Contezolid and polymyxin B nonapeptide combination reveals antibacterial synergy against multidrug-resistant Acinetobacter baumannii strains
- BMC Microbiol. 2026 May 29. doi: 10.1186/s12866-026-05237-8.
- 1. Antibiotics Innovation and Resistance Control Key Laboratory of Sichuan Province, School of Pharmacy, Chengdu University, Chengdu, 610106, China.
- 2. Affiliated Meishan Hospital of Chengdu University of Traditional Chinese Medicine/Traditional Chinese Medicine Hospital of Meishan, Meishan, 620010, China.
- 3. Antibiotics Innovation and Resistance Control Key Laboratory of Sichuan Province, School of Pharmacy, Chengdu University, Chengdu, 610106, China. [email protected].
- 4. Affiliated Meishan Hospital of Chengdu University of Traditional Chinese Medicine/Traditional Chinese Medicine Hospital of Meishan, Meishan, 620010, China. [email protected].
- 5. Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, 610072, China. [email protected].
- # Contributed equally.
Background: Acinetobacter baumannii is a notorious clinical pathogen that predominantly causes nosocomial infections. The multidrug resistant Acinetobacter baumannii clinical isolates are becoming more prevalent on a global scale. In this study, we aimed to determine the potential synergistic Antibacterial activity of contezolid in combination with polymyxin B nonapeptide (PBNP) against various A. baumannii strains.
Results: Contezolid, a commonly-used agents targeting Gram-positive bacteria, in combination with PBNP (CP) was used to explore the potential synergistic Antibacterial activity against A. baumannii in vitro and Caenorhabditis elegans models. We found that CP treatment exhibited a strong synergistic effect on A. baumannii or multidrug resistant A. baumannii. CP also inhibited the biofilm formation and alter morphology of A. baumannii compared to the control group. Moreover, the residual bacteria were significantly decreased in the CP-treated murine alveolar macrophages (MH-S). Importantly, CP treatment improved the survival of C. elegans compared to the control or monotherapy group.
Conclusions: This strategy improved Antibacterial activity spectrum of agents targeting Gram-positive bacteria like contezolid. Nevertheless, CP combination therapy requires further validation in mammalian Infection models.
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Cat. No.Product NameDescriptionTargetResearch Area
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Research Areas: Infection
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