Evidence map›Paper›PMID 29691368›Full record

ArticleEmerging microbes & infections2018

A novel SigB(Q225P) mutation in Staphylococcus aureus retains virulence but promotes biofilm formation.

Hui Liu, Weilong Shang, Zhen Hu, Ying Zheng, Jizhen Yuan, Qiwen Hu, Huagang Peng, Xinyu Cai, Li Tan, Shu Li and 6 more

Open access · goldAbstract read
In one paragraph

Article in Emerging microbes & infections, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.2field-weighted citation impact, top 13% of its field
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

26 citing papers in PubMed, 35 citations in OpenAlex.

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  12. Antibiotics Resistance and Virulence ofFoods (Basel, Switzerland) · 2022
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  14. Accessory Gene Regulator (Frontiers in microbiology · 2022
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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

16 authors at 1 institution in 1 country.

Hui LiuDepartment of Microbiology, College of Basic Medical Sciences, Third Military Medical University, 400038, Chongqing, China.
Weilong ShangDepartment of Microbiology, College of Basic Medical Sciences, Third Military Medical University, 400038, Chongqing, China.
Zhen HuDepartment of Microbiology, College of Basic Medical Sciences, Third Military Medical University, 400038, Chongqing, China.
Ying ZhengDepartment of Microbiology, College of Basic Medical Sciences, Third Military Medical University, 400038, Chongqing, China.
Jizhen YuanDepartment of Microbiology, College of Basic Medical Sciences, Third Military Medical University, 400038, Chongqing, China.
Qiwen HuDepartment of Microbiology, College of Basic Medical Sciences, Third Military Medical University, 400038, Chongqing, China.
Huagang PengDepartment of Microbiology, College of Basic Medical Sciences, Third Military Medical University, 400038, Chongqing, China.
Xinyu CaiDepartment of Emergency, Xinqiao Hospital, Third Military Medical University, 400037, Chongqing, China.
Li TanDepartment of Microbiology, College of Basic Medical Sciences, Third Military Medical University, 400038, Chongqing, China.
Shu LiDepartment of Microbiology, College of Basic Medical Sciences, Third Military Medical University, 400038, Chongqing, China.
Junmin ZhuDepartment of Microbiology, College of Basic Medical Sciences, Third Military Medical University, 400038, Chongqing, China.
Ming LiDepartment of Microbiology, College of Basic Medical Sciences, Third Military Medical University, 400038, Chongqing, China.
Xiaomei HuDepartment of Microbiology, College of Basic Medical Sciences, Third Military Medical University, 400038, Chongqing, China.
Renjie ZhouDepartment of Emergency, Xinqiao Hospital, Third Military Medical University, 400037, Chongqing, China.
Xiancai RaoDepartment of Microbiology, College of Basic Medical Sciences, Third Military Medical University, 400038, Chongqing, China. raoxiancai@126.com.
Yi YangDepartment of Microbiology, College of Basic Medical Sciences, Third Military Medical University, 400038, Chongqing, China. yangyi19871230@126.com.
Army Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Staphylococcus aureus is an important pathogen that produces abundant virulence factors, which cause various diseases that burden human health worldwide. The stress response regulon called sigma factor B (SigB) is a well-characterized global regulator that is involved in the regulation of S. aureus virulence, pigmentation, and biofilm formation. However, the regulatory network upon SigB in S. aureus is incompletely described. Here, we identified a novel substitution mutation, SigB(Q225P), which contributed the nonpigmented phenotype of S. aureus. The S. aureus mutant carrying SigB(Q225P) substitution lacks staphyloxanthin, a key virulence factor in protecting bacteria from host-oxidant killing, but retains bacterial pathogenicity with pleiotropic alterations in virulence factors, resulting in similar lethality and abscess formation ability in animal models. We also reported the SigB(Q225P) promotion of biofilm formation in S. aureus. Real-time quantitative polymerase chain reaction (RT-qPCR) revealed that the expression of nuc gene, which encodes thermonuclease, was significantly downregulated, resulting in accumulation of eDNA in the biofilm of SigB(Q225P) mutant strain. LacZ reporter assay showed that SigB(Q225P) influenced the activity of nuc promoter. Furthermore, electrophoretic mobility shift assay (EMSA) and Bio-layer interferometry (BLI) assay revealed that both SigB and SigB(Q225P) proteins could directly bind to nuc gene promoter; however, the binding activity decreased for SigB(Q225P). Our data renewed the understanding of the relationship between S. aureus golden pigment and its virulence and suggested that a single substitution mutation in SigB might enhance the biofilm formation of S. aureus by directly downregulating nuc expression.

Indexed as

MutationAnimalsBacterial ProteinsBiofilmsGene Expression Regulation, BacterialHumansMicrococcal NucleasePhenotypePromoter Regions, GeneticReal-Time Polymerase Chain ReactionSigma FactorStaphylococcal InfectionsStaphylococcus aureusVirulenceVirulence FactorsBacterial ProteinsMicrococcal Nucleasenuc protein, staphylococcusSigB protein, BacteriaSigma FactorVirulence Factors

Identifiers

PMID29691368
PMCPMC5915575
OpenAlexW2807708508

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.