Evidence map›Paper›PMID 26462916›Full record

ArticleBMC genomics2015

Association mapping by pooled sequencing identifies TOLL 11 as a protective factor against Plasmodium falciparum in Anopheles gambiae.

Seth N Redmond, Karin Eiglmeier, Christian Mitri, Kyriacos Markianos, Wamdaogo M Guelbeogo, Awa Gneme, Alison T Isaacs, Boubacar Coulibaly, Emma Brito-Fravallo, Gareth Maslen and 7 more

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

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  13. Human Genomic Loci Important in Common Infectious Diseases: Role of High-Throughput Sequencing and Genome-Wide Association Studies.The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale · 2018
    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

17 authors at 7 institutions in 5 countries.

Seth N RedmondDepartment of Parasites and Insect Vectors, Institut Pasteur, Unit of Insect Vector Genetics and Genomics, 28 rue du Docteur Roux, Paris, 75015, France. snr@sanger.ac.uk.
Karin EiglmeierDepartment of Parasites and Insect Vectors, Institut Pasteur, Unit of Insect Vector Genetics and Genomics, 28 rue du Docteur Roux, Paris, 75015, France. kei@pasteur.fr.
Christian MitriDepartment of Parasites and Insect Vectors, Institut Pasteur, Unit of Insect Vector Genetics and Genomics, 28 rue du Docteur Roux, Paris, 75015, France. cmitri@pasteur.fr.
Kyriacos MarkianosProgram in Genomics, Boston Children's Hospital, Harvard Medical School, 3 Blackfan Street, Boston, MA, 02115, USA. kmarkianos@enders.tch.harvard.edu.
Wamdaogo M GuelbeogoCentre National de Recherche et de Formation sur le Paludisme, 1487 Avenue de l'Oubritenga, 01 BP 2208, Ouagadougou, Burkina Faso. guelbeogo.cnrfp@fasonet.bf.
Awa GnemeCentre National de Recherche et de Formation sur le Paludisme, 1487 Avenue de l'Oubritenga, 01 BP 2208, Ouagadougou, Burkina Faso. gplouise@yahoo.fr.
Alison T IsaacsDepartment of Parasites and Insect Vectors, Institut Pasteur, Unit of Insect Vector Genetics and Genomics, 28 rue du Docteur Roux, Paris, 75015, France. Alison.Isaacs@lstmed.ac.uk.
Boubacar CoulibalyMalaria Research and Training Centre, Faculty of Medicine and Dentistry, University of Mali, Point G, Bamako, Mali. bcoulibaly@mrtcbko.org.
Emma Brito-FravalloDepartment of Parasites and Insect Vectors, Institut Pasteur, Unit of Insect Vector Genetics and Genomics, 28 rue du Docteur Roux, Paris, 75015, France. emma.brito-fravallo@pasteur.fr.
Gareth MaslenWellcome Trust Sanger Institute, Hinxton, Cambridge, UK. gmaslen@ebi.ac.uk.
Daniel MeadWellcome Trust Sanger Institute, Hinxton, Cambridge, UK. da2@sanger.ac.uk.
Oumou NiareMalaria Research and Training Centre, Faculty of Medicine and Dentistry, University of Mali, Point G, Bamako, Mali. niare@mrtcbko.org.
Sekou F TraoreMalaria Research and Training Centre, Faculty of Medicine and Dentistry, University of Mali, Point G, Bamako, Mali. cheick@icermali.org.
N'Fale SagnonCentre National de Recherche et de Formation sur le Paludisme, 1487 Avenue de l'Oubritenga, 01 BP 2208, Ouagadougou, Burkina Faso. n.fale.cnlp@fasonet.bf.
Dominic KwiatkowskiWellcome Trust Sanger Institute, Hinxton, Cambridge, UK. dominic@well.ox.ac.uk.
Michelle M RiehleDepartment of Microbiology, University of Minnesota, 1500 Gortner Avenue, Saint Paul, MN 55108, USA. mriehle@umn.edu.
Kenneth D VernickDepartment of Parasites and Insect Vectors, Institut Pasteur, Unit of Insect Vector Genetics and Genomics, 28 rue du Docteur Roux, Paris, 75015, France. kvernick@pasteur.fr.
University of Bamako · MLCentre National de Recherche et de Formation sur le Paludisme · BFInstitut Pasteur · FRWellcome Sanger Institute · GBCentre National de la Recherche Scientifique · FRBoston Children's Hospital · USUniversity of Minnesota · US

Funding

Genomics of Mosquito Resistance to PlasmodiumR01AI042361 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI VERNICK, KENNETH D · 1998 to 2012
$4.8M
European Research Council 323173NIAID NIH HHS R01 AI042361Wellcome Trust 090770
6 · The paper itself

Abstract

backgroundThe genome-wide association study (GWAS) techniques that have been used for genetic mapping in other organisms have not been successfully applied to mosquitoes, which have genetic characteristics of high nucleotide diversity, low linkage disequilibrium, and complex population stratification that render population-based GWAS essentially unfeasible at realistic sample size and marker density.

methodsWe designed a novel mapping strategy for the mosquito system that combines the power of linkage mapping with the resolution afforded by genetic association. We established founder colonies from West Africa, controlled for diversity, linkage disequilibrium and population stratification. Colonies were challenged by feeding on the infectious stage of the human malaria parasite, Plasmodium falciparum, mosquitoes were phenotyped for parasite load, and DNA pools for phenotypically similar mosquitoes were Illumina sequenced. Phenotype-genotype mapping was carried out in two stages, coarse and fine.

resultsIn the first mapping stage, pooled sequences were analysed genome-wide for intervals displaying relativereduction in diversity between phenotype pools, and candidate genomic loci were identified for influence upon parasite infection levels. In the second mapping stage, focused genotyping of SNPs from the first mapping stage was carried out in unpooled individual mosquitoes and replicates. The second stage confirmed significant SNPs in a locus encoding two Toll-family proteins. RNAi-mediated gene silencing and infection challenge revealed that TOLL 11 protects mosquitoes against P. falciparum infection.

conclusionsWe present an efficient and cost-effective method for genetic mapping using natural variation segregating in defined recent Anopheles founder colonies, and demonstrate its applicability for mapping in a complex non-model genome. This approach is a practical and preferred alternative to population-based GWAS for first-pass mapping of phenotypes in Anopheles. This design should facilitate mapping of other traits involved in physiology, epidemiology, and behaviour.

Indexed as

Genome-Wide Association StudyAnimalsAnophelesChromosome MappingGenome, InsectGenotypeHost-Parasite InteractionsHumansInsect VectorsMalaria, FalciparumPhenotypePlasmodium falciparumPolymorphism, Single NucleotideToll-Like ReceptorsToll-Like Receptors

Identifiers

PMID26462916
PMCPMC4603968
OpenAlexW2162384697

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.