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1.
Mem. Inst. Oswaldo Cruz ; 99(5): 493-498, Aug. 2004. ilus
Article in English | LILACS, SES-SP | ID: lil-386680

ABSTRACT

The bacterium Bacillus thuringiensis (Bt) produces parasporal crystals containing delta-endotoxins responsible for selective insecticidal activity on larvae. Upon ingestion, these crystals are solubilized in the midgut lumen and converted into active toxins that bind to receptors present on the microvilli causing serious damage to the epithelial columnar cells. We investigated the effect of these endotoxins on larvae of the Simulium pertinax, a common black fly in Brazil, using several concentrations during 4 h of the serovar israelensis strain IPS-82 (LFB-FIOCRUZ 584), serotype H-14 type strain of the Institute Pasteur, Paris. Light and electron microscope observations revealed, by time and endotoxin concentration, increasing damages of the larvae midgut epithelium. The most characteristic effects were midgut columnar cell vacuolization, microvilli damages, epithelium cell contents passing into the midgut lumen and finally the cell death. This article is the first report of the histopathological effects of the Bti endotoxins in the midgut of S. pertinax larvae and the data obtained may contribute to a better understanding of the mode of action of this bacterial strain used as bioinsecticide against black fly larvae.


Subject(s)
Animals , Simuliidae , Bacillus thuringiensis , Digestive System , Insecticides , Microscopy, Electron , Pest Control, Biological , Larva
2.
Mem. Inst. Oswaldo Cruz ; 96(8): 1069-1073, Nov. 2001. ilus, tab
Article in English | LILACS | ID: lil-304642

ABSTRACT

Between June 4th and June 20th1996 rotavirus, adenovirus, and astrovirus (HAstrV) were investigated in fecal samples from 27 children under three years old with acute diarrhea, attending the Bertha Lutz day care center, in Rio de Janeiro. All fecal samples were analyzed by polyacrylamide gel electrophoresis (PAGE), reverse transcriptase polymerase chain reaction (RT-PCR), enzyme immunoassays (EIA), and electron microscopy (EM). Nine of them (33 percent) showed positive results for HAstrV by at least one of the employed methodologies. Eight were positive by RT-PCR and EIA, and six by EM. All positive samples were inoculated onto HT-29 (human colon adenocarcinoma) cultured cells for HAstrV isolation and seven were positive after three passages. The sequencing analysis of eight RT-PCR products (449 bp) from gene that codifies VP2 protein, showed a total nucleotide identity among them and 98 percent with HAstrV-1 (strain Oxford type 1). This is the first report of a gastroenteritis outbreak associated with HAstrv-1 in a day care center in Rio de Janeiro and it reinforces the importance of this virus in association with infantile acute gastroenteritis


Subject(s)
Humans , Infant , Child, Preschool , Child Day Care Centers , Disease Outbreaks , Gastroenteritis , Astroviridae Infections/epidemiology , Mamastrovirus , Brazil , Gastroenteritis , Astroviridae Infections/complications , Astroviridae Infections/diagnosis
3.
Mem. Inst. Oswaldo Cruz ; 83(2): 207-12, abr.-jun. 1988. ilus
Article in English | LILACS | ID: lil-72557

ABSTRACT

A presença de antígeno viral em cortes de tecidos humanos fixados em formol e emblocados em parafina foi demonstrada pela digestäo com tripsina foi demonstrada pela ingestäo com tripsina seguida de imunofluorescência direta ou indireta. Os espécimens podem ser utilizados para diagnoses retrospectivas. A técnica da imunofluorescência deve ser adaptada à infecçäo viral suspeita segundo diagnosie histopatológica prévia. Os parâmetros para a digestäo do tecido pela tripsina, relacionados à concentraçäo, duraçäo de atuaçäo e temperatura, expöem diferentes antígenos virais e devem ser previamente testados para cada sistema a ser estabelecido. Uma digestäo mais intensa deve ser aplicada para a detecçäo do vírus do sarampo em tecido pulmonar do que para adenovírus ou vírus respiratório sincicial no mesmo tecido. Por outro lado, o vírus da febre amarela em tecido de fígado necessita de uma digestäo mais fraca


Subject(s)
Humans , Fluorescent Antibody Technique , Trypsin/metabolism , Virus Diseases/diagnosis , Virus Cultivation
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