Lee Jiyoung, Baek Eunyoung, Ahn Hyesun, Bae Jinyoung, Kim Sangha, Kim Sohyeong, Lee Suchan, Kim Sunghyun
Department of Research & Development, DreamDX Inc., C001, 57, Oryundae-ro, Geumjeong-gu, Busan 46252, Republic of Korea.
Joint & Arthritis Research Center, Himchan Hospital, 120, Sinmok-ro, Yangcheon-gu, Seoul 07999, Republic of Korea.
Pathogens. 2024 Sep 30;13(10):853. doi: 10.3390/pathogens13100853.
The most common antibiotic-resistant bacteria in Korea are methicillin-resistant (MRSA) and vancomycin-resistant enterococci (VRE). Pathogen identification in clinical laboratories can be divided into traditional phenotype- and genotype-based methods, both of which are complementary to each other. The genotype-based method using multiplex real-time polymerase chain reaction (PCR) is a rapid and accurate technique that analyzes material at the genetic level by targeting genes simultaneously. Accordingly, we aimed to develop a rapid method for studying the genetic characteristics of antibiotic-resistant bacteria and to provide an experimental guide for the efficient antibiotic resistance gene analysis of detection for MRSA and or detection for VRE using a one-step multiplex qPCR assay at an early stage of infection. As a result, the sensitivity and specificity of the gene for clinical isolates, including MRSA and methicillin-susceptible , were 97.44% (95% CI, 86.82-99.87%) and 96.15% (95% CI, 87.02-99.32%), respectively. The receiver operating characteristic area under the curve for the diagnosis of MRSA was 0.9798 (*** < 0.0001). Therefore, the molecular diagnostic method using this newly developed one-step multiplex qPCR assay can provide accurate and rapid results for the treatment of patients with MRSA and VRE infections.
韩国最常见的耐抗生素细菌是耐甲氧西林金黄色葡萄球菌(MRSA)和耐万古霉素肠球菌(VRE)。临床实验室中的病原体鉴定可分为基于传统表型和基因型的方法,这两种方法相互补充。使用多重实时聚合酶链反应(PCR)的基于基因型的方法是一种快速准确的技术,通过同时靶向基因在遗传水平上分析材料。因此,我们旨在开发一种快速方法来研究耐抗生素细菌的遗传特征,并为在感染早期使用一步多重定量PCR检测MRSA和/或VRE的高效抗生素抗性基因分析提供实验指导。结果,包括MRSA和甲氧西林敏感金黄色葡萄球菌在内的临床分离株的基因敏感性和特异性分别为97.44%(95%CI,86.82 - 99.87%)和96.15%(95%CI,87.02 - 99.32%)。诊断MRSA的曲线下受试者操作特征面积为0.9798(***P < 0.0001)。因此,使用这种新开发的一步多重定量PCR检测的分子诊断方法可以为MRSA和VRE感染患者的治疗提供准确快速的结果。