Evidence map›Paper›PMID 36200903›Full record

ArticleMicrobiology spectrum2022

The Bacterial Markers of Identification of Invasive CovR/CovS-Inactivated Group A

Yong-An Shi, Tzu-Ching Chen, Yan-Wen Chen, Yen-Shan Liu, Yi-Ywan M Chen, Chih-Ho Lai, Cheng-Hsun Chiu, Chuan Chiang-Ni

Open access · goldAbstract read
In one paragraph

Article in Microbiology spectrum, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. iScience · 2024
    Article
  6. Article
  7. Article
  8. RopB represses the transcription ofLife science alliance · 2023
    Article
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

8 authors at 1 institution in 1 country.

Yong-An ShiGraduate Institute of Biomedical Sciences, College of Medicine, Chang Gung Universitygrid.145695.a, Taoyuan, Taiwan.ORCID 0000-0001-5717-1255
Tzu-Ching ChenDepartment of Medical Biotechnology and Laboratory Science, College of Medicine, Chang Gung Universitygrid.145695.a, Taoyuan, Taiwan.
Yan-Wen ChenDepartment of Microbiology and Immunology, College of Medicine, Chang Gung Universitygrid.145695.a, Taoyuan, Taiwan.
Yen-Shan LiuDepartment of Microbiology and Immunology, College of Medicine, Chang Gung Universitygrid.145695.a, Taoyuan, Taiwan.
Yi-Ywan M ChenGraduate Institute of Biomedical Sciences, College of Medicine, Chang Gung Universitygrid.145695.a, Taoyuan, Taiwan.ORCID 0000-0002-8727-9811
Chih-Ho LaiGraduate Institute of Biomedical Sciences, College of Medicine, Chang Gung Universitygrid.145695.a, Taoyuan, Taiwan.
Cheng-Hsun ChiuGraduate Institute of Biomedical Sciences, College of Medicine, Chang Gung Universitygrid.145695.a, Taoyuan, Taiwan.ORCID 0000-0003-4324-7743
Chuan Chiang-NiGraduate Institute of Biomedical Sciences, College of Medicine, Chang Gung Universitygrid.145695.a, Taoyuan, Taiwan.ORCID 0000-0002-0753-035X
Chang Gung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Necrotizing fasciitis is a severe infectious disease that results in significant mortality. Streptococcus pyogenes (group A Streptococcus, GAS) is one of the most common bacterial pathogens of monomicrobial necrotizing fasciitis. The early diagnosis of necrotizing fasciitis is crucial; however, the typical cutaneous manifestations are not always presented in patients with GAS necrotizing fasciitis, which would lead to miss- or delayed diagnosis. GAS with spontaneous inactivating mutations in the CovR/CovS two-component regulatory system is significantly associated with destructive diseases such as necrotizing fasciitis and toxic shock syndrome; however, no specific marker has been used to identify these invasive clinical isolates. This study evaluated the sensitivity and specificity of using CovR/CovS-controlled phenotypes to identify CovR/CovS-inactivated isolates. Results showed that the increase of hyaluronic acid capsule production and streptolysin O expression were not consistently presented in CovS-inactivated clinical isolates. The repression of SpeB is the phenotype with 100% sensitivity of identifying in CovS-inactivated isolates among 61 clinical isolates. Nonetheless, this phenotype failed to distinguish RopB-inactivated isolates from CovS-inactivated isolates and cannot be utilized to identify CovR-inactivated mutant and RocA (

Indexed as

Fasciitis, NecrotizingShock, SepticStreptococcal InfectionsBacterial ProteinsEndopeptidasesGene Expression Regulation, BacterialHistidine KinaseHumansHyaluronic AcidRepressor ProteinsStreptococcus pyogenesBacterial ProteinsEndopeptidasesHistidine KinaseHyaluronic AcidRepressor ProteinsCovR/CovSgroup A StreptococcusPepORocASIPSpeB

Identifiers

PMID36200903
PMCPMC9603395
OpenAlexW4302762828

What OpenQuestion holds

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LicenceCC BY
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 OpenQuestion graph.