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.
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.
| 2023 | |
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Biomphalaria sudanica Biomphalaria choanomphala schistosomiasis snail vector de novo genome assembly polymorphism immunogenetics gene family evolution balancing selection pathogen recognition |
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| 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) |
| _version_ | 1875693114323107840 |
|---|---|
| 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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| collection | COLIBRI |
| 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 |
| format | preprint |
| id | COLIBRI_0eb0c217847d38cf08c058682e6a9f4c |
| 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 10.1101/2023.11.01.565203 |
| instacron_str | Universidad de la República |
| institution | Universidad de la República |
| instname_str | Universidad de la República |
| language | eng |
| language_invalid_str_mv | en |
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| publishDate | 2023 |
| reponame_str | COLIBRI |
| 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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Institucionalhttps://www.colibri.udelar.edu.uyUniversidadhttps://udelar.edu.uy/https://www.colibri.udelar.edu.uy/oai/requestkarina.camps@seciu.edu.uyUruguayopendoar:47712026-06-04T17:51COLIBRI - 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 |