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[Effects of four efflux pump inhibitors on the activities of clarithromycin against Mycobacterium abscessus].
Teng, T L; Shang, Y Y; Huang, H R; Chu, N H; Chen, S T.
Afiliación
  • Teng TL; Department of Pulmonary and Critical Care Medicine, Beijing Chest Hospital, Capital Medical University, Beijing 101149, China.
  • Shang YY; Department of Tuberculosis, Beijing Chest Hospital, Capital Medical University, Beijing 101149, China.
  • Huang HR; National Clinical Laboratory on Tuberculosis, Beijing Chest Hospital, Capital Medical University; Beijing Tuberculosis and Thoracic Tumor Research Institute, Beijing 101149, China.
  • Chu NH; Department of Tuberculosis, Beijing Chest Hospital, Capital Medical University, Beijing 101149, China.
  • Chen ST; National Clinical Laboratory on Tuberculosis, Beijing Chest Hospital, Capital Medical University; Beijing Tuberculosis and Thoracic Tumor Research Institute, Beijing 101149, China.
Zhonghua Jie He He Hu Xi Za Zhi ; 45(5): 468-474, 2022 May 12.
Article en Zh | MEDLINE | ID: mdl-35527462
ABSTRACT

Objective:

To detect the effects of four efflux pump inhibitors on the minimum inhibitory concentration of clarithromycin (CLA) against Mycobacterium abscessus (M. abscessus) in vitro, and to explore the role of efflux pump in CLA resistance of M. abscessus.

Methods:

Four frequently-used efflux pump inhibitors (Carbonyl Cyanide 3-chlorophenylhydrazone, CCCP, N, N'-dicyclohexylcarbodiimide, DCC, Verapamil, VP, Reserpine, RSP) were evaluated in this study. The minimum inhibitory concentration (MIC) values of clarithromycin against M. abscessus reference strain and 60 clinical strains with or without efflux pump inhibitors were detected by Alamar Blue method. Sequence analysis of erm(41) and rrl genes known to be associated with CLA resistance in M. abscessus was performed to analyze the correlation between the effect of efflux pump inhibitors on MIC and mutation of resistance-related genes.

Results:

CCCP, DCC, VP and RSP could reduce the MIC of M. abscessus to CLA, and the effect of RSP was weaker than the other three efflux pump inhibitors. Among the sixty M. abscessus clinical strains, ten strains were resistant to clarithromycin, seven of which had rrl gene mutation. The CLA resistance rate of smooth phenotype isolates was higher than that of rough phenotype isolates. At 3 day of clarithromycin incubation, the MICs of resistant strains were all reduced by efflux pump inhibitors. Compared with the strains with rrl gene mutation, efflux pump inhibitors had a greater effect on the strains without rrl gene mutation. At 14 day of clarithromycin incubation, 83% of M. abscessus subsp. abscessus, were induced to be resistant, and all of them were T28 sequence type of erm(41). With the occurrence of induced drug resistance, the effect of efflux pump inhibitor on CLA MIC decreased. Efflux pump inhibitors had no statistically significant diffence in the effect of effcux pump inhibitors on CLA MIC levels in different phenotypes of isolates.

Conclusions:

Efflux pump is involved in the resistance process of M. abscessus to CLA. Efflux pump inhibitors reduce the drug resistance to clarithromycin against M. abscessus in different degrees. The use of efflux pump inhibitors may provide a new way to alleviate the drug resistance of M. abscessus.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Mycobacterium abscessus / Infecciones por Mycobacterium no Tuberculosas Límite: Humans Idioma: Zh Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Mycobacterium abscessus / Infecciones por Mycobacterium no Tuberculosas Límite: Humans Idioma: Zh Año: 2022 Tipo del documento: Article