Antibiotic tolerance and the alternative lifestyles of Staphylococcus aureus
被引:48
作者:
Bui, Long M. G.
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Univ Adelaide, Sch Biol Sci, Res Ctr Infect Dis, Adelaide, SA 5005, Australia
Univ Adelaide, Australian Ctr Antimicrobial Resistance Ecol, Adelaide, SA 5005, AustraliaUniv Adelaide, Sch Biol Sci, Res Ctr Infect Dis, Adelaide, SA 5005, Australia
Bui, Long M. G.
[1
,2
]
Conlon, Brian P.
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Univ N Carolina, Sch Med, Dept Microbiol & Immunol, Chapel Hill, NC 27599 USAUniv Adelaide, Sch Biol Sci, Res Ctr Infect Dis, Adelaide, SA 5005, Australia
Conlon, Brian P.
[3
]
Kidd, Stephen P.
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Univ Adelaide, Sch Biol Sci, Res Ctr Infect Dis, Adelaide, SA 5005, Australia
Univ Adelaide, Australian Ctr Antimicrobial Resistance Ecol, Adelaide, SA 5005, AustraliaUniv Adelaide, Sch Biol Sci, Res Ctr Infect Dis, Adelaide, SA 5005, Australia
Kidd, Stephen P.
[1
,2
]
机构:
[1] Univ Adelaide, Sch Biol Sci, Res Ctr Infect Dis, Adelaide, SA 5005, Australia
[2] Univ Adelaide, Australian Ctr Antimicrobial Resistance Ecol, Adelaide, SA 5005, Australia
[3] Univ N Carolina, Sch Med, Dept Microbiol & Immunol, Chapel Hill, NC 27599 USA
Staphylococcus aureus has an incredible ability to survive, either by adapting to environmental conditions or defending against exogenous stress. Although there are certainly important genetic traits, in part this ability is provided by the breadth of modes of growth S. aureus can adopt. It has been proposed that while within their host, S. aureus survives host-generated and therapeutic antimicrobial stress via alternative lifestyles: a persister sub-population, through biofilm growth on host tissue or by growing as small colony variants (SCVs). Key to an understanding of chronic and relapsing S. aureus infections is determining the molecular basis for its switch to these quasi-dormant lifestyles. In a multicellular biofilm, the metabolically quiescent bacterial community additionally produces a highly protective extracellular polymeric substance (EPS). Furthermore, there are bacteria within a biofilm community that have an altered physiology potentially equivalent to persister cells. Recent studies have directly linked the cellular ATP production by persister cells as their key feature and the basis for their tolerance of a range of antibiotics. In clinical settings, SCVs of S. aureus have been observed for many years; when cultured, these cells form non-pigmented colonies and are approximately ten times smaller than their counterparts. Various genotypic factors have been identified in attempts to characterize S. aureus SCVs and different environmental stresses have been implicated as important inducers.
机构:
Univ Adelaide, Sch Mol & Biomed Sci, Res Ctr Infect Dis, Adelaide, SA 5005, AustraliaUniv Adelaide, Sch Mol & Biomed Sci, Res Ctr Infect Dis, Adelaide, SA 5005, Australia
Bui, Long M. G.
;
Turnidge, John D.
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Womens & Childrens Hosp, SA Pathol, Adelaide, SA 5005, AustraliaUniv Adelaide, Sch Mol & Biomed Sci, Res Ctr Infect Dis, Adelaide, SA 5005, Australia
Turnidge, John D.
;
Kidd, Stephen P.
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Univ Adelaide, Sch Mol & Biomed Sci, Res Ctr Infect Dis, Adelaide, SA 5005, AustraliaUniv Adelaide, Sch Mol & Biomed Sci, Res Ctr Infect Dis, Adelaide, SA 5005, Australia
机构:
Univ Adelaide, Sch Mol & Biomed Sci, Res Ctr Infect Dis, Adelaide, SA 5005, AustraliaUniv Adelaide, Sch Mol & Biomed Sci, Res Ctr Infect Dis, Adelaide, SA 5005, Australia
Bui, Long M. G.
;
Turnidge, John D.
论文数: 0引用数: 0
h-index: 0
机构:
Womens & Childrens Hosp, SA Pathol, Adelaide, SA 5005, AustraliaUniv Adelaide, Sch Mol & Biomed Sci, Res Ctr Infect Dis, Adelaide, SA 5005, Australia
Turnidge, John D.
;
Kidd, Stephen P.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Adelaide, Sch Mol & Biomed Sci, Res Ctr Infect Dis, Adelaide, SA 5005, AustraliaUniv Adelaide, Sch Mol & Biomed Sci, Res Ctr Infect Dis, Adelaide, SA 5005, Australia