Evidence map›Paper›PMID 28482808›Full record

ArticleBMC infectious diseases2017

Valine/isoleucine variants drive selective pressure in the VP1 sequence of EV-A71 enteroviruses.

Nghia Ngu Duy, Le Thi Thanh Huong, Patrice Ravel, Le Thi Song Huong, Ankit Dwivedi, October Michael Sessions, Yan'An Hou, Robert Chua, Guilhem Kister, Aneta Afelt and 10 more

Abstract read
In one paragraph

Article in BMC infectious diseases, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Enterovirus A71 Proteins: Structure and Function.Frontiers in microbiology · 2018
    Review
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

20 authors.

Nghia Ngu DuyNational Institute of Hygiene and Epidemiology, 1 Pho Yersin Street, Hanoi, 10000, Vietnam. nguduynghia@gmail.com.
Le Thi Thanh HuongNational Institute of Hygiene and Epidemiology, 1 Pho Yersin Street, Hanoi, 10000, Vietnam.
Patrice RavelInstitut de Recherche en Cancérologie de Montpellier (U1194), Campus Val d'Aurelle, 34298, Montpellier Cedex 5, France.
Le Thi Song HuongHai Phong Preventive Medicine Center, Hai Phong city, Vietnam.
Ankit DwivediInstitut de Biologie Computationnelle, MMVE, La Galera, CC6005, 95 rue de la Galera, 34095, Montpellier, France.
October Michael SessionsDUKE-NUS Graduate Medical School, 8 College Road, Singapore, Singapore.
Yan'An HouDUKE-NUS Graduate Medical School, 8 College Road, Singapore, Singapore.
Robert ChuaDUKE-NUS Graduate Medical School, 8 College Road, Singapore, Singapore.
Guilhem KisterFaculty of Pharmacy, University of Montpellier, 15 av Charles Flahault, BP14491, 34093, Montpellier Cedex 5, France.
Aneta AfeltFaculty of Geography and Regional Studies, University of Warsaw, Krakowskie Przedmiescie 26/28, 00-927, Warsaw, Poland.
Catherine MouliaUniversity of Montpellier, ISEM, CC063, Place E. Bataillon, 34095, Montpellier Cedex 5, France.
Duane J GublerDUKE-NUS Graduate Medical School, 8 College Road, Singapore, Singapore.
Vu Dinh ThiemNational Institute of Hygiene and Epidemiology, 1 Pho Yersin Street, Hanoi, 10000, Vietnam.
Nguyen Thi Hien ThanhNational Institute of Hygiene and Epidemiology, 1 Pho Yersin Street, Hanoi, 10000, Vietnam.
Christian DevauxInstitut de Recherche pour le Développement (IRD), Le Sextant, 44, bd de Dunkerque, CS 90009, 13572, Marseille cedex 02, France.
Tran Nhu DuongNational Institute of Hygiene and Epidemiology, 1 Pho Yersin Street, Hanoi, 10000, Vietnam.
Nguyen Tran HienNational Institute of Hygiene and Epidemiology, 1 Pho Yersin Street, Hanoi, 10000, Vietnam.
Emmanuel CornillotInstitut de Recherche en Cancérologie de Montpellier (U1194), Campus Val d'Aurelle, 34298, Montpellier Cedex 5, France.
Laurent GavotteUniversity of Montpellier, ISEM, CC063, Place E. Bataillon, 34095, Montpellier Cedex 5, France.
Roger FrutosCirad, UMR 17, Intertryp, TA-A17/G, Campus International de Baillarguet, 34398, Montpellier Cedex 5, France. roger.frutos@ies.univ-montp2.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn 2011-2012, Northern Vietnam experienced its first large scale hand foot and mouth disease (HFMD) epidemic. In 2011, a major HFMD epidemic was also reported in South Vietnam with fatal cases. This 2011-2012 outbreak was the first one to occur in North Vietnam providing grounds to study the etiology, origin and dynamic of the disease. We report here the analysis of the VP1 gene of strains isolated throughout North Vietnam during the 2011-2012 outbreak and before.

methodsThe VP1 gene of 106 EV-A71 isolates from North Vietnam and 2 from Central Vietnam were sequenced. Sequence alignments were analyzed at the nucleic acid and protein level. Gene polymorphism was also analyzed. A Factorial Correspondence Analysis was performed to correlate amino acid mutations with clinical parameters.

resultsThe sequences were distributed into four phylogenetic clusters. Three clusters corresponded to the subgenogroup C4 and the last one corresponded to the subgenogroup C5. Each cluster displayed different polymorphism characteristics. Proteins were highly conserved but three sites bearing only Isoleucine (I) or Valine (V) were characterized. The isoleucine/valine variability matched the clusters. Spatiotemporal analysis of the I/V variants showed that all variants which emerged in 2011 and then in 2012 were not the same but were all present in the region prior to the 2011-2012 outbreak. Some correlation was found between certain I/V variants and ethnicity and severity.

conclusionsThe 2011-2012 outbreak was not caused by an exogenous strain coming from South Vietnam or elsewhere but by strains already present and circulating at low level in North Vietnam. However, what triggered the outbreak remains unclear. A selective pressure is applied on I/V variants which matches the genetic clusters. I/V variants were shown on other viruses to correlate with pathogenicity. This should be investigated in EV-A71. I/V variants are an easy and efficient way to survey and identify circulating EV-A71 strains.

Indexed as

Capsid ProteinsChild, PreschoolDisease OutbreaksEnterovirusEnterovirus A, HumanEpidemicsFemaleHand, Foot and Mouth DiseaseHumansInfantIsoleucineMaleMutationPhylogenyPolymorphism, GeneticSelection, GeneticCapsid ProteinsIsoleucineValineVP1 protein, Foot-and-mouth disease virusEnterovirusEV-A71HFMDVietnamVP1

Identifiers

PMID28482808
PMCPMC5422960

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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.