从叙利亚大马士革教学医院分离出的医院获得性耐甲氧西林金黄色葡萄球菌的分子检测

Lina ALyousef, Salah Addin Shehadeh, A. Al-Mariri
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摘要

背景:耐甲氧西林金黄色葡萄球菌(MRSA)是导致医院获得性感染(HAIs)的公认病原体。准确诊断 MRSA 对促进早期有效治疗和有效控制其传播至关重要。我们研究的主要目的是通过检测 mecA 基因的存在,确定大马士革部分教学医院中医院获得性 MRSA(HA-MRSA)的准确流行率。研究方法从叙利亚大马士革三家主要教学医院(包括 Al-Moussat、Al-Assad 和 Tishreen 军事医院)住院病人的各种临床标本中收集了 100 株金黄色葡萄球菌分离物。这些患者符合既定的 HAIs 标准。分离菌株的采集时间为 2021 年 12 月至 2022 年 8 月。通过聚合酶链式反应(PCR),利用葡萄球菌属的 16SrDNA 基因和金黄色葡萄球菌的 nuc 基因进行属种确认。根据临床与实验室标准研究所(CLSI)的建议,采用头孢西丁盘扩散法(CDD)评估甲氧西林耐药性。还通过 PCR 检测了 mecA 基因的存在。结果:在收集到的分离株中,经 CDD 检测,67% 的分离株对头孢西丁具有耐药性,66% 的分离株的 mecA 基因呈阳性。CDD 的灵敏度为 100%,特异性为 97%。结论这项调查显示,在所调查的教学医院中,HA-MRSA 感染的发病率明显偏高。CDD 方法显示出显著的灵敏度和特异性,使其成为检测 MRSA 的 mecA PCR 的可靠替代方法。这一发现对于有效实施旨在根除 MRSA 并遏制其在医院设施内传播的感染控制措施和战略具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular Detection of Hospital-Acquired Methicillin-Resistant Staphylococcusaureus Isolated From Teaching Hospitals in Damascus, Syria
Background: Methicillin-resistant Staphylococcus aureus (MRSA) is an established pathogen responsible for hospital-acquired infections (HAIs). Accurate MRSA diagnosis is of paramount importance to facilitate early and effective treatment and to manage its transmission effectively. The primary objective of our study was to determine the precise prevalence of hospital-acquired MRSA (HA-MRSA) in select teaching hospitals in Damascus by detecting the presence of the mecA gene. Methods: One hundred Staphylococcus aureus isolates were collected from various clinical specimens obtained from inpatients admitted to three major teaching hospitals in Damascus, Syria, including Al-Moussat, Al-Assad, and Tishreen Military Hospitals. These patients met the established criteria for HAIs. The isolates were collected between December 2021 and August 2022. Genus and species confirmation were conducted via polymerase chain reaction (PCR), employing the 16SrDNA gene specific to the Staphylococcus genus and the nuc gene specific to S. aureus. Methicillin resistance was assessed using cefoxitin disc diffusion (CDD) in accordance with Clinical and Laboratory Standards Institute (CLSI) recommendations. The presence of the mecA gene was also detected through PCR. Results: Out of the collected isolates, 67% exhibited resistance to cefoxitin, as determined by the CDD, while 66% were found to be positive for the mecA gene. CDD demonstrated a sensitivity of 100% and a specificity of 97%. Conclusion: This investigation revealed a notably high incidence of HA-MRSA infections within the teaching hospitals under scrutiny. The CDD method displayed significant sensitivity and specificity, making it a dependable alternative to the mecA PCR for MRSA detection. This finding holds substantial importance for the effective implementation of infection control initiatives and strategies aimed at eradicating MRSA and curtailing its spread within our hospital facilities.
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