Determination of In Vitro Antimicrobial Susceptibility for Lefamulin (Pleuromutilin) for <i>Ureaplasma</i> Spp. and <i>Mycoplasma hominis</i>

Lefamulin is the first of the pleuromutilin class of antimicrobials to be available for therapeutic use in humans. Minimum inhibitory concentrations of lefamulin were determined by microbroth dilution for 90 characterised clinical isolates (25 <i>Ureaplasma</i> <i>parvum</i>,...

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Main Authors: Oliver Spiller-Boulter, Susanne Paukner, Ian Boostrom, Kirsty Sands, Edward A. R. Portal, Owen B. Spiller
Format: Article
Language:English
Published: MDPI AG 2021-11-01
Series:Antibiotics
Subjects:
Online Access:https://www.mdpi.com/2079-6382/10/11/1370
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author Oliver Spiller-Boulter
Susanne Paukner
Ian Boostrom
Kirsty Sands
Edward A. R. Portal
Owen B. Spiller
author_facet Oliver Spiller-Boulter
Susanne Paukner
Ian Boostrom
Kirsty Sands
Edward A. R. Portal
Owen B. Spiller
author_sort Oliver Spiller-Boulter
collection DOAJ
description Lefamulin is the first of the pleuromutilin class of antimicrobials to be available for therapeutic use in humans. Minimum inhibitory concentrations of lefamulin were determined by microbroth dilution for 90 characterised clinical isolates (25 <i>Ureaplasma</i> <i>parvum</i>, 25 <i>Ureaplasma urealyticum,</i> and 40 <i>Mycoplasma hominis</i>). All <i>Mycoplasma hominis</i> isolates possessed lefamulin MICs of ≤0.25 mg/L after 48 h (MIC<sub>50/90</sub> of 0.06/0.12 mg/L), despite an inherent resistance to macrolides; while <i>Ureaplasma</i> isolates had MICs of ≤2 mg/L after 24 h (MIC<sub>50/90</sub> of 0.25/1 mg/L), despite inherent resistance to clindamycin. Two <i>U. urealyticum</i> isolates with additional A2058G mutations of 23S rRNA, and one <i>U. parvum</i> isolate with a R66Q67 deletion (all of which had a combined resistance to macrolides and clindamycin) only showed a 2-fold increase in lefamulin MIC (1–2 mg/L) relative to macrolide-susceptible strains. Lefamulin could be an effective alternative antimicrobial for treating <i>Ureaplasma</i> spp. and <i>Mycoplasma hominis</i> infections irrespective of intrinsic or acquired resistance to macrolides, lincosamides, and ketolides. Based on this potent in vitro activity and the known good, rapid, and homogenous tissue penetration of female and male urogenital tissues and glands, further exploration of clinical efficacy of lefamulin for the treatment of <i>Mycoplasma</i> and <i>Ureaplasma</i> urogenital infections is warranted.
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spelling doaj.art-bc719c3f63ca4dcc8b8fbc8c3bbac62d2023-11-22T22:10:38ZengMDPI AGAntibiotics2079-63822021-11-011011137010.3390/antibiotics10111370Determination of In Vitro Antimicrobial Susceptibility for Lefamulin (Pleuromutilin) for <i>Ureaplasma</i> Spp. and <i>Mycoplasma hominis</i>Oliver Spiller-Boulter0Susanne Paukner1Ian Boostrom2Kirsty Sands3Edward A. R. Portal4Owen B. Spiller5HealthFirst Consulting, Research Division, Blackwood NP12 3RF, UKNabriva Theraputics AG, 1110 Vienna, AustriaDivision of Infection and Immunity, Department of Medical Microbiology, Cardiff University, 6th Floor University Hospital of Wales, Cardiff CF14 4XN, UKDivision of Infection and Immunity, Department of Medical Microbiology, Cardiff University, 6th Floor University Hospital of Wales, Cardiff CF14 4XN, UKDivision of Infection and Immunity, Department of Medical Microbiology, Cardiff University, 6th Floor University Hospital of Wales, Cardiff CF14 4XN, UKDivision of Infection and Immunity, Department of Medical Microbiology, Cardiff University, 6th Floor University Hospital of Wales, Cardiff CF14 4XN, UKLefamulin is the first of the pleuromutilin class of antimicrobials to be available for therapeutic use in humans. Minimum inhibitory concentrations of lefamulin were determined by microbroth dilution for 90 characterised clinical isolates (25 <i>Ureaplasma</i> <i>parvum</i>, 25 <i>Ureaplasma urealyticum,</i> and 40 <i>Mycoplasma hominis</i>). All <i>Mycoplasma hominis</i> isolates possessed lefamulin MICs of ≤0.25 mg/L after 48 h (MIC<sub>50/90</sub> of 0.06/0.12 mg/L), despite an inherent resistance to macrolides; while <i>Ureaplasma</i> isolates had MICs of ≤2 mg/L after 24 h (MIC<sub>50/90</sub> of 0.25/1 mg/L), despite inherent resistance to clindamycin. Two <i>U. urealyticum</i> isolates with additional A2058G mutations of 23S rRNA, and one <i>U. parvum</i> isolate with a R66Q67 deletion (all of which had a combined resistance to macrolides and clindamycin) only showed a 2-fold increase in lefamulin MIC (1–2 mg/L) relative to macrolide-susceptible strains. Lefamulin could be an effective alternative antimicrobial for treating <i>Ureaplasma</i> spp. and <i>Mycoplasma hominis</i> infections irrespective of intrinsic or acquired resistance to macrolides, lincosamides, and ketolides. Based on this potent in vitro activity and the known good, rapid, and homogenous tissue penetration of female and male urogenital tissues and glands, further exploration of clinical efficacy of lefamulin for the treatment of <i>Mycoplasma</i> and <i>Ureaplasma</i> urogenital infections is warranted.https://www.mdpi.com/2079-6382/10/11/1370lefamulin<i>Mycoplasma hominis</i><i>Ureaplasma</i> spp.pleuromutilinsusceptibility testing
spellingShingle Oliver Spiller-Boulter
Susanne Paukner
Ian Boostrom
Kirsty Sands
Edward A. R. Portal
Owen B. Spiller
Determination of In Vitro Antimicrobial Susceptibility for Lefamulin (Pleuromutilin) for <i>Ureaplasma</i> Spp. and <i>Mycoplasma hominis</i>
Antibiotics
lefamulin
<i>Mycoplasma hominis</i>
<i>Ureaplasma</i> spp.
pleuromutilin
susceptibility testing
title Determination of In Vitro Antimicrobial Susceptibility for Lefamulin (Pleuromutilin) for <i>Ureaplasma</i> Spp. and <i>Mycoplasma hominis</i>
title_full Determination of In Vitro Antimicrobial Susceptibility for Lefamulin (Pleuromutilin) for <i>Ureaplasma</i> Spp. and <i>Mycoplasma hominis</i>
title_fullStr Determination of In Vitro Antimicrobial Susceptibility for Lefamulin (Pleuromutilin) for <i>Ureaplasma</i> Spp. and <i>Mycoplasma hominis</i>
title_full_unstemmed Determination of In Vitro Antimicrobial Susceptibility for Lefamulin (Pleuromutilin) for <i>Ureaplasma</i> Spp. and <i>Mycoplasma hominis</i>
title_short Determination of In Vitro Antimicrobial Susceptibility for Lefamulin (Pleuromutilin) for <i>Ureaplasma</i> Spp. and <i>Mycoplasma hominis</i>
title_sort determination of in vitro antimicrobial susceptibility for lefamulin pleuromutilin for i ureaplasma i spp and i mycoplasma hominis i
topic lefamulin
<i>Mycoplasma hominis</i>
<i>Ureaplasma</i> spp.
pleuromutilin
susceptibility testing
url https://www.mdpi.com/2079-6382/10/11/1370
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