Molecular Epidemiology, Ecology, and Evolution of Group A Streptococci

被引:36
作者
Bessen, Debra E. [1 ]
Smeesters, Pierre R. [2 ,3 ]
Beall, Bernard W. [4 ]
机构
[1] New York Med Coll, Dept Microbiol & Immunol, Valhalla, NY 10595 USA
[2] Univ Libre Bruxelles, Dept Pediat, Queen Fabiola Childrens Univ Hosp, B-1020 Brussels, Belgium
[3] Univ Libre Bruxelles, Mol Bacteriol Lab, B-1020 Brussels, Belgium
[4] Ctr Dis Control & Prevent, Natl Ctr Immunizat & Resp Dis, Atlanta, GA 30333 USA
关键词
ACUTE RHEUMATIC-FEVER; FIBRONECTIN-BINDING PROTEIN; SERUM OPACITY FACTOR; BETA-HEMOLYTIC STREPTOCOCCI; C-REPEAT REGION; POPULATION GENETIC-STRUCTURE; AMINO-ACID REPLACEMENT; CLUSTER TYPING SYSTEM; EMM TYPE DISTRIBUTION; SCARLET FEVER;
D O I
10.1128/microbiolspec.CPP3-0009-2018
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The clinico-epidemiological features of diseases caused by group A streptococci (GAS) is presented through the lens of the ecology, population genetics, and evolution of the organism. The serological targets of three typing schemes (M, T, SOF) are themselves GAS cell surface proteins that have a myriad of virulence functions and a diverse array of structural forms. Horizontal gene transfer expands the GAS antigenic cell surface repertoire by generating numerous combinations of M, T, and SOF antigens. However, horizontal gene transfer of the serotype determinant genes is not unconstrained, and therein lies a genetic organization that may signify adaptations to a narrow ecological niche, such as the primary tissue reservoirs of the human host. Adaptations may be further shaped by selection pressures such as herd immunity. Understanding the molecular evolution of GAS on multiple levels-short, intermediate, and long term-sheds insight on mechanisms of host-pathogen interactions, the emergence and spread of new clones, rational vaccine design, and public health interventions.
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页数:33
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