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1.
Mem. Inst. Oswaldo Cruz ; 100(7): 709-714, Nov. 2005. tab, graf
Article in English | LILACS | ID: lil-419692

ABSTRACT

Human astroviruses (HAstV) have been increasingly identified as important etiological agents of acute gastroenteritis in children up to five years old. The aim of this study was to determine the prevalence and genotype diversity of HAstV in children with symptomatic and asymptomatic infections in São Luís, Maranhão, Brazil. From June 1997 to July 1999 a total of 183 fecal samples 84 from symptomatic and 99 from asymptomatic children were tested by enzyme immunoassay for HAstV. Prevalence rates were found to be 11 and 3 percent for symptomatic and asymptomatic children, respectively. Reverse transcription-polymerase chain reaction (RT-PCR) was carried out in 46 specimens (26 symptomatic and 20 asymptomatic) including the 12 samples that were positive by enzyme immunoassay (EIA). The overall positivity yielded by both methods was 8 percent (15/184); of these, 11 percent (9/84) for symptomatic and 5 percent (5/99) for those without symptoms or signs. Sequence analysis of amplicons revealed that HAstV-1 genotype was the most prevalent, accounting for 60 percent of isolates. Genotypes 2, 3, 4, and 5 were also detected, as one single isolate (10 percent) for each type. Variations in the sequences were observed when Brazilian isolates were compared to prototype strains identified in the United Kingdom. No seasonal pattern of occurrence was observed during these two years of study, and peak detection rate was observed in children aged between 3 and 6 months in the symptomatic group, and between 18 and 24 months in the controls.


Subject(s)
Infant, Newborn , Infant , Child, Preschool , Humans , Male , Female , Astroviridae Infections/epidemiology , Diarrhea, Infantile/virology , Genetic Variation , Gastroenteritis/virology , Mamastrovirus , Acute Disease , Base Sequence , Brazil/epidemiology , Case-Control Studies , Diarrhea, Infantile/epidemiology , Feces/virology , Genotype , Gastroenteritis/epidemiology , Immunoenzyme Techniques , Mamastrovirus , Phylogeny , Prevalence , Reverse Transcriptase Polymerase Chain Reaction , RNA, Viral/genetics , Sequence Analysis, RNA
2.
Rev. Inst. Med. Trop. Säo Paulo ; 44(1): 13-16, Jan.-Feb. 2002. tab
Article in English | LILACS | ID: lil-307236

ABSTRACT

The rhesus-human reassortant, tetravalent rotavirus vaccine (RRV-TV) was licensed for routine use in the United States of America but it was recently withdrawn from the market because of its possible association with intussusception as an adverse event. The protective efficacy of 3 doses of RRV-TV, in its lower-titer (4 x 10(4) pfu/dose) formulation, was evaluated according to the nutritional status of infants who participated in a phase III trial in Belém, Northern Brazil. A moderate protection conferred by RRV-TV was related to weight-for-age Z-scores (WAZ) greater than -1 only, with rates of 38 percent (p = 0.04) and 40 percent (p = 0.04) for all- and- pure rotavirus diarrhoeal cases, respectively. In addition, there was a trend for greater efficacy (43 percent, p = 0.05) among infants reaching an height-for-age Z-score (HAZ) of > -1. Taking WAZ, HAZ and weight-for-height Z-score (WHZ) indices <= -1 together, there was no significant protection (p > 0.05) if both placebo and vaccine groups are compared. There was no significant difference if rates of mixed and pure rotavirus diarrhoeal cases are compared in relation to HAZ, WAZ and weight-for-height Z-score (WHZ) indices. Although a low number of malnourished infants could be identified in the present study, our data show some evidence that malnutrition may interfere with the efficacy of rotavirus vaccines in developing countries


Subject(s)
Humans , Animals , Infant, Newborn , Infant , Diarrhea , Nutritional Status , Rotavirus , Rotavirus Infections , Rotavirus Vaccines , Vaccines, Attenuated , Anthropometry , Brazil , Developed Countries , Diarrhea , Double-Blind Method , Gastroenteritis , Reassortant Viruses , Rotavirus Vaccines , Vaccination , Vaccines, Attenuated , Vaccines, Combined
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