• Occurrence of Schistosoma bovis on Pemba Island, Zanzibar: implications for urogenital schistosomiasis transmission monitoring - CORRIGENDUM (vol 145, pg 1727, 2018)

      Pennance, T; Ame, SM; Amour, AK; Suleiman, KR; Allan, F; Rollinson, D; Webster, BL (Cambridge University Press, 2018-11)
    • Preliminary survival and movement data for a declining population of Flesh-footed Shearwater Ardenna carneipes in Western Australia provides insights into marine threats

      Lavers, J; Lisovski, S; Bond, A (Cambridge University Press, 2018-08-31)
      Seabirds face diverse threats on their breeding islands and while at sea. Human activities have been linked to the decline of seabird populations, yet over-wintering areas typically receive little or no protection. Adult survival rates, a crucial parameter for population persistence in long-lived species, tend to be spatially or temporally restricted for many seabird species, limiting our understanding of factors driving population trends at some sites. We used bio-loggers to study the migration of Western Australian Flesh-footed Shearwaters Ardenna carneipes carneipes and estimated adult survival over five years. Western Australia is home to around 35% of the world’s breeding Flesh-footed Shearwaters, a population which was up-listed to Vulnerable in 2015. During the austral winter, shearwaters migrated across the central Indian Ocean to their non-breeding grounds off western Sri Lanka. Low site fidelity on breeding islands, mortality of adult birds at sea (e.g. fisheries bycatch), and low annual breeding frequency likely contributed to the low estimated annual adult survival (2011–2015: ϕ = 0.634-0.835).
    • Whole genome amplification and exome sequencing of archived schistosome miracidia

      Le Clec'h, W; Chevalier, FD; McDew-White, M; Allan, F; Webster, BL; Gouvras, AN; Kinunghi, S; Tchuem Tchuenté, L-A; Garba, A; Mohammed, KA; et al. (Cambridge University Press, 2018-05-28)
      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.