Evidence map›Paper›PMID 35062237›Full record

ArticleViruses2021

Genetic Diversity and Molecular Epidemiology of Circulating Respiratory Syncytial Virus in Central Taiwan, 2008-2017.

Chun-Yi Lee, Yu-Ping Fang, Li-Chung Wang, Teh-Ying Chou, Hsin-Fu Liu

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

19 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Observational
  4. Article
  5. Article
  6. Article
  7. Article
  8. Phylogenetic and phylodynamic analysis of respiratory syncytial virus strains circulating in children less than five years of age in Karachi-Pakistan.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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 4 institutions in 1 country.

Chun-Yi LeeDepartment of Pediatrics, Chang Bing Show Chwan Memorial Hospital, Changhua 505029, Taiwan.ORCID 0000-0002-4210-206X
Yu-Ping FangDepartment of Pediatrics, Chang Bing Show Chwan Memorial Hospital, Changhua 505029, Taiwan.
Li-Chung WangDepartment of Pathology and Laboratory Medicine, Taichung Veterans General Hospital, Taichung 40705, Taiwan.
Teh-Ying ChouInstitute of Clinical Medicine, National Yang Ming Chiao Tung University, Taipei 112304, Taiwan.
Hsin-Fu LiuDepartment of Medical Research, Mackay Memorial Hospital, Taipei 25160, Taiwan.ORCID 0000-0003-0082-2269
National Yang Ming Chiao Tung University · TWChang Bing Show Chwan Memorial Hospital · TWNational Taiwan Ocean University · TWTaichung Veterans General Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, we investigated the molecular evolution and phylodynamics of respiratory syncytial virus (RSV) over 10 consecutive seasons (2008-2017) and the genetic variability of the RSV genotypes ON1 and BA in central Taiwan. The ectodomain region of the G gene was sequenced for genotyping. The nucleotide and deduced amino acid sequences of the second hypervariable region of the G protein in RSV ON1 and BA were analyzed. A total of 132 RSV-A and 81 RSV-B isolates were obtained. Phylogenetic analysis revealed that the NA1, ON1, and BA9 genotypes were responsible for the RSV epidemics in central Taiwan in the study period. For RSV-A, the NA1 genotype predominated during the 2008-2011 seasons. The ON1 genotype was first detected in 2011 and replaced NA1 after 2012. For RSV-B, the BA9 and BA10 genotypes cocirculated from 2008 to 2010, but the BA9 genotype has predominated since 2012. Amino acid sequence alignments revealed the continuous evolution of the G gene in the ectodomain region. The predicted N-glycosylation sites were relatively conserved in the ON1 (site 237 and 318) and BA9 (site 296 and 310) genotype strains. Our results contribute to the understanding and prediction of the temporal evolution of RSV at the local level.

Indexed as

Genetic VariationAdultChildChild, PreschoolEvolution, MolecularGenes, ViralGenotypeGlycosylationHumansInfantMolecular EpidemiologyPhylogenyRespiratory Syncytial Virus, HumanRespiratory Syncytial Virus InfectionsSelection, GeneticTaiwanG glycoprotein, Respiratory syncytial virusViral Fusion ProteinsgenotypeG proteinrespiratory syncytial virusTaiwan

Identifiers

PMID35062237
PMCPMC8777914
OpenAlexW4205262835

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.