Antimicrobial susceptibility and minimum inhibitory concentration distribution of common clinically relevant non-tuberculous mycobacterial isolates from the respiratory tract

Ann Med. 2022 Dec;54(1):2500-2510. doi: 10.1080/07853890.2022.2121984.

Abstract

Objective: To determine the minimum inhibitory concentration (MIC) distribution of antibacterial drugs and the susceptibility of non-tuberculous mycobacterial (NTM) isolates to provide a reference basis for the clinical selection of an effective starting regimen.Methods: The common clinical isolates of NTM in the respiratory tract, which met the standards of the American Thoracic Society for NTM lung disease, were collected. The MICs of 81 isolates were determined using the microbroth dilution method (Thermo Fisher Scientific, USA), as recommended by the Clinical and Laboratory Standards Institute, USA.Results: Included were 43 Mycobacterium avium complex (MAC) strains, 24 M. abscessus complex (MAB) strains, and 14 M. kansasii strains. The sensitivity rates of MAC to clarithromycin and amikacin were 81.4% and 79.1%, respectively, while the sensitivity rates to linezolid and moxifloxacin were only 20.9% and 9.3%; the MIC of rifabutin was the lowest (MIC50% was just 2 μg/mL). After incubation for 3-5 days, the sensitivity rate of MAB to clarithromycin was 87.5%; this decreased to 50% after 14 days' incubation. Most of them were susceptible to amikacin (91.6%), and most were resistant to moxifloxacin (95.8%), ciprofloxacin (95.8%), imipenem (95.8%), amoxicillin/clavulanate (95.8%), tobramycin (79.1%), doxycycline (95.8%) and trimethoprim/sulfamethoxazole (95.8%). intermediate (83.3%) and resistant (16.7%) to cefoxitin. The susceptibility to linezolid was only 33.3%. The sensitivity and resistance breakpoints of tigecycline were set to ≤0.5 and ≥8 μg/mL, respectively, and the sensitivity and resistance rates were 50% and 0%, respectively. M. kansasii was susceptible to clarithromycin, amikacin, linezolid, moxifloxacin, rifampicin and rifabutin (100%).Discussion: In Wenzhou, clarithromycin, amikacin and rifabutin have good antibacterial activity against MAC, while linezolid and moxifloxacin have high resistance. Amikacin and tigecycline have strong antibacterial activity against MAB, while most other antibacterial drugs are resistant to varying degrees. Most antibacterial drugs are susceptible to M. kansasii and have good antibacterial activity.Conclusion: The identification of NTM species and the detection of their MICs have certain guiding values for the treatment of NTM lung disease.Key MessageThe three most common respiratory non-tuberculous mycobacterial (NTM) isolates with clinical significance in the Wenzhou area were tested for drug susceptibility. The broth microdilution method was used to determine the minimum inhibitory concentration distribution of antibacterial drugs and the susceptibility of NTM isolates to provide a reference basis for the clinical selection of an effective starting regimen.

Keywords: Drug susceptibility; Mycobacterium abscessus complex (MAB); Mycobacterium avium complex (MAC); Mycobacterium kansasii (M. kansasii); Non-tuberculous mycobacteria (NTM).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amikacin / pharmacology
  • Amikacin / therapeutic use
  • Amoxicillin
  • Anti-Bacterial Agents / pharmacology
  • Anti-Bacterial Agents / therapeutic use
  • Cefoxitin / pharmacology
  • Cefoxitin / therapeutic use
  • Ciprofloxacin / pharmacology
  • Ciprofloxacin / therapeutic use
  • Clarithromycin / pharmacology
  • Clavulanic Acid / pharmacology
  • Clavulanic Acid / therapeutic use
  • Doxycycline / pharmacology
  • Doxycycline / therapeutic use
  • Humans
  • Imipenem / pharmacology
  • Imipenem / therapeutic use
  • Linezolid / pharmacology
  • Linezolid / therapeutic use
  • Lung Diseases*
  • Microbial Sensitivity Tests
  • Moxifloxacin / pharmacology
  • Moxifloxacin / therapeutic use
  • Mycobacterium Infections, Nontuberculous* / drug therapy
  • Mycobacterium Infections, Nontuberculous* / microbiology
  • Nontuberculous Mycobacteria
  • Respiratory System
  • Rifabutin / pharmacology
  • Rifabutin / therapeutic use
  • Rifampin / pharmacology
  • Rifampin / therapeutic use
  • Sulfamethoxazole / pharmacology
  • Sulfamethoxazole / therapeutic use
  • Tigecycline / pharmacology
  • Tigecycline / therapeutic use
  • Tobramycin / pharmacology
  • Tobramycin / therapeutic use
  • Trimethoprim / pharmacology
  • Trimethoprim / therapeutic use

Substances

  • Anti-Bacterial Agents
  • Rifabutin
  • Clavulanic Acid
  • Ciprofloxacin
  • Cefoxitin
  • Tigecycline
  • Imipenem
  • Amoxicillin
  • Amikacin
  • Trimethoprim
  • Clarithromycin
  • Linezolid
  • Sulfamethoxazole
  • Doxycycline
  • Moxifloxacin
  • Rifampin
  • Tobramycin

Grants and funding

This work was supported by Wenzhou Science and Technology Plan Project [grant no.: Y20180192] and the Basic Public Welfare Research Project of Zhejiang Province [grant no.: LGF20H010003].