Full-Genome Dissection of an Epidemic of Severe Invasive Disease Caused by a Hypervirulent, Recently Emerged Clone of Group A Streptococcus

被引:59
作者
Fittipaldi, Nahuel [1 ,2 ]
Beres, Stephen B. [1 ,2 ]
Olsen, Randall J. [1 ,2 ]
Kapur, Vivek [3 ]
Shea, Patrick R. [1 ,2 ]
Watkins, M. Ebru [1 ,2 ]
Cantu, Concepcion C. [1 ,2 ]
Laucirica, Daniel R. [1 ,2 ]
Jenkins, Leslie [1 ,2 ]
Flores, Anthony R. [1 ,2 ]
Lovgren, Marguerite [4 ,5 ]
Ardanuy, Carmen [6 ]
Linares, Josefina [6 ]
Low, Donald E. [7 ,8 ]
Tyrrell, Gregory J. [4 ,5 ]
Musser, James M. [1 ,2 ]
机构
[1] Methodist Hosp Syst, Dept Pathol & Genom Med, Houston, TX 77030 USA
[2] Methodist Hosp Syst, Ctr Mol & Translat Human Infect Dis Res, Houston, TX 77030 USA
[3] Penn State Univ, Dept Vet & Biomed Sci, University Pk, PA 16802 USA
[4] Natl Ctr Streptococcus, Edmonton, AB, Canada
[5] Prov Lab Publ Hlth, Edmonton, AB, Canada
[6] Univ Barcelona, Dept Microbiol, Hosp Univ Bellvitge, Hosp Ilobregat, Barcelona, Spain
[7] Ontario Agcy Hlth Protect & Promot, Toronto, ON, Canada
[8] Univ Toronto, Toronto, ON, Canada
基金
加拿大健康研究院;
关键词
M-PROTEIN; PHARYNGITIS; GENERATION; EVOLUTION; SURVEILLANCE; PATHOGENESIS; INFECTIONS; OUTBREAK; BACTERIA; MUTATION;
D O I
10.1016/j.ajpath.2011.12.037
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Group A Streptococcus (GAS) causes an exceptionally broad range of infections in humans, from relatively mild pharyngitis and skin infections to fife-threatening necrotizing fasciitis and toxic shock syndrome. An epidemic of severe invasive human infections caused by type emm59 GAS, heretofore an exceedingly rare cause of disease, spread west to east across Canada over a 3-year period (2006 to 2008). By sequencing the genomes of 601 epidemic, historic, and other emm59 organisms, we discovered that a recently emerged, genetically distinct emm59 done is responsible for the Canadian epidemic. Using near-real-time genome sequencing, we were able to show spread of the Canadian epidemic clone into the United States. The extensive genome data permitted us to identify patterns of geographic dissemination as well as links between emm59 subclonal lineages that cause infections. Mouse and nonhuman primate models of infection demonstrated that the emerged done is unusually virulent Transmission of epidemic emm59 strains may have occurred primarily by skin contact, as suggested by an experimental model of skin transmission. In addition, the emm59 strains had a significantly impaired ability to persist in human saliva and to colonize the oropharynx of mice, and seldom caused human pharyngitis. Our study contributes new information to the rapidly emerging field of molecular pathogenomics of bacterial epidemics and illustrates how full-genome data can be used to precisely illuminate the landscape of strain dissemination during a bacterial epidemic. (Am J Pathol 2012, 180:1522-1534; DOI: 10.1016/j.ajpath.2011.12.037)
引用
收藏
页码:1522 / 1534
页数:13
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