Shin Jeong-Ih, Ha Jong-Hun, Kim Kyu-Min, Choi Jeong-Gyu, Park Seo-Rin, Park Hyun-Eui, Park Jin-Sik, Byun Jung-Hyun, Jung Myunghwan, Baik Seung-Chul, Lee Woo-Kon, Kang Hyung-Lyun, Yoo Jung-Wan, Shin Min-Kyoung
Department of Microbiology and Convergence Medical Sciences, Institute of Health Sciences, College of Medicine, Gyeongsang National University, Jinju, Republic of Korea.
Fastidious Specialized Pathogen Resources Bank, A Member of the National Culture Collection for Pathogens, Gyeongsang National University Hospital, Jinju, Republic of Korea.
Front Microbiol. 2023 Apr 6;14:1161194. doi: 10.3389/fmicb.2023.1161194. eCollection 2023.
Repetitive sequence-based PCR (rep-PCR) is a potential epidemiological technique that can provide high-throughput genotype fingerprints of heterogeneous strains rapidly. Previously published rep-PCR primers, which are based on nucleotide sequences of Gram-negative bacteria may have low specificity for mycobacteria. Moreover, it was difficult to ensure the continuity of the study after the commercial rep-PCR kit was discontinued. Here, we designed a novel rep-PCR for , a major cause of nontuberculous mycobacterial pulmonary disease with frequent recurrence. We screened the 7,645 repeat sequences for 200 fragments from the genome of ATCC 13950 , finally generating five primers with more than 90% identity for a total of 226 loci in the genome. The five primers could make different band patterns depending on the genome of three different strains using an test. The novel rep-PCR with the five primers was conducted using 34 bacterial samples of 7 species containing 25 clinical isolates, compared with previous published rep-PCRs. This shows distinguished patterns depending on species and blotting assay for 6 species implied the sequence specificity of the five primers. The Designed rep-PCR had a 95-98% of similarity value in the reproducibility test and showed 7 groups of fingerprints in strains. Designed rep-PCR had a correlation value of 0.814 with VNTR, reference epidemiological method. This study provides a promising genotype fingerprinting method for tracing the recurrence of heterogeneous .
基于重复序列的聚合酶链反应(rep-PCR)是一种潜在的流行病学技术,能够快速提供异质菌株的高通量基因型指纹图谱。先前发表的基于革兰氏阴性菌核苷酸序列的rep-PCR引物对分枝杆菌可能特异性较低。此外,在商业rep-PCR试剂盒停产之后,很难确保研究的连续性。在此,我们针对非结核分枝杆菌肺病的主要病因且频繁复发的[具体菌种]设计了一种新型rep-PCR。我们从[具体菌种]ATCC 13950基因组的200个片段中筛选了7645个重复序列,最终生成了五个与基因组中总共226个位点具有90%以上同源性的引物。使用[具体检测方法]检测时,这五个引物根据三种不同[具体菌种]的基因组可产生不同的条带模式。使用包含25株临床分离株的7个物种的34个细菌样本进行新型rep-PCR检测,并与先前发表的rep-PCR进行比较。结果显示,根据物种不同呈现出不同模式,6个物种的印迹分析表明了这五个引物的序列特异性。在重复性测试中,设计的rep-PCR相似性值为95 - 98%,在[具体菌种]中显示出7组指纹图谱。设计的rep-PCR与参考流行病学方法可变数目串联重复序列(VNTR)的相关值为0.814。本研究为追踪异质[具体菌种]的复发提供了一种有前景的基因型指纹图谱方法。