Evidence map›Paper›PMID 27348299›Full record

ArticleNature genetics2016

Genomic analysis of local variation and recent evolution in Plasmodium vivax.

Richard D Pearson, Roberto Amato, Sarah Auburn, Olivo Miotto, Jacob Almagro-Garcia, Chanaki Amaratunga, Seila Suon, Sivanna Mao, Rintis Noviyanti, Hidayat Trimarsanto and 34 more

Open access · greenAbstract read
In one paragraph

Article in Nature genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 145 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
145citing papers in PubMed, 2 pooled it
25.1field-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

145 citing papers in PubMed, 2 syntheses or guidelines pooled it, 232 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Observational
  6. Article
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85 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

44 authors at 16 institutions in 13 countries.

Richard D PearsonWellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Roberto Amato *Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Sarah Auburn *Global and Tropical Health Division, Menzies School of Health Research and Charles Darwin University, Darwin, Northern Territories 0811, Australia.
Olivo MiottoWellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Jacob Almagro-GarciaMRC Centre for Genomics and Global Health, Wellcome Trust Centre for Human Genetics, Oxford OX3 7BN, UK.
Chanaki AmaratungaNational Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, Maryland 20852, USA.
Seila SuonNational Centre for Parasitology, Entomology, and Malaria Control, Phnom Penh, Cambodia.
Sivanna MaoSampov Meas Referral Hospital, Pursat, Cambodia.
Rintis NoviyantiEijkman Institute for Molecular Biology, Jakarta 10430, Indonesia.
Hidayat TrimarsantoEijkman Institute for Molecular Biology, Jakarta 10430, Indonesia.
Jutta MarfurtGlobal and Tropical Health Division, Menzies School of Health Research and Charles Darwin University, Darwin, Northern Territories 0811, Australia.
Nicholas M AnsteyGlobal and Tropical Health Division, Menzies School of Health Research and Charles Darwin University, Darwin, Northern Territories 0811, Australia.
Timothy WilliamInfectious Diseases Society Sabah-Menzies School of Health Research Clinical Research Unit and Queen Elizabeth Hospital Clinical Research Centre, Kota Kinabalu, Sabah, Malaysia.
Maciej F BoniOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Christiane DolecekOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Tinh Tran HienOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Nicholas J WhiteMahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok 10400, Thailand.
Pascal MichonPapua New Guinea Institute of Medical Research, Madang, Papua New Guinea.
Peter SibaPapua New Guinea Institute of Medical Research, Madang, Papua New Guinea.
Livingstone TavulPapua New Guinea Institute of Medical Research, Madang, Papua New Guinea.
Gabrielle HarrisonDivision of Population Health and Immunity, The Walter and Eliza Hall Institute for Medical Research, Parkville, Victoria, Australia.
Alyssa BarryDivision of Population Health and Immunity, The Walter and Eliza Hall Institute for Medical Research, Parkville, Victoria, Australia.
Ivo MuellerDivision of Population Health and Immunity, The Walter and Eliza Hall Institute for Medical Research, Parkville, Victoria, Australia.
Marcelo U FerreiraDepartment of Parasitology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazil.
Nadira KarunaweeraDepartment of Parasitology, Faculty of Medicine, University of Colombo, Sri Lanka.
Milijaona RandrianarivelojosiaInstitut Pasteur de Madagascar, Antananarivo, Madagascar.
Qi GaoJiangsu Institute of Parasitic Diseases, Key Laboratory of Parasitic Disease Control and Prevention (Ministry of Health), Jiangsu Provincial Key Laboratory of Parasite Molecular Biology, Wuxi, Jiangsu, People's Republic of China.
Christina HubbartMRC Centre for Genomics and Global Health, Wellcome Trust Centre for Human Genetics, Oxford OX3 7BN, UK.
Lee HartMRC Centre for Genomics and Global Health, Wellcome Trust Centre for Human Genetics, Oxford OX3 7BN, UK.
Ben JefferyMRC Centre for Genomics and Global Health, Wellcome Trust Centre for Human Genetics, Oxford OX3 7BN, UK.
Eleanor DruryWellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Daniel MeadWellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Mihir KekreWellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Susana CampinoWellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Magnus ManskeWellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Victoria J CorneliusWellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Bronwyn MacInnisWellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Kirk A RockettWellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Alistair MilesWellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Julian C RaynerWellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Rick M FairhurstNational Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, Maryland 20852, USA.
Francois NostenMahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok 10400, Thailand.
Ric N PriceGlobal and Tropical Health Division, Menzies School of Health Research and Charles Darwin University, Darwin, Northern Territories 0811, Australia.
Dominic P KwiatkowskiWellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1SA, UK.
Centre for Human Genetics · GBWellcome Sanger Institute · GBCharles Darwin University · AUOxford University Clinical Research Unit · VNThe University of Melbourne · AUEijkman Institute for Molecular Biology · IDMahidol University · THNational Institutes of Health · USPapua New Guinea Institute of Medical Research · PGCambodia National Malaria Center · KHDivine Word University · PGInstitut Pasteur de Madagascar · MGJiangsu Institute of Parasitic Diseases · CNQueen Elizabeth Hospital · MYUniversidade de São Paulo · BRUniversity of Colombo · LK

Funding

International Research in Cambodia: Tropical Medicine and Vector Research ZIAAI001066 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI YEK, CHRISTINA · 2009 to 2025
$10.8M
Malaria Pathogenesis and Human ImmunityZIAAI001000 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI FAIRHURST, RICK · 2009 to 2017
$9.3M
Medical Research Council G0600718Medical Research Council MR/M006212/1RRD VA I01 RX000265Wellcome Trust 082370Wellcome Trust 090770Wellcome Trust 091625Wellcome Trust 098051
6 · The paper itself

Abstract

The widespread distribution and relapsing nature of Plasmodium vivax infection present major challenges for the elimination of malaria. To characterize the genetic diversity of this parasite in individual infections and across the population, we performed deep genome sequencing of >200 clinical samples collected across the Asia-Pacific region and analyzed data on >300,000 SNPs and nine regions of the genome with large copy number variations. Individual infections showed complex patterns of genetic structure, with variation not only in the number of dominant clones but also in their level of relatedness and inbreeding. At the population level, we observed strong signals of recent evolutionary selection both in known drug resistance genes and at new loci, and these varied markedly between geographical locations. These findings demonstrate a dynamic landscape of local evolutionary adaptation in the parasite population and provide a foundation for genomic surveillance to guide effective strategies for control and elimination of P. vivax.

Indexed as

Biological EvolutionGenetic MarkersGenetic VariationGenomicsHumansMalaria, VivaxPlasmodium vivaxGenetic Markers

Identifiers

PMID27348299
PMCPMC4966634
OpenAlexW2462219738

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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.