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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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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. |
format | Online Article Text |
id | pubmed-4361660 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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