Felgate Heather, Crossman Lisa C, Gray Elizabeth, Clifford Rebecca, Correia Annapaula, Dean Rachael, Wain John, Langridge Gemma C
Medical Microbiology Research Laboratory, Norwich Medical School, University of East Anglia, Norwich Research Park, Norwich, NR4 7UQ, UK.
Quadram Institute Bioscience, Norwich Research Park, Norwich, NR4 7UQ, UK.
NPJ Antimicrob Resist. 2023 Nov 13;1(1):15. doi: 10.1038/s44259-023-00008-1.
Non-aureus staphylococci (NAS) are implicated in many healthcare-acquired infections and an understanding of the genetics of antimicrobial resistance is important in relation to both clinical intervention and the role of NAS as a reservoir of resistance genes. Gap statement: The burden of antimicrobial resistance in NAS, particularly to clinically relevant antimicrobials, is under-recognised. We sourced 394 NAS isolates from clinical samples, healthy human volunteers, animals and type cultures and subjected them to minimum inhibitory concentration (MIC) testing by agar dilution using eight antimicrobials. Cefoxitin was used to screen for methicillin resistance, as it stimulates the expression of mecA in S. aureus. We performed whole genome sequencing on 366 isolates and analysed these genotypically for the presence of genetic mechanisms responsible for the phenotypic levels of reduced antimicrobial susceptibility. We observed 175 sequenced isolates with a MIC ≥ 4 µg/ml to cefoxitin, of which 50% did not harbour a known mec homologue. Eight clinical NAS isolates displayed high daptomycin MICs (>4 µg/ml), with no known mechanism identified. Differences in MICs against erythromycin were attributable to the presence of different resistance genes (msrA and ermC). In total, 49% of isolates displayed reduced susceptibility to three or more of the antimicrobials tested. The widespread presence of reduced antimicrobial susceptibility in NAS is concerning. An increased likelihood of harder-to-treat infections caused directly by NAS with acquired resistance genes has clinical implications for AMR detection, the horizontal resistance gene pool and the management of patients.
非金黄色葡萄球菌(NAS)与许多医疗保健相关感染有关,了解其抗菌药物耐药性的遗传学对于临床干预以及NAS作为耐药基因储存库的作用都很重要。差距陈述:NAS中抗菌药物耐药性的负担,尤其是对临床相关抗菌药物的耐药性负担,尚未得到充分认识。我们从临床样本、健康人类志愿者、动物和标准菌株中获取了394株NAS分离株,并使用八种抗菌药物通过琼脂稀释法对它们进行最低抑菌浓度(MIC)测试。使用头孢西丁筛选耐甲氧西林情况,因为它能刺激金黄色葡萄球菌中mecA的表达。我们对366株分离株进行了全基因组测序,并对这些分离株进行基因型分析,以确定导致抗菌药物敏感性降低表型水平的遗传机制的存在情况。我们观察到175株测序分离株对头孢西丁的MIC≥4μg/ml,其中50%没有已知的mec同源物。八株临床NAS分离株对达托霉素的MIC较高(>4μg/ml),未发现已知机制。对红霉素的MIC差异归因于不同耐药基因(msrA和ermC)的存在。总体而言,49%的分离株对三种或更多测试抗菌药物的敏感性降低。NAS中广泛存在的抗菌药物敏感性降低令人担忧。由带有获得性耐药基因的NAS直接引起的更难治疗感染的可能性增加,这对AMR检测、水平耐药基因库和患者管理具有临床意义。