Evidence map›Paper›PMID 27536288›Full record

ArticleFrontiers in microbiology2016

Typing of Panton-Valentine Leukocidin-Encoding Phages and lukSF-PV Gene Sequence Variation in Staphylococcus aureus from China.

Huanqiang Zhao, Fupin Hu, Shu Jin, Xiaogang Xu, Yuhan Zou, Baixing Ding, Chunyan He, Fang Gong, Qingzhong Liu

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

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  8. Examination ofViruses · 2021
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  9. Panton-Valentine leukocidin (PVL) isoforms among Staphylococcus aureus lineages isolated from hospitals in Rio de Janeiro, Brazil.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2020
    Article
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  11. Temperate Phages ofMicrobiology spectrum · 2019
    Review
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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

9 authors at 5 institutions in 1 country.

Huanqiang ZhaoDepartment of Clinical Laboratory, Shanghai General Hospital, School of Medicine, Shanghai Jiaotong University Shanghai, China.
Fupin HuInstitute of Antibiotics, Huashan Hospital, Fudan University Shanghai, China.
Shu JinExperimental Research Center, Shanghai People's Hospital of Putuo District Shanghai, China.
Xiaogang XuInstitute of Antibiotics, Huashan Hospital, Fudan University Shanghai, China.
Yuhan ZouExperimental Research Center, Shanghai People's Hospital of Putuo District Shanghai, China.
Baixing DingInstitute of Antibiotics, Huashan Hospital, Fudan University Shanghai, China.
Chunyan HeDepartment of Clinical Laboratory, Shanghai General Hospital, School of Medicine, Shanghai Jiaotong University Shanghai, China.
Fang GongDepartment of Clinical Laboratory, The Third Hospital Affiliated to Nantong University Wuxi, China.
Qingzhong LiuDepartment of Clinical Laboratory, Shanghai General Hospital, School of Medicine, Shanghai Jiaotong University Shanghai, China.
Shanghai First People's Hospital · CNCentral Hospital of Putuo District · CNFudan University · CNHuashan Hospital · CNWuxi Third People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Panton-Valentine leukocidin (PVL, encoded by lukSF-PV genes), a bi-component and pore-forming toxin, is carried by different staphylococcal bacteriophages. The prevalence of PVL in Staphylococcus aureus has been reported around the globe. However, the data on PVL-encoding phage types, lukSF-PV gene variation and chromosomal phage insertion sites for PVL-positive S. aureus are limited, especially in China. In order to obtain a more complete understanding of the molecular epidemiology of PVL-positive S. aureus, an integrated and modified PCR-based scheme was applied to detect the PVL-encoding phage types. Phage insertion locus and the lukSF-PV variant were determined by PCR and sequencing. Meanwhile, the genetic background was characterized by staphylococcal cassette chromosome mec (SCCmec) typing, staphylococcal protein A (spa) gene polymorphisms typing, pulsed-field gel electrophoresis (PFGE) typing, accessory gene regulator (agr) locus typing and multilocus sequence typing (MLST). Seventy eight (78/1175, 6.6%) isolates possessed the lukSF-PV genes and 59.0% (46/78) of PVL-positive strains belonged to CC59 lineage. Eight known different PVL-encoding phage types were detected, and Φ7247PVL/ΦST5967PVL (n = 13) and ΦPVL (n = 12) were the most prevalent among them. While 25 (25/78, 32.1%) isolates, belonging to ST30, and ST59 clones, were unable to be typed by the modified PCR-based scheme. Single nucleotide polymorphisms (SNPs) were identified at five locations in the lukSF-PV genes, two of which were non-synonymous. Maximum-likelihood tree analysis of attachment sites sequences detected six SNP profiles for attR and eight for attL, respectively. In conclusion, the PVL-positive S. aureus mainly harbored Φ7247PVL/ΦST5967PVL and ΦPVL in the regions studied. lukSF-PV gene sequences, PVL-encoding phages, and phage insertion locus generally varied with lineages. Moreover, PVL-positive clones that have emerged worldwide likely carry distinct phages.

Indexed as

genetic backgroundPanton-Valentine leukocidinphage typingsequence variationStaphylococcus aureus

Identifiers

PMID27536288
PMCPMC4971802
OpenAlexW2487630870

What OpenQuestion holds

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LicenceCC BY
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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.