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Cited 5 time in webofscience Cited 4 time in scopus
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Bigger problems from smaller colonies: emergence of antibiotic-tolerant small colony variants of <i>Mycobacterium avium</i> complex in MAC-pulmonary disease patientsopen access

Authors
Park, Hyun-EuiKim, Kyu-MinYoo, Jung-WanTrinh, Minh PhuongShin, Sung JaeShin, Min-Kyoung
Issue Date
Mar-2024
Publisher
BioMed Central
Keywords
Non-tuberculous mycobacteria; Mycobacterium avium complex; Small colony variant; Revertant colony; Antibiotic-tolerance
Citation
Annals of Clinical Microbiology and Antimicrobials, v.23, no.1
Indexed
SCIE
SCOPUS
Journal Title
Annals of Clinical Microbiology and Antimicrobials
Volume
23
Number
1
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/70063
DOI
10.1186/s12941-024-00683-6
ISSN
1476-0711
1476-0711
Abstract
Background Mycobacterium avium complex (MAC) is a group of slow-growing mycobacteria that includes Mycobacterium avium and Mycobacterium intracellulare. MAC pulmonary disease (MAC-PD) poses a threat to immunocompromised individuals and those with structural pulmonary diseases worldwide. The standard treatment regimen for MAC-PD includes a macrolide in combination with rifampicin and ethambutol. However, the treatment failure and disease recurrence rates after successful treatment remain high. Results In the present study, we investigated the unique characteristics of small colony variants (SCVs) isolated from patients with MAC-PD. Furthermore, revertant (RVT) phenotype, emerged from the SCVs after prolonged incubation on 7H10 agar. We observed that SCVs exhibited slower growth rates than wild-type (WT) strains but had higher minimum inhibitory concentrations (MICs) against multiple antibiotics. However, some antibiotics showed low MICs for the WT, SCVs, and RVT phenotypes. Additionally, the genotypes were identical among SCVs, WT, and RVT. Based on the MIC data, we conducted time-kill kinetic experiments using various antibiotic combinations. The response to antibiotics varied among the phenotypes, with RVT being the most susceptible, WT showing intermediate susceptibility, and SCVs displaying the lowest susceptibility. Conclusions In conclusion, the emergence of the SCVs phenotype represents a survival strategy adopted by MAC to adapt to hostile environments and persist during infection within the host. Additionally, combining the current drugs in the treatment regimen with additional drugs that promote the conversion of SCVs to RVT may offer a promising strategy to improve the clinical outcomes of patients with refractory MAC-PD.
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