Evidence map›Paper›PMID 29897905›Full record

ArticlePLoS computational biology2018

Identifying functional groups among the diverse, recombining antigenic var genes of the malaria parasite Plasmodium falciparum from a local community in Ghana.

Mary M Rorick, Edward B Baskerville, Thomas S Rask, Karen P Day, Mercedes Pascual

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 25% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
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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

5 authors at 4 institutions in 2 countries.

Mary M RorickDepartment of Ecology and Evolution, University of Chicago, Chicago, IL, United States of America.ORCID 0000-0001-7332-1065
Edward B BaskervilleDepartment of Ecology and Evolution, University of Chicago, Chicago, IL, United States of America.ORCID 0000-0003-4124-6472
Thomas S RaskSchool of Biosciences, Bio21 Institute, The University of Melbourne, Melbourne, AU.
Karen P DaySchool of Biosciences, Bio21 Institute, The University of Melbourne, Melbourne, AU.
Mercedes PascualDepartment of Ecology and Evolution, University of Chicago, Chicago, IL, United States of America.ORCID 0000-0003-3575-7233
The University of Melbourne · AUSanta Fe Institute · USUniversity of Chicago · USUniversity of Utah · US

Funding

P.falciparum var gene diversity and malaria controlR01AI084156 · NIAID · UNIVERSITY OF MELBOURNE · PI DAY, KAREN PATRICIA · 2010 to 2014
$1.9M
The impact of seasonality and vector control on the population structure of Plasmodium falciparumR01TW009670 · FIC · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAY, KAREN PATRICIA, KORAM, KWADWO ANSAH · 2013 to 2016
$1.8M
FIC NIH HHS R01 TW009670NIAID NIH HHS R01 AI084156
6 · The paper itself

Abstract

A challenge in studying diverse multi-copy gene families is deciphering distinct functional types within immense sequence variation. Functional changes can in some cases be tracked through the evolutionary history of a gene family; however phylogenetic approaches are not possible in cases where gene families diversify primarily by recombination. We take a network theoretical approach to functionally classify the highly recombining var antigenic gene family of the malaria parasite Plasmodium falciparum. We sample var DBLα sequence types from a local population in Ghana, and classify 9,276 of these variants into just 48 functional types. Our approach is to first decompose each sequence type into its constituent, recombining parts; we then use a stochastic block model to identify functional groups among the parts; finally, we classify the sequence types based on which functional groups they contain. This method for functional classification does not rely on an inferred phylogenetic history, nor does it rely on inferring function based on conserved sequence features. Instead, it infers functional similarity among recombining parts based on the sharing of similar co-occurrence interactions with other parts. This method can therefore group sequences that have undetectable sequence homology or even distinct origination. Describing these 48 var functional types allows us to simplify the antigenic diversity within our dataset by over two orders of magnitude. We consider how the var functional types are distributed in isolates, and find a nonrandom pattern reflecting that common var functional types are non-randomly distinct from one another in terms of their functional composition. The coarse-graining of var gene diversity into biologically meaningful functional groups has important implications for understanding the disease ecology and evolution of this system, as well as for designing effective epidemiological monitoring and intervention.

Indexed as

AnimalsAntigenic VariationAntigens, ProtozoanComputational BiologyConserved SequenceFemaleGenetic VariationGhanaHumansMalaria, FalciparumMaleParasitesPlasmodium falciparumProtozoan ProteinsSequence Analysis, DNAAntigens, Protozoanerythrocyte membrane protein 1, Plasmodium falciparumProtozoan Proteins

Identifiers

PMID29897905
PMCPMC6016947
OpenAlexW2808064078

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.