Identification of novel virulence-associated genes via genome analysis of hypothetical genes

被引:33
作者
Garbom, S
Forsberg, Å
Wolf-Watz, H
Kihlberg, BM
机构
[1] Umea Univ, Dept Mol Biol, S-90187 Umea, Sweden
[2] Swedish Def Res Agcy, Div NBC Def, Dept Med Countermeasures, S-90182 Umea, Sweden
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
D O I
10.1128/IAI.72.3.1333-1340.2004
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 sequencing of bacterial genomes has opened new perspectives for identification of targets for treatment of infectious diseases. We have identified a set of novel virulence-associated genes (vag genes) by comparing the genome sequences of six human pathogens that are known to cause persistent or chronic infections in humans: Yersinia pestis, Neisseria gonorrhoeae, Helicobacter pylori, Borrelia burgdorferi, Streptococcus pneumoniae, and Treponema pallidum. This comparison was limited to genes annotated as hypothetical in the T. pallidum genome project. Seventeen genes with unknown functions were found to be conserved among these pathogens. Insertional inactivation of 14 of these genes generated nine mutants that were attenuated for virulence in a mouse infection model. Out of these nine genes, five were found to be specifically associated with virulence in mice as demonstrated by infection with Yersinia pseudotuberculosis in-frame deletion mutants. In addition, these five vag genes were essential only in vivo, since all the mutants were able to grow in vitro. These genes are broadly conserved among bacteria. Therefore, we propose that the corresponding vag gene products may constitute novel targets for antimicrobial therapy and that some vag mutants could serve as carrier strains for live vaccines.
引用
收藏
页码:1333 / 1340
页数:8
相关论文
共 60 条
[1]   Yersinia pestis, the cause of plague, is a recently emerged clone of Yersinia pseudotuberculosis [J].
Achtman, M ;
Zurth, K ;
Morelli, C ;
Torrea, G ;
Guiyoule, A ;
Carniel, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (24) :14043-14048
[2]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[3]   HP0333, a member of the dprA family, is involved in natural transformation in Helicobacter pylori [J].
Ando, T ;
Israel, DA ;
Kusugami, K ;
Blaser, MJ .
JOURNAL OF BACTERIOLOGY, 1999, 181 (18) :5572-5580
[4]   A genome-based approach for the identification of essential bacterial genes [J].
Arigoni, F ;
Talabot, F ;
Peitsch, M ;
Edgerton, MD ;
Meldrum, E ;
Allet, E ;
Fish, R ;
Jamotte, T ;
Curchod, ML ;
Loferer, H .
NATURE BIOTECHNOLOGY, 1998, 16 (09) :851-856
[5]  
BJORK GR, 1995, TRNA STRUCTURE BIOSY, P165
[6]   FACTORS PROMOTING ACUTE AND CHRONIC DISEASES CAUSED BY YERSINIAE [J].
BRUBAKER, RR .
CLINICAL MICROBIOLOGY REVIEWS, 1991, 4 (03) :309-324
[7]   Concordance analysis of microbial genomes [J].
Bruccoleri, RE ;
Dougherty, TJ ;
Davison, DB .
NUCLEIC ACIDS RESEARCH, 1998, 26 (19) :4482-4486
[8]   Evolution of a molecular switch: universal bacterial GTPases regulate ribosome function [J].
Caldon, CE ;
Yoong, P ;
March, PE .
MOLECULAR MICROBIOLOGY, 2001, 41 (02) :289-297
[9]   A competence regulon in Streptococcus pneumoniae revealed by genomic analysis [J].
Campbell, EA ;
Choi, SY ;
Masure, HR .
MOLECULAR MICROBIOLOGY, 1998, 27 (05) :929-939
[10]  
Charette M, 2000, IUBMB LIFE, V49, P341