Evidence map›Paper›PMID 19131083›Full record

ArticleVirology2009

Characterization of novel VP7, VP4, and VP6 genotypes of a previously untypeable group A rotavirus.

Owen D Solberg, Maria Eloisa Hasing, Gabriel Trueba, Joseph N S Eisenberg

Open access · greenAbstract read
In one paragraph

Article in Virology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
12.4field-weighted citation impact, top 1% 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

33 citing papers in PubMed, 123 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Identification of a new bovine picornavirus (Journal of veterinary science · 2024
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Molecular characterization of a human G20P[28] rotavirus a strain with multiple genes related to bat rotaviruses.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2018
    Article
  11. Identification of two novel Rotavirus A genotypes, G35 and P[50], from Peruvian alpaca faeces.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2017
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Molecular surveillance of rotavirus strains circulating in Yaoundé, Cameroon, September 2007-December 2012.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2014
    Article
  19. Article
  20. 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

4 authors at 3 institutions in 2 countries.

Owen D SolbergDepartment of Integrative Biology, University of California, Berkeley, 94720, USA. solberg@cal.berkeley.edu
Maria Eloisa Hasing
Gabriel Trueba
Joseph N S Eisenberg
Universidad San Francisco de Quito · ECAcupuncture & Integrative Medicine College · USUniversity of Michigan · US

Funding

Environment Change and Diarrheal Disease: A Natural ExperimentR01AI050038 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI EISENBERG, JOSEPH N. S. · 2003 to 2012
$6.1M
NIAID NIH HHS R01 AI050038NIAID NIH HHS R01-AI050038
6 · The paper itself

Abstract

Rotavirus is the most common cause of acute gastroenteritis among infants and young children throughout the world, but rotavirus cases in developing countries account for nearly all of the approximately 600,000 annual deaths. We studied the epidemiology of rotavirus in 22 rural communities in northern coastal Ecuador over a five-year period. From 250 rotavirus positive stool specimens, the percentage that could not be RT-PCR genotyped for VP4 and VP7 was 77% and 63%, respectively. The possibility of sample degradation was considered but discounted after an experimental examination of rotavirus stability and EM visualization of rotavirus-like particles in several untypeable samples. Finally, alternate primers were used to amplify Ecu534, a sample that was untypeable using most published VP4 and VP7 primers. Characterization of the VP7, VP4, and VP6 full gene segments revealed novel genotypes and nucleotide mismatches with most published primer sequences. When considered with other findings, our results suggest that primer mismatch may be a widespread cause of genotyping failure, and might be particularly problematic in countries with greater rotavirus diversity. The novel sequences described in this study have been given GenBank accession numbers EU805775 (VP7), EU805773 (VP4), EU805774 (VP6) and the RCWG has assigned them novel genotypes G20P[28]I13, respectively.

Indexed as

Antigens, ViralCapsid ProteinsChild, PreschoolDNA PrimersEcuadorFecesGastroenteritisGenotypeHumansInfantMolecular Sequence DataRotavirusRotavirus InfectionsAntigens, ViralCapsid ProteinsDNA PrimersVP4 protein, RotavirusVP6 protein, RotavirusVP7 protein, Rotavirus

Identifiers

PMID19131083
PMCPMC2729439
OpenAlexW2009147787

What OpenQuestion holds

Textmetadata
LicenceTDM
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.