| Literature DB >> 32209228 |
Susanne U Franssen1, Caroline Durrant1, Olivia Stark2, Bettina Moser2, Tim Downing1,3, Hideo Imamura4, Jean-Claude Dujardin4,5, Mandy J Sanders1, Isabel Mauricio6, Michael A Miles7, Lionel F Schnur8, Charles L Jaffe8, Abdelmajeed Nasereddin8, Henk Schallig9, Matthew Yeo7, Tapan Bhattacharyya7, Mohammad Z Alam10, Matthew Berriman1, Thierry Wirth11,12, Gabriele Schönian2, James A Cotton1.
Abstract
Protozoan parasites of the Leishmania donovani complex - L. donovani and L. infantum - cause the fatal disease visceral leishmaniasis. We present the first comprehensive genome-wide global study, with 151 cultured field isolates representing most of the geographical distribution. L. donovani isolates separated into five groups that largely coincide with geographical origin but vary greatly in diversity. In contrast, the majority of L. infantum samples fell into one globally-distributed group with little diversity. This picture is complicated by several hybrid lineages. Identified genetic groups vary in heterozygosity and levels of linkage, suggesting different recombination histories. We characterise chromosome-specific patterns of aneuploidy and identified extensive structural variation, including known and suspected drug resistance loci. This study reveals greater genetic diversity than suggested by geographically-focused studies, provides a resource of genomic variation for future work and sets the scene for a new understanding of the evolution and genetics of the Leishmania donovani complex.Entities:
Keywords: Leishmania donovani / infantum; aneuploidy; genetics; genomics; hybridisation; infectious disease; microbiology; neglected tropical disease; visceral leishmaniasis
Year: 2020 PMID: 32209228 PMCID: PMC7105377 DOI: 10.7554/eLife.51243
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140