Phages and the evolution of bacterial pathogens:: From genomic rearrangements to lysogenic conversion

被引:1169
作者
Brüssow, H
Canchaya, C
Hardt, WD
机构
[1] Nestec Ltd, Nestle Res Ctr, CH-1000 Lausanne, Switzerland
[2] ETH, Inst Microbiol, CH-8092 Zurich, Switzerland
关键词
D O I
10.1128/MMBR.68.3.560-602.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Comparative genomics demonstrated that the chromosomes from bacteria and their viruses (bacteriophages) are coevolving. This process is most evident for bacterial pathogens where the majority contain prophages or phage remnants integrated into the bacterial DNA. Many prophages from bacterial pathogens encode virulence factors. Two situations can be distinguished: Vibrio cholerae, Shiga toxin-producing Escherichia coli, Corynebacterium diphtheriae, and Clostridium botulinum depend on a specific prophage-encoded toxin for causing a specific disease, whereas Staphylococcus aureus, Streptococcus pyogenes, and Salmonella enterica serovar Typhimurium harbor a multitude of prophages and each phage-encoded virulence or fitness factor makes an incremental contribution to the fitness of the lysogen. These prophages behave like "swarms" of related prophages. Prophage diversification seems to be fueled by the frequent transfer of phage material by recombination with superinfecting phages, resident prophages, or occasional acquisition of other mobile DNA elements or bacterial chromosomal genes. Prophages also contribute to the diversification of the bacterial genome architecture. In many cases, they actually represent a large fraction of the strain-specific DNA sequences. In addition, they can serve as anchoring points for genome inversions. The current review presents the available genomics and biological data on prophages from bacterial pathogens in an evolutionary framework.
引用
收藏
页码:560 / +
页数:44
相关论文
共 264 条
[1]  
Acheson DWK, 1998, INFECT IMMUN, V66, P4496
[2]   CURING AND INDUCTION OF THE FELS-1 AND FELS-2 PROPHAGES IN THE AMES MUTAGEN TESTER STRAINS OF SALMONELLA-TYPHIMURIUM [J].
AFFOLTER, M ;
PARENTVAUGEOIS, C ;
ANDERSON, A .
MUTATION RESEARCH, 1983, 110 (02) :243-262
[3]   Complete genomic sequence of SfV, a serotype-converting temperate bacteriophage of Shigella flexneri [J].
Allison, GE ;
Angeles, D ;
Tran-Dinh, N ;
Verma, NK .
JOURNAL OF BACTERIOLOGY, 2002, 184 (07) :1974-1987
[4]   Morphology of temperate bacteriophage SfV and characterisation of the DNA packaging and capsid genes: the structural genes evolved from two different phage families [J].
Allison, GE ;
Angeles, DC ;
Huan, PT ;
Verma, NK .
VIROLOGY, 2003, 308 (01) :114-127
[5]   Cloning and characterization of the region III flagellar operons of the four Shigella subgroups: Genetic defects that cause loss of flagella of Shigella boydii and Shigella sonnei [J].
AlMamun, AAM ;
Tominaga, A ;
Enomoto, M .
JOURNAL OF BACTERIOLOGY, 1997, 179 (14) :4493-4500
[6]  
[Anonymous], 1992, CHOLERA
[7]   Invasive M1T1 group A Streptococcus undergoes a phase-shift in vivo to prevent proteolytic degradation of multiple virulence factors by SpeB [J].
Aziz, RK ;
Pabst, MJ ;
Jeng, A ;
Kansal, R ;
Low, DE ;
Nizet, V ;
Kotb, M .
MOLECULAR MICROBIOLOGY, 2004, 51 (01) :123-134
[8]   Genome and virulence determinants of high virulence community-acquired MRSA [J].
Baba, T ;
Takeuchi, F ;
Kuroda, M ;
Yuzawa, H ;
Aoki, K ;
Oguchi, A ;
Nagai, Y ;
Iwama, N ;
Asano, K ;
Naimi, T ;
Kuroda, H ;
Cui, L ;
Yamamoto, K ;
Hiramatsu, K .
LANCET, 2002, 359 (9320) :1819-1827
[9]   Identification of SopE2, a Salmonella secreted protein which is highly homologous to SopE and involved in bacterial invasion of epithelial cells [J].
Bakshi, CS ;
Singh, VP ;
Wood, MW ;
Jones, PW ;
Wallis, TS ;
Galyov, EE .
JOURNAL OF BACTERIOLOGY, 2000, 182 (08) :2341-2344
[10]   Prophage induction and expression of prophage-encoded virulence factors in group A Streptococcus serotype M3 strain MGAS315 [J].
Banks, DJ ;
Lei, BF ;
Musser, JM .
INFECTION AND IMMUNITY, 2003, 71 (12) :7079-7086