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2023-10-14Zeitschriftenartikel
Cryptic susceptibility to penicillin/β-lactamase inhibitor combinations in emerging multidrug-resistant, hospital-adapted Staphylococcus epidermidis lineages
dc.contributor.authorBa, Xiaoliang
dc.contributor.authorRaisen, Claire L.
dc.contributor.authorRestif, Olivier
dc.contributor.authorCavaco, Lina Maria
dc.contributor.authorVingsbo Lundberg, Carina
dc.contributor.authorLee, Jean Y. H.
dc.contributor.authorHowden, Benjamin P.
dc.contributor.authorBartels, Mette D.
dc.contributor.authorStrommenger, Birgit
dc.contributor.authorHarrison, Ewan M.
dc.contributor.authorLarsen, Anders Rhod
dc.contributor.authorHolmes, Mark A.
dc.contributor.authorLarsen, Jesper
dc.date.accessioned2026-01-23T09:20:13Z
dc.date.available2026-01-23T09:20:13Z
dc.date.issued2023-10-14none
dc.identifier.other10.1038/s41467-023-42245-y
dc.identifier.urihttp://edoc.rki.de/176904/13189
dc.description.abstractGlobal spread of multidrug-resistant, hospital-adapted Staphylococcus epidermidis lineages underscores the need for new therapeutic strategies. Here we show that many S. epidermidis isolates belonging to these lineages display cryptic susceptibility to penicillin/β-lactamase inhibitor combinations under in vitro conditions, despite carrying the methicillin resistance gene mecA. Using a mouse thigh model of S. epidermidis infection, we demonstrate that single-dose treatment with amoxicillin/clavulanic acid significantly reduces methicillin-resistant S. epidermidis loads without leading to detectable resistance development. On the other hand, we also show that methicillin-resistant S. epidermidis is capable of developing increased resistance to amoxicillin/clavulanic acid during long-term in vitro exposure to these drugs. These findings suggest that penicillin/β-lactamase inhibitor combinations could be a promising therapeutic candidate for treatment of a high proportion of methicillin-resistant S. epidermidis infections, although the in vivo risk of resistance development needs to be further addressed before they can be incorporated into clinical trials.eng
dc.language.isoengnone
dc.publisherRobert Koch-Institut
dc.rights(CC BY 3.0 DE) Namensnennung 3.0 Deutschlandger
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/de/
dc.subjectBacterial genomicseng
dc.subjectBacterial infectioneng
dc.subject.ddc610 Medizin und Gesundheitnone
dc.titleCryptic susceptibility to penicillin/β-lactamase inhibitor combinations in emerging multidrug-resistant, hospital-adapted Staphylococcus epidermidis lineagesnone
dc.typearticle
dc.identifier.urnurn:nbn:de:0257-176904/13189-0
dc.type.versionpublishedVersionnone
local.edoc.container-titleNature Communicationsnone
local.edoc.type-nameZeitschriftenartikel
local.edoc.container-typeperiodical
local.edoc.container-type-nameZeitschrift
local.edoc.container-publisher-nameSpringer Naturenone
local.edoc.container-reportyear2023none
local.edoc.container-firstpage1none
local.edoc.container-lastpage12none
dc.description.versionPeer Reviewednone

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