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Major Histocompatibility Complex Based Resistance to a Common Bacterial Pathogen of Amphibians

Given their well-developed systems of innate and adaptive immunity, global population declines of amphibians are particularly perplexing. To investigate the role of the major histocompatibilty complex (MHC) in conferring pathogen resistance, we challenged Xenopus laevis tadpoles bearing different co...

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Detalles Bibliográficos
Autores principales: Barribeau, Seth M., Villinger, Jandouwe, Waldman, Bruce
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2443284/
https://www.ncbi.nlm.nih.gov/pubmed/18629002
http://dx.doi.org/10.1371/journal.pone.0002692
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author Barribeau, Seth M.
Villinger, Jandouwe
Waldman, Bruce
author_facet Barribeau, Seth M.
Villinger, Jandouwe
Waldman, Bruce
author_sort Barribeau, Seth M.
collection PubMed
description Given their well-developed systems of innate and adaptive immunity, global population declines of amphibians are particularly perplexing. To investigate the role of the major histocompatibilty complex (MHC) in conferring pathogen resistance, we challenged Xenopus laevis tadpoles bearing different combinations of four MHC haplotypes (f, g, j, and r) with the bacterial pathogen Aeromonas hydrophila in two experiments. In the first, we exposed ff, fg, gg, gj, and jj tadpoles, obtained from breeding MHC homozygous parents, to one of three doses of A. hydrophila or heat-killed bacteria as a control. In the second, we exposed ff, fg, fr, gg, rg, and rr tadpoles, obtained from breeding MHC heterozygous parents and subsequently genotyped by PCR, to A. hydrophila, heat-killed bacteria or media alone as controls. We thereby determined whether the same patterns of MHC resistance emerged within as among families, independent of non-MHC heritable differences. Tadpoles with r or g MHC haplotypes were more likely to die than were those with f or j haplotypes. Growth rates varied among MHC types, independent of exposure dose. Heterozygous individuals with both susceptible and resistant haplotypes were intermediate to either homozygous genotype in both size and survival. The effect of the MHC on growth and survival was consistent between experiments and across families. MHC alleles differentially confer resistance to, or tolerance of, the bacterial pathogen, which affects tadpoles' growth and survival.
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spelling pubmed-24432842008-07-16 Major Histocompatibility Complex Based Resistance to a Common Bacterial Pathogen of Amphibians Barribeau, Seth M. Villinger, Jandouwe Waldman, Bruce PLoS One Research Article Given their well-developed systems of innate and adaptive immunity, global population declines of amphibians are particularly perplexing. To investigate the role of the major histocompatibilty complex (MHC) in conferring pathogen resistance, we challenged Xenopus laevis tadpoles bearing different combinations of four MHC haplotypes (f, g, j, and r) with the bacterial pathogen Aeromonas hydrophila in two experiments. In the first, we exposed ff, fg, gg, gj, and jj tadpoles, obtained from breeding MHC homozygous parents, to one of three doses of A. hydrophila or heat-killed bacteria as a control. In the second, we exposed ff, fg, fr, gg, rg, and rr tadpoles, obtained from breeding MHC heterozygous parents and subsequently genotyped by PCR, to A. hydrophila, heat-killed bacteria or media alone as controls. We thereby determined whether the same patterns of MHC resistance emerged within as among families, independent of non-MHC heritable differences. Tadpoles with r or g MHC haplotypes were more likely to die than were those with f or j haplotypes. Growth rates varied among MHC types, independent of exposure dose. Heterozygous individuals with both susceptible and resistant haplotypes were intermediate to either homozygous genotype in both size and survival. The effect of the MHC on growth and survival was consistent between experiments and across families. MHC alleles differentially confer resistance to, or tolerance of, the bacterial pathogen, which affects tadpoles' growth and survival. Public Library of Science 2008-07-16 /pmc/articles/PMC2443284/ /pubmed/18629002 http://dx.doi.org/10.1371/journal.pone.0002692 Text en Barribeau 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Barribeau, Seth M.
Villinger, Jandouwe
Waldman, Bruce
Major Histocompatibility Complex Based Resistance to a Common Bacterial Pathogen of Amphibians
title Major Histocompatibility Complex Based Resistance to a Common Bacterial Pathogen of Amphibians
title_full Major Histocompatibility Complex Based Resistance to a Common Bacterial Pathogen of Amphibians
title_fullStr Major Histocompatibility Complex Based Resistance to a Common Bacterial Pathogen of Amphibians
title_full_unstemmed Major Histocompatibility Complex Based Resistance to a Common Bacterial Pathogen of Amphibians
title_short Major Histocompatibility Complex Based Resistance to a Common Bacterial Pathogen of Amphibians
title_sort major histocompatibility complex based resistance to a common bacterial pathogen of amphibians
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2443284/
https://www.ncbi.nlm.nih.gov/pubmed/18629002
http://dx.doi.org/10.1371/journal.pone.0002692
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