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Staphylococcus aureus mutants resistant to the feed-additive monensin show increased virulence and altered purine metabolism

Warsi, Omar M. (författare)
Department of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden
Upterworth, Lina M. (författare)
Department of Evolutionary Ecology and Genetics, Zoological Institute, Kiel University, Kiel, Germany
Breidenstein, Annika (författare)
Umeå universitet,Institutionen för medicinsk kemi och biofysik
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Lustig, Ulrika (författare)
Department of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden
Mikkelsen, Kasper (författare)
Department of Veterinary and Animal Sciences, University of Copenhagen, Copenhagen, Denmark
Nagy, Tamás (författare)
Department of Laboratory Medicine, Medical School, University of Pécs, Pécs, Hungary
Szatmari, Dávid (författare)
Department of Biophysics, Medical School, University of Pécs, Pécs, Hungary
Ingmer, Hanne (författare)
Department of Veterinary and Animal Sciences, University of Copenhagen, Copenhagen, Denmark
Andersson, Dan I. (författare)
Department of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden
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 (creator_code:org_t)
American Society for Microbiology, 2024
2024
Engelska.
Ingår i: mBio. - : American Society for Microbiology. - 2161-2129 .- 2150-7511. ; 15:2
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Ionophores are antibacterial compounds that affect bacterial growth by changing intracellular concentrations of the essential cations, sodium and potassium. They are extensively used in animal husbandry to increase productivity and reduce infectious diseases, but our understanding of the potential for and effects of resistance development to ionophores is poorly known. Thus, given their widespread global usage, it is important to determine the potential negative consequences of ionophore use on human and animal health. In this study, we demonstrate that exposure to the ionophore monensin can select for resistant mutants in the human and animal pathogen Staphylococcus aureus, with a majority of the resistant mutants showing increased growth rates in vitro and/or in mice. Whole-genome sequencing and proteomic analysis of the resistant mutants show that the resistance phenotype is associated with de-repression of de novo purine synthesis, which could be achieved through mutations in different transcriptional regulators including mutations in the gene purR, the repressor of the purine de novo synthesis pathway. This study shows that mutants with reduced susceptibility to the ionophore monensin can be readily selected and highlights an unexplored link between ionophore resistance, purine metabolism, and fitness in pathogenic bacteria.IMPORTANCEThis study demonstrates a novel link between ionophore resistance, purine metabolism, and virulence/fitness in the key human and animal pathogen Staphylococcus aureus. The results show that mutants with reduced susceptibility to the commonly used ionophore monensin can be readily selected and that the reduced susceptibility observed is associated with an increased expression of the de novo purine synthesis pathway. This study increases our understanding of the impact of the use of animal feed additives on both human and veterinary medicine.

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

cross-resistance
drug resistance evolution
drug resistance mechanisms
fitness
ionophore
mouse experiment
purine metabolism

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