Evidence map›Paper›PMID 27464503›Full record

ArticleVirology journal2016

Characterization of VP1 sequence of Coxsackievirus A16 isolates by Bayesian evolutionary method.

Guolian Zhao, Xun Zhang, Changmin Wang, Guoqing Wang, Fan Li

Open access · goldAbstract read
In one paragraph

Article in Virology journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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

5 authors at 1 institution in 1 country.

Guolian ZhaoDepartment of Pathogenobiology, The Key Laboratory of Zoonosis, Chinese Ministry of Education, Norman Bethune College of Basic Medicine, Jilin University, Changchun, Jilin, 130021, China.
Xun ZhangDepartment of Pathogenobiology, The Key Laboratory of Zoonosis, Chinese Ministry of Education, Norman Bethune College of Basic Medicine, Jilin University, Changchun, Jilin, 130021, China.
Changmin WangDepartment of Pathogenobiology, The Key Laboratory of Zoonosis, Chinese Ministry of Education, Norman Bethune College of Basic Medicine, Jilin University, Changchun, Jilin, 130021, China.
Guoqing WangDepartment of Pathogenobiology, The Key Laboratory of Zoonosis, Chinese Ministry of Education, Norman Bethune College of Basic Medicine, Jilin University, Changchun, Jilin, 130021, China.
Fan LiDepartment of Pathogenobiology, The Key Laboratory of Zoonosis, Chinese Ministry of Education, Norman Bethune College of Basic Medicine, Jilin University, Changchun, Jilin, 130021, China. lifan@jlu.edu.cn.
Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCoxsackievirus A16 (CV-A16), a major etiopathologic cause of pediatric hand, foot, and mouth disease (HFMD) worldwide, has been reported to have caused several fatalities. Revealing the evolutionary and epidemiologic dynamics of CV-A16 across time and space is central to understanding its outbreak potential.

methodsIn this study, we isolated six CV-A16 strains in China's Jilin province and construct a maximum clade credibility (MCC) tree for CV-A16 VP1 gene by the Bayesian Markov Chain Monte Carlo method using 708 strains from GenBank with epidemiological information. The evolution characteristics of CV-A16 VP1 gene was also analysed dynamicly through Bayesian skyline plot.

resultsAll CV-A16 strains identified could be classified into five major genogroups, denoted by GI-GV. GIV and GV have co-circulated in China since 2007, and the CV-A16 epidemic strain isolated in the Jilin province, China, can be classified as GIV-3. The CV-A16 genogroups circulating recently in China have the same ancestor since 2007. The genetic diversity of the CV-A16 VP1 gene shows a continuous increase since the mid-1990s, with sharp increases in genetic diversity in 1997 and 2007 and reached peak in 2007. Very low genetic diversity existed after 2010. The CV-A16 VP1 gene evolutionary rate was 6.656E-3 substitutions per site per year.

conclusionsWe predicted the dynamic phylogenetic trends, which indicate outbreak trends of CV-A16, and provide theoretical foundations for clinical prevention and treatment of HFMD which caused by a CV-A16.

Indexed as

Bayes TheoremChinaEnterovirus A, HumanEnterovirus InfectionsEvolution, MolecularGenetic VariationHumansPhylogenyViral ProteinsViral ProteinsBayesian methodCoxsackievirus A16Genetic diversityHFMDMolecular evolution

Identifiers

PMID27464503
PMCPMC4963925
OpenAlexW2493154784

What OpenQuestion holds

Textmetadata
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.