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Within-Host Competition Drives Selection for the Capsule Virulence Determinant of Streptococcus pneumoniae

For many opportunistic pathogens, it is unclear why their virulence determinants and expression of pathogenic behavior have evolved when damage or death of their host offers no obvious selective advantage to microbial growth or survival [1–3]. Many pathogens initiate interactions with their host on...

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Detalles Bibliográficos
Autores principales: Lysenko, Elena S., Lijek, Rebeccah S., Brown, Sam P., Weiser, Jeffrey N.
Formato: Texto
Lenguaje:English
Publicado: Cell Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2913241/
https://www.ncbi.nlm.nih.gov/pubmed/20619820
http://dx.doi.org/10.1016/j.cub.2010.05.051
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author Lysenko, Elena S.
Lijek, Rebeccah S.
Brown, Sam P.
Weiser, Jeffrey N.
author_facet Lysenko, Elena S.
Lijek, Rebeccah S.
Brown, Sam P.
Weiser, Jeffrey N.
author_sort Lysenko, Elena S.
collection PubMed
description For many opportunistic pathogens, it is unclear why their virulence determinants and expression of pathogenic behavior have evolved when damage or death of their host offers no obvious selective advantage to microbial growth or survival [1–3]. Many pathogens initiate interactions with their host on mucosal surfaces and must compete with other members of the microflora for the same niche. Here we explore whether competitive interactions between microbes promote the acquisition of virulence characteristics. During model murine nasal colonization, Haemophilus influenzae outcompetes another member of the local flora, Streptococcus pneumoniae, by recruiting neutrophils and stimulating the killing of complement-opsonized pneumococci [4]. For S. pneumoniae, resistance to opsonophagocytic killing is determined by its polysaccharide capsule [5, 6]. Although there are many capsule types among different S. pneumoniae isolates that allow for efficient colonization, virulent pneumococci express capsules that confer resistance to opsonophagocytic clearance. Modeling of interspecies interaction predicts that these more virulent S. pneumoniae will prevail during competition with H. influenzae, even if production of a capsule is otherwise costly. Experimental colonization studies confirmed the increased survival of the more virulent S. pneumoniae type during competition. Our findings demonstrate that competition between microbes during their commensal state may underlie selection for characteristics that allow invasive disease.
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spelling pubmed-29132412010-09-03 Within-Host Competition Drives Selection for the Capsule Virulence Determinant of Streptococcus pneumoniae Lysenko, Elena S. Lijek, Rebeccah S. Brown, Sam P. Weiser, Jeffrey N. Curr Biol Report For many opportunistic pathogens, it is unclear why their virulence determinants and expression of pathogenic behavior have evolved when damage or death of their host offers no obvious selective advantage to microbial growth or survival [1–3]. Many pathogens initiate interactions with their host on mucosal surfaces and must compete with other members of the microflora for the same niche. Here we explore whether competitive interactions between microbes promote the acquisition of virulence characteristics. During model murine nasal colonization, Haemophilus influenzae outcompetes another member of the local flora, Streptococcus pneumoniae, by recruiting neutrophils and stimulating the killing of complement-opsonized pneumococci [4]. For S. pneumoniae, resistance to opsonophagocytic killing is determined by its polysaccharide capsule [5, 6]. Although there are many capsule types among different S. pneumoniae isolates that allow for efficient colonization, virulent pneumococci express capsules that confer resistance to opsonophagocytic clearance. Modeling of interspecies interaction predicts that these more virulent S. pneumoniae will prevail during competition with H. influenzae, even if production of a capsule is otherwise costly. Experimental colonization studies confirmed the increased survival of the more virulent S. pneumoniae type during competition. Our findings demonstrate that competition between microbes during their commensal state may underlie selection for characteristics that allow invasive disease. Cell Press 2010-07-13 /pmc/articles/PMC2913241/ /pubmed/20619820 http://dx.doi.org/10.1016/j.cub.2010.05.051 Text en © 2010 ELL & Excerpta Medica. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Report
Lysenko, Elena S.
Lijek, Rebeccah S.
Brown, Sam P.
Weiser, Jeffrey N.
Within-Host Competition Drives Selection for the Capsule Virulence Determinant of Streptococcus pneumoniae
title Within-Host Competition Drives Selection for the Capsule Virulence Determinant of Streptococcus pneumoniae
title_full Within-Host Competition Drives Selection for the Capsule Virulence Determinant of Streptococcus pneumoniae
title_fullStr Within-Host Competition Drives Selection for the Capsule Virulence Determinant of Streptococcus pneumoniae
title_full_unstemmed Within-Host Competition Drives Selection for the Capsule Virulence Determinant of Streptococcus pneumoniae
title_short Within-Host Competition Drives Selection for the Capsule Virulence Determinant of Streptococcus pneumoniae
title_sort within-host competition drives selection for the capsule virulence determinant of streptococcus pneumoniae
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2913241/
https://www.ncbi.nlm.nih.gov/pubmed/20619820
http://dx.doi.org/10.1016/j.cub.2010.05.051
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