Distinct diversity of the cag pathogenicity island among Helicobacter pylori strains in Japan

被引:69
作者
Azuma, T [1 ]
Yamakawa, A
Yamazaki, S
Ohtani, M
Ito, Y
Muramatsu, A
Suto, H
Yamazaki, Y
Keida, Y
Higashi, H
Hatakeyama, M
机构
[1] Univ Fukui, Fac Med Sci, Dept Internal Med 2, Fukui 9101193, Japan
[2] Univ Fukui, Dept Endoscop Med, Fukui 9101193, Japan
[3] Okinawa Chubu Hosp, Div Internal Med, Okinawa, Japan
[4] Hokkaido Univ, Inst Genet Med, Div Mol Oncol, Sapporo, Hokkaido, Japan
[5] Hokkaido Univ, Grad Sch Sci, Sapporo, Hokkaido, Japan
关键词
D O I
10.1128/JCM.42.6.2508-2517.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The severity of Helicobacter pylori-related disease is correlated with the presence of a cag pathogenicity island (PAI). Genetic diversity within the cag PAI may have a modifying effect on the pathogenic potential of the infecting strain. We analyzed the complete cag PAI sequences of 11 representative Japanese strains according to their vacA genotypes and clinical effects and examined the relationship between the diversity of the cag PAI and clinical features. The cag PAI genes were divided into two major groups, a Western and a Japanese group, by phylogenetic analysis based on the entire cag PAI sequences. The predominant Japanese strains formed a Japanese cluster which was different from the cluster formed by Western strains. The diversity of the cag PAI was associated with the vacA and cagA genotypes. All strains with the s1c vacA genotype were in the Japanese cluster. In addition, all strains with the East Asian-type cagA genotype were also in the Japanese cluster. Patients infected with the Japanese-cluster strain had high-grade gastric mucosal atrophy. These results suggest that a distinct diversity of the cag PAI of H. pylori is present among Japanese strains and that this diversity may be involved in the development of atrophic gastritis and may increase the risk for gastric cancer.
引用
收藏
页码:2508 / 2517
页数:10
相关论文
共 33 条
[21]   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
[22]   HELICOBACTER-PYLORI INFECTION AND THE RISK OF GASTRIC-CARCINOMA [J].
PARSONNET, J ;
FRIEDMAN, GD ;
VANDERSTEEN, DP ;
CHANG, Y ;
VOGELMAN, JH ;
ORENTREICH, N ;
SIBLEY, RK .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (16) :1127-1131
[23]   Altered states:: Involvement of phosphorylated CagA in the induction of host cellular growth changes by Helicobacter pylori [J].
Segal, ED ;
Cha, J ;
Lo, J ;
Falkow, S ;
Tompkins, LS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (25) :14559-14564
[24]   Tyrosine phosphorylation of the Helicobacter pylori CagA antigen after cag-driven host cell translocation [J].
Stein, M ;
Rappuoli, R ;
Covacci, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (03) :1263-1268
[25]   The complete genome sequence of the gastric pathogen Helicobacter pylori [J].
Tomb, JF ;
White, O ;
Kerlavage, AR ;
Clayton, RA ;
Sutton, GG ;
Fleischmann, RD ;
Ketchum, KA ;
Klenk, HP ;
Gill, S ;
Dougherty, BA ;
Nelson, K ;
Quackenbush, J ;
Zhou, LX ;
Kirkness, EF ;
Peterson, S ;
Loftus, B ;
Richardson, D ;
Dodson, R ;
Khalak, HG ;
Glodek, A ;
McKenney, K ;
Fitzegerald, LM ;
Lee, N ;
Adams, MD ;
Hickey, EK ;
Berg, DE ;
Gocayne, JD ;
Utterback, TR ;
Peterson, JD ;
Kelley, JM ;
Cotton, MD ;
Weldman, JM ;
Fujii, C ;
Bowman, C ;
Watthey, L ;
Wallin, E ;
Hayes, WS ;
Weidman, JM ;
Fujii, C ;
Borodovsky, M ;
Karp, PD ;
Smith, HO ;
Fraser, CM ;
Venter, JC .
NATURE, 1997, 388 (6642) :539-547
[26]   Expanding allelic diversity of Helicobacter pylori vacA [J].
van Doorn, LJ ;
Figueiredo, C ;
Sanna, R ;
Pena, S ;
Midolo, P ;
Ng, EKW ;
Atherton, JC ;
Blaser, MJ ;
Quint, WGV .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (09) :2597-2603
[27]   Geographic distribution of vacA allelic types of Helicobacter pylori [J].
van Doorn, LJ ;
Figueiredo, C ;
Mégraud, F ;
Pena, S ;
Midolo, P ;
Queiroz, DMD .
GASTROENTEROLOGY, 1999, 116 (04) :823-830
[28]  
WARREN JR, 1983, LANCET, V1, P1273
[29]   HELICOBACTER-PYLORI-ASSOCIATED GASTRITIS AND PRIMARY B-CELL GASTRIC LYMPHOMA [J].
WOTHERSPOON, AC ;
ORTIZHIDALGO, C ;
FALZON, MR ;
ISAACSON, PG .
LANCET, 1991, 338 (8776) :1175-1176
[30]   ANALYSIS OF EXPRESSION OF CAGA AND VACA VIRULENCE FACTORS IN 43 STRAINS OF HELICOBACTER-PYLORI REVEALS THAT CLINICAL ISOLATES CAN BE DIVIDED INTO 2 MAJOR TYPES AND THAT CAGA IS NOT NECESSARY FOR EXPRESSION OF THE VACUOLATING CYTOTOXIN [J].
XIANG, ZY ;
CENSINI, S ;
BAYELI, PF ;
TELFORD, JL ;
FIGURA, N ;
RAPPUOLI, R ;
COVACCI, A .
INFECTION AND IMMUNITY, 1995, 63 (01) :94-98