| Literature DB >> 33514858 |
Philipp Schwabl1, Mariana C Boité2, Giovanni Bussotti3,4, Arne Jacobs1, Bjorn Andersson5, Otacilio Moreira6, Anita L Freitas-Mesquita7, Jose Roberto Meyer-Fernandes7, Erich L Telleria8,9, Yara Traub-Csekö8, Slavica Vaselek9, Tereza Leštinová9, Petr Volf9, Fernanda N Morgado10, Renato Porrozzi10, Martin Llewellyn1, Gerald F Späth4, Elisa Cupolillo10.
Abstract
Leishmania infantum causes visceral leishmaniasis, a deadly vector-borne disease introduced to the Americas during the colonial era. This non-native trypanosomatid parasite has since established widespread transmission cycles using alternative vectors, and human infection has become a significant concern to public health, especially in Brazil. A multi-kilobase deletion was recently detected in Brazilian L. infantum genomes and is suggested to reduce susceptibility to the anti-leishmanial drug miltefosine. We show that deletion-carrying strains occur in at least 15 Brazilian states and describe diversity patterns suggesting that these derive from common ancestral mutants rather than from recurrent independent mutation events. We also show that the deleted locus and associated enzymatic activity is restored by hybridization with non-deletion type strains. Genetic exchange appears common in areas of secondary contact but also among closely related parasites. We examine demographic and ecological scenarios underlying this complex L. infantum population structure and discuss implications for disease control.Entities:
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Year: 2021 PMID: 33514858 PMCID: PMC7846609 DOI: 10.1038/s42003-021-01658-5
Source DB: PubMed Journal: Commun Biol ISSN: 2399-3642