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Hyperdiverse Gene Cluster in Snail Host Conveys Resistance to Human Schistosome Parasites

Schistosomiasis, a neglected global pandemic, may be curtailed by blocking transmission of the parasite via its intermediate hosts, aquatic snails. Elucidating the genetic basis of snail-schistosome interaction is a key to this strategy. Here we map a natural parasite-resistance polymorphism from a...

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Autores principales: Tennessen, Jacob A., Théron, André, Marine, Melanie, Yeh, Jan-Ying, Rognon, Anne, Blouin, Michael S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4361660/
https://www.ncbi.nlm.nih.gov/pubmed/25775214
http://dx.doi.org/10.1371/journal.pgen.1005067
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author Tennessen, Jacob A.
Théron, André
Marine, Melanie
Yeh, Jan-Ying
Rognon, Anne
Blouin, Michael S.
author_facet Tennessen, Jacob A.
Théron, André
Marine, Melanie
Yeh, Jan-Ying
Rognon, Anne
Blouin, Michael S.
author_sort Tennessen, Jacob A.
collection PubMed
description Schistosomiasis, a neglected global pandemic, may be curtailed by blocking transmission of the parasite via its intermediate hosts, aquatic snails. Elucidating the genetic basis of snail-schistosome interaction is a key to this strategy. Here we map a natural parasite-resistance polymorphism from a Caribbean population of the snail Biomphalaria glabrata. In independent experimental evolution lines, RAD genotyping shows that the same genomic region responds to selection for resistance to the parasite Schistosoma mansoni. A dominant allele in this region conveys an 8-fold decrease in the odds of infection. Fine-mapping and RNA-Seq characterization reveal a <1Mb region, the Guadeloupe Resistance Complex (GRC), with 15 coding genes. Seven genes are single-pass transmembrane proteins with putative immunological roles, most of which show strikingly high nonsynonymous divergence (5-10%) among alleles. High linkage disequilibrium among three intermediate-frequency (>25%) haplotypes across the GRC, a significantly non-neutral pattern, suggests that balancing selection maintains diversity at the GRC. Thus, the GRC resembles immune gene complexes seen in other taxa and is likely involved in parasite recognition. The GRC is a potential target for controlling transmission of schistosomiasis, including via genetic manipulation of snails.
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spelling pubmed-43616602015-03-23 Hyperdiverse Gene Cluster in Snail Host Conveys Resistance to Human Schistosome Parasites Tennessen, Jacob A. Théron, André Marine, Melanie Yeh, Jan-Ying Rognon, Anne Blouin, Michael S. PLoS Genet Research Article Schistosomiasis, a neglected global pandemic, may be curtailed by blocking transmission of the parasite via its intermediate hosts, aquatic snails. Elucidating the genetic basis of snail-schistosome interaction is a key to this strategy. Here we map a natural parasite-resistance polymorphism from a Caribbean population of the snail Biomphalaria glabrata. In independent experimental evolution lines, RAD genotyping shows that the same genomic region responds to selection for resistance to the parasite Schistosoma mansoni. A dominant allele in this region conveys an 8-fold decrease in the odds of infection. Fine-mapping and RNA-Seq characterization reveal a <1Mb region, the Guadeloupe Resistance Complex (GRC), with 15 coding genes. Seven genes are single-pass transmembrane proteins with putative immunological roles, most of which show strikingly high nonsynonymous divergence (5-10%) among alleles. High linkage disequilibrium among three intermediate-frequency (>25%) haplotypes across the GRC, a significantly non-neutral pattern, suggests that balancing selection maintains diversity at the GRC. Thus, the GRC resembles immune gene complexes seen in other taxa and is likely involved in parasite recognition. The GRC is a potential target for controlling transmission of schistosomiasis, including via genetic manipulation of snails. Public Library of Science 2015-03-16 /pmc/articles/PMC4361660/ /pubmed/25775214 http://dx.doi.org/10.1371/journal.pgen.1005067 Text en © 2015 Tennessen 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
Tennessen, Jacob A.
Théron, André
Marine, Melanie
Yeh, Jan-Ying
Rognon, Anne
Blouin, Michael S.
Hyperdiverse Gene Cluster in Snail Host Conveys Resistance to Human Schistosome Parasites
title Hyperdiverse Gene Cluster in Snail Host Conveys Resistance to Human Schistosome Parasites
title_full Hyperdiverse Gene Cluster in Snail Host Conveys Resistance to Human Schistosome Parasites
title_fullStr Hyperdiverse Gene Cluster in Snail Host Conveys Resistance to Human Schistosome Parasites
title_full_unstemmed Hyperdiverse Gene Cluster in Snail Host Conveys Resistance to Human Schistosome Parasites
title_short Hyperdiverse Gene Cluster in Snail Host Conveys Resistance to Human Schistosome Parasites
title_sort hyperdiverse gene cluster in snail host conveys resistance to human schistosome parasites
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4361660/
https://www.ncbi.nlm.nih.gov/pubmed/25775214
http://dx.doi.org/10.1371/journal.pgen.1005067
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