Genetics and genetic manipulation in Francisella tularensis

被引:22
作者
Frank, Dara W.
Zahrt, Thomas C.
机构
[1] Med Coll Wisconsin, Dept Microbiol & Mol Genet, Milwaukee, WI 53226 USA
[2] Med Coll Wisconsin, Ctr Biopreparedness & Infect Dis, Dept Microbiol & Mol Genet, Milwaukee, WI 53226 USA
来源
FRANCISELLA TULARENSIS: BIOLOGY, PATHOGENICITY, EPIDEMIOLOGY, AND BIODEFENSE | 2007年 / 1105卷
关键词
Francisella; genetics; shuttle vectors; allelic exchange; transposon mutagenesis; complementation;
D O I
10.1196/annals.1409.008
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Francisella tularensis is a gram-negative coccobacillus and the etiological agent of tularemia. The limited knowledge regarding the interaction of F. tularensis with its host is due in part to the previous lack of tools for genetically manipulating the organism. During the past 10 years, the field of F tularensis genetics has seen a rapid expansion. Plasmids capable of stable or conditional replication in Francisella have been constructed. Methods for the efficient introduction of DNA into Francisella have been developed or optimized. Genetic platforms and procedures for transposon mutagenesis and allelic exchange have been adapted for use in Francisella. Finally, selectable, counterselectable, and screenable genetic markers amenable for use in a variety of F. tularensis species, including highly virulent clinical isolates, have been described. Collectively, these advances have aided in the construction of defined Francisella mutants and helped investigators begin to define the mechanism(s) employed by these organisms to cause disease in the host. In this article, we describe the history of genetic manipulation in Francisella and summarize the current tools and techniques for conducting genetic studies in this organism.
引用
收藏
页码:67 / 97
页数:31
相关论文
共 59 条
[1]   Survival and growth of Francisella tularensis in Acanthamoeba castellanii [J].
Abd, H ;
Johansson, T ;
Golovliov, I ;
Sandström, G ;
Forsman, M .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2003, 69 (01) :600-606
[2]   TRANSFORMATION AND ALLELIC REPLACEMENT IN FRANCISELLA SPP [J].
ANTHONY, LSD ;
GU, M ;
COWLEY, SC ;
LEUNG, WWS ;
NANO, FE .
JOURNAL OF GENERAL MICROBIOLOGY, 1991, 137 :2697-2703
[3]   GROWTH OF FRANCISELLA-SPP IN RODENT MACROPHAGES [J].
ANTHONY, LSD ;
BURKE, RD ;
NANO, FE .
INFECTION AND IMMUNITY, 1991, 59 (09) :3291-3296
[4]  
ANTHONY LSD, 1994, FEMS MICROBIOL LETT, V124, P157, DOI 10.1111/j.1574-6968.1994.tb07278.x
[5]   ANTIMICROBIAL SUSCEPTIBILITY TESTING OF FRANCISELLA-TULARENSIS WITH A MODIFIED MUELLER-HINTON BROTH [J].
BAKER, CN ;
HOLLIS, DG ;
THORNSBERRY, C .
JOURNAL OF CLINICAL MICROBIOLOGY, 1985, 22 (02) :212-215
[6]   Superoxide dismutase B gene (sodB)-deficient mutants of Francisella tularensis demonstrate hypersensitivity to oxidative stress and attenuated virulence [J].
Bakshi, Chandra Shekhar ;
Malik, Meenakshi ;
Regan, Kevin ;
Melendez, J. Andres ;
Metzger, Dennis W. ;
Pavlov, Vitaly M. ;
Sellati, Timothy J. .
JOURNAL OF BACTERIOLOGY, 2006, 188 (17) :6443-6448
[7]  
Baron G S, 1995, Methods Mol Biol, V47, P149
[8]  
Baron GS, 1999, FEMS MICROBIOL LETT, V176, P85, DOI 10.1111/j.1574-6968.1999.tb13646.x
[9]   MgIA and MgIB are required for the intramacrophage growth of Francisella novicida [J].
Baron, GS ;
Nano, FE .
MOLECULAR MICROBIOLOGY, 1998, 29 (01) :247-259
[10]   MOLECULAR-CLONING OF THE RECA GENE AND CONSTRUCTION OF A RECA STRAIN OF FRANCISELLA-NOVICIDA [J].
BERG, JM ;
MDLULI, KE ;
NANO, FE .
INFECTION AND IMMUNITY, 1992, 60 (02) :690-693