Helicobacter pylori strain ATCC700392 encodes a methyl-accepting chemotaxis receptor protein (MCP) for arginine and sodium bicarbonate

被引:64
作者
Cerda, O [1 ]
Rivas, A [1 ]
Toledo, H [1 ]
机构
[1] Univ Chile, Fac Med, ICBM, Programa Biol Celular & Mol, Santiago 7, Chile
关键词
chemotaxis; signal transduction; HP0099; IS605; Helicobacter pylori;
D O I
10.1016/S0378-1097(03)00423-3
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Helicobacter pylori ATCC43504 responds chemotactically to aspartic acid and serine, but not to arginine, nor to sodium bicarbonate. In contrast, H. pylori ATCC700392 (strain 26695) shows chemotaxis to all four attractants. Open reading frame HP0099 from H. pylori 26695 is predicted to encode one of three methyl-accepting chernotaxis receptor proteins (MCPs). When Escherichia coli is transformed with a plasmid carrying HP0099 from strain 26695, the recombinants acquire chernotaxis to arginine, bicarbonate, and urea. In H. pylori 43504, the HP0099 gene is interrupted with a mini-IS605 insertion, which accounts for its inability to recognize arginine and bicarbonate as attractants. Together, these results argue that the H. pylori HP0099 gene encodes an MCP for arginine and bicarbonate. (C) 2003 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:175 / 181
页数:7
相关论文
共 29 条
[1]   METHOD FOR MEASURING CHEMOTAXIS AND USE OF METHOD TO DETERMINE OPTIMUM CONDITIONS FOR CHEMOTAXIS BY ESCHERICHIA-COLI [J].
ADLER, J .
JOURNAL OF GENERAL MICROBIOLOGY, 1973, 74 (JAN) :77-91
[2]   Analyses of the cag pathogenicity island of Helicobacter pylori [J].
Akopyants, NS ;
Clifton, SW ;
Kersulyte, D ;
Crabtree, JE ;
Youree, BE ;
Reece, CA ;
Bukanov, NO ;
Drazek, ES ;
Roe, BA ;
Berg, DE .
MOLECULAR MICROBIOLOGY, 1998, 28 (01) :37-53
[3]   DNA DIVERSITY AMONG CLINICAL ISOLATES OF HELICOBACTER-PYLORI DETECTED BY PCR-BASED RAPD FINGERPRINTING [J].
AKOPYANZ, N ;
BUKANOV, NO ;
WESTBLOM, TU ;
KRESOVICH, S ;
BERG, DE .
NUCLEIC ACIDS RESEARCH, 1992, 20 (19) :5137-5142
[4]   Genomic-sequence comparison of two unrelated isolates of the human gastric pathogen Helicobacter pylori [J].
Alm, RA ;
Ling, LSL ;
Moir, DT ;
King, BL ;
Brown, ED ;
Doig, PC ;
Smith, DR ;
Noonan, B ;
Guild, BC ;
deJonge, BL ;
Carmel, G ;
Tummino, PJ ;
Caruso, A ;
Uria-Nickelsen, M ;
Mills, DM ;
Ives, C ;
Gibson, R ;
Merberg, D ;
Mills, SD ;
Jiang, Q ;
Taylor, DE ;
Vovis, GF ;
Trost, TJ .
NATURE, 1999, 397 (6715) :176-180
[5]   Two predicted chemoreceptors of Helicobacter pylori promote stomach infection [J].
Andermann, TM ;
Chen, YT ;
Ottemann, KM .
INFECTION AND IMMUNITY, 2002, 70 (10) :5877-5881
[6]   cag, a pathogenicity island of Helicobacter pylori, encodes type I-specific and disease-associated virulence factors [J].
Censini, S ;
Lange, C ;
Xiang, ZY ;
Crabtree, JE ;
Ghiara, P ;
Borodovsky, M ;
Rappuoli, R ;
Covacci, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) :14648-14653
[7]   EVOLUTION OF CHEMOTACTIC-SIGNAL TRANSDUCERS IN ENTERIC BACTERIA [J].
DAHL, MK ;
BOOS, W ;
MANSON, MD .
JOURNAL OF BACTERIOLOGY, 1989, 171 (05) :2361-2371
[8]  
Delgado M, 1998, APPL ENVIRON MICROB, V64, P2380
[9]   Helicobacter pylori [J].
Dunn, BE ;
Cohen, H ;
Blaser, MJ .
CLINICAL MICROBIOLOGY REVIEWS, 1997, 10 (04) :720-+
[10]   Colonization of gnotobiotic piglets by Helicobacter pylori deficient in two flagellin genes [J].
Eaton, KA ;
Suerbaum, S ;
Josenhans, C ;
Krakowka, S .
INFECTION AND IMMUNITY, 1996, 64 (07) :2445-2448