Comparative sequence analysis of the icm/dot genes in Legionella

被引:38
作者
Morozova, I
Qu, XY
Shi, SD
Asamani, G
Greenberg, JE
Shuman, HA
Russo, JJ
机构
[1] Columbia Univ Coll Phys & Surg, Columbia Genome Ctr, New York, NY 10032 USA
[2] Columbia Univ Coll Phys & Surg, Dept Microbiol, New York, NY 10032 USA
基金
美国国家卫生研究院;
关键词
Legionella pneumophila; icm/dot genes; evolution; phylogenetic analysis; virulence;
D O I
10.1016/j.plasmid.2003.12.004
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The icm/dot genes in Legionella pneumophila are essential for the ability of the bacteria to survive within macrophages in lung infections such as Legionnaires' disease, or amoebae in nature. The 22 genes of the complex, thought to encode a transport apparatus for transfer of effector molecules into the host cell cytoplasm, are located in two chromosomal loci. We demonstrate that these genes are present in all the L. pneumophila strains examined herein, but display a wide range of sequence variation among the different strains, none of which are clearly associated with virulence potential. The strains fall within seven phylogenetic groups, but discrepancies among the gene trees indicate a complicated evolutionary history for the icm/dot loci, with perhaps two independent gene acquisition events and subsequent genomic rearrangements. Significant findings include a probable t-SNARE domain in IcmG that may indicate a direct role for this putative inner membrane protein in altering the host's membrane fusion machinery, a potential functional domain in the central hydrophobic portion of IcmK that may allow it to participate in forming the pore of the secretion complex, and strict conservation of the amino acid physicochemical characteristics in the IcmP region corresponding to the trbA domain that could play a role in molecular transfer. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:127 / 147
页数:21
相关论文
共 70 条
[1]   Legionella-like amebal pathogens - Phylogenetic status and possible role in respiratory disease [J].
Adeleke, A ;
Pruckler, J ;
Benson, R ;
Rowbotham, T ;
Halablab, M ;
Fields, B .
EMERGING INFECTIOUS DISEASES, 1996, 2 (03) :225-230
[2]   Comparative assessment of virulence traits in Legionella spp. [J].
Alli, OAT ;
Zink, S ;
von Lackum, NK ;
Abu-Kwaik, Y .
MICROBIOLOGY-SGM, 2003, 149 :631-641
[3]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[4]   Identification of linked Legionella pneumophila genes essential for intracellular growth and evasion of the endocytic pathway [J].
Andrews, HL ;
Vogel, JP ;
Isberg, RR .
INFECTION AND IMMUNITY, 1998, 66 (03) :950-958
[5]   Sequence and genome context analysis of a new molecular class D β-lactamase gene from Legionella pneumophila [J].
Avison, MB ;
Simm, AM .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2002, 50 (03) :331-338
[6]  
Bateman A, 2004, NUCLEIC ACIDS RES, V32, pD138, DOI [10.1093/nar/gkp985, 10.1093/nar/gkr1065, 10.1093/nar/gkh121]
[7]   Structure determination of human and murine β-defensins reveals structural conservation in the absence of significant sequence similarity [J].
Bauer, F ;
Schweimer, K ;
Klüver, E ;
Conejo-Garcia, JR ;
Forssmann, WG ;
Rösch, P ;
Adermann, K ;
Sticht, H .
PROTEIN SCIENCE, 2001, 10 (12) :2470-2479
[8]  
Benson R F, 1998, Semin Respir Infect, V13, P90
[9]   2 DISTINCT DEFECTS IN INTRACELLULAR GROWTH COMPLEMENTED BY A SINGLE GENETIC-LOCUS IN LEGIONELLA-PNEUMOPHILA [J].
BERGER, KH ;
ISBERG, RR .
MOLECULAR MICROBIOLOGY, 1993, 7 (01) :7-19
[10]   EVOLUTION OF THE AMINO-ACID SUBSTITUTION IN THE MAMMALIAN MYOGLOBIN GENE [J].
BOGARDT, RA ;
JONES, BN ;
DWULET, FE ;
GARNER, WH ;
LEHMAN, LD ;
GURD, FRN .
JOURNAL OF MOLECULAR EVOLUTION, 1980, 15 (03) :197-218