Please use this identifier to cite or link to this item: https://doi.org/10.1099/mgen.0.000708
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dc.titleMolecular epidemiology and phylogenomic analysis of Mycobacterium abscessus clinical isolates in an Asian population
dc.contributor.authorChew, Ka Lip
dc.contributor.authorOctavia, Sophie
dc.contributor.authorJureen, Roland
dc.contributor.authorNg, Oon Tek
dc.contributor.authorMarimuthu, Kalisvar
dc.contributor.authorLin, Raymond Tzer Pin
dc.contributor.authorTeo, Jeanette W. P.
dc.date.accessioned2022-10-11T08:03:55Z
dc.date.available2022-10-11T08:03:55Z
dc.date.issued2021-11-30
dc.identifier.citationChew, Ka Lip, Octavia, Sophie, Jureen, Roland, Ng, Oon Tek, Marimuthu, Kalisvar, Lin, Raymond Tzer Pin, Teo, Jeanette W. P. (2021-11-30). Molecular epidemiology and phylogenomic analysis of Mycobacterium abscessus clinical isolates in an Asian population. Microbial Genomics 7 (11) : 708. ScholarBank@NUS Repository. https://doi.org/10.1099/mgen.0.000708
dc.identifier.issn2057-5858
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/232148
dc.description.abstractMycobacterium abscessus comprises three subspecies: M. abscessus subsp. abscessus, M. abscessus subsp. bolletii, and M. abscessus subsp. massiliense. These closely related strains are typically multi-drug-resistant and can cause difficult-to-treat infections. Dominant clusters of isolates with increased pathogenic potential have been demonstrated in pulmonary infections in the global cystic fibrosis (CF) population. An investigation was performed on isolates cultured from an Asian, predominantly non-CF population to explore the phylogenomic relationships within our population and compare it to global M. abscessus isolates. Whole-genome-sequencing was performed on M. abscessus isolates between 2017 and 2019. Bioinformatic analysis was performed to determine multi-locus-sequence-type, to establish the phylogenetic relationships between isolates, and to identify virulence and resistance determinants in these isolates. A total of 210 isolates were included, of which 68.5% (144/210) were respiratory samples. These isolates consisted of 140 (66.6%) M. abscessus subsp. massiliense, 67 (31.9%) M. abscessus subsp. abscessus, and three (1.4%) M. abscessus subsp. bolletii. Dominant sequence-types in our population were similar to those of global CF isolates, but SNP differences in our population were comparatively wider despite the isolates being from the same geographical region. ESX (ESAT-6 secretory) cluster three appeared to occur most commonly in ST4 and ST6 M. abscessus subsp. massiliense, but other virulence factors did not demonstrate an association with isolate subspecies or sample source. We demonstrate that although similar predominant sequence-types are seen in our patient population, crosstransmission is absent. The risk of patient-to-patient transmission appears to be largely limited to the vulnerable CF population, indicating infection from environmental sources remains more common than human-to-human transmission. Resistance and virulence factors are largely consistent across the subspecies with the exception of clarithromycin susceptibility and ESX-3. © 2021 The Authors.
dc.publisherMicrobiology Society
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2021
dc.subjectGenomic epidemiology
dc.subjectMycobacterium abscessus complex
dc.subjectMycobacterium bolletii
dc.subjectMycobacterium massiliense
dc.subjectWhole genome sequencing
dc.typeArticle
dc.contributor.departmentMEDICINE
dc.contributor.departmentPATHOLOGY
dc.description.doi10.1099/mgen.0.000708
dc.description.sourcetitleMicrobial Genomics
dc.description.volume7
dc.description.issue11
dc.description.page708
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