Identification of a new segment involved in cagA 3′ region variation of Helicobacter pylori

被引:5
作者
Dong, QJ [1 ]
O'Sullivan, M
Hall, W
Herra, C
Kean, C
O'Morain, C
Buckley, M
机构
[1] Univ Dublin Trinity Coll, St James Hosp, Dept Microbiol, Dublin, Ireland
[2] Univ Dublin Trinity Coll, Adelaide Hosp, Dept Gastroenterol, Dublin, Ireland
[3] Univ Dublin Trinity Coll, Meath Hosp, Dept Gastroenterol, Dublin, Ireland
来源
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY | 2002年 / 33卷 / 01期
关键词
cagA; tyrosine phosphorylation; Helicobacter pylori;
D O I
10.1016/S0928-8244(02)00272-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The cagA 3' region shows marked variation among Helicobacter pylori strains. Two segments of 102 bp and 57 bp are reportedly responsible for this variation. We analysed the cagA 3' region in 70 H. pylori strains using polymerase chain reaction and sequencing. We found that another segment, namely beta segment, was also involved in the variation of this region. The beta segment was 105 bp long and located between the aforementioned two segments. Six genotypes were identified based on the structure of the cagA 3' region. No relationship was found between these genotypes and the clinical outcomes or vacA genotypes. The numbers of tyrosine phosphorylation sites within the cagA 3' region varied among strains, but this was not related to the cagA genotypes. Our data suggest that the cagA 3' region is significantly variable. It appears that the variation of the cagA 3' region might contribute to the modification of virulence. (C) 2002 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:51 / 55
页数:5
相关论文
共 18 条
[1]  
Atherton JC, 1998, BRIT MED BULL, V54, P105
[2]  
BLASER MJ, 1995, CANCER RES, V55, P2111
[3]   MOLECULAR CHARACTERIZATION OF THE 128-KDA IMMUNODOMINANT ANTIGEN OF HELICOBACTER-PYLORI-ASSOCIATED WITH CYTOTOXICITY AND DUODENAL-ULCER [J].
COVACCI, A ;
CENSINI, S ;
BUGNOLI, M ;
PETRACCA, R ;
BURRONI, D ;
MACCHIA, G ;
MASSONE, A ;
PAPINI, E ;
XIANG, ZY ;
FIGURA, N ;
RAPPUOLI, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (12) :5791-5795
[4]   SEROLOGIC DETECTION OF INFECTION WITH CAGA(+) HELICOBACTER-PYLORI STRAINS [J].
COVER, TL ;
GLUPCZYNSKI, Y ;
LAGE, AP ;
BURETTE, A ;
TUMMURU, MKR ;
PEREZPEREZ, GI ;
BLASER, MJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (06) :1496-1500
[5]   High seropositivity of anti-CagA antibody in Helicobacter pylori-infected patients irrelevant to peptic ulcers and normal mucosa in Japan [J].
Maeda, S ;
Kanai, F ;
Ogura, K ;
Yoshida, H ;
Ikenoue, T ;
Takahashi, M ;
Kawabe, T ;
Shiratori, Y ;
Omata, M .
DIGESTIVE DISEASES AND SCIENCES, 1997, 42 (09) :1841-1847
[6]   Major virulence factors, VacA and CagA, are commonly positive in Helicobacter pylori isolates in Japan [J].
Maeda, S ;
Ogura, K ;
Yoshida, H ;
Kanai, F ;
Ikenoue, T ;
Kato, N ;
Shiratori, Y ;
Omata, M .
GUT, 1998, 42 (03) :338-343
[7]   Composition and gene expression of the cag pathogenicity island in Helicobacter pylori strains isolated from gastric carcinoma and gastritis patients in Costa Rica [J].
Occhialini, A ;
Marais, A ;
Urdaci, M ;
Sierra, R ;
Muñoz, N ;
Covacci, A ;
Mégraud, F .
INFECTION AND IMMUNITY, 2001, 69 (03) :1902-1908
[8]   Translocation of Helicobacter pylori CagA into gastric epithelial cells by type IV secretion [J].
Odenbreit, S ;
Püls, J ;
Sedlmaier, B ;
Gerland, E ;
Fischer, W ;
Haas, R .
SCIENCE, 2000, 287 (5457) :1497-1500
[9]   Equally high prevalences of infection with cagA-positive Helicobacter pylori in Chinese patients with peptic ulcer disease and those with chronic gastritis-associated dyspepsia [J].
Pan, ZJ ;
vanderHulst, RWM ;
Feller, M ;
Xiao, SD ;
Tytgat, GNJ ;
Dankert, J ;
vanderEnde, A .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (06) :1344-1347
[10]   Risk for gastric cancer in people with CagA positive or CagA negative Helicobacter pylori infection [J].
Parsonnet, J ;
Friedman, GD ;
Orentreich, N ;
Vogelman, H .
GUT, 1997, 40 (03) :297-301