Accurate Subspecies-Level Identification of Clinically Significant Mycobacterium Avium and Mycobacterium Intracellulare by Whole-Genome Sequencing
Document Type
Article
Publication Date
5-2023
Publication Title
Journal of Microbiological Methods
Abstract
Whole genome sequencing (WGS) of Mycobacterium avium complex (MAC) isolates in the clinical laboratory setting allows for rapid and reliable subspecies identification of a closely related complex of human pathogens. We developed a bioinformatics pipeline for accurate subspecies identification and tested 74 clinical MAC isolates from various anatomical sites. We demonstrate that reliable subspecies level identification of these common and clinically significant MAC isolates, including M. avium subsp. hominissuis (most dominant in causing lower respiratory tract infections in our cohort), M. avium subsp. avium, M. intracellulare subsp. intracellulare, and M. intracellulare subsp. chimaera, can be achieved by analysis of only two marker genes (rpoB and groEL/hsp65). We then explored the relationship between these subspecies and anatomical site of infection. Further, we conducted an in silico analysis and showed our algorithm also performed well for M. avium subsp. paratuberculosis but failed to consistently identify M. avium subsp. silvaticum and M. intracellulare subsp. yongonense, likely due to a lack of available reference genome sequences; all the 3 subspecies were not found in our clinical isolates and rarely reported to cause human infections. Accurate MAC subspecies identification may provide the tool and opportunity for better understanding of the disease-subspecies dynamics in MAC infections.
Volume
208
First Page
106726
Recommended Citation
Chawla R, Shaw B, von Bredow B, Chong C, Garner OB, Zangwill KM, et al. Accurate subspecies-level identification of clinically significant Mycobacterium avium and Mycobacterium intracellulare by whole-genome sequencing. J Microbiol Methods. 2023 May;208:106726. doi: 10.1016/j.mimet.2023.106726. PMID: 37120137.
DOI
10.1016/j.mimet.2023.106726
ISSN
1872-8359
PubMed ID
37120137