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Comparative proteomic analysis of passaged Helicobacter pylori
Author(s) -
Zhang MaoJun,
Zhao Fei,
Xiao Di,
Gu YiXin,
Meng FanLiang,
He liHua,
Zhang JianZhong
Publication year - 2009
Publication title -
journal of basic microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.58
H-Index - 54
eISSN - 1521-4028
pISSN - 0233-111X
DOI - 10.1002/jobm.200800372
Subject(s) - downregulation and upregulation , membrane protein , proteome , bacterial adhesin , biology , bacterial outer membrane , virulence , microbiology and biotechnology , helicobacter pylori , gel electrophoresis , hypothetical protein , biochemistry , genetics , gene , escherichia coli , membrane
In order to identify the proteins associated with Helicobacter pylori colonization in mice, we used 2‐dimensional gel electrophoresis (2‐DE) to analyze the membrane‐ and soluble‐cellular proteins extracted from H. pylori strain 26695 and the mouse‐passaged homolog 88‐3887. We defined 2‐ and 3‐fold changes in protein expression as the threshold values for differential expression in the membrane‐protein and whole‐cell‐protein fractions, respectively. The differentially expressed proteins were identified by matrix‐assisted laser desorption/ionization time‐of‐flight mass spectrometry (MALDI‐TOF/TOF). A total of 29 proteins, including 16 membrane‐ or membrane‐associated proteins (13 upregulated, 3 downregulated) and 13 cellular proteins (10 upregulated, 3 downregulated) were differentially expressed between the strains 26695 and 88‐3887. Among the upregulated proteins, 10 proteins had been previously shown to be associated with the mouse colonization, and 13 upregulated proteins were shown to be associated with the adaptation of H. pylori in murine hosts for the first time in this study. The identified proteins were classified as proteins related to metabolism, stress response, virulence, or adhesion. The data presented in this report indicated that there were subsets of upregulated proteins in mouse‐adapted H. pylori . In particular, the adhesins, virulence factors, and stress‐response proteins are likely to contribute to colonization in mice. (© 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)