Evidence map›Paper›PMID 41082411›Full record

ArticleFuture microbiology2025

Synergistic drug strategy against mastitis-associated MRSA strains.

Xiaoyan Li, Li Yao, Lisha Qian

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Article in Future microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Xiaoyan LiDepartment of Thyroid and Breast Surgery, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Li YaoDepartment of Thyroid and Breast Surgery, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Lisha QianDepartment of Thyroid and Breast Surgery, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsTo investigate the resistance profiles of mastitis-associated methicillin-resistant Staphylococcus aureus (MRSA) and to evaluate the synergistic antibacterial effects of antibiotic combinations.

methodsTwenty clinical isolates obtained from patients with lactational mastitis underwent antimicrobial susceptibility testing. Six multidrug-resistant (MDR) isolates were selected to assess pairwise combinations of 10 antibiotics by checkerboard assays and to confirm bactericidal synergy via time-kill testing. In vivo efficacy of the combinations was assessed in a Galleria mellonella infection model.

resultsOver 90% of the isolates were MRSA, with high resistance to oxacillin, clindamycin, and gentamicin; several also displayed elevated minimum inhibitory concentrations (MICs) of vancomycin. Vancomycin plus oxacillin (VAN+OXA) or rifampicin (VAN+RIF) showed consistent in vitro synergy. VAN+OXA produced the greatest killing, reducing bacterial counts by > 3 log₁₀ CFU/mL at 24 h. In vivo, both combinations significantly improved larval survival versus monotherapy across multiple strains.

conclusionsVAN combined with OXA or RIF exhibited robust synergy against mastitis-linked MDR-MRSA in vitro and in vivo. These findings highlight that the combination of VAN with OXA or RIF could be a promising strategy for treating mastitis caused by drug-resistant MRSA.

Indexed as

Anti-Bacterial AgentsDrug SynergismMastitisMethicillin-Resistant Staphylococcus aureusStaphylococcal InfectionsAnimalsDisease Models, AnimalDrug Resistance, Multiple, BacterialDrug Therapy, CombinationFemaleHumansLarvaMicrobial Sensitivity TestsMicrobial ViabilityMothsOxacillinAnti-Bacterial AgentsOxacillinRifampincombination treatmentMastitisMRSAoxacillinvancomycin

Identifiers

PMID41082411
PMCPMC12667645

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.