Literature DB >> 10921938

vacA genotypes in Helicobacter pylori strains isolated from children with and without duodenal ulcer in Brazil.

V R De Gusmão1, E Nogueira Mendes, D M De Magalhães Queiroz, G Aguiar Rocha, A M Camargos Rocha, A A Ramadan Ashour, A S Teles Carvalho.   

Abstract

Data concerning the association between vacA genotypes and disease in children in both developed and developing countries are scarce, especially because of the small number of children with a duodenal ulcer studied. The vacA genotypes of Helicobacter pylori strains obtained from 65 children (24 with a duodenal ulcer and 41 without a duodenal ulcer; 33 girls; mean age, 10.2 years; age range, 1 to 17 years) were investigated as described by J. C. Atherton et al. (J. Clin. Microbiol. 37:2979-2982, 1999). Ten (15.4%) children were infected with more than one H. pylori strain. None of these patients were included in our analysis of the relationship between gastric disorders and specific vacA genotypes. The s1 allele was detected in all H. pylori strains isolated from patients with a duodenal ulcer and from 21 (58.3%) patients without a duodenal ulcer (P = 0.003). Strains with the s2 allele were found only in patients without ulcer (n = 15; 41.7%). Most s1 strains had the s1b allele (97.5%), a result similar to that reported for adults from the Iberian peninsula, which could reflect the Brazilian population origin. One untypeable s1 strain was isolated. The m1 allele was also more frequently found in strains obtained from duodenal ulcer patients (P = 0.028). The m2 allele was found in strains obtained from 20 (36. 4%) children, 3 (15.8%) with an ulcer and 17 (47.2%) without an ulcer. Only one m hybrid strain (m1 and m2 hybrid) was detected. It was demonstrated for the first time that the frequencies of colonization with strains with the s1 allele (14.3% in children up to 8 years of age and 85.7% in older patients; P = 0.012) and of strains with the m1 allele (11.1% in patients up to the age 8 years and 88.9% in older children; P = 0.013) increase with age.

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Year:  2000        PMID: 10921938      PMCID: PMC87127     

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  37 in total

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6.  Intracellular Campylobacter-like organism from ferrets and hamsters with proliferative bowel disease is a Desulfovibrio sp.

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Journal:  Cancer Res       Date:  1995-05-15       Impact factor: 12.701

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  27 in total

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Journal:  J Clin Microbiol       Date:  2001-05       Impact factor: 5.948

2.  Mucosal lymphocyte subsets and HLA-DR antigen expression in paediatric Helicobacter pylori-associated gastritis.

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4.  Helicobacter pylori virulence genes detected by string PCR in children from an urban community in northeastern Brazil.

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5.  New pathogenicity marker found in the plasticity region of the Helicobacter pylori genome.

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6.  Association between vacA genotypes and the risk of duodenal ulcer: a meta-analysis.

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7.  Cytokine expression in pediatric Helicobacter pylori infection.

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8.  Regional variation among vacA alleles of Helicobacter pylori in China.

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9.  Analysis of Helicobacter pylori genotypes and correlation with clinical outcome in Turkey.

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10.  Infection with cagA-positive and cagA-negative types of Helicobacter pylori among children and adolescents with gastrointestinal symptoms in Latvia.

Authors:  I Daugule; I Rumba; L Engstrand; J Ejderhamn
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