Laboratoire de Référence MRSA-Staphylocoques, Service de Microbiologie, Université Libre de Bruxelles, Hôpital Erasme, Brussels, Belgium.
J Antimicrob Chemother. 2011 Nov;66(11):2455-9. doi: 10.1093/jac/dkr348. Epub 2011 Aug 25.
Methicillin-resistant Staphylococcus aureus (MRSA) and methicillin-susceptible S. aureus (MSSA), collected from 109 Belgian acute-care hospitals during a national survey in 2008, were investigated for macrolide-lincosamide (ML) resistance with particular emphasis on the analysis of erm(T)-carrying isolates.
In total, 314 MRSA and 212 MSSA were collected and characterized by spa typing. The SCCmec type of MRSA was determined. Resistance to ML antibiotics was detected by agar dilution and resistant strains were screened by PCR for erm(A), erm(C) and msr(A). Five ML-resistant MSSA isolates, negative by PCR for the aforementioned genes, were further characterized.
Half of all MRSA isolates (n = 157; 50.0%) were resistant to erythromycin and harboured the gene erm(A) (n = 112), erm(C) (n = 41), erm(A) + erm(C) (n = 3) or msr(A) (n = 1). The erm(A) gene was mainly present in MRSA spa-CC002-ST5-SCCmec II and spa-CC008-ST8-SCCmec IV (where CC stands for clonal complex and ST stands for sequence type); the distribution of erm(C) was more diverse. Thirty-five of the 40 erythromycin-resistant MSSA (18.9%) carried the gene erm(A) (n = 17), erm(C) (n = 9) or msr(A) (n = 9). The remaining five MSSA were ST398-t571 isolates, which exhibited closely related ApaI PFGE patterns, harboured the gene erm(T) in the chromosomal DNA and did not exhibit additional resistances. These isolates were from severe infections in patients, of whom four had no contact and one had only indirect contact with livestock via a family member working in animal husbandry.
The ML-streptogramin B ('MLS(B)') resistance genes erm(A) or erm(C) were detected in the majority of ML-resistant MRSA and MSSA isolates. The erm(T) gene was identified in MSSA ST398 isolates from five independent patients who lacked direct contact with livestock.
从 2008 年全国调查中收集的 109 家比利时急性护理医院的耐甲氧西林金黄色葡萄球菌(MRSA)和甲氧西林敏感金黄色葡萄球菌(MSSA)进行大环内酯-林可酰胺(ML)耐药性研究,特别强调分析携带 erm(T)的分离株。
共收集 314 株 MRSA 和 212 株 MSSA,并通过 spa 分型进行特征描述。确定 MRSA 的 SCCmec 类型。通过琼脂稀释法检测 ML 抗生素的耐药性,并用 PCR 筛选 erm(A)、erm(C) 和 msr(A) 来筛选耐药株。对 5 株经上述基因 PCR 检测呈阴性的 ML 耐药 MSSA 分离株进行进一步特征描述。
所有 MRSA 分离株中有一半(n=157;50.0%)对红霉素耐药,携带 erm(A)基因(n=112)、erm(C)基因(n=41)、erm(A)+erm(C)基因(n=3)或 msr(A)基因(n=1)。erm(A)基因主要存在于 MRSA spa-CC002-ST5-SCCmec II 和 spa-CC008-ST8-SCCmec IV 中(CC 代表克隆复合体,ST 代表序列类型);erm(C)的分布更为多样化。40 株红霉素耐药 MSSA 中有 35 株(18.9%)携带 erm(A)基因(n=17)、erm(C)基因(n=9)或 msr(A)基因(n=9)。其余 5 株 MSSA 为 ST398-t571 分离株,其 ApaI PFGE 图谱密切相关,染色体 DNA 中携带 erm(T)基因,且无其他耐药性。这些分离株来自于 5 位重症感染患者,其中 4 位患者与家畜无直接接触,1 位患者仅通过从事畜牧业的家庭成员间接接触家畜。
在大多数 ML 耐药性 MRSA 和 MSSA 分离株中检测到大环内酯-林可酰胺-链阳菌素 B(MLS(B))耐药基因 erm(A)或 erm(C)。在 5 位来自不同患者的 MSSA ST398 分离株中鉴定出 erm(T)基因,这些患者均与家畜无直接接触。