Evidence map›Paper›PMID 28748110›Full record

ArticleVirus evolution2016

Unbiased whole-genome deep sequencing of human and porcine stool samples reveals circulation of multiple groups of rotaviruses and a putative zoonotic infection.

My V T Phan, Pham Hong Anh, Nguyen Van Cuong, Bas B Oude Munnink, Lia van der Hoek, Phuc Tran My, Tue Ngo Tri, Juliet E Bryant, Stephen Baker, Guy Thwaites and 5 more

Open access · goldAbstract read
In one paragraph

Article in Virus evolution, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.0field-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

38 citing papers in PubMed, 66 citations in OpenAlex.

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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

15 authors at 7 institutions in 3 countries.

My V T PhanVirus Genomics, Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Pham Hong AnhOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Nguyen Van CuongOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Bas B Oude MunninkVirus Genomics, Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Lia van der HoekLaboratory of Experimental Virology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Phuc Tran MyOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Tue Ngo TriOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Juliet E BryantOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Stephen BakerOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Guy ThwaitesOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Mark WoolhouseCentre for Immunity, Infection & Evolution, University of Edinburgh, Edinburgh, UK.
Paul KellamKymab Inc., Cambridge, UK.
Maia A RabaaOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Matthew CottenVirus Genomics, Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
VIZIONS Consortium
Oxford University Clinical Research Unit · VNWellcome Sanger Institute · GBNuffield Orthopaedic Centre · GBUniversity of Oxford · GBCentre for Immunity, Infection and Evolution · GBImperial College London · GBUniversity of Amsterdam · NL

Funding

Medical Research Council MC_UU_12014/12Wellcome Trust
6 · The paper itself

Abstract

Coordinated and synchronous surveillance for zoonotic viruses in both human clinical cases and animal reservoirs provides an opportunity to identify interspecies virus movement. Rotavirus (RV) is an important cause of viral gastroenteritis in humans and animals. In this study, we document the RV diversity within co-located humans and animals sampled from the Mekong delta region of Vietnam using a primer-independent, agnostic, deep sequencing approach. A total of 296 stool samples (146 from diarrhoeal human patients and 150 from pigs living in the same geographical region) were directly sequenced, generating the genomic sequences of sixty human rotaviruses (all group A) and thirty-one porcine rotaviruses (thirteen group A, seven group B, six group C, and five group H). Phylogenetic analyses showed the co-circulation of multiple distinct RV group A (RVA) genotypes/strains, many of which were divergent from the strain components of licensed RVA vaccines, as well as considerable virus diversity in pigs including full genomes of rotaviruses in groups B, C, and H, none of which have been previously reported in Vietnam. Furthermore, the detection of an atypical RVA genotype constellation (G4-P[6]-I1-R1-C1-M1-A8-N1-T7-E1-H1) in a human patient and a pig from the same region provides some evidence for a zoonotic event.

Indexed as

deep sequencingrotavirusvirus surveillancewhole genomeszoonotic infection

Identifiers

PMID28748110
PMCPMC5522372
OpenAlexW2951729100

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.