Evidence map›Paper›PMID 26085170›Full record

ArticleJournal of virology2015

Phylodynamics of Enterovirus A71-Associated Hand, Foot, and Mouth Disease in Viet Nam.

Jemma L Geoghegan, Le Van Tan, Denise Kühnert, Rebecca A Halpin, Xudong Lin, Ari Simenauer, Asmik Akopov, Suman R Das, Timothy B Stockwell, Susmita Shrivastava and 22 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of virology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

41 citing papers in PubMed, 53 citations in OpenAlex.

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  7. Markov genealogy processes.Theoretical population biology · 2022
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  8. Global emergence of Enterovirus 71: a systematic review.Beni-Suef University journal of basic and applied sciences · 2022
    Review
  9. Article
  10. Article
  11. Coxsackievirus A16 in Southern Vietnam.Frontiers in microbiology · 2021
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Observational
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

32 authors at 10 institutions in 5 countries.

Jemma L GeogheganMarie Bashir Institute for Infectious Diseases and Biosecurity, Charles Perkins Centre, School of Biological Sciences and Sydney Medical School, The University of Sydney, Sydney, Australia jemma.geoghegan@sydney.edu.au tanlv@oucru.org.
Le Van TanOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam jemma.geoghegan@sydney.edu.au tanlv@oucru.org.
Denise KühnertDepartment of Environmental Systems Science, ETH Zurich, Zurich, Switzerland Swiss Institute of Bioinformatics, Lausanne, Switzerland.
Rebecca A HalpinJ. Craig Venter Institute, Rockville, Maryland, USA.
Xudong LinJ. Craig Venter Institute, Rockville, Maryland, USA.
Ari SimenauerJ. Craig Venter Institute, Rockville, Maryland, USA.
Asmik AkopovJ. Craig Venter Institute, Rockville, Maryland, USA.
Suman R DasJ. Craig Venter Institute, Rockville, Maryland, USA.
Timothy B StockwellJ. Craig Venter Institute, Rockville, Maryland, USA.
Susmita ShrivastavaJ. Craig Venter Institute, Rockville, Maryland, USA.
Nghiem My NgocHospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Le Thi Tam UyenHospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Nguyen Thi Kim TuyenOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
Tran Tan ThanhOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
Vu Thi Ty HangOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
Phan Tu QuiHospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Nguyen Thanh HungChildren's Hospital 1, Ho Chi Minh City, Vietnam.
Truong Huu KhanhChildren's Hospital 1, Ho Chi Minh City, Vietnam.
Le Quoc ThinhChildren's Hospital 1, Ho Chi Minh City, Vietnam.
Le Nguyen Thanh NhanChildren's Hospital 1, Ho Chi Minh City, Vietnam.
Hoang Minh Tu VanCentre for Tropical Medicine, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
Do Chau VietChildren's Hospital 2, Ho Chi Minh City, Vietnam.
Ha Manh TuanChildren's Hospital 2, Ho Chi Minh City, Vietnam.
Ho Lu VietChildren's Hospital 2, Ho Chi Minh City, Vietnam.
Tran Tinh HienOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam.
Nguyen Van Vinh ChauHospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Guy ThwaitesOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam Centre for Tropical Medicine, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
Bryan T GrenfellDepartment of Ecology and Evolutionary Biology, Princeton University, Princeton, New Jersey, USA Fogarty International Center, National Institutes of Health, Bethesda, Maryland, USA.
Tanja StadlerSwiss Institute of Bioinformatics, Lausanne, Switzerland Department of Biosystems Science and Engineering, ETH Zurich, Zurich, Switzerland.
David E WentworthCenters for Disease Control and Prevention, Atlanta, Georgia, USA.
Edward C HolmesMarie Bashir Institute for Infectious Diseases and Biosecurity, Charles Perkins Centre, School of Biological Sciences and Sydney Medical School, The University of Sydney, Sydney, Australia.
H Rogier Van DoornOxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam Centre for Tropical Medicine, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
J. Craig Venter Institute · USOxford University Clinical Research Unit · VNChildren's Hospital 1 · VNHospital for Tropical Diseases · VNChildren's Hospital 2 · VNSIB Swiss Institute of Bioinformatics · CHUniversity of Sydney · AUCenters for Disease Control and Prevention · USFogarty International Center · USUniversity of Oxford · GB

Funding

The J. Craig Venter Institute Genome Center for Infectious DiseasesU19AI110819 · NIAID · J. CRAIG VENTER INSTITUTE, INC. · PI TAN, GENE · 2014 to 2018
$29.7M
Scientific and Technical Computing CoreP2CHD047879 · NICHD · PRINCETON UNIVERSITY · PI SALGANIK, MATTHEW J. · 2014 to 2018
$2.0M
NIAID NIH HHS HHSN272200900007CNIAID NIH HHS U19 AI110819NICHD NIH HHS P2C HD047879Wellcome Trust 089276Wellcome Trust 089276/Z/09/ZWellcome Trust 101104/Z/13/Z
6 · The paper itself

Abstract

unlabelledEnterovirus A71 (EV-A71) is a major cause of hand, foot, and mouth disease (HFMD) and is particularly prevalent in parts of Southeast Asia, affecting thousands of children and infants each year. Revealing the evolutionary and epidemiological dynamics of EV-A71 through time and space is central to understanding its outbreak potential. We generated the full genome sequences of 200 EV-A71 strains sampled from various locations in Viet Nam between 2011 and 2013 and used these sequence data to determine the evolutionary history and phylodynamics of EV-A71 in Viet Nam, providing estimates of the effective reproduction number (Re) of the infection through time. In addition, we described the phylogeography of EV-A71 throughout Southeast Asia, documenting patterns of viral gene flow. Accordingly, our analysis reveals that a rapid genogroup switch from C4 to B5 likely took place during 2012 in Viet Nam. We show that the Re of subgenogroup C4 decreased during the time frame of sampling, whereas that of B5 increased and remained >1 at the end of 2013, corresponding to a rise in B5 prevalence. Our study reveals that the subgenogroup B5 virus that emerged into Viet Nam is closely related to variants that were responsible for large epidemics in Malaysia and Taiwan and therefore extends our knowledge regarding its associated area of endemicity. Subgenogroup B5 evidently has the potential to cause more widespread outbreaks across Southeast Asia. IMPORTANCE: EV-A71 is one of many viruses that cause HFMD, a common syndrome that largely affects infants and children. HFMD usually causes only mild illness with no long-term consequences. Occasionally, however, severe infection may arise, especially in very young children, causing neurological complications and even death. EV-A71 is highly contagious and is associated with the most severe HFMD cases, with large and frequent epidemics of the virus recorded worldwide. Although major advances have been made in the development of a potential EV-A71 vaccine, there is no current prevention and little is known about the patterns and dynamics of EV-A71 spread. In this study, we utilize full-length genome sequence data obtained from HFMD patients in Viet Nam, a geographical region where the disease has been endemic since 2003, to characterize the phylodynamics of this important emerging virus.

Indexed as

Base SequenceChildDisease OutbreaksEnterovirus A, HumanEpidemicsGene FlowGenome, ViralHand, Foot and Mouth DiseaseHumansMolecular Sequence DataPhylogeographySequence Analysis, RNAVietnamVirus Replication

Identifiers

PMID26085170
PMCPMC4524079
OpenAlexW1949590888

What OpenQuestion holds

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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.