Stress conditions promote the mating competency of Leishmania promastigotes in vitro marked by expression of the ancestral gamete fusogen HAP2
Stress conditions promote the mating competency of Leishmania promastigotes in vitro marked by expression of the ancestral gamete fusogen HAP2
Abstract Leishmania are protozoan parasites transmitted by the bite of sand fly vectors producing a wide spectrum of diseases in their mammalian hosts. These diverse clinical outcomes are directly associated with parasite strain and species diversity. Although Leishmania reproduction is mainly clonal, a cryptic sexual cycle capable of producing hybrid genotypes has been inferred from population genetic studies, and directly demonstrated by laboratory crosses. Experimentally, mating competency has been largely confined to promastigotes developing in the sand fly midgut. The ability to hybridize culture promastigotes in vitro has been limited so far to low efficiency mating between two L. tropica strains, L747 and MA37, that mate with high efficiency in flies. Here, we show that exposure of promastigote cultures to DNA damage stress produces a remarkably enhanced efficiency of in vitro hybridization of the L. tropica strains, and extends to other species, including L. donovani, L. infantum, and L. braziliensis, a capacity to generate intra- and interspecific hybrids. Whole genome sequencing and total DNA content analyses indicate that the hybrids are in each case full genome, polyploid hybrids. Single-cell RNA sequencing of the L747 and MA37 parental lines highlights the transcriptome heterogeneity of culture promastigotes and reveals discrete clusters that emerge post-irradiation in which genes potentially involved in genetic exchange are expressed, including the ancestral gamete fusogen HAP2. By generating reporter constructs for HAP2, we could select for mating-competent and mating-incompetent promastigotes. Overall, this work reveals that there are specific populations involved in Leishmania mating associated with a discernible transcriptomic signature, and that stress facilitated in vitro hybridization can be a transformative approach to generate large numbers of hybrid genotypes between diverse species and strains.
Louradour Isabelle、Duge Emma、Paun Andrea、Karunaweera Nadira、Sacks David、Ferreira Tiago Rodrigues
Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of HealthLaboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of HealthLaboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of HealthDepartment of Parasitology, Faculty of Medicine, University of ColomboLaboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of HealthLaboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health
微生物学分子生物学遗传学
Louradour Isabelle,Duge Emma,Paun Andrea,Karunaweera Nadira,Sacks David,Ferreira Tiago Rodrigues.Stress conditions promote the mating competency of Leishmania promastigotes in vitro marked by expression of the ancestral gamete fusogen HAP2[EB/OL].(2025-03-28)[2025-05-25].https://www.biorxiv.org/content/10.1101/2021.08.31.458317.点此复制
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