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沃尔巴克氏体在黑腹果蝇中细胞间水平转移的机制

Mechanisms of Horizontal Cell-to-Cell Transfer of Wolbachia spp. in Drosophila melanogaster.

作者信息

White Pamela M, Pietri Jose E, Debec Alain, Russell Shelbi, Patel Bhavin, Sullivan William

机构信息

Department of Molecular, Cell & Developmental Biology, University of California, Santa Cruz, California, USA.

Department of Molecular, Cell & Developmental Biology, University of California, Santa Cruz, California, USA

出版信息

Appl Environ Microbiol. 2017 Mar 17;83(7). doi: 10.1128/AEM.03425-16. Print 2017 Apr 1.

Abstract

is an intracellular endosymbiont present in most arthropod and filarial nematode species. Transmission between hosts is primarily vertical, taking place exclusively through the female germ line, although horizontal transmission has also been documented. The results of several studies indicate that spp. can undergo transfer between somatic and germ line cells during nematode development and in adult flies. However, the mechanisms underlying horizontal cell-to-cell transfer remain largely unexplored. Here, we establish a tractable system for probing horizontal transfer of cells between cells in culture using fluorescence hybridization (FISH). First, we show that horizontal transfer is independent of cell-to-cell contact and can efficiently take place through the culture medium within hours. Further, we demonstrate that efficient transfer utilizes host cell phagocytic and clathrin/dynamin-dependent endocytic machinery. Lastly, we provide evidence that this process is conserved between species, showing that horizontal transfer from mosquito to cells takes place in a similar fashion. Altogether, our results indicate that utilizes host internalization machinery during infection, and this mechanism is conserved across insect species. Our work has broad implications for the control and treatment of tropical diseases. can confer resistance against a variety of human pathogens in mosquito vectors. Elucidating the mechanisms of horizontal transfer will be useful for efforts to more efficiently infect nonnatural insect hosts with as a biological control agent. Further, as is essential for the survival of filarial nematodes, understanding horizontal transfer might provide new approaches to treating human infections by targeting Finally, this work provides a key first step toward the genetic manipulation of .

摘要

是一种存在于大多数节肢动物和丝虫线虫物种中的细胞内共生体。宿主之间的传播主要是垂直传播,仅通过雌性生殖系进行,不过水平传播也有记录。多项研究结果表明,[物种名称]在秀丽隐杆线虫发育过程中和成年果蝇中可在体细胞和生殖系细胞之间转移。然而,水平细胞间转移的潜在机制在很大程度上仍未得到探索。在此,我们建立了一个易于处理的系统,利用荧光原位杂交(FISH)来探究培养物中[物种名称]细胞在[另一物种名称]细胞之间的水平转移。首先,我们表明水平转移不依赖细胞间接触,并且能在数小时内通过培养基高效发生。此外,我们证明高效转移利用宿主细胞的吞噬作用以及网格蛋白/发动蛋白依赖性内吞机制。最后,我们提供证据表明这个过程在物种间是保守的,显示从蚊子到[另一物种名称]细胞的水平转移以类似方式发生。总之,我们的结果表明[物种名称]在感染过程中利用宿主内化机制,并且这种机制在昆虫物种间是保守的。我们的工作对热带疾病的控制和治疗具有广泛意义。[物种名称]可使蚊子媒介对多种人类病原体产生抗性。阐明水平转移机制将有助于更有效地用[物种名称]作为生物控制剂感染非天然昆虫宿主。此外,由于[物种名称]对丝虫线虫的生存至关重要,了解水平转移可能为通过靶向[物种名称]治疗人类感染提供新方法。最后,这项工作为[物种名称]的基因操作迈出了关键的第一步。

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