Multilocus sequence typing of Streptococcus pyogenes representing most known emm types and distinctions among subpopulation genetic structures

被引:101
作者
McGregor, KF
Spratt, BG
Kalia, A
Bennett, A
Bilek, N
Beall, B
Bessen, DE [1 ]
机构
[1] New York Med Coll, Dept Microbiol & Immunol, Valhalla, NY 10595 USA
[2] Ctr Dis Control & Prevent, Resp Dis Branch, Atlanta, GA USA
[3] Yale Univ, Dept Ecol & Evolutionary Biol, New Haven, CT USA
[4] Washington Univ, Sch Med, Dept Mol Microbiol, St Louis, MO 63110 USA
[5] Univ London Imperial Coll Sci Technol & Med, Dept Infect Dis Epidemiol, London, England
基金
英国惠康基金;
关键词
D O I
10.1128/JB.186.13.4285-4294.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A long-term goal is to characterize the full range of genetic diversity within Streptococcus pyogenes as it exists in the world today. Since the emm locus is subject to strong diversifying selection, emm type was used as a guide for identifying a genetically diverse set of strains. This report contains a description of multilocus sequence typing based on seven housekeeping loci for 495 isolates representing 158 emm types, yielding 238 unique combinations of sequence type and emm type. A genotypic marker for tissue site preference (emm pattern) revealed that only 17% of the emm types displayed the marker representing strong preference for infection at the throat and that 39% of emm types had the marker for skin tropism, whereas 41% of emm types harbored the marker for no obvious tissue site preference. As a group, the emm types bearing the emm pattern marker indicative of no obvious tissue site preference were far less likely to have two distinct emm types associated with the same sequence type than either of the two subpopulations having markers for strong tissue tropisms (P < 0.002). In addition, all genetic diversification events clearly ascribed to a recombinational mechanism involved strains of only two of the emm pattern-defined subpopulations, those representing skin specialists and generalists. The findings suggest that the population genetic structure differs for the tissue-defined subpopulations of S. pyogenes. The observed differences may partly reflect differential host immune selection pressures.
引用
收藏
页码:4285 / 4294
页数:10
相关论文
共 34 条
[1]  
Anderson RM, 1998, BIOMED RES REP, P23
[2]   TYPE-SPECIFIC PROTECTIVE IMMUNITY EVOKED BY SYNTHETIC PEPTIDE OF STREPTOCOCCUS-PYOGENES M-PROTEIN [J].
BEACHEY, EH ;
SEYER, JM ;
DALE, JB ;
SIMPSON, WA ;
KANG, AH .
NATURE, 1981, 292 (5822) :457-459
[3]   Sequencing emm-specific PCR products for routine and accurate typing of group a streptococci [J].
Beall, B ;
Facklam, R ;
Thompson, T .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (04) :953-958
[4]   Genetic correlates of throat and skin isolates of group A streptococci [J].
Bessen, DE ;
Sotir, CM ;
Readdy, TL ;
Hollingshead, SK .
JOURNAL OF INFECTIOUS DISEASES, 1996, 173 (04) :896-900
[5]   Genomic localization of a T serotype locus to a recombinatorial zone encoding extracellular matrix-binding proteins in Streptococcus pyogenes [J].
Bessen, DE ;
Kalia, A .
INFECTION AND IMMUNITY, 2002, 70 (03) :1159-1167
[6]   Contrasting molecular epidemiology of group A streptococci causing tropical and nontropical infections of the skin and throat [J].
Bessen, DE ;
Carapetis, JR ;
Beall, B ;
Katz, R ;
Hibble, M ;
Currie, BJ ;
Collingridge, T ;
Izzo, MW ;
Scaramuzzino, DA ;
Sriprakash, KS .
JOURNAL OF INFECTIOUS DISEASES, 2000, 182 (04) :1109-1116
[7]  
Bisno AL, 2000, PRINCIPLES PRACTICE, V2, P2101
[8]   Database-driven multi locus sequence typing (MLST) of bacterial pathogens [J].
Chan, MS ;
Maiden, MCJ ;
Spratt, BG .
BIOINFORMATICS, 2001, 17 (11) :1077-1083
[9]   LOCALIZATION OF PROTECTIVE EPITOPES OF THE AMINO TERMINUS OF TYPE-5 STREPTOCOCCAL M-PROTEIN [J].
DALE, JB ;
BEACHEY, EH .
JOURNAL OF EXPERIMENTAL MEDICINE, 1986, 163 (05) :1191-1202
[10]   Group A streptococcal genotypes from pediatric throat isolates in Rome, Italy [J].
Dicuonzo, G ;
Gherardi, G ;
Lorino, G ;
Angeletti, S ;
De Cesaris, M ;
Fiscarelli, E ;
Bessen, DE ;
Beall, B .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (05) :1687-1690