Helicobacter pylori vacA genotypes, cagA status and ureA-B polymorphism in isolates recovered from an Argentine population

被引:17
作者
Catalano, M [1 ]
Matteo, M
Barbolla, RE
Vega, DEJ
Crespo, O
Leanza, AG
Toppor, J
Antelo, P
机构
[1] Univ Buenos Aires, Fac Med, Dept Microbiol Immunol & Parasitol, Buenos Aires, DF, Argentina
[2] Hosp Escuela Don Jose San Martin, Fac Med, Serv Gastroenterol, Buenos Aires, DF, Argentina
关键词
D O I
10.1016/S0732-8893(01)00307-8
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Several reports have evidenced geographic differences in the prevalence of vacA (vacuolating cytotoxin gene) alleles and cagA (cytotoxin-associated gene) status among Helicobacter pylori isolates. We investigated the occurrence of these virulence-associated genes status among our isolates, and their relationship with ulcer disease outcome. Besides, ureA-B polymorphism was studied. One hundred isolates, comprising 32 from patients with ulcer disease (UD) and 68 from patients with non-ulcer dyspepsia (NUD), were analyzed. Eighty-four percent of isolates were cagA-positive without statistically significant difference in prevalence between patients with UD or NUD. Genotype vacA-s1m1 was predominant, although unlike other South American regions, subtype s1am1 occurrence was higher than sib. The multivariate model used to estimate the predictive value of cagA and vacA status for UD development disclosed infection with vacA-slam I isolates as the only variable that increased the risk of UD onset. ureAB fingerprinting showed considerable genetic divergence among isolates, however, confirmed that certain DNA banding profiles are conserved worldwide. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:205 / 210
页数:6
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