A novel repeat sequence-based PCR (rep-PCR) using specific repeat sequences of Mycobacterium intracellulare as a DNA fingerprinting

• Published in: Frontiers in microbiology Vol. 14; p. 1161194
• Main Authors: 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
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 06.04.2023
• Subjects: diagnostics; epidemiology; Microbiology; mycobacterial pulmonary disease; Mycobacterium intracellulre; nontuberculous mycobacteria; repetitive sequences based-PCR (rep-PCR); epidemiology; diagnostics; mycobacterial pulmonary disease; genotype fingerprinting; mycobacterium strain typing; nontuberculous mycobacteria; repetitive sequences based-PCR (rep-PCR); Mycobacterium intracellulre
• ISSN: 1664-302X; 1664-302X
• DOI: 10.3389/fmicb.2023.1161194

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 .