Laboratory of Parasitic Diseases, National Institutes of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, United States of America.
Department of Molecular Microbiology, Washington University School of Medicine in St Louis, St Louis, Missouri, United States of America.
PLoS Genet. 2019 May 15;15(5):e1008042. doi: 10.1371/journal.pgen.1008042. eCollection 2019 May.
Hybrid genotypes have been repeatedly described among natural isolates of Leishmania, and the recovery of experimental hybrids from sand flies co-infected with different strains or species of Leishmania has formally demonstrated that members of the genus possess the machinery for genetic exchange. As neither gamete stages nor cell fusion events have been directly observed during parasite development in the vector, we have relied on a classical genetic analysis to determine if Leishmania has a true sexual cycle. Here, we used whole genome sequencing to follow the chromosomal inheritance patterns of experimental hybrids generated within and between different strains of L. major and L. infantum. We also generated and sequenced the first experimental hybrids in L. tropica. We found that in each case the parental somy and allele contributions matched the inheritance patterns expected under meiosis 97-99% of the time. The hybrids were equivalent to F1 progeny, heterozygous throughout most of the genome for the markers that were homozygous and different between the parents. Rare, non-Mendelian patterns of chromosomal inheritance were observed, including a gain or loss of somy, and loss of heterozygosity, that likely arose during meiosis or during mitotic divisions of the progeny clones in the fly or culture. While the interspecies hybrids appeared to be sterile, the intraspecies hybrids were able to produce backcross and outcross progeny. Analysis of 5 backcross and outcross progeny clones generated from an L. major F1 hybrid, as well as 17 progeny clones generated from backcrosses involving a natural hybrid of L. tropica, revealed genome wide patterns of recombination, demonstrating that classical crossing over occurs at meiosis, and allowed us to construct the first physical and genetic maps in Leishmania. Altogether, the findings provide strong evidence for meiosis-like sexual recombination in Leishmania, presenting clear opportunities for forward genetic analysis and positional cloning of important genes.
杂种基因型在天然分离的利什曼原虫中反复被描述,并且从同时感染不同利什曼原虫株或种的沙蝇中回收的实验杂种正式证明该属具有遗传交换的机制。由于在媒介中寄生虫发育过程中既没有观察到配子阶段也没有观察到细胞融合事件,因此我们依赖经典的遗传分析来确定利什曼原虫是否具有真正的有性周期。在这里,我们使用全基因组测序来跟踪在不同利什曼原虫株和种内和之间产生的实验杂种的染色体遗传模式。我们还在 L. tropica 中生成并测序了第一个实验杂种。我们发现,在每种情况下,亲本 somy 和等位基因贡献与减数分裂中预期的遗传模式一致,97-99%的情况下符合预期。杂种与 F1 后代相当,在大多数基因组中对于标记都是杂合的,而这些标记在亲本之间是纯合的。观察到罕见的、非孟德尔的染色体遗传模式,包括 somy 的增益或损失,以及杂合性的丧失,这些可能是在减数分裂期间或在后代克隆的有丝分裂分裂期间发生的。虽然种间杂种似乎是不育的,但种内杂种能够产生回交和杂交后代。对来自 L. major F1 杂种的 5 个回交和杂交后代克隆以及涉及 L. tropica 天然杂种的回交涉及的 17 个后代克隆的分析表明,重组具有全基因组模式,证明经典交叉发生在减数分裂期间,并且使我们能够构建在利什曼原虫中的第一个物理和遗传图谱。总的来说,这些发现为利什曼原虫中的减数分裂样性重组提供了有力的证据,为正向遗传分析和重要基因的定位克隆提供了明确的机会。