Evidence map›Paper›PMID 42226113›Full record

ArticleBMC microbiology2026

Unveiling the antibacterial activity and mechanisms of BMS-303141 against Staphylococcus aureus.

Junhua Ma, Qiqi Lan, Xuancheng Huang, Zhichao Xu, Zhijian Yu, Zewen Wen, Xiaoju Liu, Zhong Chen, Duoyun Li, Bing Bai and 2 more

Abstract read
In one paragraph

Article in BMC microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Junhua Ma *Department of Infectious Diseases and Shenzhen Key Laboratory for Endogenous Infections, Shenzhen Nanshan People's Hospital, Affiliated Nanshan Hospital of Shenzhen University, Shenzhen, 518052, China.
Qiqi Lan *Department of Infectious Diseases and Shenzhen Key Laboratory for Endogenous Infections, Shenzhen Nanshan People's Hospital, Affiliated Nanshan Hospital of Shenzhen University, Shenzhen, 518052, China.
Xuancheng Huang *Department of Infectious Diseases and Shenzhen Key Laboratory for Endogenous Infections, Shenzhen Nanshan People's Hospital, Affiliated Nanshan Hospital of Shenzhen University, Shenzhen, 518052, China.
Zhichao XuDepartment of Infectious Diseases and Shenzhen Key Laboratory for Endogenous Infections, Shenzhen Nanshan People's Hospital, Affiliated Nanshan Hospital of Shenzhen University, Shenzhen, 518052, China.
Zhijian YuDepartment of Infectious Diseases and Shenzhen Key Laboratory for Endogenous Infections, Shenzhen Nanshan People's Hospital, Affiliated Nanshan Hospital of Shenzhen University, Shenzhen, 518052, China.
Zewen WenDepartment of Infectious Diseases and Shenzhen Key Laboratory for Endogenous Infections, Shenzhen Nanshan People's Hospital, Affiliated Nanshan Hospital of Shenzhen University, Shenzhen, 518052, China.
Xiaoju LiuDepartment of Infectious Diseases and Shenzhen Key Laboratory for Endogenous Infections, Shenzhen Nanshan People's Hospital, Affiliated Nanshan Hospital of Shenzhen University, Shenzhen, 518052, China.
Zhong ChenDepartment of Infectious Diseases and Shenzhen Key Laboratory for Endogenous Infections, Shenzhen Nanshan People's Hospital, Affiliated Nanshan Hospital of Shenzhen University, Shenzhen, 518052, China.
Duoyun LiDepartment of Infectious Diseases and Shenzhen Key Laboratory for Endogenous Infections, Shenzhen Nanshan People's Hospital, Affiliated Nanshan Hospital of Shenzhen University, Shenzhen, 518052, China. liduoyun94@163.com.
Bing BaiDepartment of Infectious Diseases and Shenzhen Key Laboratory for Endogenous Infections, Shenzhen Nanshan People's Hospital, Affiliated Nanshan Hospital of Shenzhen University, Shenzhen, 518052, China. 568646535@qq.com.
Tieying HouDepartment of Infectious Diseases and Shenzhen Key Laboratory for Endogenous Infections, Shenzhen Nanshan People's Hospital, Affiliated Nanshan Hospital of Shenzhen University, Shenzhen, 518052, China. sz_houtieying@yeah.net.
Peiyu LiDepartment of Infectious Diseases and Shenzhen Key Laboratory for Endogenous Infections, Shenzhen Nanshan People's Hospital, Affiliated Nanshan Hospital of Shenzhen University, Shenzhen, 518052, China. jewelry199@126.com.

Funding

Guangdong Basic and Applied Basic Research Foundation Enterprise Joint Fund 2023A1515220082Medical Scientific Research Foundation of Guangdong Province A2023468Medical Scientific Research Foundation of Guangdong Province A2025089National Natural Science Foundation of China 32570223National Natural Science Foundation of China 82572621Sanming Project of Medicine in Shenzhen SZSM202303037Science, Technology and Innovation Commission of Shenzhen Municipality Basic Research Funds JCYJ20220530141614034Science, Technology and Innovation Commission of Shenzhen Municipality Basic Research Funds JCYJ20230807115814030Shenzhen Nanshan District Scientific Research Program NS2023008Shenzhen Nanshan District Scientific Research Program NS2024007, NSZD2024023, NSZD2025005Shenzhen Nanshan District Scientific Research Program NS2024014, NSZD2023035Shenzhen Nanshan District Scientific Research Program NSZD2024032Shenzhen Nanshan District Scientific Research Program NSZD2024036Shenzhen Nanshan District Scientific Research Program NSZD2024038Shenzhen Science and Technology Program KJZD20240903103500002
6 · The paper itself

Abstract

The rising prevalence of multidrug-resistant (MDR) Staphylococcus aureus (S. aureus), particularly methicillin-resistant S. aureus (MRSA), poses ongoing clinical challenges, driving an urgent need for novel antibacterial agents. Here, we report the first identification of BMS-303141 (an ATP-citrate lyase inhibitor) as a potent anti-staphylococcal compound that induces multi-pathway cellular disruption. BMS-303141 exhibited potent antibacterial activity against MRSA, with the minimum inhibitory concentration (MIC) ranging from 6.25 to 12.5 μM (2.65-5.30 μg/mL) and inhibited biofilm formation at sub-MIC concentrations. Integrative proteomics and whole-genome sequencing revealed multi-pathway cellular disruption involving cell wall integrity and protein synthesis pathways, as indicated by differentially expressed proteins and mutated genes (Atl, LytH, Rot, OatA, Asd, ClfA, FnbA, SdrD, dltB). Mechanistic studies further demonstrated disruption of membrane phospholipid homeostasis and peptidoglycan homeostasis by BMS-303141. Critically, in mouse wound and thigh muscle infection models, BMS-303141 significantly reduced bacterial burden and accelerated healing, demonstrating therapeutic potential against S. aureus. Together, these findings indicate that BMS-303141 is a promising lead for developing new antibacterial agents against S. aureus and its resistant strains.

Indexed as

Anti-Bacterial AgentsMethicillin-Resistant Staphylococcus aureusStaphylococcus aureusAnimalsBacterial ProteinsBiofilmsCell WallMiceMicrobial Sensitivity TestsProteomicsStaphylococcal InfectionsAnti-Bacterial AgentsBacterial ProteinsAntibacterial activityBMS-303141Cell wallMembraneMRSAProteomicsRibosomeStaphylococcus aureus

Identifiers

PMID42226113
PMCPMC13440227

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 Socratic graph.