Whole-genome sequence of the bovine blood fluke Schistosoma bovis supports interspecific hybridization with S. haematobium.


Journal

PLoS pathogens
ISSN: 1553-7374
Titre abrégé: PLoS Pathog
Pays: United States
ID NLM: 101238921

Informations de publication

Date de publication:
01 2019
Historique:
received: 05 06 2018
accepted: 07 12 2018
revised: 04 02 2019
pubmed: 24 1 2019
medline: 19 3 2019
entrez: 24 1 2019
Statut: epublish

Résumé

Mesenteric infection by the parasitic blood fluke Schistosoma bovis is a common veterinary problem in Africa and the Middle East and occasionally in the Mediterranean Region. The species also has the ability to form interspecific hybrids with the human parasite S. haematobium with natural hybridisation observed in West Africa, presenting possible zoonotic transmission. Additionally, this exchange of alleles between species may dramatically influence disease dynamics and parasite evolution. We have generated a 374 Mb assembly of the S. bovis genome using Illumina and PacBio-based technologies. Despite infecting different hosts and organs, the genome sequences of S. bovis and S. haematobium appeared strikingly similar with 97% sequence identity. The two species share 98% of protein-coding genes, with an average sequence identity of 97.3% at the amino acid level. Genome comparison identified large continuous parts of the genome (up to several 100 kb) showing almost 100% sequence identity between S. bovis and S. haematobium. It is unlikely that this is a result of genome conservation and provides further evidence of natural interspecific hybridization between S. bovis and S. haematobium. Our results suggest that foreign DNA obtained by interspecific hybridization was maintained in the population through multiple meiosis cycles and that hybrids were sexually reproductive, producing viable offspring. The S. bovis genome assembly forms a highly valuable resource for studying schistosome evolution and exploring genetic regions that are associated with species-specific phenotypic traits.

Identifiants

pubmed: 30673782
doi: 10.1371/journal.ppat.1007513
pii: PPATHOGENS-D-18-01153
pmc: PMC6361461
doi:

Substances chimiques

Proteome 0
DNA 9007-49-2

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1007513

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Harald Oey (H)

The University of Queensland Diamantina Institute, The University of Queensland, Brisbane, QLD, Australia.

Martha Zakrzewski (M)

Genetics & Computational Biology Department, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.

Kerstin Gravermann (K)

Faculty of Technology and Center for Biotechnology (CeBiTec), Bielefeld University, Bielefeld, Germany.

Neil D Young (ND)

Faculty of Veterinary and Agricultural Sciences, The University of Melbourne, Parkville, VIC, Australia.

Pasi K Korhonen (PK)

Faculty of Veterinary and Agricultural Sciences, The University of Melbourne, Parkville, VIC, Australia.

Geoffrey N Gobert (GN)

Immunology Department, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
School of Biological Sciences, Queen's University Belfast, Belfast, Northern Ireland, United Kingdom.

Sujeevi Nawaratna (S)

Immunology Department, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.

Shihab Hasan (S)

The University of Queensland Diamantina Institute, The University of Queensland, Brisbane, QLD, Australia.
Genetics & Computational Biology Department, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.

David M Martínez (DM)

Immunology Department, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.

Hong You (H)

Immunology Department, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.

Martin Lavin (M)

UQ Centre for Clinical Research, The University of Queensland, Brisbane, QLD, Australia.

Malcolm K Jones (MK)

Immunology Department, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
School of Veterinary Science, University of Queensland, Gatton, QLD, Australia.

Mark A Ragan (MA)

Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, Australia.

Jens Stoye (J)

Faculty of Technology and Center for Biotechnology (CeBiTec), Bielefeld University, Bielefeld, Germany.

Ana Oleaga (A)

Institute of Natural Resources and Agrobiology (IRNASA, CSIC), Cordel de Merinas, Salamanca, Spain.

Aidan M Emery (AM)

Natural History Museum, Life Sciences Department, Parasites and Vectors Division, Cromwell Road, London, United Kingdom.

Bonnie L Webster (BL)

Natural History Museum, Life Sciences Department, Parasites and Vectors Division, Cromwell Road, London, United Kingdom.

David Rollinson (D)

Natural History Museum, Life Sciences Department, Parasites and Vectors Division, Cromwell Road, London, United Kingdom.

Robin B Gasser (RB)

Faculty of Veterinary and Agricultural Sciences, The University of Melbourne, Parkville, VIC, Australia.

Donald P McManus (DP)

Immunology Department, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.

Lutz Krause (L)

The University of Queensland Diamantina Institute, The University of Queensland, Brisbane, QLD, Australia.
Genetics & Computational Biology Department, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.

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