. Several different serotypes exist.
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.
A genus of the family POXVIRIDAE, subfamily CHORDOPOXVIRINAE, which infect ungulates and may infect humans. ORF VIRUS is the type species.
The measurement of infection-blocking titer of ANTISERA by testing a series of dilutions for a given virus-antiserum interaction end-point, which is generally the dilution at which tissue cultures inoculated with the serum-virus mixtures demonstrate cytopathology (CPE) or the dilution at which 50% of test animals injected with serum-virus mixtures show infectivity (ID50) or die (LD50).
Substances elaborated by viruses that have antigenic activity.
Immunoglobulins produced in response to VIRAL ANTIGENS.

Identification of neutralizing epitopes on a European strain of swine vesicular disease virus. (1/32)

Six neutralizing monoclonal antibodies (MAbs) were used to isolate MAb neutralization-resistant (MAR) mutants from a recent European strain of swine vesicular disease virus (SVDV), ITL/9/93. Sequencing of MAR mutants identified two epitopes located at positions analogous to sites 2A (VP2) and 3B (VP3) on poliovirus (PV) which have been previously identified on a Japanese strain of SVDV. A third epitope near to the C terminus of VP1, not previously recognized on SVDV, was tentatively identified in a region analogous to site 1 of PV. A fourth epitope, located in the C-terminal region of VP3, has never before been recognized as a site of neutralization on picornaviruses. All four epitopes were predicted to be surface-exposed.  (+info)

Molecular evolution of swine vesicular disease virus. (2/32)

Phylogenetic analysis was used to examine the evolutionary relationships within a group of coxsackie B viruses that contained representatives of the major serotypes of this group and 45 isolates of swine vesicular disease virus (SVDV) from Asia and Europe. Separate analyses of sequence data from two regions of the viral genomes encoding the VP1 and 3BC genes both revealed that the SVDV belonged to a single monophyletic group which could be clearly distinguished from all other sampled coxsackieviruses. Regression analysis revealed that within the SVDV clade at least 80% of the synonymous variation in evolutionary divergence between isolates was explained by time, indicating the existence of an approximate molecular clock. Calibration of this clock according to synonymous substitutions per year indicated the date of occurrence of a common ancestor for the SVDV clade to be between 1945 and 1965.  (+info)

Immune recognition of swine vesicular disease virus structural proteins: novel antigenic regions that are not exposed in the capsid. (3/32)

Swine vesicular disease virus (SVDV) is an enterovirus of the Picornaviridae family that belongs to the coxsackievirus B group. A number of antigenic sites have been identified in SVDV by analysis of neutralizing monoclonal antibody-resistant mutants and shown to be exposed on the surface of the capsid. In this paper we have identified seven new immunodominant antigenic regions in SVDV capsid proteins by a peptide scanning method, using a panel of sera from infected pigs. When these antigenic regions were located in the capsid by using a computer-generated three-dimensional model of the virion, one was readily exposed on the surface of the virus and the remaining sites were located facing the inner side of the capsid shell, at subunit contacts, or in the interior of the subunit structure.  (+info)

The coxsackie-adenovirus receptor (CAR) is used by reference strains and clinical isolates representing all six serotypes of coxsackievirus group B and by swine vesicular disease virus. (4/32)

Group B coxsackieviruses are etiologically linked to many human diseases, and cell surface receptors are postulated to play an important role in mediating their pathogenesis. The coxsackievirus adenovirus receptor (CAR) has been shown to function as a receptor for selected strains of coxsackievirus group B (CVB) serotypes 3, 4, and 5 and is postulated to serve as a receptor for all six serotypes. In this study, we demonstrate that CAR can serve as a receptor for laboratory reference strains and clinical isolates of all six CVB serotypes. Infection of CHO cells expressing human CAR results in a 1000-fold increase in CVB progeny virus titer compared to mock transfected cells. CAR was shown to be a functional receptor for swine vesicular disease virus (SVDV), as CHO-CAR cells but not CHO mock transfected controls were susceptible to SVDV infection, produced progeny SVDV, and developed cytopathic effects. Moreover, SVDV infection could be specifically blocked by monoclonal antibody to CAR (RmcB). SVDV infection of HeLa cells was also inhibited by an anti-CD55 MAb, suggesting that this virus, like some CVB, may interact with CD55 (decay accelerating factor) in addition to CAR. Finally, pretreatment of CVB or SVDV with soluble CAR effectively blocks virus infection of HeLa cell monolayers.  (+info)

Construction of a full-length infectious cDNA clone of swine vesicular disease virus strain NET/1/92 and analysis of new antigenic variants derived from it. (5/32)

The Dutch swine vesicular disease virus (SVDV) isolate NET/1/92 was one of the first isolates belonging to a new SVDV antigenic group. This strain was completely sequenced and was shown to have 93% similarity with the UKG/27/72 isolate. To enable antigenicity, replication, maturation and pathogenicity studies of NET/1/92, an infectious full-length cDNA clone, designated pSVD146, was prepared. The in vitro and in vivo biological properties of the virus derived from pSVD146 were studied by analysing antigenicity, plaque morphology, growth curves and virulence in pigs. The epitopes of newly prepared monoclonal antibodies were roughly mapped by fusion-PCR. Fine mapping of epitopes at the amino acid level was achieved by introducing single amino acid mutations in pSVD146. Two new amino acids important in epitope formation were located in VP1; one was mapped in the C-terminal end and the second is thought to be located in the H-I loop. Growth curve and plaque sizes in vitro were similar between virus derived from pSVD146 and the parent wild-type virus. In virulence studies in pigs, the lesions score, neutralization titres and the seroconversion rates were comparable between virus derived from pSVD146 and the parent strain. Since virus derived from pSVD146 had the same biological properties as the parent strain NET/1/92, the full-length infectious cDNA clone pSVD146 will be very useful in studies of the antigenicity, virulence, pathogenesis, maturation and replication of SVDV.  (+info)

The N-terminal region of the VP1 protein of swine vesicular disease virus contains a neutralization site that arises upon cell attachment and is involved in viral entry. (6/32)

The N-terminal region of VP1 of swine vesicular disease virus (SVDV) is highly antigenic in swine, despite its internal location in the capsid. Here we show that antibodies to this region can block infection and that allowing the virus to attach to cells increases this blockage significantly. The results indicate that upon binding to the cell, SVDV capsid undergoes a conformational change that is temperature independent and that exposes the N terminus of VP1. This process makes this region accessible to antibodies which block virus entry.  (+info)

Persistent infection is a rare sequel following infection of pigs with swine vesicular disease virus. (7/32)

Nine isolates from pigs persistently infected with a recent Italian isolate of swine vesicular disease (SVD) virus, ITL/9/93, were collected sequentially over 121 days and were characterized antigenically and biochemically. There was an accumulation of amino acid (aa) substitutions in the capsid proteins throughout the carrier state that could be correlated with alterations in antigenicity in virus isolates collected late stage in infection. The aa substitutions detected mainly occurred in VPI and antigenic changes were detected in late isolates both at antigenic site 1, resulting in loss of binding of Mab 4GO7, and at a closely located site which has not yet been named, recognized by Mab C29. In further experiments groups of pigs were exposed to a range of SVD viruses, but no virus was isolated beyond 16 days post infection (dpi) nor viral RNA detected beyond 42 dpi. Attempts to transfer infection to sentinel pigs introduced some time after initial infection of the original pigs were largely unsuccessful. The carrier state was established in only one out of five experimental infections of pigs with SVD virus and can therefore be considered a rare sequel toinfection with SVD virus and is of limited significance in the epidemiology of the disease.  (+info)

Crystal structure of Swine vesicular disease virus and implications for host adaptation. (8/32)

Swine vesicular disease virus (SVDV) is an Enterovirus of the family Picornaviridae that causes symptoms indistinguishable from those of foot-and-mouth disease virus. Phylogenetic studies suggest that it is a recently evolved genetic sublineage of the important human pathogen coxsackievirus B5 (CBV5), and in agreement with this, it has been shown to utilize the coxsackie and adenovirus receptor (CAR) for cell entry. The 3.0-A crystal structure of strain UK/27/72 SVDV (highly virulent) reveals the expected similarity in core structure to those of other picornaviruses, showing most similarity to the closest available structure to CBV5, that of coxsackievirus B3 (CBV3). Features that help to cement together and rigidify the protein subunits are extended in this virus, perhaps explaining its extreme tolerance of environmental factors. Using the large number of capsid sequences available for both SVDV and CBV5, we have mapped the amino acid substitutions that may have occurred during the supposed adaptation of SVDV to a new host onto the structure of SVDV and a model of the SVDV/CAR complex generated by reference to the cryo-electron microscopy-visualized complex of CBV3 and CAR. The changes fall into three clusters as follows: one lines the fivefold pore, a second maps to the CAR-binding site and partially overlaps the site for decay accelerating factor (DAF) to bind to echovirus 7 (ECHO7), and the third lies close to the fivefold axis, where the low-density lipoprotein receptor binds to the minor group of rhinoviruses. Later changes in SVDV (post-1971) map to the first two clusters and may, by optimizing recognition of a pig CAR and/or DAF homologue, have improved the adaptation of the virus to pigs.  (+info)

Swine Vesicular Disease (SVD) is a contagious viral disease affecting pigs, caused by the Swine Vesicular Disease Virus (SVDV), which is closely related to human, bovine, and enteric cytopathic types of Coxsackie B virus. The disease is characterized by the sudden onset of fever, lameness, and the development of vesicles or blisters on the snout, mouth, and hooves of infected animals. It can result in significant economic losses to the swine industry due to reduced growth rates, decreased feed conversion efficiency, and trade restrictions on affected herds.

SVD is primarily spread through the ingestion of contaminated food or water, direct contact with infected pigs, or indirectly through fomites such as vehicles, equipment, and clothing. The virus can also be transmitted via aerosolized particles, making it highly contagious in susceptible populations.

While SVD is not considered a significant threat to human health, its clinical signs are similar to those of Foot-and-Mouth Disease (FMD), which can have severe consequences for both animal and human health. As such, SVD is often reported to the World Organization for Animal Health (OIE) and is subject to strict control measures in affected countries.

Enteroviruses, Porcine are a group of viruses that belong to the family Picornaviridae and include several species that can infect pigs. These viruses are typically associated with respiratory and gastrointestinal illnesses in pigs, although some strains have been linked to reproductive problems and neurological disorders as well.

Some of the enteroviruses that can infect pigs include Porcine Enterovirus A (PEVA), Porcine Enterovirus B (PEVB), Porcine Enterovirus C (PEVC), Porcine Enterovirus D (PEVD), and Porcine Enterovirus E (PEVE). These viruses are usually spread through the fecal-oral route, and they can cause a range of clinical signs depending on the specific virus and the age and health status of the infected pig.

In general, porcine enteroviruses are not considered to be a significant threat to human health, although there have been rare reports of transmission from pigs to humans in cases where proper biosecurity measures were not followed. However, further research is needed to fully understand the potential risks associated with these viruses and their impact on both animal and human health.

Enterovirus B, Human (HEVB) is a type of enterovirus that infects humans. Enteroviruses are small viruses that belong to the Picornaviridae family and are named after the Greek word "pico" meaning small. They are further classified into several species, including Human Enterovirus B (HEV-B).

HEVB includes several serotypes, such as Coxsackievirus A9, A16, and B types, and Echoviruses. These viruses are typically transmitted through the fecal-oral route or respiratory droplets and can cause a range of illnesses, from mild symptoms like fever, rash, and sore throat to more severe diseases such as meningitis, myocarditis, and paralysis.

HEVB infections are common worldwide, and people of all ages can be affected. However, young children and individuals with weakened immune systems are at higher risk for severe illness. Prevention measures include good hygiene practices, such as washing hands frequently and avoiding close contact with sick individuals. There is no specific treatment for HEVB infections, and most cases resolve on their own within a few days to a week. However, hospitalization may be necessary for severe cases.

Vesicular Exanthema of Swine (VES) is a viral disease that affects pigs, characterized by the formation of blisters or vesicles on the skin and mucous membranes. The causative agent is an RNA virus known as Vesicular Exanthema of Swine Virus (VESV), which belongs to the family Caliciviridae.

The disease is primarily transmitted through direct contact with infected pigs or contaminated fomites, and it can also be spread through the ingestion of contaminated food or water. The incubation period for VES ranges from 2-6 days, after which affected animals develop fever, lethargy, loss of appetite, and lameness.

The most notable clinical sign of VES is the development of vesicles on the snout, coronary bands, and hooves of infected pigs. These lesions can rupture and form crusts or scabs, leading to secondary bacterial infections. In severe cases, lameness can progress to the point where affected animals are unable to stand or walk.

VES is a highly contagious disease that can cause significant economic losses for pig farmers. While it does not pose a direct threat to human health, VESV can cause a mild self-limiting illness in humans who come into contact with infected pigs or their secretions.

It's worth noting that Vesicular Exanthema of Swine has been eradicated from the United States since 1952, and it is now considered a foreign animal disease. However, it remains a significant concern for the global swine industry due to its potential to cause significant economic losses.

Enterovirus infections are viral illnesses caused by enteroviruses, which are a type of picornavirus. These viruses commonly infect the gastrointestinal tract and can cause a variety of symptoms depending on the specific type of enterovirus and the age and overall health of the infected individual.

There are over 100 different types of enteroviruses, including polioviruses, coxsackieviruses, echoviruses, and newer enteroviruses such as EV-D68 and EV-A71. Some enterovirus infections may be asymptomatic or cause only mild symptoms, while others can lead to more severe illnesses.

Common symptoms of enterovirus infections include fever, sore throat, runny nose, cough, muscle aches, and skin rashes. In some cases, enteroviruses can cause more serious complications such as meningitis (inflammation of the membranes surrounding the brain and spinal cord), encephalitis (inflammation of the brain), myocarditis (inflammation of the heart muscle), and paralysis.

Enterovirus infections are typically spread through close contact with an infected person, such as through respiratory droplets or fecal-oral transmission. They can also be spread through contaminated surfaces or objects. Preventive measures include good hygiene practices, such as washing hands frequently and avoiding close contact with sick individuals.

There are no specific antiviral treatments for enterovirus infections, and most cases resolve on their own within a few days to a week. However, severe cases may require hospitalization and supportive care, such as fluids and medication to manage symptoms. Prevention efforts include vaccination against poliovirus and surveillance for emerging enteroviruses.

"Swine" is a common term used to refer to even-toed ungulates of the family Suidae, including domestic pigs and wild boars. However, in a medical context, "swine" often appears in the phrase "swine flu," which is a strain of influenza virus that typically infects pigs but can also cause illness in humans. The 2009 H1N1 pandemic was caused by a new strain of swine-origin influenza A virus, which was commonly referred to as "swine flu." It's important to note that this virus is not transmitted through eating cooked pork products; it spreads from person to person, mainly through respiratory droplets produced when an infected person coughs or sneezes.

An enterovirus is a type of virus that primarily infects the gastrointestinal tract. There are over 100 different types of enteroviruses, including polioviruses, coxsackieviruses, echoviruses, and newer enteroviruses such as EV-D68 and EV-A71. These viruses are typically spread through close contact with an infected person, or by consuming food or water contaminated with the virus.

While many people infected with enteroviruses may not experience any symptoms, some may develop mild to severe illnesses such as hand, foot and mouth disease, herpangina, meningitis, encephalitis, myocarditis, and paralysis (in case of poliovirus). Infection can occur in people of all ages, but young children are more susceptible to infection and severe illness.

Prevention measures include practicing good hygiene, such as washing hands frequently with soap and water, avoiding close contact with sick individuals, and not sharing food or drinks with someone who is ill. There are also vaccines available to prevent poliovirus infection.

Vesicular exanthema of swine (VES) is a viral disease that affects pigs, characterized by the formation of blisters or vesicles on the skin and mucous membranes. The causative agent of VES is a member of the Caliciviridae family, specifically the vesicular exanthema of swine virus (VESV).

The disease is highly contagious and can spread rapidly in pig populations through direct contact with infected animals or contaminated fomites. The incubation period for VES is typically 2-6 days, after which affected pigs may develop fever, lethargy, loss of appetite, and lameness. Within a few days, small fluid-filled vesicles appear on the snout, lips, ears, and coronary bands of the hooves. These vesicles can rupture, leading to the formation of raw, painful erosions that may become secondarily infected with bacteria.

While VES is not a direct threat to human health, it can cause significant economic losses in the swine industry due to decreased growth rates, reduced feed conversion, and increased mortality in affected animals. Additionally, the clinical signs of VES are similar to those of other vesicular diseases, such as foot-and-mouth disease (FMD), which can lead to costly trade restrictions and quarantines.

Historically, VES was a significant problem in the United States swine industry, but extensive vaccination programs and eradication efforts have largely eliminated the disease from domestic pig populations. However, VESV continues to circulate in wild pig populations and remains a potential threat to the swine industry.

Picornaviridae is a family of small, single-stranded RNA viruses that are non-enveloped and have an icosahedral symmetry. The name "picornavirus" is derived from "pico," meaning small, and "RNA." These viruses are responsible for a variety of human and animal diseases, including the common cold, poliomyelitis, hepatitis A, hand-foot-and-mouth disease, and myocarditis. The genome of picornaviruses is around 7.5 to 8.5 kilobases in length and encodes a single polyprotein that is processed into structural and nonstructural proteins by viral proteases. Picornaviridae includes several important genera, such as Enterovirus, Rhinovirus, Hepatovirus, Cardiovirus, Aphthovirus, and Erbovirus.

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.

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.

Parapoxvirus is a genus of viruses in the Poxviridae family, which includes several species that can infect mammals such as sheep, goats, and humans. These viruses are characterized by causing localized, papular, and pustular skin lesions in their hosts. The most common species that infect humans are Orf virus and Parapoxvirus ovis (also known as contagious ecthyma virus or pseudocowpox virus).

Human infections with parapoxviruses typically occur through direct contact with infected animals or their products, such as wool, hair, or milk. The incubation period for these viruses ranges from 3 to 10 days after exposure, and the infection usually manifests as a single, painful, red, and fluid-filled lesion that progresses into a scab over time.

Parapoxvirus infections are generally self-limiting and resolve within 4-6 weeks without specific treatment. However, secondary bacterial infections can occur and may require antibiotics. It is essential to prevent transmission of the virus through good hygiene practices and avoiding contact with infected animals or their products.

Neutralization tests are a type of laboratory assay used in microbiology and immunology to measure the ability of a substance, such as an antibody or antitoxin, to neutralize the activity of a toxin or infectious agent. In these tests, the substance to be tested is mixed with a known quantity of the toxin or infectious agent, and the mixture is then incubated under controlled conditions. After incubation, the mixture is tested for residual toxicity or infectivity using a variety of methods, such as cell culture assays, animal models, or biochemical assays.

The neutralization titer is then calculated based on the highest dilution of the test substance that completely neutralizes the toxin or infectious agent. Neutralization tests are commonly used in the diagnosis and evaluation of immune responses to vaccines, as well as in the detection and quantification of toxins and other harmful substances.

Examples of neutralization tests include the serum neutralization test for measles antibodies, the plaque reduction neutralization test (PRNT) for dengue virus antibodies, and the cytotoxicity neutralization assay for botulinum neurotoxins.

An antigen is any substance that can stimulate an immune response, particularly the production of antibodies. Viral antigens are antigens that are found on or produced by viruses. They can be proteins, glycoproteins, or carbohydrates present on the surface or inside the viral particle.

Viral antigens play a crucial role in the immune system's recognition and response to viral infections. When a virus infects a host cell, it may display its antigens on the surface of the infected cell. This allows the immune system to recognize and target the infected cells for destruction, thereby limiting the spread of the virus.

Viral antigens are also important targets for vaccines. Vaccines typically work by introducing a harmless form of a viral antigen to the body, which then stimulates the production of antibodies and memory T-cells that can recognize and respond quickly and effectively to future infections with the actual virus.

It's worth noting that different types of viruses have different antigens, and these antigens can vary between strains of the same virus. This is why there are often different vaccines available for different viral diseases, and why flu vaccines need to be updated every year to account for changes in the circulating influenza virus strains.

Antibodies, viral are proteins produced by the immune system in response to an infection with a virus. These antibodies are capable of recognizing and binding to specific antigens on the surface of the virus, which helps to neutralize or destroy the virus and prevent its replication. Once produced, these antibodies can provide immunity against future infections with the same virus.

Viral antibodies are typically composed of four polypeptide chains - two heavy chains and two light chains - that are held together by disulfide bonds. The binding site for the antigen is located at the tip of the Y-shaped structure, formed by the variable regions of the heavy and light chains.

There are five classes of antibodies in humans: IgA, IgD, IgE, IgG, and IgM. Each class has a different function and is distributed differently throughout the body. For example, IgG is the most common type of antibody found in the bloodstream and provides long-term immunity against viruses, while IgA is found primarily in mucous membranes and helps to protect against respiratory and gastrointestinal infections.

In addition to their role in the immune response, viral antibodies can also be used as diagnostic tools to detect the presence of a specific virus in a patient's blood or other bodily fluids.

Swine vesicular disease (SVD) is an acute, contagious viral disease of swine caused by swine vesicular disease virus, an ... Swine vesicular disease virus is a variant of coxsackievirus B5 and causes a vesicular disease in pigs clinically ... and vesicular disease in pigs caused by Seneca Valley virus (genus Senecavirus). "Technical disease card: Swine vesicular ... Swine vesicular disease was first identified in Italy in 1966. In 1971, an outbreak occurred in Hong Kong, and the disease was ...
It is generally a mild disease that was endemic in Italy until recently; it has occurred only sporadically in other countries. ... Its importance is as a differential diagnosis for foot-and-mouth disease, from which it is clinically indistinguishable. ... Swine vesicular disease is a viral vesicular disease of pigs caused by an enterovirus closely related to human coxsackie virus ...
... according to an organization that monitors swine health. ... Cases of vesicular swine disease appeared to be increasing this ... Cases of vesicular swine disease appeared to be increasing this summer, according to an organization that monitors swine health ... The vesicular disease caused by the Seneca Valley virus, also known as Senecavirus A, produces clinical signs similar to those ... The swine industry also is investigating a novel virus that could cause neurologic disease. ...
Novel Senecavirus A in Swine with Vesicular Disease, United States, July 2015 Baoqing Guo, Pablo E. Piñeyro, Christopher ... Novel Senecavirus A in Swine with Vesicular Disease, United States, July 2015. ... a 2011 Canada swine SVA isolate (11-55910-3), and 2015 Brazil swine SVA isolates (SVV-BRA-G03-2015, SVV-BRA-MG1-2015, and SVV- ... The Centers for Disease Control and Prevention (CDC) cannot attest to the accuracy of a non-federal website. ...
Swine Vesicular Disease (SVD). SVD is well recognized in Taiwan. It is characterized by vesicular lesions on the snout, teats ... Clinical Disease. The incubation period was short and appeared to be approximately 1-4 days. Only swine were affected. The ... Laboratory work-up was completed over the weekend and all other swine diseases were excluded. The FMD diagnostic kit was opened ... 6) lack of complete laboratory confirmation of vesicular diseases. Figures available to us as of June 17, 1997, indicated that ...
Swine vesicular disease virus. Contamination by food and water. Water can become a major source of contamination in both ... There are many diseases on the farm that result from contaminated skin damage. These include tail biting, ear nibbling, greasy ... can be carriers of some infectious agents and act as mechanical vectors or indirect hosts in diseases such as African swine ... Opportunist invaders are those organisms that normally on their own would not cause disease but given the opportunity by ...
Foot and Mouth Disease (FMD). Swine Vesicular Disease (SVD). Bluetongue. African Horse Sickness (AHS). ...
Categories: Swine Vesicular Disease Image Types: Photo, Illustrations, Video, Color, Black&White, PublicDomain, ... The Centers for Disease Control and Prevention (CDC) cannot attest to the accuracy of a non-federal website. ... Centers for Disease Control and Prevention. CDC twenty four seven. Saving Lives, Protecting People ...
Swine vesicular disease virus (cultures only). Vesicular stomatitis virus (cultures only). 6.2.2.2.2 Category B:. An infectious ... Classical swine fever virus (cultures only). Foot and mouth disease virus (cultures only). Goatpox virus (cultures only). Lumpy ... African swine fever virus (cultures only). Avian paramyxovirus Type 1 - Velogenic Newcastle disease virus (cultures only). ... 6.2.2.3.1 Substances which do not contain infectious substances or substances which are unlikely to cause disease in humans or ...
A notifiable disease is any disease that is required by law to be reported to government authorities. The collation of ... Swine Vesicular Disease(external link opens in a new window / tab). Pigs. Never. ... which species are affected by the disease and the last known occurrence of the disease in NI. The diseases are categorised in ... Vesicular Exanthema. Pigs (very rarely horses). Never. Vesicular Stomatitis(external link opens in a new window / tab). All. ...
Kenya is affected by diseases such as African swine fever, Newcastle disease, foot and mouth disease, and swine vesicular ... CBP agriculture specialists ensure these diseases dont enter the U.S. by thoroughly inspecting travelers belongings. ... there is high possibility a person could have contracted a disease from this jewelry and developed serious health issues." ...
China has lifted its 17-year-old trade ban on Italian pork imports, in place since 1999 over swine vesicular disease (SVD) ... Xylella fastidiosa disease could cost olive oil producing regions billions of euros over the next 50 years, according to fresh ... Women, who have more reactive immune systems than men, are more susceptible to coeliac disease, says the Italian Ministry of ...
Additionally, in Canada, reportable swine diseases include African swine fever (ASF), swine vesicular disease and ... reportable swine diseases include classical swine fever (CSF), porcine epidemic diarrhea (PED), foot-and-mouth (FMD) disease, ... Environmental swine disease surveillance. Disease surveillance plays an essential role in protecting the health and welfare of ... Swine disease outbreaks on-farm. Animal diseases are considered either "reportable" or "notifiable" on the provincial and ...
Directives 64/432/EEC and 72/461/EEC as regards certain measures relating to foot-and-mouth disease and swine vesicular disease ... Council Directive of 21 December 1982 on the notification of animal diseases within the Community ... Decision of 21 December 1982 on a financial contribution from the Community to the campaign against foot-and-mouth disease in ...
I sat through many discussions about sugar beet yields or swine vesicular disease, waiting impatiently for the football to ...
... j PP 0413-0422 FIRST APPEARANCE 0 SWINE VESICULAR DISEASE ---IN SWITZERLAND 11 PP ACSI K-6318 POHLMAN Re //FASE4 FOR $CHUNG UND ... IN0004f PP 0118-0119 VESICULAR DISEASE OF SWINE IN GREAT BRITAIN 4 PP CSO: 834412079 COMPLETED SPECIAL pusmKov" B. //ECON.- ... ADDITIONAL CASES OF FOOT AND MOUTH DISEASE FOOT AND MOUTH DISEASE INFECTIONS IN MAN *NTIS TT 76-53022 PIMENOV M. K. f ... INDUCED DEAFNESS AS OCCUPATIONAL DISEASE IN ACCORDANCE WITH SUBPARAGRAPH 26 OF THE 7TH OCCUPATIONAL DISEASE ORDINANCE 15 PP GUO ...
Whereas, in view of the development of foot-and-mouth disease and swine vesicular disease in the Community, the Community ... Directives 64/432/EEC and 72/461/EEC as regards certain measures relating to foot-and-mouth disease and swine vesicular disease ... Directives 64/432/EEC and 72/461/EEC as regards certain measures relating to foot-and-mouth disease and swine vesicular disease ... Directives 64/432/EEC and 72/461/EEC as regards certain measures relating to foot-and-mouth disease and swine vesicular disease ...
African swine fever, classical swine fever, Newcastle disease, foot-and-mouth disease and swine vesicular disease are among ... there is high possibility a person could have contracted a disease from this jewelry and developed serious health issues." ...
Notice of Availability of an Evaluation of the Classical Swine Fever, Foot-and-Mouth Disease, Swine Vesicular Disease, and ... and swine vesicular disease, and as low risk for classical swine fever. This proposed recognition is based on evaluations we ... an unlicensed Bursal Disease-Mareks Disease-Newcastle Disease Vaccine, Serotype 3, Live Mareks Disease Vector. Based on the ... We are advising the public that we are proposing to recognize Cyprus as being free of foot-and-mouth disease, rinderpest, ...
African swine fever, classical swine fever, Newcastle disease, foot-and-mouth disease and swine vesicular disease are among ... First human case of swine flu strain detected in … 1 week ago. ... is high possibility a person could have contracted a disease ...
African swine fever, classical swine fever, Newcastle disease, foot-and-mouth disease and swine vesicular disease are among ... there is high possibility a person could have contracted a disease from this jewelry and developed serious health issues." ...
... of a ban by China on imports of fresh pork from northern Italy that was imposed in 1999 over fears of swine vesicular disease. ...
The effort to understand and combat infectious diseases has, during the centuries, produced many key ad... ... Swine vesicular disease virus. Vesicular stomatitis virus (exotic): Indiana subtypes VSV-IN2, VSV-IN3 ... Centers for Disease Control and Prevention CDC is currently developing a personnel screening program and monitoring program for ... BSL-4 laboratories are for working with agents or toxins that pose a high risk of life threatening disease that may be aerosol ...
Here we investigated the role of PI4KIII in foot-and-mouth disease virus (FMDV) replication. Our results showed that, in ... Subcellular distribution of swine vesicular disease virus proteins and alterations induced in infected cells: a comparative ... Moffat K., Howell G., Knox C., Belsham G. J., Monaghan P., Ryan M. D., Wileman T. 2005; Effects of foot-and-mouth disease virus ... Knox C., Moffat K., Ali S., Ryan M., Wileman T. 2005; Foot-and-mouth disease virus replication sites form next to the nucleus ...
... vesicular stomatitis (VS), vesicular exanthema of swine (VES), and swine vesicular disease (SVD). FMD, VES, and SVD are exotic ... Swine Vesicular Disease Edit SVD is a moderately contagious disease of swine. Mice may be infected experimentally. Persons ... Vesicular exanthema of swine. Bacteriol Rev 19:6-19.. Mann, J. A., and Hutchings, G. H. 1980. Swine vesicular disease: Pathways ... Diseases of Swine Vesicular Diseases by J. A. House and C. A. House ...
ABSTRACT Foot-and-mouth disease virus (FMDV) nonstructural protein 3A plays important roles in virus replication, virulence, ... Subcellular distribution of swine vesicular disease virus proteins and alterations induced in infected cells: a comparative ... Foot-and-mouth disease, p 333-363. In Gibbs EPJ (ed), Virus diseases of food animals. Academic Press Inc., London, United ... Foot-and-mouth disease virus proteinases. In Sobrino F and Domingo E (ed), Foot and mouth disease: current perspectives. ...

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