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
相关论文
共 31 条
  • [1] CagA: a role at last
    Atherton, JC
    [J]. GUT, 2000, 47 (03) : 330 - 331
  • [2] Clinical and pathological importance of heterogeneity in vacA, the vacuolating cytotoxin gene of Helicobacter pylori
    Atherton, JC
    Peek, RM
    Tham, KT
    Cover, TL
    Blaser, MJ
    [J]. GASTROENTEROLOGY, 1997, 112 (01) : 92 - 99
  • [3] PARASITISM BY THE SLOW BACTERIUM HELICOBACTER-PYLORI LEADS TO ALTERED GASTRIC HOMEOSTASIS AND NEOPLASIA
    BLASER, MJ
    PARSONNET, J
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (01) : 4 - 8
  • [4] CARRATOLIL A, 2000, EUROPEAN J GASTROENT, V12, P1207
  • [5] MOLECULAR CHARACTERIZATION OF THE 128-KDA IMMUNODOMINANT ANTIGEN OF HELICOBACTER-PYLORI-ASSOCIATED WITH CYTOTOXICITY AND DUODENAL-ULCER
    COVACCI, A
    CENSINI, S
    BUGNOLI, M
    PETRACCA, R
    BURRONI, D
    MACCHIA, G
    MASSONE, A
    PAPINI, E
    XIANG, ZY
    FIGURA, N
    RAPPUOLI, R
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (12) : 5791 - 5795
  • [6] De Gusmao VR, 2000, J CLIN MICROBIOL, V38, P2853
  • [7] DICE RL, 1945, J ECOL, V36, P297
  • [8] DUNN BE, 1999, CLIN MICROBIOLOGIC R, V10, P720
  • [9] Helicobacter pylori vacA and cagA genotypes in Mexican adults and children
    González-Valencia, G
    Atherton, JC
    Muñoz, O
    Dehesa, M
    Madrazo-de la Garza, A
    Torres, J
    [J]. JOURNAL OF INFECTIOUS DISEASES, 2000, 182 (05) : 1450 - 1454
  • [10] H-pylori and cagA: Relationships with gastric cancer, duodenal ulcer, and reflux esophagitis and its complications
    Graham, DY
    Yamaoka, Y
    [J]. HELICOBACTER, 1998, 3 (03) : 145 - 151