A large genomic island allows Neisseria meningitidis to utilize propionic acid, with implications for colonization of the human nasopharynx. Issue 2 (27th June 2014)
- Record Type:
- Journal Article
- Title:
- A large genomic island allows Neisseria meningitidis to utilize propionic acid, with implications for colonization of the human nasopharynx. Issue 2 (27th June 2014)
- Main Title:
- A large genomic island allows Neisseria meningitidis to utilize propionic acid, with implications for colonization of the human nasopharynx
- Authors:
- Catenazzi, Maria Chiara E.
Jones, Helen
Wallace, Iain
Clifton, Jacqueline
Chong, James P. J.
Jackson, Matthew A.
Macdonald, Sandy
Edwards, James
Moir, James W. B. - Abstract:
- <abstract abstract-type="main"> <title>Summary</title> <p> <italic>N</italic> <italic>eisseria meningitidis</italic> is an important human pathogen that is capable of killing within hours of infection. Its normal habitat is the nasopharynx of adult humans. Here we identify a genomic island (the <italic>prp</italic> gene cluster) in <italic>N</italic><italic>. meningitidis</italic> that enables this species to utilize propionic acid as a supplementary carbon source during growth, particularly under nutrient poor growth conditions. The <italic>prp</italic> gene cluster encodes enzymes for a methylcitrate cycle. Novel aspects of the methylcitrate cycle in <italic>N</italic><italic>. meningitidis</italic> include a propionate kinase which was purified and characterized, and a putative propionate transporter. This genomic island is absent from the close relative of <italic>N</italic><italic>. meningitidis</italic>, the commensal <italic>N</italic><italic>eisseria lactamica</italic>, which chiefly colonizes infants not adults. We reason that the possession of the <italic>prp</italic> genes provides a metabolic advantage to <italic>N</italic><italic>. meningitidis</italic> in the adult oral cavity, which is rich in propionic acid‐generating bacteria. Data from classical microbiological and sequence‐based microbiome studies provide several lines of supporting evidence that <italic>N</italic><italic>. meningitidis</italic> colonization is correlated with propionic acid generating<abstract abstract-type="main"> <title>Summary</title> <p> <italic>N</italic> <italic>eisseria meningitidis</italic> is an important human pathogen that is capable of killing within hours of infection. Its normal habitat is the nasopharynx of adult humans. Here we identify a genomic island (the <italic>prp</italic> gene cluster) in <italic>N</italic><italic>. meningitidis</italic> that enables this species to utilize propionic acid as a supplementary carbon source during growth, particularly under nutrient poor growth conditions. The <italic>prp</italic> gene cluster encodes enzymes for a methylcitrate cycle. Novel aspects of the methylcitrate cycle in <italic>N</italic><italic>. meningitidis</italic> include a propionate kinase which was purified and characterized, and a putative propionate transporter. This genomic island is absent from the close relative of <italic>N</italic><italic>. meningitidis</italic>, the commensal <italic>N</italic><italic>eisseria lactamica</italic>, which chiefly colonizes infants not adults. We reason that the possession of the <italic>prp</italic> genes provides a metabolic advantage to <italic>N</italic><italic>. meningitidis</italic> in the adult oral cavity, which is rich in propionic acid‐generating bacteria. Data from classical microbiological and sequence‐based microbiome studies provide several lines of supporting evidence that <italic>N</italic><italic>. meningitidis</italic> colonization is correlated with propionic acid generating bacteria, with a strong correlation between <italic>prp</italic>‐containing <italic>N</italic><italic>eisseria</italic> and propionic acid generating bacteria from the genus <italic>P</italic><italic>orphyromonas</italic>, and that this may explain adolescent/adult colonization by <italic>N</italic><italic>. meningitidis</italic>.</p> </abstract> … (more)
- Is Part Of:
- Molecular microbiology. Volume 93:Issue 2(2014)
- Journal:
- Molecular microbiology
- Issue:
- Volume 93:Issue 2(2014)
- Issue Display:
- Volume 93, Issue 2 (2014)
- Year:
- 2014
- Volume:
- 93
- Issue:
- 2
- Issue Sort Value:
- 2014-0093-0002-0000
- Page Start:
- 346
- Page End:
- 355
- Publication Date:
- 2014-06-27
- Subjects:
- Molecular microbiology -- Periodicals
572.829 - Journal URLs:
- http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=mmi&close=2003#C2003 ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2958 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/mmi.12664 ↗
- Languages:
- English
- ISSNs:
- 0950-382X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5900.817960
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3093.xml