Phage 3396 from a Streptococcus dysgalactiae subsp equisimilis pathovar may have its origins in Streptococcus pyogenes

被引:22
作者
Davies, Mark R.
McMillan, David J.
Van Domselaar, Gary H.
Jones, Malcolm K.
Sriprakash, Kadaba S. [1 ]
机构
[1] Queensland Inst Med Res, Bacterial Pathogenesis Lab, Brisbane, Qld 4029, Australia
[2] Queensland Inst Med Res, Australian Ctr Int Trop Hlth & Nutr, Brisbane, Qld 4029, Australia
[3] Queensland Inst Med Res, Cooperat Res Ctr Vaccine Technol, Brisbane, Qld 4029, Australia
[4] Publ Hlth Agcy Canada, Natl Microbiol Lab, Winnipeg, MB R3E 3R2, Canada
[5] Univ Manitoba, Fac Pharm, Winnipeg, MB R3T 2N2, Canada
[6] Queensland Inst Med Res, Mol Parasitol Lab, Brisbane, Qld 4029, Australia
关键词
D O I
10.1128/JB.01590-06
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Streptococcus dysgalactiae subsp. equisimilis strains (group G streptococcus [GGS]) are largely defined as commensal organisms, which are closely related to the well-defined human pathogen, the group A streptococcus (GAS). While lateral gene transfers are emerging as a common theme in these species, little is known about the mechanisms and role of these transfers and their effect on the population structure of streptococci in nature. It is now becoming evident that bacteriophages are major contributors to the genotypic diversity of GAS and, consequently, are pivotal to the GAS strain structure. Furthermore, bacteriophages are strongly associated with altering the pathogenic potential of GAS. In contrast, little is know about phages from GGS and their role in the population dynamics of GGS. In this study we report the first complete genome sequence of a GGS phage, Phi 3396. Exhibiting high homology to the GAS phage Phi 315.1, the chimeric nature of Phi 3396 is unraveled to reveal evidence of extensive ongoing genetic diversity and dissemination of streptococcal phages in nature. Furthermore, we expand on our recent findings to identify inducible Phi 3396 homologues in GAS from a region of endemicity for GAS and GGS infection. Together, these findings provide new insights into not only the population structure of GGS but also the overall population structure of the streptococcal genus and the emergence of pathogenic variants.
引用
收藏
页码:2646 / 2652
页数:7
相关论文
共 40 条
[1]   Mosaic prophages with horizontally acquired genes account for the emergence and diversification of the globally disseminated M1T1 clone of Streptococcus pyogenes [J].
Aziz, RK ;
Edwards, RA ;
Taylor, WW ;
Low, DE ;
McGeer, A ;
Kotb, M .
JOURNAL OF BACTERIOLOGY, 2005, 187 (10) :3311-3318
[2]   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
[3]   The fundamental contribution of phages to GAS evolution, genome diversification and strain emergence [J].
Banks, DJ ;
Beres, SB ;
Musser, JM .
TRENDS IN MICROBIOLOGY, 2002, 10 (11) :515-521
[4]   Genome sequence of a serotype M3 strain of group A Streptococcus:: Phage-encoded toxins, the high-virulence phenotype, and clone emergence [J].
Beres, SB ;
Sylva, GL ;
Barbian, KD ;
Lei, BF ;
Hoff, JS ;
Mammarella, ND ;
Liu, MY ;
Smoot, JC ;
Porcella, SF ;
Parkins, LD ;
Campbell, DS ;
Smith, TM ;
McCormick, JK ;
Leung, DYM ;
Schlievert, PM ;
Musser, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (15) :10078-10083
[5]   A new DNA sequence assembly program [J].
Bonfield, JK ;
Smith, KF ;
Staden, R .
NUCLEIC ACIDS RESEARCH, 1995, 23 (24) :4992-4999
[6]   Phages and the evolution of bacterial pathogens:: From genomic rearrangements to lysogenic conversion [J].
Brüssow, H ;
Canchaya, C ;
Hardt, WD .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2004, 68 (03) :560-+
[7]   Prophage genomics [J].
Canchaya, C ;
Proux, C ;
Fournous, G ;
Bruttin, A ;
Brüssow, H .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2003, 67 (02) :238-+
[8]   ACT: the Artemis comparison tool [J].
Carver, TJ ;
Rutherford, KM ;
Berriman, M ;
Rajandream, MA ;
Barrell, BG ;
Parkhill, J .
BIOINFORMATICS, 2005, 21 (16) :3422-3423
[9]   VIRULENT HUMAN STRAINS OF GROUP-G STREPTOCOCCI EXPRESS A C5A PEPTIDASE ENZYME SIMILAR TO THAT PRODUCED BY GROUP-A STREPTOCOCCI [J].
CLEARY, PP ;
PETERSON, J ;
CHEN, C ;
NELSON, C .
INFECTION AND IMMUNITY, 1991, 59 (07) :2305-2310
[10]   Group G streptococcal bacteremia in Jerusalem [J].
Cohen-Poradosu, R ;
Jaffe, J ;
Lavi, D ;
Grisariu-Greenzaid, S ;
Nir-Paz, R ;
Valinsky, L ;
Dan-Goor, M ;
Block, C ;
Beall, B ;
Moses, AE .
EMERGING INFECTIOUS DISEASES, 2004, 10 (08) :1455-1460