Evidence map›Paper›PMID 39632874›Full record

ArticleScientific reports2024

Combined transcriptome and metabolome analysis revealed the antimicrobial mechanism of Griseorhodin C against Methicillin-resistant Staphylococcus aureus.

Jingyang Liao, Jinli Tan, Xiaobo Li, Dan Huang, Lijun Wang, Liuchong Zhu, Zhiyu Chen, Lin Gan, Wenbin Liu, Xiaobao Jin

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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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

2 citing papers in PubMed.

  1. Article
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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

10 authors.

Jingyang Liao *School of basic medical sciences, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China.
Jinli Tan *School of basic medical sciences, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China.
Xiaobo Li *School of basic medical sciences, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China.
Dan HuangSchool of basic medical sciences, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China.
Lijun WangSchool of basic medical sciences, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China.
Liuchong ZhuSchool of basic medical sciences, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China.
Zhiyu ChenSchool of basic medical sciences, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China.
Lin GanGuangdong Provincial Key Laboratory of Pharmaceutical Bioactive Substances, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China.
Wenbin LiuSchool of basic medical sciences, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China. 408011126@gdpu.edu.cn.
Xiaobao JinSchool of basic medical sciences, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China. jinxf2001@163.com.

Funding

Guangdong Medical Science and Technology Research Foundation A2024478Guangdong Medical Science and Technology Research Foundation B2023440Guangzhou Science and technology planning project 202201010357
6 · The paper itself

Abstract

The global rise of multidrug-resistant pathogens, particularly Methicillin-resistant Staphylococcus aureus (MRSA), has become a critical public health concern, necessitating the urgent discovery of new antimicrobial agents. Griseorhodin C, a hydroxyquinone compound isolated from Streptomyces, has demonstrated significant inhibitory effects against MRSA. In this study, we employed a comprehensive approach combining transcriptome and metabolome analyses to investigate the underlying antimicrobial mechanism of Griseorhodin C. Our findings reveal that Griseorhodin C interferes with multiple bacterial metabolic pathways, including those essential for the biosynthesis and metabolism of amino acids, purine metabolism and energy metabolism, ultimately leading to bacterial growth inhibition and cell death. Notably, Griseorhodin C showed superior inhibitory effects compared to the clinical standard, vancomycin, both in vivo and vitro. These results highlight the potential of Griseorhodin C as a promising candidate for the development of new therapeutic strategies aimed at combating MRSA infections. The study underscores the importance of exploring natural products as sources of novel antibiotics in the ongoing fight against antimicrobial resistance.

Indexed as

Anti-Bacterial AgentsMetabolomeMethicillin-Resistant Staphylococcus aureusTranscriptomeAnimalsAnthraquinonesGene Expression ProfilingMetabolomicsMiceMicrobial Sensitivity TestsStaphylococcal InfectionsAnthraquinonesAnti-Bacterial AgentsAntimicrobial mechanismGriseorhodin CMetabonomicsMRSATranscriptomic

Identifiers

PMID39632874
PMCPMC11618768

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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.