全代谢昆虫与半代谢昆虫变态过程中肠道内的免疫基因调控

IF 2.7 3区 医学 Q3 VIROLOGY
Retrovirology Pub Date : 2019-10-14 Epub Date: 2019-08-26 DOI:10.1098/rstb.2019.0073
Paul R Johnston, Véronique Paris, Jens Rolff
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引用次数: 0

摘要

在变态过程中,全变态昆虫完全取代了幼虫的肠道,必须控制微生物群以避免败血症。蛹开始时昆虫肠道中杀菌活性的快速诱导在全变态昆虫的许多目中都有描述,鳞翅目昆虫的研究最为深入,因为它受 20-hydroxyecdysone (20E) 蜕皮途径的控制。在这里,我们利用 RNAseq 比较了全代谢昆虫(Galleria mellonella)和半代谢昆虫(Gryllus bimaculatus)在蜕皮过程中肠道中免疫效应基因的表达。我们发现,在G. mellonella中,许多免疫效应因子和转录因子GmEts的表达上调,其中三种抗菌肽(AMPs)和一种溶菌酶的表达峰值与幼虫肠道分层相吻合。与此相反,在半代谢性的双尾蝇(Gr. bimaculatus)中却检测不到这种上调。这些发现支持了这样一种观点,即完全变态开始时免疫效应因子的上调是一种适应性反应,它在肠道更换过程中控制微生物群。本文是主题 "完全变态的进化 "的一部分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immune gene regulation in the gut during metamorphosis in a holo- versus a hemimetabolous insect.

During metamorphosis, holometabolous insects completely replace the larval gut and must control the microbiota to avoid septicaemia. Rapid induction of bactericidal activity in the insect gut at the onset of pupation has been described in numerous orders of the Holometabola and is best-studied in the Lepidoptera where it is under control of the 20-hydroxyecdysone (20E) moulting pathway. Here, using RNAseq, we compare the expression of immune effector genes in the gut during metamorphosis in a holometabolous (Galleria mellonella) and a hemimetabolous insect (Gryllus bimaculatus). We find that in G. mellonella, the expression of numerous immune effectors and the transcription factor GmEts are upregulated, with peak expression of three antimicrobial peptides (AMPs) and a lysozyme coinciding with delamination of the larval gut. By contrast, no such upregulation was detectable in the hemimetabolous Gr. bimaculatus. These findings support the idea that the upregulation of immune effectors at the onset of complete metamorphosis is an adaptive response, which controls the microbiota during gut replacement. This article is part of the theme issue 'The evolution of complete metamorphosis'.

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来源期刊
Retrovirology
Retrovirology 医学-病毒学
CiteScore
5.80
自引率
3.00%
发文量
24
审稿时长
>0 weeks
期刊介绍: Retrovirology is an open access, online journal that publishes stringently peer-reviewed, high-impact articles on host-pathogen interactions, fundamental mechanisms of replication, immune defenses, animal models, and clinical science relating to retroviruses. Retroviruses are pleiotropically found in animals. Well-described examples include avian, murine and primate retroviruses. Two human retroviruses are especially important pathogens. These are the human immunodeficiency virus, HIV, and the human T-cell leukemia virus, HTLV. HIV causes AIDS while HTLV-1 is the etiological agent for adult T-cell leukemia and HTLV-1-associated myelopathy/tropical spastic paraparesis. Retrovirology aims to cover comprehensively all aspects of human and animal retrovirus research.
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