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从英国和丹麦分离出的新兴人类呼吸道病原体弯曲菌属的表型和基因型抗菌药物敏感性模式。

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

机构信息

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

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

出版信息

J Antimicrob Chemother. 2022 Oct 28;77(11):3126-3129. doi: 10.1093/jac/dkac293.

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.

摘要

目的

确定从英国和丹麦患者中分离的变形支原体分离株的表型和基因型抗生素敏感性。

方法

使用肉汤微量稀释法根据 CLSI 支原体指南对七种抗生素对七种变形支原体分离株进行抗菌药物敏感性检测。每个分离株还进行 WGS 以鉴定耐药相关突变。基于基因组数据的共识序列,设计并测试了用于扩增 parC 基因内 QRDR 的 PCR 引物。

结果

在所研究的七种分离株中,有四种(57%)对莫西沙星(0.5-1mg/L)和左氧氟沙星(1-2mg/L)耐药,而敏感株的相应浓度分别为 0.03-0.06mg/L 和 0.006mg/L。分离株 H29 对测试的七种抗生素中的五种耐药:莫西沙星,0.5mg/L;左氧氟沙星,2mg/L;阿奇霉素,64mg/L;红霉素,128mg/L;克林霉素,64mg/L。所有分离株均对四环素(0.06mg/L)和 lefamulin(0.001-0.004mg/L)敏感。来自基因组数据的突变证实了所有氟喹诺酮类耐药分离株中 ParC 蛋白内 S89F 突变的存在,以及大环内酯类和林可酰胺类耐药分离株 H29 中 23S rRNA 基因的 A2059G 突变。

结论

据我们所知,这是首次将表型和基因型耐药数据配对用于变形支原体,证实了两者之间的相关性。鉴于抗微生物药物耐药率较高,这些数据表明需要对高风险患者的分离株进行有针对性的测试和耐药性确定。

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