Phenotypic and genotypic antimicrobial susceptibility patterns of the emerging human respiratory pathogen Mycoplasma amphoriforme isolated from the UK and Denmark

Author:

Day Jessica1,Afshar Baharak1,Rowlands Richard S2,Umer Taiba S2,Windsor Helena3,Paukner Susanne4,Jensen Jorgen S5ORCID,Spiller Owen B16,Chalker Victoria J1,Beeton Michael L12ORCID,Beeton Michael,Jensen Jorgen Skov,Mestrovic Tomislav,Pereyre Sabine,Van Der Pol Barbara,

Affiliation:

1. United Kingdom Health Security Agency, Colindale , London , UK

2. Microbiology and Infection Research Group, Cardiff School of Sport and Health Sciences, Cardiff Metropolitan University , Cardiff , UK

3. Mycoplasma Experience, Brewer Street Dairy Business Park , Bletchingley, Surrey , UK

4. Nabriva Therapeutics GmbH , 1110 Vienna , Austria

5. Research Unit for Reproductive Microbiology, Statens Serum Institut , Copenhagen, DK-2300 , Denmark

6. Cardiff University, Division of Infection and Immunity, Department of Medical Microbiology, University Hospital of Wales , Cardiff , UK

Abstract

Abstract Objectives To determine the phenotypic and genotypic antibiotic susceptibility of Mycoplasma amphoriforme isolates recovered from patients in the UK and Denmark. Methods Seven isolates of M. amphoriforme were examined for antimicrobial susceptibility to seven antibiotics using the microbroth dilution assay in line with the CLSI guidelines for mycoplasmas. Each isolate was additionally subjected to WGS to identify resistance-associated mutations. Based on the consensus sequences from the genomic data, PCR primers were designed, and tested, for the amplification of the QRDR within the parC gene. Results Of the seven isolates investigated, four (57%) were resistant to moxifloxacin (0.5–1 mg/L) and levofloxacin (1–2 mg/L), compared with those that were susceptible (0.03–0.06 and 0.006 mg/L, respectively). Isolate H29 was resistant to five of the seven antibiotics tested: moxifloxacin, 0.5 mg/L; levofloxacin, 2 mg/L; azithromycin, 64 mg/L; erythromycin, 128 mg/L; and clindamycin, 64 mg/L. All isolates were susceptible to tetracycline (0.06 mg/L) and lefamulin (0.001–0.004 mg/L). Mutations from genomic data confirmed the presence of an S89F mutation within the ParC protein among all fluoroquinolone-resistant isolates and an A2059G mutation in the 23S rRNA gene in the macrolide- and lincosamide-resistant isolate H29. Conclusions To the best of our knowledge, this is the first time where phenotypic and genotypic resistance data have been paired for M. amphoriforme confirming a correlation between the two. These data suggest the need for focused testing and resistance determination of isolates from high-risk patients given the backdrop of a high prevalence of antimicrobial resistance.

Funder

Research and Innovation Services fund and Development of Impactful Research fund at Cardiff Metropolitan University

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology,Microbiology (medical)

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Mycoplasma;Bergey's Manual of Systematics of Archaea and Bacteria;2024-07-31

2. Safety and Pharmacokinetics Following Oral or Intravenous Lefamulin in Adults With Cystic Fibrosis;Clinical Therapeutics;2024-02

3. A case of diffuse panbronchiolitis caused by Mycoplasma amphoriforme;Diagnostic Microbiology and Infectious Disease;2023-08

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