RESUMO
In the Kyasanur Forest disease area two species of wild monkeys, Presbytis entellus and Macaca radiata, succumb to the natural infection with Kyasanur Forest disease (KFD) virus (family Flaviviridae). Between October 1964 and September 1973, 1046 monkeys (860 P. entellus and 186 M. radiata) died. Of these, KFD virus was isolated from 118 P. entellus and 13 M. radiata. Maximum mortality of monkeys was reported during December through May coinciding with the season of activity of immature stages of Haemaphysalis ticks, incriminated vectors of KFD. The epizootic showed an initial spread of the disease to the areas contiguous with the original focus of infection. This was followed by the recognition of epizootics and epidemics in three new foci, removed from the original focus, by the end of 1973. It was also observed that, in certain localities in the original focus, KFD virus activity persisted over several years.
Assuntos
Surtos de Doenças/veterinária , Doença da Floresta de Kyasanur/veterinária , Doenças dos Macacos/mortalidade , Animais , Cercopithecidae , Índia , Doença da Floresta de Kyasanur/mortalidade , Doença da Floresta de Kyasanur/transmissão , Macaca radiata , Doenças dos Macacos/transmissão , Estações do AnoRESUMO
Hepatitis A is highly endemic in India. The surveillance reports for the disease from this region are primarily based on the demonstration of hepatitis A virus (HAV) specific serum IgM and IgG antibodies. The present study was conducted to assess the presence and duration of fecal shedding of HAV in patients with hepatitis A and in an experimentally infected rhesus monkey. Nested reverse transcription polymerase chain reaction (RT-PCR) was applied to fecal specimens from 67 sporadic cases of hepatitis A. Recent infection with HAV in these cases was evidenced by the presence of serum anti-HAV IgM. Fecal HAV RNA positivity was observed in nearly 40% patients. The proportion of HAV RNA positivity in fecal specimens obtained within the first week (36.58%) was not different from those collected in 2-12 weeks post onset (42.42%) (P>0.05). A significant number of HAV RNA positive stool specimens showed presence of full virus particles by immune electron microscopy (IEM). Extended fecal shedding of HAV could be a major contributory factor for high circulation of virus thereby maintaining hyperendemicity of the disease. One of the IEM positive samples was inoculated into an anti-HAV negative rhesus monkey. Serum alanine amino transferase levels of the monkey remained within the normal limits. However, HAV RNA positivity in the feces was noted from 3 to 50 days post inoculation. The monkey seroconverted to anti-HAV IgM on day 31. This study records prolonged excretion of HAV in humans as well as in experimentally infected rhesus monkey.