Multilocus Sequence Typing of Streptococcus pyogenes Representing Most Known emm Types and Distinctions among Subpopulation Genetic Structures
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Published in | Journal of Bacteriology Vol. 186; no. 13; pp. 4285 - 4294 |
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Main Authors | , , , , , , |
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American Society for Microbiology
01.07.2004
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AbstractList | 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. 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. Article Usage Stats Services JB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon Twitter current issue JB About JB Subscribers Authors Reviewers Advertisers Inquiries from the Press Permissions & Commercial Reprints ASM Journals Public Access Policy JB RSS Feeds 1752 N Street N.W. • Washington DC 20036 202.737.3600 • 202.942.9355 fax • journals@asmusa.org Print ISSN: 0021-9193 Online ISSN: 1098-5530 Copyright © 2014 by the American Society for Microbiology. For an alternate route to JB .asm.org, visit: JB 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. [PUBLICATION ABSTRACT] |
Author | Bernard Beall Alicia Bennett Awdhesh Kalia Debra E. Bessen Brian G. Spratt Nicole Bilek Karen F. McGregor |
AuthorAffiliation | Department of Infectious Disease Epidemiology, Imperial College London, London, United Kingdom, 1 Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri, 2 Department of Ecology and Evolutionary Biology, Yale University, New Haven, Connecticut, 3 Respiratory Diseases Branch, Centers for Disease Control and Prevention, Atlanta, Georgia, 4 Department of Microbiology and Immunology, New York Medical College, Valhalla, New York 5 |
AuthorAffiliation_xml | – name: Department of Infectious Disease Epidemiology, Imperial College London, London, United Kingdom, 1 Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri, 2 Department of Ecology and Evolutionary Biology, Yale University, New Haven, Connecticut, 3 Respiratory Diseases Branch, Centers for Disease Control and Prevention, Atlanta, Georgia, 4 Department of Microbiology and Immunology, New York Medical College, Valhalla, New York 5 |
Author_xml | – sequence: 1 givenname: Karen F. surname: McGregor fullname: McGregor, Karen F. organization: Department of Infectious Disease Epidemiology, Imperial College London, London, United Kingdom – sequence: 2 givenname: Brian G. surname: Spratt fullname: Spratt, Brian G. organization: Department of Infectious Disease Epidemiology, Imperial College London, London, United Kingdom – sequence: 3 givenname: Awdhesh surname: Kalia fullname: Kalia, Awdhesh organization: Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri, Department of Ecology and Evolutionary Biology, Yale University, New Haven, Connecticut – sequence: 4 givenname: Alicia surname: Bennett fullname: Bennett, Alicia organization: Department of Ecology and Evolutionary Biology, Yale University, New Haven, Connecticut – sequence: 5 givenname: Nicole surname: Bilek fullname: Bilek, Nicole organization: Department of Infectious Disease Epidemiology, Imperial College London, London, United Kingdom – sequence: 6 givenname: Bernard surname: Beall fullname: Beall, Bernard organization: Respiratory Diseases Branch, Centers for Disease Control and Prevention, Atlanta, Georgia – sequence: 7 givenname: Debra E. surname: Bessen fullname: Bessen, Debra E. organization: Department of Ecology and Evolutionary Biology, Yale University, New Haven, Connecticut, Department of Microbiology and Immunology, New York Medical College, Valhalla, New York |
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Keywords | Streptococcaceae Microbiology Bacteria Micrococcales Genotype Genetics Streptococcus pyogenes Bacteriology |
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Notes | SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 14 ObjectType-Article-2 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 Corresponding author. Mailing address: New York Medical College, Department of Microbiology & Immunology, Valhalla, NY 10595. Phone: (914) 594-4193. Fax: (914) 594-4176. E-mail: debra_bessen@nymc.edu. |
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Mendeley... 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... 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... |
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SubjectTerms | Antigens, Bacterial - classification Bacterial Outer Membrane Proteins - classification Bacteriology Biological and medical sciences Carrier Proteins - classification Chromosome Mapping Fundamental and applied biological sciences. Psychology Gene loci Genetic diversity Genetic structure Genetic Variation Microbiology Miscellaneous Population genetics Population Genetics and Evolution Streptococcus pyogenes Streptococcus pyogenes - classification Streptococcus pyogenes - genetics Subpopulations Tissues |
Title | Multilocus Sequence Typing of Streptococcus pyogenes Representing Most Known emm Types and Distinctions among Subpopulation Genetic Structures |
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