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Immunogenetic response of the bananaquit in the face of malarial parasites

BACKGROUND: In the arms race between hosts and parasites, genes involved in the immune response are targets for natural selection. Toll-Like Receptor (TLR) genes play a role in parasite detection as part of the innate immune system whereas Major Histocompatibility Complex (MHC) genes encode proteins...

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Autores principales: Antonides, Jennifer, Mathur, Samarth, Sundaram, Mekala, Ricklefs, Robert, DeWoody, J. Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6529992/
https://www.ncbi.nlm.nih.gov/pubmed/31113360
http://dx.doi.org/10.1186/s12862-019-1435-y
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author Antonides, Jennifer
Mathur, Samarth
Sundaram, Mekala
Ricklefs, Robert
DeWoody, J. Andrew
author_facet Antonides, Jennifer
Mathur, Samarth
Sundaram, Mekala
Ricklefs, Robert
DeWoody, J. Andrew
author_sort Antonides, Jennifer
collection PubMed
description BACKGROUND: In the arms race between hosts and parasites, genes involved in the immune response are targets for natural selection. Toll-Like Receptor (TLR) genes play a role in parasite detection as part of the innate immune system whereas Major Histocompatibility Complex (MHC) genes encode proteins that display antigens as part of the vertebrate adaptive immune system. Thus, both gene families are under selection pressure from pathogens. The bananaquit (Coereba flaveola) is a passerine bird that is a common host of avian malarial parasites (Plasmodium sp. and Haemoproteus sp.). We assessed molecular variation of TLR and MHC genes in a wild population of bananaquits and identified allelic associations with resistance/susceptibility to parasitic infection to address hypotheses of avian immune response to haemosporidian parasites. RESULTS: We found that allele frequencies are associated with infection status at the immune loci studied. A consistent general trend showed the infected groups possessed more alleles at lower frequencies, and exhibited unique alleles, compared to the uninfected group. CONCLUSIONS: Our results support the theory of natural selection favoring particular alleles for resistance while maintaining overall genetic diversity in the population, a mechanism which has been demonstrated in some systems in MHC previously but understudied in TLRs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12862-019-1435-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-65299922019-05-28 Immunogenetic response of the bananaquit in the face of malarial parasites Antonides, Jennifer Mathur, Samarth Sundaram, Mekala Ricklefs, Robert DeWoody, J. Andrew BMC Evol Biol Research Article BACKGROUND: In the arms race between hosts and parasites, genes involved in the immune response are targets for natural selection. Toll-Like Receptor (TLR) genes play a role in parasite detection as part of the innate immune system whereas Major Histocompatibility Complex (MHC) genes encode proteins that display antigens as part of the vertebrate adaptive immune system. Thus, both gene families are under selection pressure from pathogens. The bananaquit (Coereba flaveola) is a passerine bird that is a common host of avian malarial parasites (Plasmodium sp. and Haemoproteus sp.). We assessed molecular variation of TLR and MHC genes in a wild population of bananaquits and identified allelic associations with resistance/susceptibility to parasitic infection to address hypotheses of avian immune response to haemosporidian parasites. RESULTS: We found that allele frequencies are associated with infection status at the immune loci studied. A consistent general trend showed the infected groups possessed more alleles at lower frequencies, and exhibited unique alleles, compared to the uninfected group. CONCLUSIONS: Our results support the theory of natural selection favoring particular alleles for resistance while maintaining overall genetic diversity in the population, a mechanism which has been demonstrated in some systems in MHC previously but understudied in TLRs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12862-019-1435-y) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-22 /pmc/articles/PMC6529992/ /pubmed/31113360 http://dx.doi.org/10.1186/s12862-019-1435-y Text en © The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Antonides, Jennifer
Mathur, Samarth
Sundaram, Mekala
Ricklefs, Robert
DeWoody, J. Andrew
Immunogenetic response of the bananaquit in the face of malarial parasites
title Immunogenetic response of the bananaquit in the face of malarial parasites
title_full Immunogenetic response of the bananaquit in the face of malarial parasites
title_fullStr Immunogenetic response of the bananaquit in the face of malarial parasites
title_full_unstemmed Immunogenetic response of the bananaquit in the face of malarial parasites
title_short Immunogenetic response of the bananaquit in the face of malarial parasites
title_sort immunogenetic response of the bananaquit in the face of malarial parasites
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6529992/
https://www.ncbi.nlm.nih.gov/pubmed/31113360
http://dx.doi.org/10.1186/s12862-019-1435-y
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