Cargando…
Exome-wide association study reveals largely distinct gene sets underlying specific resistance to dengue virus types 1 and 3 in Aedes aegypti
Although specific interactions between host and pathogen genotypes have been well documented in invertebrates, the identification of host genes involved in discriminating pathogen genotypes remains a challenge. In the mosquito Aedes aegypti, the main dengue virus (DENV) vector worldwide, statistical...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7282673/ https://www.ncbi.nlm.nih.gov/pubmed/32463828 http://dx.doi.org/10.1371/journal.pgen.1008794 |
_version_ | 1783544164455022592 |
---|---|
author | Dickson, Laura B. Merkling, Sarah H. Gautier, Mathieu Ghozlane, Amine Jiolle, Davy Paupy, Christophe Ayala, Diego Moltini-Conclois, Isabelle Fontaine, Albin Lambrechts, Louis |
author_facet | Dickson, Laura B. Merkling, Sarah H. Gautier, Mathieu Ghozlane, Amine Jiolle, Davy Paupy, Christophe Ayala, Diego Moltini-Conclois, Isabelle Fontaine, Albin Lambrechts, Louis |
author_sort | Dickson, Laura B. |
collection | PubMed |
description | Although specific interactions between host and pathogen genotypes have been well documented in invertebrates, the identification of host genes involved in discriminating pathogen genotypes remains a challenge. In the mosquito Aedes aegypti, the main dengue virus (DENV) vector worldwide, statistical associations between host genetic markers and DENV types or strains were previously detected, but the host genes underlying this genetic specificity have not been identified. In particular, it is unknown whether DENV type- or strain-specific resistance relies on allelic variants of the same genes or on distinct gene sets. Here, we investigated the genetic architecture of DENV resistance in a population of Ae. aegypti from Bakoumba, Gabon, which displays a stronger resistance phenotype to DENV type 1 (DENV-1) than to DENV type 3 (DENV-3) infection. Following experimental exposure to either DENV-1 or DENV-3, we sequenced the exomes of large phenotypic pools of mosquitoes that are either resistant or susceptible to each DENV type. Using variation in single-nucleotide polymorphism (SNP) frequencies among the pools, we computed empirical p values based on average gene scores adjusted for the differences in SNP counts, to identify genes associated with infection in a DENV type-specific manner. Among the top 5% most significant genes, 263 genes were significantly associated with resistance to both DENV-1 and DENV-3, 287 genes were only associated with DENV-1 resistance and 290 were only associated with DENV-3 resistance. The shared significant genes were enriched in genes with ATP binding activity and sulfur compound transmembrane transporter activity, whereas the genes uniquely associated with DENV-3 resistance were enriched in genes with zinc ion binding activity. Together, these results indicate that specific resistance to different DENV types relies on largely non-overlapping sets of genes in this Ae. aegypti population and pave the way for further mechanistic studies. |
format | Online Article Text |
id | pubmed-7282673 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-72826732020-06-17 Exome-wide association study reveals largely distinct gene sets underlying specific resistance to dengue virus types 1 and 3 in Aedes aegypti Dickson, Laura B. Merkling, Sarah H. Gautier, Mathieu Ghozlane, Amine Jiolle, Davy Paupy, Christophe Ayala, Diego Moltini-Conclois, Isabelle Fontaine, Albin Lambrechts, Louis PLoS Genet Research Article Although specific interactions between host and pathogen genotypes have been well documented in invertebrates, the identification of host genes involved in discriminating pathogen genotypes remains a challenge. In the mosquito Aedes aegypti, the main dengue virus (DENV) vector worldwide, statistical associations between host genetic markers and DENV types or strains were previously detected, but the host genes underlying this genetic specificity have not been identified. In particular, it is unknown whether DENV type- or strain-specific resistance relies on allelic variants of the same genes or on distinct gene sets. Here, we investigated the genetic architecture of DENV resistance in a population of Ae. aegypti from Bakoumba, Gabon, which displays a stronger resistance phenotype to DENV type 1 (DENV-1) than to DENV type 3 (DENV-3) infection. Following experimental exposure to either DENV-1 or DENV-3, we sequenced the exomes of large phenotypic pools of mosquitoes that are either resistant or susceptible to each DENV type. Using variation in single-nucleotide polymorphism (SNP) frequencies among the pools, we computed empirical p values based on average gene scores adjusted for the differences in SNP counts, to identify genes associated with infection in a DENV type-specific manner. Among the top 5% most significant genes, 263 genes were significantly associated with resistance to both DENV-1 and DENV-3, 287 genes were only associated with DENV-1 resistance and 290 were only associated with DENV-3 resistance. The shared significant genes were enriched in genes with ATP binding activity and sulfur compound transmembrane transporter activity, whereas the genes uniquely associated with DENV-3 resistance were enriched in genes with zinc ion binding activity. Together, these results indicate that specific resistance to different DENV types relies on largely non-overlapping sets of genes in this Ae. aegypti population and pave the way for further mechanistic studies. Public Library of Science 2020-05-28 /pmc/articles/PMC7282673/ /pubmed/32463828 http://dx.doi.org/10.1371/journal.pgen.1008794 Text en © 2020 Dickson et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Dickson, Laura B. Merkling, Sarah H. Gautier, Mathieu Ghozlane, Amine Jiolle, Davy Paupy, Christophe Ayala, Diego Moltini-Conclois, Isabelle Fontaine, Albin Lambrechts, Louis Exome-wide association study reveals largely distinct gene sets underlying specific resistance to dengue virus types 1 and 3 in Aedes aegypti |
title | Exome-wide association study reveals largely distinct gene sets underlying specific resistance to dengue virus types 1 and 3 in Aedes aegypti |
title_full | Exome-wide association study reveals largely distinct gene sets underlying specific resistance to dengue virus types 1 and 3 in Aedes aegypti |
title_fullStr | Exome-wide association study reveals largely distinct gene sets underlying specific resistance to dengue virus types 1 and 3 in Aedes aegypti |
title_full_unstemmed | Exome-wide association study reveals largely distinct gene sets underlying specific resistance to dengue virus types 1 and 3 in Aedes aegypti |
title_short | Exome-wide association study reveals largely distinct gene sets underlying specific resistance to dengue virus types 1 and 3 in Aedes aegypti |
title_sort | exome-wide association study reveals largely distinct gene sets underlying specific resistance to dengue virus types 1 and 3 in aedes aegypti |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7282673/ https://www.ncbi.nlm.nih.gov/pubmed/32463828 http://dx.doi.org/10.1371/journal.pgen.1008794 |
work_keys_str_mv | AT dicksonlaurab exomewideassociationstudyrevealslargelydistinctgenesetsunderlyingspecificresistancetodenguevirustypes1and3inaedesaegypti AT merklingsarahh exomewideassociationstudyrevealslargelydistinctgenesetsunderlyingspecificresistancetodenguevirustypes1and3inaedesaegypti AT gautiermathieu exomewideassociationstudyrevealslargelydistinctgenesetsunderlyingspecificresistancetodenguevirustypes1and3inaedesaegypti AT ghozlaneamine exomewideassociationstudyrevealslargelydistinctgenesetsunderlyingspecificresistancetodenguevirustypes1and3inaedesaegypti AT jiolledavy exomewideassociationstudyrevealslargelydistinctgenesetsunderlyingspecificresistancetodenguevirustypes1and3inaedesaegypti AT paupychristophe exomewideassociationstudyrevealslargelydistinctgenesetsunderlyingspecificresistancetodenguevirustypes1and3inaedesaegypti AT ayaladiego exomewideassociationstudyrevealslargelydistinctgenesetsunderlyingspecificresistancetodenguevirustypes1and3inaedesaegypti AT moltiniconcloisisabelle exomewideassociationstudyrevealslargelydistinctgenesetsunderlyingspecificresistancetodenguevirustypes1and3inaedesaegypti AT fontainealbin exomewideassociationstudyrevealslargelydistinctgenesetsunderlyingspecificresistancetodenguevirustypes1and3inaedesaegypti AT lambrechtslouis exomewideassociationstudyrevealslargelydistinctgenesetsunderlyingspecificresistancetodenguevirustypes1and3inaedesaegypti |