Comparison of two-drug combinations, amikacin/tigecycline/imipenem and amikacin/tigecycline/clarithromycin against Mycobacteroides abscessus subsp. abscessus using the in vitro time-kill assay
- PMID: 33420382
- PMCID: PMC8005373
- DOI: 10.1038/s41429-020-00392-0
Comparison of two-drug combinations, amikacin/tigecycline/imipenem and amikacin/tigecycline/clarithromycin against Mycobacteroides abscessus subsp. abscessus using the in vitro time-kill assay
Abstract
Nontuberculous mycobacteria include 198 mycobacterial species. Among these, Mycobacteroides abscessus is a rapidly growing mycobacteria that causes lung and skin infections. M. abscessus lung infections are difficult to treat due to the high levels of resistance to several classes of antibiotics. The current treatment is based on combining at least two or three antibiotics. However, treatment outcomes remain very poor. The objective was to compare the in vitro activity of amikacin, tigecycline, imipenem, and clarithromycin, alone and in two different three-drug combinations (amikacin/tigecycline/imipenem and amikacin/tigecycline/clarithromycin) against seven M. abscessus subsp. abscessus clinical isolates using the time-kill assay. The two combinations showed greater activity than the antibiotics tested individually. Even though both combinations showed similar activity as well as no antagonistic activity, the combination including imipenem could not be an alternative treatment against M. abscessus subsp. abscessus lung infections caused by clarithromycin susceptible isolates. However, this combination could be considered against clarithromycin resistant isolates. Future studies are necessary to confirm this hypothesis.
Conflict of interest statement
The authors declare that they have no conflict of interest.
Similar articles
-
The synergetic effect of Imipenem-clarithromycin combination in the Mycobacteroides abscessus complex.BMC Microbiol. 2020 Oct 19;20(1):316. doi: 10.1186/s12866-020-02000-5. BMC Microbiol. 2020. PMID: 33076820 Free PMC article.
-
In Vitro Synergism of Rifabutin with Clarithromycin, Imipenem, and Tigecycline against the Mycobacterium abscessus Complex.Antimicrob Agents Chemother. 2019 Mar 27;63(4):e02234-18. doi: 10.1128/AAC.02234-18. Print 2019 Apr. Antimicrob Agents Chemother. 2019. PMID: 30670428 Free PMC article.
-
Rifabutin Acts in Synergy and Is Bactericidal with Frontline Mycobacterium abscessus Antibiotics Clarithromycin and Tigecycline, Suggesting a Potent Treatment Combination.Antimicrob Agents Chemother. 2018 Jul 27;62(8):e00283-18. doi: 10.1128/AAC.00283-18. Print 2018 Aug. Antimicrob Agents Chemother. 2018. PMID: 29760147 Free PMC article.
-
Skin and soft-tissue infections due to rapidly growing mycobacteria: An overview.Int J Mycobacteriol. 2021 Jul-Sep;10(3):293-300. doi: 10.4103/ijmy.ijmy_110_21. Int J Mycobacteriol. 2021. PMID: 34494569 Review.
-
Dual β-lactam therapy to improve treatment outcome in Mycobacterium abscessus disease.Clin Microbiol Infect. 2024 Jun;30(6):738-742. doi: 10.1016/j.cmi.2024.03.019. Epub 2024 Mar 23. Clin Microbiol Infect. 2024. PMID: 38527611 Review.
Cited by
-
Antimicrobial resistance of rapidly growing mycobacteria isolated from companion animals in Taiwan.Microbiol Spectr. 2025 Jul;13(7):e0307424. doi: 10.1128/spectrum.03074-24. Epub 2025 May 19. Microbiol Spectr. 2025. PMID: 40387379 Free PMC article.
-
Omadacycline for management of Mycobacterium abscessus infections: a review of its effectiveness, place in therapy, and considerations for use.BMC Infect Dis. 2022 Nov 22;22(1):874. doi: 10.1186/s12879-022-07857-7. BMC Infect Dis. 2022. PMID: 36419143 Free PMC article. Review.
-
VLX600, an anticancer iron chelator, exerts antimicrobial effects on Mycobacterium abscessus infections.Microbiol Spectr. 2025 Aug 5;13(8):e0071925. doi: 10.1128/spectrum.00719-25. Epub 2025 Jun 20. Microbiol Spectr. 2025. PMID: 40539807 Free PMC article.
References
-
- Parte AC. LPSN — List of Prokaryotic names with Standing in Nomenclature (bacterio.net), 20 years on. Int J Syst Evol Microbiol. 2018;68:1825–9. doi: 10.1099/ijsem.0.002786. - DOI - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical