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Epistasis analysis uncovers hidden antibiotic resistance-associated fitness costs hampering the evolution of MRSA

Yokoyama, Maho (författare)
University of Bath
Stevens, Emily (författare)
University of Bristol
Laabei, Maisem (författare)
Lund University,Lunds universitet,Proteinkemi, Malmö,Forskargrupper vid Lunds universitet,Protein Chemistry, Malmö,Lund University Research Groups
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Bacon, Leann (författare)
University of Bristol
Heesom, Kate (författare)
University of Bristol
Bayliss, Sion (författare)
University of Bath
Ooi, Nicola (författare)
University of Leeds
O'Neill, Alex J. (författare)
University of Leeds
Murray, Ewan (författare)
University of Nottingham
Williams, Paul (författare)
University of Nottingham
Lubben, Anneke (författare)
University of Bath
Reeksting, Shaun (författare)
University of Bath
Meric, Guillaume (författare)
University of Bath
Pascoe, Ben (författare)
University of Bath
Sheppard, Samuel K. (författare)
University of Bath
Recker, Mario (författare)
University of Exeter
Hurst, Laurence D. (författare)
University of Bath
Massey, Ruth C. (författare)
University of Bristol
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 (creator_code:org_t)
2018-07-18
2018
Engelska.
Ingår i: Genome Biology. - : Springer Science and Business Media LLC. - 1474-7596 .- 1474-760X. ; 19:1
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Background: Fitness costs imposed on bacteria by antibiotic resistance mechanisms are believed to hamper their dissemination. The scale of these costs is highly variable. Some, including resistance of Staphylococcus aureus to the clinically important antibiotic mupirocin, have been reported as being cost-free, which suggests that there are few barriers preventing their global spread. However, this is not supported by surveillance data in healthy communities, which indicate that this resistance mechanism is relatively unsuccessful. Results: Epistasis analysis on two collections of MRSA provides an explanation for this discord, where the mupirocin resistance-conferring mutation of the ileS gene appears to affect the levels of toxins produced by S. aureus when combined with specific polymorphisms at other loci. Proteomic analysis demonstrates that the activity of the secretory apparatus of the PSM family of toxins is affected by mupirocin resistance. As an energetically costly activity, this reduction in toxicity masks the fitness costs associated with this resistance mutation, a cost that becomes apparent when toxin production becomes necessary. This hidden fitness cost provides a likely explanation for why this mupirocin-resistance mechanism is not more prevalent, given the widespread use of this antibiotic. Conclusions: With dwindling pools of antibiotics available for use, information on the fitness consequences of the acquisition of resistance may need to be considered when designing antibiotic prescribing policies. However, this study suggests there are levels of depth that we do not understand, and that holistic, surveillance and functional genomics approaches are required to gain this crucial information.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Mikrobiologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Microbiology in the medical area (hsv//eng)

Nyckelord

Epistasis
Fitness costs
GWAS
MRSA
Mupirocin resistance

Publikations- och innehållstyp

art (ämneskategori)
ref (ämneskategori)

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