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Contribuição ao estudo da hepatite A em primatas neotropicais
| Content Provider | Semantic Scholar |
|---|---|
| Author | Setzer, Ariela Priscila |
| Copyright Year | 2003 |
| Abstract | SETZER, A. P. Contribution to the study of hepatitis A in New World primates.[Contribuição ao estudo da hepatite A em primatas neotropicais]. 2003. 135 f. Dissertação (Mestrado em Patologia) – Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo, São Paulo, 2003. Hepatitis A virus (HAV) is a picornavirus that causes hepatitis A, a zoonotic disease. This virus has only humans and nonhumans primates as its natural hosts. Just one serotype is known, but several strains have been recognized. Those strains are divided into 7 genotypes, 3 of them being exclusively from human strains, other 3 exclusively from Old World primates strains and the genotype III that has human and primate strains. The maximum genetic difference between strains from the same genotype is 15% and the antigenic difference between all strains is almost none. This is why it is possible to use human diagnostic tests for nonhuman primates. The infection route of the HAV is fecal-oral. After the ingestion of the virus by infected food or contaminated objects, the virus replicates in the liver of the animal and reaches the intestines through the bile, being eliminated with the feces. The disease in primates and children is assymptomatic, but when present, it is unspecific and varies from mild signs to death. The diagnosis is made by serological tests or identification from the viral antigen in sera or feces at the acute phase from the disease. The presence of anti-HAV IgM shows acute or recent infection. On the other hand, anti-HAV IgG is found from the convalescent phase of the disease on, through several years. The aim of this project was to research the seroprevalence of anti-HAV antibodies in New World primates and detect the viral antigen in feces from those animals that had acute infection. Sera from 421 animals of 32 different species were tested. From these animals, 13,5% (57/421) were wild animals, 29,7% (125/421) were from the Centro de Primatologia do Rio de Janeiro (CPRJ), 4% (17/421) from breeders, 3,8% (16/421) from Departamento de Parques e Áreas Verdes (DEPAVE) and 48,9% (206/421) were zoo animals. The sera were tested, by immune-enzymatic tests, for the presence of IgM and total anti-HAV antibodies. All the sera were negative for IgM, which means that no animal had acute infection when tested. All wild animals were negative for total anti-HAV, as were the animals from DEPAVE. Four percent (5/125) from the CPRJ animals and 7,6% (17/223) from the zoos’/breeders’ animals were positive for total antiHAV, showing that a number of captive animals have already been in contact with the virus. The prevalence of anti-HAV antibodies found in this study was lower than expected, as it is known that the number of positive animals in captivity is high. The possible reasons for such low prevalence are discussed. Since humans are the major risk factor for primate infection with HAV, the lower prevalence found at the CPRJ was predictable, because this is a research center, where visitors are not allowed, so the animals have less contact with humans in there, than they do in zoos. Our results lead us to think that hepatitis A is not a disease of high risk for either wild or zoo New World primates. |
| File Format | PDF HTM / HTML |
| DOI | 10.11606/D.10.2003.tde-07062004-155248 |
| Alternate Webpage(s) | https://teses.usp.br/teses/disponiveis/10/10133/tde-07062004-155248/publico/arielasetzer.pdf |
| Alternate Webpage(s) | https://doi.org/10.11606/D.10.2003.tde-07062004-155248 |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |