Evidence map›Paper›PMID 41413337›Full record

ArticleNPJ biofilms and microbiomes2025

The role of nitric oxide synthase in biofilm formation by Staphylococcus aureus.

Yi Huang, Yu Cheng, Yingying Shi, Xiaoqiong Wang, Samira Khodi Aghmiuni, Ayesha Serwat, Zhengliang Zhang, Xueqin Shu, Baolin Sun

Abstract read
In one paragraph

Article in NPJ biofilms and microbiomes, 2025. 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

9 authors.

Yi HuangState Key Laboratory of Immune Response and Immunotherapy, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui Province, China.
Yu ChengState Key Laboratory of Immune Response and Immunotherapy, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui Province, China.
Yingying ShiState Key Laboratory of Immune Response and Immunotherapy, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui Province, China.
Xiaoqiong WangDepartment of Respiratory and Critical Care Medicine, The Second People's Hospital of Hefei, Hefei Hospital Affilianted to Anhui Medical University, Hefei City, Anhui Province, China.
Samira Khodi AghmiuniState Key Laboratory of Immune Response and Immunotherapy, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui Province, China.
Ayesha SerwatState Key Laboratory of Immune Response and Immunotherapy, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui Province, China.
Zhengliang ZhangAnhui Kemen Biotechnology Co., Ltd. Room A304, Future Center, Advanced Technology Research Institute, University of Science and Technology of China, No. 5089 Wangjiang West Road, High-tech Zone, Hefei City, Anhui Province, China.
Xueqin ShuSichuan Institute of Edible Fungi, Chengdu, China. shirleys@mail.ustc.edu.cn.
Baolin SunState Key Laboratory of Immune Response and Immunotherapy, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui Province, China. sunb@ustc.edu.cn.

Funding

Foundation for Innovative Research Groups of the National Natural Science Foundation of China 32370184the Fundamental Research Funds for the Central Universities WK9100000080the National Natural Science Foundation of China 32070132the USTC Research Funds of the Double First-Class Initiative YD9100002063
6 · The paper itself

Abstract

Staphylococcus aureus is capable of colonizing diverse environments and forming biofilms. In this study, we found that the knockout of NO synthase (NOS) impaired biofilm integrity, resulting in weakened biofilms. We found the deletion of the nos reduced intracellular NO levels, which subsequently altered the S-nitrosylation modification levels of the proteome. This alteration was particularly pronounced in the S-nitrosylation modification of the cysteine residue at position 12 of the MgrA. This modification reduced the binding affinity of MgrA to the promoter of the acetyltransferase gene (icaA), resulting in reduced levels of poly-N-acetyl-β-(1-6)-glucosamine (PIA), a key component of biofilms formed by S. aureus, thereby further weakening biofilm formation. Consequently, we conclude that NOS in S. aureus S-nitrosylates the MgrA through the synthesis of endogenous NO. This process strengthens the interaction between MgrA and the icaA promoter (P

Indexed as

BiofilmsNitric Oxide SynthaseStaphylococcus aureusAcetylglucosamineAcetyltransferasesBacterial Proteinsbeta-GlucansGene Expression Regulation, BacterialGene Knockout TechniquesNitric OxidePromoter Regions, GeneticAcetylglucosamineAcetyltransferasesBacterial Proteinsbeta-GlucansNitric OxideNitric Oxide Synthasepoly-N-acetyl-1-6-glucosamine

Identifiers

PMID41413337
PMCPMC12770482

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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.