Susceptibilidade de Biomphalaria tenagophila (d'Orbigny, 1835), de Itajubá (MG), à infecção pela cepa "LE" de Schistosoma mansoni Sambon, 1907, de Belo Horizonte, MG (Brasil)

Infecções experimentais de descendentes de Biomphalaria tenagophila de Itajubá, MG (Brasil) foram realizadas utilizando-se a conhecida cepa "LE" de Schistosoma mansoni, isolada em Belo Horizonte. Como controle, utilizou-se B. glabrata de Belo Horizonte, MG. Em conseqüência, assinalou-se, pela primeira vez, a infecção de B. tenagophila de Itajubá, à cepa de S. mansoni adaptada à B. glabrata de Belo Horizonte. Isto é, ao final do experimento, 5 (3,3%) entre os 149 exemplares sobreviventes, infectaram-se. Face ao atual surto industrial da região, com grande aporte de migrantes, foi chamada a atenção para a necessidade de medidas profiláticas, em decorrência da possibilidade de instalação de foco da doença no Sul de Minas Gerais.

Suscetibilidade de "híbridos" de Biomphalaria tenagophila à cepa LE (BH) do Schistosoma mansoni

"Híbridos" de Biomphalaria tenagophila provenientes dos cruzamentos de linhagens albinas de Belo Horizonte (BH) ou de Joinvile (SC), com melânicos de Cabo Frio (CF), do Taim (Ta) ou de Curitiba (PR), submetidos à infecção pela cepa do Schistosoma mansoni de Belo Horizonte (=LE), apresentaram os seguintes resultados: em F1, os "híbridos" TaSC, PRSC e CFTa exibiram taxas de 4,5%, 12,5% e 11,2% de suscetibilidade; em F2, todos os "híbridos" foram negativos e em F3, um exemplar albino, filho de (CFBH) ². TaBH se infectou com a LE. Dentre os controles, a B. glabrata apresentou taxas de 66,7 a 93,6% de suscetibilidade à LE e a B. tenagophila de Joinvile exibiu taxas de infecção de 17,1 e 33,3% pela cepa SJ; e os "híbridos" BHTa e BHCF, taxas de 6,0 a 53,8% também pela cepa SJ. Houve grande influência da linhagem materna nas taxas de suscetibilidade. Devido ao fato de descendentes do cruzamento de linhagens refratárias a LE (CF, Ta e BH), terem se infectado, é recomendado o uso de "híbridos" para a detecção de gens de suscetibilidade em tais linhagens. São ainda discutidas, a necessidade do uso de maior número de miracídios nos testes de infecção e a falta de relação entre a freqüência de contatos parasitas-hospedeiros e as taxas de infectividade. Considerando que estas dependem de características genéticas preexistentes na população, a cepa LE seria uma variedade genética (ou raça) distinta da cepa SJ, dotada de pouca aptidão em infectar as diversas populações de B. tenagophila, exceto a de Joinvile (SC).

Hepatitis G virus / GB virus C in Brazil. Preliminary report

Hepatitis G virus/ GB virus C is a novel flavivirus recently detected in hepatitis non A-E cases. In this study, the presence of this virus in chronic non-B, non-C hepatitis patients was evaluated using GBV-C specific PCR and this virus was detected in one out of thirteen patients. This patient has presented a severe liver failure, has lived for a long time in the Western Amazon basin and no other cause for this clinical picture was reported. The impact of the discovery of this new agent is still under evaluation throughout the world. The study of the prevalence of this virus among chronic hepatitis patients and healthy individuals (as blood donors) will furnish subside to evaluate its real pathogenicity.

GB virus C/Hepatitis G virus and other putative hepatitis non A-E viruses

The identification of the major agents causing human hepatitis (Hepatitis A, B, C, D and E Viruses) was achieved during the last 30 years. These viruses are responsible for the vast majority of human viral hepatitis cases, but there are still some cases epidemiologically related to infectious agents without any evidence of infection with known virus, designated as hepatitis non A - E. Those cases are considered to be associated with at least three different viruses: 1 - Hepatitis B Virus mutants expressing its surface antigen (HBsAg) with altered epitopes or in low quantities; 2 - Another virus probably associated with enteral transmitted non A-E hepatitis, called Hepatitis F Virus. Still more studies are necessary to better characterize this agent; 3 - Hepatitis G Virus or GB virus C, recently identified throughout the world (including Brazil) as a Flavivirus responsible for about 10% of parenteral transmitted hepatitis non A-E. Probably still other unknown viruses are responsible for human hepatitis cases without evidence of infection by any of these viruses, that could be called as non A-G hepatitis.

High prevalence of GB Virus C/Hepatitis G Virus RNA among Brazilian blood donors

The aim of this study was to investigate the presence of the Hepatitis G Virus on a population of blood donors from São Paulo, Brazil and to evaluate its association to sociodemographic variables. Two RT-PCR systems targeting the putative 5'NCR and NS3 regions were employed and the former has shown a higher sensitivity. The observed prevalence of HGV-RNA on 545 blood donors was 9.7% (CI 95% 7.4;12.5). Statistical analysis depicted an association with race/ethnicity, black and mulatto donors being more frequently infected; and also with years of education, less educated donors presenting higher prevalences. No association was observed with other sociodemographic parameters as age, gender, place of birth and of residence. DNA sequencing of nine randomly chosen isolates demonstrated the presence of genotypes 1, 2 and 3 among our population but clustering of these Brazilian isolates was not detected upon phylogenetic analysis.

Genotype distribution of the GB virus C in citizens of São Paulo City, Brazil

There has been several studies worldwide on phylogenetics and genotype distribution of the GB-virus C / Hepatitis G virus (GBV-C/HGV). However, in their great majority, those investigations were based on some epidemiologically linked group, rather than on a representative sampling of the general population. The present is a continuation of the first study in Brazil with such a population; it addresses the GBV-C/HGV phylogenetics and genotype distribution based on samples identified among more than 1,000 individuals of the city of São Paulo. For this purpose, a 728 bp fragment of the 5´non-coding region (5´NCR) of the viral genome, from 24 isolates, was sequenced and subjected to phylogenetic analysis. Genotypes 1, 2a and 2b were found at 8.3% (2/24), 50% (12/24) and 41.7% (10/24), respectively. In conclusion São Paulo displays a genotype distribution similar to the published data for other States and Regions of Brazil, endorsing the notion that types 1 and 2 would have entered the country with African and European people, respectively, since its earliest formation.

Comportamento da cepa LE de Schistosoma mansoni, após passagem em hospedeiro humano infectado acidentalmente

Uma auxiliar de laboratório infectou-se acidentalmente, com cercárias de Schistosoma mansoni, cepa LE, mantida rotineiramente em nossos laboratórios. Decorridos 5 meses, o exame parasitológico de fezes revelou 108 ovos/g . A pacientefoi tratada com oxamniquine, porém a infecção continuou ativa (6 ovos/g). Foi então obtido o isolado SSF mantido no modelo Biomphalaria glabrata - camundongo albino. Os resultados obtidos no estudo comparativo, entre o isolado SSF e a cepa LE, que lhe deu origem, mostraram que a duração do período pré-patente e o índice de infectividade em camundongos, bem como a resposta aos agentes esquistossomicidas (hycanthone, oxamniquine epraziquantel) não apresentaram diferenças estatisticamente significativas. Por outro lado, o número de miracídios obtidos dos intestinos e fígados dos camundongos infectados foi o dobro com a cepa LE, quando comparados com aquele do isolado SSF. Também a variação do peso dos animais foi bastante diferente. Concluiu-se que apenas uma passagem pelo hospedeiro humano não mudou substancialmente as características da cepa estudada.