The genome and transcriptome of the snail Biomphalaria sudanica s.l.: Immune gene diversification and highly polymorphic genomic regions in an important African vector of Schistosoma mansoni.

Pennance, Tom - Calvelo, Javier - Tennessen, Jacob A. - Burd, Ryan - Cayton, Jared - Bollmann, Stephanie R. - Blouin, Michael S. - Spaan, Johannie M. - Hoffmann, Federico G. - Ogara, George - Rawago, Fredrick - Andiego, Kennedy - Mulonga, Boaz - Odhiambo, Meredith - Loker, Eric S. - Laidemitt, Martina R. - Lu, Lijun - Iriarte, Andrés - Odiere, Maurice - Steinauer, Michelle L.

Resumen:

Background: Control and elimination of schistosomiasis is an arduous task, with current strategies proving inadequate to break transmission. Exploration of genetic approaches to interrupt Schistosoma mansoni transmission, the causative agent for human intestinal schistosomiasis in sub-Saharan Africa and South America, has led to genomic research of the snail vector hosts of the genus Biomphalaria. Few complete genomic resources exist, with African Biomphalaria species being particularly underrepresented despite this being where the majority of S. mansoni infections occur. Here we generate and annotate the first genome assembly of Biomphalaria sudanica sensu lato, a species responsible for S. mansoni transmission in lake and marsh habitats of the African Rift Valley. Supported by whole-genome diversity data among five inbred lines, we describe orthologs of immune-relevant gene regions in the South American vector B. glabrata and present a bioinformatic pipeline to identify candidate novel pathogen recognition receptors (PRRs). Results: De novo genome and transcriptome assembly of inbred B. sudanica originating from the shoreline of Lake Victoria (Kisumu, Kenya) resulted in a haploid genome size of ~944.2 Mb (6732 fragments, N50=1.067 Mb), comprising 23,598 genes (BUSCO=93.6% complete). The B. sudanica genome contains orthologues to all described immune genes/regions tied to protection against S. mansoni in B. glabrata. The B. sudanica PTC2 candidate immune genomic region contained many PRR-like genes across a much wider genomic region than has been shown in B. glabrata, as well as a large inversion between species. High levels of intra-species nucleotide diversity were seen in PTC2, as well as in regions linked to PTC1 and RADres orthologues. Immune related and putative PRR gene families were significantly over-represented in the sub-set of B. sudanica genes determined as hyperdiverse, including high extracellular diversity in transmembrane genes, which could be under pathogen-mediated balancing selection. However, no overall expansion in immunity related genes were seen in African compared to South American lineages. Conclusions: The B. sudanica genome and analyses presented here will facilitate future research in vector immune defense mechanisms against pathogens. This genomic/transcriptomic resource provides necessary data for the future development of molecular snail vector control/surveillance tools, facilitating schistosome transmission interruption mechanisms in Africa.

Detalles Bibliográficos
2023
Biomphalaria sudanica
Biomphalaria choanomphala
schistosomiasis
snail vector
de novo genome assembly
polymorphism
immunogenetics
gene family evolution
balancing selection
pathogen recognition
Inglés
Universidad de la República
COLIBRI
https://hdl.handle.net/20.500.12008/55369
Acceso abierto
Licencia Creative Commons Atribución - No Comercial - Sin Derivadas (CC - By-NC-ND 4.0)
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author Pennance, Tom
author2 Calvelo, Javier
Tennessen, Jacob A.
Burd, Ryan
Cayton, Jared
Bollmann, Stephanie R.
Blouin, Michael S.
Spaan, Johannie M.
Hoffmann, Federico G.
Ogara, George
Rawago, Fredrick
Andiego, Kennedy
Mulonga, Boaz
Odhiambo, Meredith
Loker, Eric S.
Laidemitt, Martina R.
Lu, Lijun
Iriarte, Andrés
Odiere, Maurice
Steinauer, Michelle L.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author_facet Pennance, Tom
Calvelo, Javier
Tennessen, Jacob A.
Burd, Ryan
Cayton, Jared
Bollmann, Stephanie R.
Blouin, Michael S.
Spaan, Johannie M.
Hoffmann, Federico G.
Ogara, George
Rawago, Fredrick
Andiego, Kennedy
Mulonga, Boaz
Odhiambo, Meredith
Loker, Eric S.
Laidemitt, Martina R.
Lu, Lijun
Iriarte, Andrés
Odiere, Maurice
Steinauer, Michelle L.
author_role author
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dc.contributor.filiacion.none.fl_str_mv Pennance Tom, Western University of Health Sciences (Estados Unidos). College of Osteopathic Medicine of the Pacific – Northwest.
Calvelo Javier, Universidad de la República (Uruguay). Facultad de Medicina. Instituto de Higiene. Unidad Académica Desarrollo Biotecnológico. Laboratorio Biología Computacional
Tennessen Jacob A., Harvard T.H. Chan School of Public Health (Estados Unidos)
Burd Ryan, Western University of Health Sciences (Estados Unidos). College of Osteopathic Medicine of the Pacific – Northwest.
Cayton Jared, Western University of Health Sciences (Estados Unidos). College of Osteopathic Medicine of the Pacific – Northwest.
Bollmann Stephanie R., Oregon State University (Estados Unidos)
Blouin Michael S., Oregon State University (Estados Unidos)
Spaan Johannie M., Western University of Health Sciences (Estados Unidos). College of Osteopathic Medicine of the Pacific – Northwest.
Hoffmann Federico G., Mississippi State University (Estados Unidos). Department of Biochemistry, Molecular Biology, Entomology, and Plant Pathology
Ogara George, Kenya Medical Research Institute (KEMRI) (Kenia). Centre for Global Health Research
Rawago Fredrick, Kenya Medical Research Institute (KEMRI) (Kenia). Centre for Global Health Research
Andiego Kennedy, Kenya Medical Research Institute (KEMRI) (Kenia). Centre for Global Health Research
Mulonga Boaz, Kenya Medical Research Institute (KEMRI) (Kenia). Centre for Global Health Research
Odhiambo Meredith, Kenya Medical Research Institute (KEMRI) (Kenia). Centre for Global Health Research
Loker Eric S., University of New Mexico (Estados Unidos). Parasite Division Museum of Southwestern Biology. Center for Evolutionary and Theoretical Immunology. Department of Biology
Laidemitt Martina R., University of New Mexico (Estados Unidos). Parasite Division Museum of Southwestern Biology. Center for Evolutionary and Theoretical Immunology. Department of Biology
Lu Lijun, University of New Mexico (Estados Unidos). Parasite Division Museum of Southwestern Biology. Center for Evolutionary and Theoretical Immunology. Department of Biology
Iriarte Andrés, Universidad de la República (Uruguay). Facultad de Medicina. Instituto de Higiene. Unidad Académica Desarrollo Biotecnológico. Laboratorio Biología Computacional
Odiere Maurice, Mississippi State University (Estados Unidos). Department of Biochemistry, Molecular Biology, Entomology, and Plant Pathology
Steinauer Michelle L., Western University of Health Sciences (Estados Unidos). College of Osteopathic Medicine of the Pacific – Northwest.
dc.creator.none.fl_str_mv Pennance, Tom
Calvelo, Javier
Tennessen, Jacob A.
Burd, Ryan
Cayton, Jared
Bollmann, Stephanie R.
Blouin, Michael S.
Spaan, Johannie M.
Hoffmann, Federico G.
Ogara, George
Rawago, Fredrick
Andiego, Kennedy
Mulonga, Boaz
Odhiambo, Meredith
Loker, Eric S.
Laidemitt, Martina R.
Lu, Lijun
Iriarte, Andrés
Odiere, Maurice
Steinauer, Michelle L.
dc.date.accessioned.none.fl_str_mv 2026-06-04T17:51:00Z
dc.date.available.none.fl_str_mv 2026-06-04T17:51:00Z
dc.date.issued.none.fl_str_mv 2023
dc.description.abstract.none.fl_txt_mv Background: Control and elimination of schistosomiasis is an arduous task, with current strategies proving inadequate to break transmission. Exploration of genetic approaches to interrupt Schistosoma mansoni transmission, the causative agent for human intestinal schistosomiasis in sub-Saharan Africa and South America, has led to genomic research of the snail vector hosts of the genus Biomphalaria. Few complete genomic resources exist, with African Biomphalaria species being particularly underrepresented despite this being where the majority of S. mansoni infections occur. Here we generate and annotate the first genome assembly of Biomphalaria sudanica sensu lato, a species responsible for S. mansoni transmission in lake and marsh habitats of the African Rift Valley. Supported by whole-genome diversity data among five inbred lines, we describe orthologs of immune-relevant gene regions in the South American vector B. glabrata and present a bioinformatic pipeline to identify candidate novel pathogen recognition receptors (PRRs). Results: De novo genome and transcriptome assembly of inbred B. sudanica originating from the shoreline of Lake Victoria (Kisumu, Kenya) resulted in a haploid genome size of ~944.2 Mb (6732 fragments, N50=1.067 Mb), comprising 23,598 genes (BUSCO=93.6% complete). The B. sudanica genome contains orthologues to all described immune genes/regions tied to protection against S. mansoni in B. glabrata. The B. sudanica PTC2 candidate immune genomic region contained many PRR-like genes across a much wider genomic region than has been shown in B. glabrata, as well as a large inversion between species. High levels of intra-species nucleotide diversity were seen in PTC2, as well as in regions linked to PTC1 and RADres orthologues. Immune related and putative PRR gene families were significantly over-represented in the sub-set of B. sudanica genes determined as hyperdiverse, including high extracellular diversity in transmembrane genes, which could be under pathogen-mediated balancing selection. However, no overall expansion in immunity related genes were seen in African compared to South American lineages. Conclusions: The B. sudanica genome and analyses presented here will facilitate future research in vector immune defense mechanisms against pathogens. This genomic/transcriptomic resource provides necessary data for the future development of molecular snail vector control/surveillance tools, facilitating schistosome transmission interruption mechanisms in Africa.
dc.format.mimetype.es.fl_str_mv application/pdf
dc.identifier.citation.es.fl_str_mv PENNANCE, T., CLAVELO, J., TENNESSEN, JA., y otros. The genome and transcriptome of the snail Biomphalaria sudanica s.l.: Immune gene diversification and highly polymorphic genomic regions in an important African vector of Schistosoma mansoni. bioRxiv [en línea] 2023. DOI: 10.1101/2023.11.01.565203
dc.identifier.doi.none.fl_str_mv 10.1101/2023.11.01.565203
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/20.500.12008/55369
dc.language.iso.none.fl_str_mv en
eng
dc.relation.none.fl_str_mv bioRxiv. 2023
dc.rights.license.none.fl_str_mv Licencia Creative Commons Atribución - No Comercial - Sin Derivadas (CC - By-NC-ND 4.0)
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
dc.source.none.fl_str_mv reponame:COLIBRI
instname:Universidad de la República
instacron:Universidad de la República
dc.subject.es.fl_str_mv Biomphalaria sudanica
Biomphalaria choanomphala
schistosomiasis
snail vector
de novo genome assembly
polymorphism
immunogenetics
gene family evolution
balancing selection
pathogen recognition
dc.title.none.fl_str_mv The genome and transcriptome of the snail Biomphalaria sudanica s.l.: Immune gene diversification and highly polymorphic genomic regions in an important African vector of Schistosoma mansoni.
dc.type.es.fl_str_mv Preprint
dc.type.none.fl_str_mv info:eu-repo/semantics/preprint
dc.type.version.none.fl_str_mv info:eu-repo/semantics/submittedVersion
description Background: Control and elimination of schistosomiasis is an arduous task, with current strategies proving inadequate to break transmission. Exploration of genetic approaches to interrupt Schistosoma mansoni transmission, the causative agent for human intestinal schistosomiasis in sub-Saharan Africa and South America, has led to genomic research of the snail vector hosts of the genus Biomphalaria. Few complete genomic resources exist, with African Biomphalaria species being particularly underrepresented despite this being where the majority of S. mansoni infections occur. Here we generate and annotate the first genome assembly of Biomphalaria sudanica sensu lato, a species responsible for S. mansoni transmission in lake and marsh habitats of the African Rift Valley. Supported by whole-genome diversity data among five inbred lines, we describe orthologs of immune-relevant gene regions in the South American vector B. glabrata and present a bioinformatic pipeline to identify candidate novel pathogen recognition receptors (PRRs). Results: De novo genome and transcriptome assembly of inbred B. sudanica originating from the shoreline of Lake Victoria (Kisumu, Kenya) resulted in a haploid genome size of ~944.2 Mb (6732 fragments, N50=1.067 Mb), comprising 23,598 genes (BUSCO=93.6% complete). The B. sudanica genome contains orthologues to all described immune genes/regions tied to protection against S. mansoni in B. glabrata. The B. sudanica PTC2 candidate immune genomic region contained many PRR-like genes across a much wider genomic region than has been shown in B. glabrata, as well as a large inversion between species. High levels of intra-species nucleotide diversity were seen in PTC2, as well as in regions linked to PTC1 and RADres orthologues. Immune related and putative PRR gene families were significantly over-represented in the sub-set of B. sudanica genes determined as hyperdiverse, including high extracellular diversity in transmembrane genes, which could be under pathogen-mediated balancing selection. However, no overall expansion in immunity related genes were seen in African compared to South American lineages. Conclusions: The B. sudanica genome and analyses presented here will facilitate future research in vector immune defense mechanisms against pathogens. This genomic/transcriptomic resource provides necessary data for the future development of molecular snail vector control/surveillance tools, facilitating schistosome transmission interruption mechanisms in Africa.
eu_rights_str_mv openAccess
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identifier_str_mv PENNANCE, T., CLAVELO, J., TENNESSEN, JA., y otros. The genome and transcriptome of the snail Biomphalaria sudanica s.l.: Immune gene diversification and highly polymorphic genomic regions in an important African vector of Schistosoma mansoni. bioRxiv [en línea] 2023. DOI: 10.1101/2023.11.01.565203
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instacron_str Universidad de la República
institution Universidad de la República
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repository.mail.fl_str_mv karina.camps@seciu.edu.uy
repository.name.fl_str_mv COLIBRI - Universidad de la República
repository_id_str 4771
rights_invalid_str_mv Licencia Creative Commons Atribución - No Comercial - Sin Derivadas (CC - By-NC-ND 4.0)
spelling Pennance Tom, Western University of Health Sciences (Estados Unidos). College of Osteopathic Medicine of the Pacific – Northwest.Calvelo Javier, Universidad de la República (Uruguay). Facultad de Medicina. Instituto de Higiene. Unidad Académica Desarrollo Biotecnológico. Laboratorio Biología ComputacionalTennessen Jacob A., Harvard T.H. Chan School of Public Health (Estados Unidos)Burd Ryan, Western University of Health Sciences (Estados Unidos). College of Osteopathic Medicine of the Pacific – Northwest.Cayton Jared, Western University of Health Sciences (Estados Unidos). College of Osteopathic Medicine of the Pacific – Northwest.Bollmann Stephanie R., Oregon State University (Estados Unidos)Blouin Michael S., Oregon State University (Estados Unidos)Spaan Johannie M., Western University of Health Sciences (Estados Unidos). College of Osteopathic Medicine of the Pacific – Northwest.Hoffmann Federico G., Mississippi State University (Estados Unidos). Department of Biochemistry, Molecular Biology, Entomology, and Plant PathologyOgara George, Kenya Medical Research Institute (KEMRI) (Kenia). Centre for Global Health ResearchRawago Fredrick, Kenya Medical Research Institute (KEMRI) (Kenia). Centre for Global Health ResearchAndiego Kennedy, Kenya Medical Research Institute (KEMRI) (Kenia). Centre for Global Health ResearchMulonga Boaz, Kenya Medical Research Institute (KEMRI) (Kenia). Centre for Global Health ResearchOdhiambo Meredith, Kenya Medical Research Institute (KEMRI) (Kenia). Centre for Global Health ResearchLoker Eric S., University of New Mexico (Estados Unidos). Parasite Division Museum of Southwestern Biology. Center for Evolutionary and Theoretical Immunology. Department of BiologyLaidemitt Martina R., University of New Mexico (Estados Unidos). Parasite Division Museum of Southwestern Biology. Center for Evolutionary and Theoretical Immunology. Department of BiologyLu Lijun, University of New Mexico (Estados Unidos). Parasite Division Museum of Southwestern Biology. Center for Evolutionary and Theoretical Immunology. Department of BiologyIriarte Andrés, Universidad de la República (Uruguay). Facultad de Medicina. Instituto de Higiene. Unidad Académica Desarrollo Biotecnológico. Laboratorio Biología ComputacionalOdiere Maurice, Mississippi State University (Estados Unidos). Department of Biochemistry, Molecular Biology, Entomology, and Plant PathologySteinauer Michelle L., Western University of Health Sciences (Estados Unidos). College of Osteopathic Medicine of the Pacific – Northwest.2026-06-04T17:51:00Z2026-06-04T17:51:00Z2023PENNANCE, T., CLAVELO, J., TENNESSEN, JA., y otros. The genome and transcriptome of the snail Biomphalaria sudanica s.l.: Immune gene diversification and highly polymorphic genomic regions in an important African vector of Schistosoma mansoni. bioRxiv [en línea] 2023. DOI: 10.1101/2023.11.01.565203https://hdl.handle.net/20.500.12008/5536910.1101/2023.11.01.565203Background: Control and elimination of schistosomiasis is an arduous task, with current strategies proving inadequate to break transmission. Exploration of genetic approaches to interrupt Schistosoma mansoni transmission, the causative agent for human intestinal schistosomiasis in sub-Saharan Africa and South America, has led to genomic research of the snail vector hosts of the genus Biomphalaria. Few complete genomic resources exist, with African Biomphalaria species being particularly underrepresented despite this being where the majority of S. mansoni infections occur. Here we generate and annotate the first genome assembly of Biomphalaria sudanica sensu lato, a species responsible for S. mansoni transmission in lake and marsh habitats of the African Rift Valley. Supported by whole-genome diversity data among five inbred lines, we describe orthologs of immune-relevant gene regions in the South American vector B. glabrata and present a bioinformatic pipeline to identify candidate novel pathogen recognition receptors (PRRs). Results: De novo genome and transcriptome assembly of inbred B. sudanica originating from the shoreline of Lake Victoria (Kisumu, Kenya) resulted in a haploid genome size of ~944.2 Mb (6732 fragments, N50=1.067 Mb), comprising 23,598 genes (BUSCO=93.6% complete). The B. sudanica genome contains orthologues to all described immune genes/regions tied to protection against S. mansoni in B. glabrata. The B. sudanica PTC2 candidate immune genomic region contained many PRR-like genes across a much wider genomic region than has been shown in B. glabrata, as well as a large inversion between species. High levels of intra-species nucleotide diversity were seen in PTC2, as well as in regions linked to PTC1 and RADres orthologues. Immune related and putative PRR gene families were significantly over-represented in the sub-set of B. sudanica genes determined as hyperdiverse, including high extracellular diversity in transmembrane genes, which could be under pathogen-mediated balancing selection. However, no overall expansion in immunity related genes were seen in African compared to South American lineages. Conclusions: The B. sudanica genome and analyses presented here will facilitate future research in vector immune defense mechanisms against pathogens. This genomic/transcriptomic resource provides necessary data for the future development of molecular snail vector control/surveillance tools, facilitating schistosome transmission interruption mechanisms in Africa.Submitted by Haller Mariana (mhaller@higiene.edu.uy) on 2026-06-04T16:58:12Z No. of bitstreams: 2 license_rdf: 27293 bytes, checksum: d62648cf14c1e37917d392ac87012955 (MD5) The genome and transcriptome of the snail Biomphalaria sudanica s.l. Immune gene diversification and highly polymorphic genomic regions in an important African vector of Schistosoma mansoni.pdf: 8868366 bytes, checksum: aee6548fc2279e79649ad118abcd00e2 (MD5)Made available in DSpace by Luna Fabiana (fabiana.luna@seciu.edu.uy) on 2026-06-04T17:51:00Z (GMT). No. of bitstreams: 2 license_rdf: 27293 bytes, checksum: d62648cf14c1e37917d392ac87012955 (MD5) The genome and transcriptome of the snail Biomphalaria sudanica s.l. Immune gene diversification and highly polymorphic genomic regions in an important African vector of Schistosoma mansoni.pdf: 8868366 bytes, checksum: aee6548fc2279e79649ad118abcd00e2 (MD5) Previous issue date: 2023application/pdfenengbioRxiv. 2023Las obras depositadas en el Repositorio se rigen por la Ordenanza de los Derechos de la Propiedad Intelectual de la Universidad de la República.(Res. Nº 91 de C.D.C. de 8/III/1994 – D.O. 7/IV/1994) y por la Ordenanza del Repositorio Abierto de la Universidad de la República (Res. Nº 16 de C.D.C. de 07/10/2014)info:eu-repo/semantics/openAccessLicencia Creative Commons Atribución - No Comercial - Sin Derivadas (CC - By-NC-ND 4.0)Biomphalaria sudanicaBiomphalaria choanomphalaschistosomiasissnail vectorde novo genome assemblypolymorphismimmunogeneticsgene family evolutionbalancing selectionpathogen recognitionThe genome and transcriptome of the snail Biomphalaria sudanica s.l.: Immune gene diversification and highly polymorphic genomic regions in an important African vector of Schistosoma mansoni.Preprintinfo:eu-repo/semantics/preprintinfo:eu-repo/semantics/submittedVersionreponame:COLIBRIinstname:Universidad de la Repúblicainstacron:Universidad de la RepúblicaPennance, TomCalvelo, JavierTennessen, Jacob A.Burd, RyanCayton, JaredBollmann, Stephanie R.Blouin, Michael S.Spaan, Johannie M.Hoffmann, Federico G.Ogara, GeorgeRawago, FredrickAndiego, KennedyMulonga, BoazOdhiambo, MeredithLoker, Eric S.Laidemitt, Martina R.Lu, LijunIriarte, AndrésOdiere, MauriceSteinauer, Michelle L.LICENSElicense.txtlicense.txttext/plain; charset=utf-84267http://localhost:8080/xmlui/bitstream/20.500.12008/55369/5/license.txt6429389a7df7277b72b7924fdc7d47a9MD55CC-LICENSElicense_urllicense_urltext/plain; charset=utf-850http://localhost:8080/xmlui/bitstream/20.500.12008/55369/2/license_urla006180e3f5b2ad0b88185d14284c0e0MD52license_textlicense_texttext/html; charset=utf-835935http://localhost:8080/xmlui/bitstream/20.500.12008/55369/3/license_text00c6a163e62314ee9d2a181a90bf9e84MD53license_rdflicense_rdfapplication/rdf+xml; charset=utf-827293http://localhost:8080/xmlui/bitstream/20.500.12008/55369/4/license_rdfd62648cf14c1e37917d392ac87012955MD54ORIGINALThe genome and transcriptome of the snail Biomphalaria sudanica s.l. Immune gene diversification and highly polymorphic genomic regions in an important African vector of Schistosoma mansoni.pdfThe genome and transcriptome of the snail Biomphalaria sudanica s.l. Immune gene diversification and highly polymorphic genomic regions in an important African vector of Schistosoma mansoni.pdfapplication/pdf8868366http://localhost:8080/xmlui/bitstream/20.500.12008/55369/1/The+genome+and+transcriptome+of+the+snail+Biomphalaria+sudanica+s.l.+Immune+gene+diversification+and+highly+polymorphic+genomic+regions+in+an+important+African+vector+of+Schistosoma+mansoni.pdfaee6548fc2279e79649ad118abcd00e2MD5120.500.12008/553692026-06-04 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- Universidad de la Repúblicafalse
spellingShingle The genome and transcriptome of the snail Biomphalaria sudanica s.l.: Immune gene diversification and highly polymorphic genomic regions in an important African vector of Schistosoma mansoni.
Pennance, Tom
Biomphalaria sudanica
Biomphalaria choanomphala
schistosomiasis
snail vector
de novo genome assembly
polymorphism
immunogenetics
gene family evolution
balancing selection
pathogen recognition
status_str submittedVersion
title The genome and transcriptome of the snail Biomphalaria sudanica s.l.: Immune gene diversification and highly polymorphic genomic regions in an important African vector of Schistosoma mansoni.
title_full The genome and transcriptome of the snail Biomphalaria sudanica s.l.: Immune gene diversification and highly polymorphic genomic regions in an important African vector of Schistosoma mansoni.
title_fullStr The genome and transcriptome of the snail Biomphalaria sudanica s.l.: Immune gene diversification and highly polymorphic genomic regions in an important African vector of Schistosoma mansoni.
title_full_unstemmed The genome and transcriptome of the snail Biomphalaria sudanica s.l.: Immune gene diversification and highly polymorphic genomic regions in an important African vector of Schistosoma mansoni.
title_short The genome and transcriptome of the snail Biomphalaria sudanica s.l.: Immune gene diversification and highly polymorphic genomic regions in an important African vector of Schistosoma mansoni.
title_sort The genome and transcriptome of the snail Biomphalaria sudanica s.l.: Immune gene diversification and highly polymorphic genomic regions in an important African vector of Schistosoma mansoni.
topic Biomphalaria sudanica
Biomphalaria choanomphala
schistosomiasis
snail vector
de novo genome assembly
polymorphism
immunogenetics
gene family evolution
balancing selection
pathogen recognition
url https://hdl.handle.net/20.500.12008/55369