Evidence map›Paper›PMID 38572320›Full record

ArticleFrontiers in cellular and infection microbiology2024

Isolation and identification of a novel phage targeting clinical multidrug-resistant

Jiao Wang, Meng Zhang, Jiao Pei, Wei Yi, Li Fan, Chunhua Wang, Xiao Xiao

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
4.6field-weighted citation impact, top 6% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Contribution of the Mobilome to the Configuration of the Resistome ofInternational journal of molecular sciences · 2024
    Article
  8. Review
  9. Rising prevalence and drug resistance ofFrontiers in cellular and infection microbiology · 2024
    Review
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

7 authors at 2 institutions in 1 country.

Jiao WangDepartment of Pathogen Biology, School of Basic Medicine, Hubei University of Arts and Science, Xiangyang, China.
Meng ZhangDepartment of Pathogen Biology, School of Basic Medicine, Hubei University of Arts and Science, Xiangyang, China.
Jiao PeiXiangyang Central Hospital, Affiliated Hospital of Hubei University of Arts and Science, Xiangyang, China.
Wei YiDepartment of Pathogen Biology, School of Basic Medicine, Hubei University of Arts and Science, Xiangyang, China.
Li FanDepartment of Pathogen Biology, School of Basic Medicine, Hubei University of Arts and Science, Xiangyang, China.
Chunhua WangDepartment of Clinical Laboratory, Xiangyang No.1 People's Hospital, Hubei University of Medicine, Xiangyang, China.
Xiao XiaoDepartment of Pathogen Biology, School of Basic Medicine, Hubei University of Medicine, Shiyan, China.
Hubei University of Arts and Science · CNHubei University of Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Over the past decade, Corynebacterium striatum (C. striatum), an emerging multidrug-resistant (MDR) pathogen, has significantly challenged healthcare settings, especially those involving individuals with weakened immune systems. The rise of these superbugs necessitates innovative solutions. Methods: This study aimed to isolate and characterize bacteriophages targeting MDR-C. striatum. Utilizing 54 MDR-C. striatum isolates from a local hospital as target strains, samples were collected from restroom puddles for phage screening. Dot Plaque and Double-layer plate Assays were employed for screening. Results: A novel temperate bacteriophage, named CSP1, was identified through a series of procedures, including purification, genome extraction, sequencing, and one-step growth curves. CSP1 possesses a 39,752 base pair circular double-stranded DNA genome with HK97-like structural proteins and potential for site-specific recombination. It represents a new species within the unclassified Caudoviricetes class, as supported by transmission electron microscopy, genomic evolutionary analysis, and collinearity studies. Notably, CSP1 infected and lysed 21 clinical MDR-C. striatum isolates, demonstrating a wide host range. The phage remained stable in conditions ranging from -40 to 55°C, pH 4 to 12, and in 0.9% NaCl buffer, showing no cytotoxicity. Discussion: The identification of CSP1 as the first phage targeting clinical C. striatum strains opens new possibilities in bacteriophage therapy research, and the development of diagnostic and therapeutic tools against pathogenic bacteria.

Indexed as

BacteriophagesCorynebacterium InfectionsAnti-Bacterial AgentsCorynebacteriumGenomicsHumansAnti-Bacterial AgentsCaudoviricetesgenome analysismultidrug-resistance Corynebacterium striatum (MDR-C. striatum)site-specific recombination elementtemperate phage

Identifiers

PMID38572320
PMCPMC10987712
OpenAlexW4393015670

What OpenQuestion holds

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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 OpenQuestion graph.