Evidence map›Paper›PMID 31318956›Full record

ArticlePloS one2019

Sequencing and analysis of globally obtained human parainfluenza viruses 1 and 3 genomes.

Michael E Bose, Susmita Shrivastava, Jie He, Martha I Nelson, Jayati Bera, Nadia Fedorova, Rebecca Halpin, Christopher D Town, Hernan A Lorenzi, Paolo Amedeo and 9 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. 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
1.1field-weighted citation impact, top 22% 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, 21 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

19 authors at 9 institutions in 7 countries.

Michael E BoseMidwest Respiratory Virus Program, Medical College of Wisconsin, Milwaukee, WI, United States of America.ORCID 0000-0001-9759-499X
Susmita ShrivastavaJ. Craig Venter Institute, Rockville, MD, United States of America.
Jie HeMidwest Respiratory Virus Program, Medical College of Wisconsin, Milwaukee, WI, United States of America.
Martha I NelsonFogarty International Center, National Institutes of Health, Bethesda, MD, United States of America.
Jayati BeraJ. Craig Venter Institute, Rockville, MD, United States of America.
Nadia FedorovaJ. Craig Venter Institute, Rockville, MD, United States of America.
Rebecca HalpinJ. Craig Venter Institute, Rockville, MD, United States of America.
Christopher D TownJ. Craig Venter Institute, Rockville, MD, United States of America.
Hernan A LorenziJ. Craig Venter Institute, Rockville, MD, United States of America.
Paolo AmedeoJ. Craig Venter Institute, Rockville, MD, United States of America.ORCID 0000-0002-9338-1724
Neha GuptaJ. Craig Venter Institute, Rockville, MD, United States of America.
Daniel E NoyolaDepartamento de Microbiología, Facultad de Medicina, Universidad Autónoma de San Luis Potosí, San Luis Potosí, Mexico.
Cristina VidelaClinical Virology Laboratory, Centro de Educación Médica e Investigaciones Clínicas (CEMIC) University Hospital, Buenos Aires, Argentina.
Tuckweng KokSchool of Molecular and Biomedical Science, University of Adelaide, Adelaide, Australia.
Amelia BuysCentre for Respiratory Diseases and Meningitis, National Institute for Communicable Diseases, Sandringham, South Africa.
Marietjie VenterCentre for Respiratory Diseases and Meningitis, National Institute for Communicable Diseases, Sandringham, South Africa.
Astrid VabretNormandie Université, Caen, France.
Samuel CordeyDivision of Infectious Diseases and Laboratory of Virology, University of Geneva Hospitals, Geneva, Switzerland.
Kelly J HenricksonMidwest Respiratory Virus Program, Medical College of Wisconsin, Milwaukee, WI, United States of America.
J. Craig Venter Institute · USMedical College of Wisconsin · USRespiratory and Meningeal Pathogens Research Unit · ZAAutonomous University of San Luis Potosí · MXCentro de Educación Médica e Investigaciones Clínicas Norberto Quirno · ARNational Institutes of Health · USNormandie Université · FRThe University of Adelaide · AUUniversity of Geneva · CH

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
Rapid point-of-care diagnostic for bioterrorism "A" agents and Pandemic influenzaU01AI070428 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI HENRICKSON, KELLY J. · 2006 to 2010
$8.5M
Multipled POC device for antigen/molecular detection of influenza & other virusesU01AI077988 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI HENRICKSON, KELLY J. · 2008 to 2011
$1.9M
NIAID NIH HHS HHSN272200900007CNIAID NIH HHS U01 AI070428NIAID NIH HHS U01 AI077988NIAID NIH HHS U19 AI110819
6 · The paper itself

Abstract

Human Parainfluenza viruses (HPIV) type 1 and 3 are important causes of respiratory tract infections in young children globally. HPIV infections do not confer complete protective immunity so reinfections occur throughout life. Since no effective vaccine is available for the two virus subtypes, comprehensive understanding of HPIV-1 and HPIV-3 genetic and epidemic features is important for diagnosis, prevention, and treatment of HPIV-1 and HPIV-3 infections. Relatively few whole genome sequences are available for both HPIV-1 and HPIV-3 viruses, so our study sought to provide whole genome sequences from multiple countries to further the understanding of the global diversity of HPIV at a whole-genome level. We collected HPIV-1 and HPIV-3 samples and isolates from Argentina, Australia, France, Mexico, South Africa, Switzerland, and USA from the years 2003-2011 and sequenced the genomes of 40 HPIV-1 and 75 HPIV-3 viruses with Sanger and next-generation sequencing with the Ion Torrent, Illumina, and 454 platforms. Phylogenetic analysis showed that the HPIV-1 genome is evolving at an estimated rate of 4.97 × 10-4 mutations/site/year (95% highest posterior density 4.55 × 10-4 to 5.38 × 10-4) and the HPIV-3 genome is evolving at a similar rate (3.59 × 10-4 mutations/site/year, 95% highest posterior density 3.26 × 10-4 to 3.94 × 10-4). There were multiple genetically distinct lineages of both HPIV-1 and 3 circulating on a global scale. Further surveillance and whole-genome sequencing are greatly needed to better understand the spatial dynamics of these important respiratory viruses in humans.

Indexed as

Genome, ViralGenomicsEvolution, MolecularHigh-Throughput Nucleotide SequencingHumansParainfluenza Virus 1, HumanParainfluenza Virus 3, HumanPhylogenyRecombination, GeneticSelection, GeneticSequence Analysis, DNA

Identifiers

PMID31318956
PMCPMC6638977
OpenAlexW2963454145

What OpenQuestion holds

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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.