Inbar Ehud, Hughitt V Keith, Dillon Laura A L, Ghosh Kashinath, El-Sayed Najib M, Sacks David L
Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, Maryland, USA.
mBio. 2017 Apr 4;8(2):e00029-17. doi: 10.1128/mBio.00029-17.
The life cycle of the parasite in the sand fly vector involves differentiation into several distinctive forms, each thought to represent an adaptation to specific microenvironments in the midgut of the fly. Based on transcriptome sequencing (RNA-Seq) results, we describe the first high-resolution analysis of the transcriptome dynamics of four distinct stages of as they develop in a natural vector, The early transformation from tissue amastigotes to procyclic promastigotes in the blood-fed midgut was accompanied by the greatest number of differentially expressed genes, including the downregulation of amastins, and upregulation of multiple cell surface proteins, sugar and amino acid transporters, and genes related to glucose metabolism and cell cycle progression. The global changes accompanying post-blood meal differentiation of procyclic promastigotes to the nectomonad and metacyclic stages were less extensive, though each displayed a unique signature. The transcriptome of nectomonads, which has not been studied previously, revealed changes consistent with cell cycle arrest and the upregulation of genes associated with starvation and stress, including autophagic pathways of protein recycling. Maturation to the infective, metacyclic stage was accompanied by changes suggesting preadaptation to the intracellular environment of the mammalian host, demonstrated by the amastigote-like profiles of surface proteins and metabolism-related genes. Finally, a direct comparison between sand fly-derived and culture-derived metacyclics revealed a reassuring similarity between the two forms, with the forms distinguished mainly by a stronger upregulation of transcripts associated with nutrient stress. The life cycle of parasites in the sand fly vector includes their growth and development as morphologically distinct forms of extracellular promastigotes found within the different microenvironments of the gut. Based on RNA-Seq, we provide here the first high-resolution, transcriptomic analysis of insect stages during their cyclical development , from tissue amastigotes ingested with the blood meal to infective, metacyclic promastigotes that initiate infection in the mammalian host. The most extensive genetic reprogramming occurred during the early transformation of amastigotes to rapidly dividing procyclic promastigotes in the blood-fed midgut, with major changes in the abundance of mRNAs for surface proteins and metabolism. The post-blood meal-adapted nectomonad stage was characterized by the downregulation of cell cycle-related genes and the upregulation of stress- and starvation-related genes. Finally, the transcriptome of metacyclic promastigotes shifted to a more amastigote-like profile, suggesting their preadaptation to the intracellular host environment.
寄生虫在白蛉传播媒介中的生命周期涉及分化为几种不同的形式,每种形式都被认为是对蛉中肠特定微环境的一种适应。基于转录组测序(RNA测序)结果,我们首次对白蛉自然传播媒介中寄生虫发育的四个不同阶段的转录组动态进行了高分辨率分析。在吸食血液的中肠中,从组织型无鞭毛体向前鞭毛体的早期转变伴随着数量最多的差异表达基因,包括无鞭毛体蛋白的下调,以及多种细胞表面蛋白、糖和氨基酸转运蛋白以及与葡萄糖代谢和细胞周期进程相关基因的上调。前鞭毛体在吸食血液后分化为 nectomonad 和成熟循环体阶段的整体变化程度较小,不过每个阶段都有独特的特征。此前未被研究过的 nectomonad 的转录组显示出与细胞周期停滞以及与饥饿和应激相关基因上调一致的变化,包括蛋白质循环利用的自噬途径。发育到具有感染性的成熟循环体阶段伴随着一些变化,这些变化表明其对哺乳动物宿主细胞内环境的预适应,表面蛋白和代谢相关基因呈现出类似无鞭毛体的特征。最后,对白蛉来源的和培养来源的成熟循环体进行直接比较发现,这两种形式之间存在令人安心的相似性,主要区别在于与营养应激相关的转录本上调程度更强。寄生虫在白蛉传播媒介中的生命周期包括它们以形态不同的细胞外前鞭毛体形式在肠道不同微环境中的生长和发育。基于RNA测序,我们在此首次对白蛉传播媒介中寄生虫从随血液摄入的组织型无鞭毛体到在哺乳动物宿主中引发感染的具有感染性的成熟循环体前鞭毛体的周期性发育过程中的昆虫阶段进行了高分辨率的转录组分析。最广泛的基因重编程发生在无鞭毛体在吸食血液的中肠中向快速分裂的前鞭毛体的早期转变过程中,表面蛋白和代谢相关mRNA丰度发生了重大变化。吸食血液后适应的 nectomonad 阶段的特征是与细胞周期相关基因的下调以及与应激和饥饿相关基因的上调。最后,成熟循环体前鞭毛体的转录组转变为更类似无鞭毛体的特征,表明它们对宿主细胞内环境的预适应。