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Whole genome amplification and exome sequencing of archived schistosome miracidia.
Le Clec'h, Winka; Chevalier, Frédéric D; McDew-White, Marina; Allan, Fiona; Webster, Bonnie L; Gouvras, Anouk N; Kinunghi, Safari; Tchuem Tchuenté, Louis-Albert; Garba, Amadou; Mohammed, Khalfan A; Ame, Shaali M; Webster, Joanne P; Rollinson, David; Emery, Aidan M; Anderson, Timothy J C.
Afiliação
  • Le Clec'h W; Department of Genetics,Texas Biomedical Research Institute,PO Box 760549, San Antonio, TX 78245-0549,USA.
  • Chevalier FD; Department of Genetics,Texas Biomedical Research Institute,PO Box 760549, San Antonio, TX 78245-0549,USA.
  • McDew-White M; Department of Genetics,Texas Biomedical Research Institute,PO Box 760549, San Antonio, TX 78245-0549,USA.
  • Allan F; Department of Life Sciences,The Natural History Museum,Cromwell Road, London SW7 5BD,UK.
  • Webster BL; Department of Life Sciences,The Natural History Museum,Cromwell Road, London SW7 5BD,UK.
  • Gouvras AN; Department of Life Sciences,The Natural History Museum,Cromwell Road, London SW7 5BD,UK.
  • Kinunghi S; National Institute for Medical Research, Mwanza Research Centre,Mwanza,United Republic of Tanzania.
  • Tchuem Tchuenté LA; Laboratoire de Parasitologie et Ecologie,Université de Yaoundé I,Yaoundé,Cameroon.
  • Garba A; Réseau International Schistosomoses, Environnement, Aménagement et Lutte (RISEAL-Niger),333, Avenue des Zarmakoye, B.P. 13724, Niamey,Niger.
  • Mohammed KA; Ministry of Health,Helminth Control Laboratory Unguja,Zanzibar,United Republic of Tanzania.
  • Ame SM; Public Health Laboratory - Ivo de Carneri,Pemba,United Republic of Tanzania.
  • Webster JP; Department of Pathobiology and Population Sciences,Centre for Emerging, Endemic and Exotic Diseases,Royal Veterinary College, University of London,AL9 7TA,UK.
  • Rollinson D; Department of Life Sciences,The Natural History Museum,Cromwell Road, London SW7 5BD,UK.
  • Emery AM; Department of Life Sciences,The Natural History Museum,Cromwell Road, London SW7 5BD,UK.
  • Anderson TJC; Department of Genetics,Texas Biomedical Research Institute,PO Box 760549, San Antonio, TX 78245-0549,USA.
Parasitology ; 145(13): 1739-1747, 2018 11.
Article em En | MEDLINE | ID: mdl-29806576
ABSTRACT
Adult schistosomes live in the blood vessels and cannot easily be sampled from humans, so archived miracidia larvae hatched from eggs expelled in feces or urine are commonly used for population genetic studies. Large collections of archived miracidia on FTA cards are now available through the Schistosomiasis Collection at the Natural History Museum (SCAN). Here we describe protocols for whole genome amplification of Schistosoma mansoni and Schistosome haematobium miracidia from these cards, as well as real time PCR quantification of amplified schistosome DNA. We used microgram quantities of DNA obtained for exome capture and sequencing of single miracidia, generating dense polymorphism data across the exome. These methods will facilitate the transition from population genetics, using limited numbers of markers to population genomics using genome-wide marker information, maximising the value of collections such as SCAN.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Schistosoma haematobium / Schistosoma mansoni / Técnicas de Amplificação de Ácido Nucleico / Genoma Helmíntico / Sequenciamento do Exoma Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Schistosoma haematobium / Schistosoma mansoni / Técnicas de Amplificação de Ácido Nucleico / Genoma Helmíntico / Sequenciamento do Exoma Idioma: En Ano de publicação: 2018 Tipo de documento: Article