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西花蓟马茧蜂寄生对水稻二化螟脂肪体和血细胞基因表达的影响。

Parasitization by Cotesia chilonis influences gene expression in fatbody and hemocytes of Chilo suppressalis.

机构信息

State Key Laboratory of Rice Biology and Key Laboratory of Agricultural Entomology of Ministry of Agriculture, Institute of Insect Sciences, Zhejiang University, Hangzhou, Zhejiang, China.

出版信息

PLoS One. 2013 Sep 23;8(9):e74309. doi: 10.1371/journal.pone.0074309. eCollection 2013.

Abstract

BACKGROUND

During oviposition many parasitoid wasps inject various factors, such as polydnaviruses (PDVs), along with eggs that manipulate the physiology and development of their hosts. These manipulations are thought to benefit the parasites. However, the detailed mechanisms of insect host-parasitoid interactions are not fully understood at the molecular level. Based on recent findings that some parasitoids influence gene expression in their hosts, we posed the hypothesis that parasitization by a braconid wasp, Cotesia chilonis, influences the expression of genes responsible for development, metabolism and immune functions in the fatbody and hemocytes of its host, Chilo suppressalis.

METHODOLOGY/PRINCIPAL FINDINGS: We obtained 39,344,452 reads, which were assembled into 146,770 scaffolds, and 76,016 unigenes. Parasitization impacted gene expression in fatbody and hemocytes. Of these, 8096 fatbody or 5743 hemocyte unigenes were down-regulated, and 2572 fatbody or 1452 hemocyte unigenes were up-regulated. Gene ontology data showed that the majority of the differentially expressed genes are involved in enzyme-regulated activity, binding, transcription regulator activity and catalytic activity. qPCR results show that most anti-microbial peptide transcription levels were up-regulated after parasitization. Expression of bracovirus genes was detected in parasitized larvae with 19 unique sequences identified from six PDV gene families including ankyrin, CrV1 protein, cystatin, early-expressed (EP) proteins, lectin, and protein tyrosine phosphatase.

CONCLUSIONS

The current study supports our hypothesis that parasitization influences the expression of fatbody and hemocyte genes in the host, C. suppressalis. The general view is that manipulation of host metabolism and immunity benefits the development and emergence of the parasitoid offsprings. The accepted beneficial mechanisms include the direct impact of parasitoid-associated virulence factors such as venom and polydnavirus on host tissues (such as cell damage) and, more deeply, the ability of these factors to influence gene expression. We infer that insect parasitoids generally manipulate their environments, the internal milieu of their hosts.

摘要

背景

在产卵过程中,许多寄生蜂会随着卵一起注入各种因子,如多粒包埋病毒(PDV),这些因子会操纵宿主的生理和发育。这些操纵被认为有利于寄生虫。然而,昆虫宿主-寄生蜂相互作用的详细机制在分子水平上还不完全清楚。基于最近的一些发现,即一些寄生蜂会影响宿主的基因表达,我们假设,一种姬蜂,Cotesia chilonis,寄生会影响其宿主斜纹夜蛾(Chilo suppressalis)的脂肪体和血细胞中负责发育、代谢和免疫功能的基因表达。

方法/主要发现:我们获得了 39344452 条reads,组装成 146770 个scaffolds 和 76016 个 unigenes。寄生作用影响了脂肪体和血细胞中的基因表达。其中,8096 个脂肪体或 5743 个血细胞 unigenes下调,2572 个脂肪体或 1452 个血细胞 unigenes上调。GO 数据显示,大多数差异表达基因参与酶调节活性、结合、转录调控活性和催化活性。qPCR 结果表明,大多数抗菌肽转录水平在寄生后上调。在被寄生的幼虫中检测到了 bracovirus 基因的表达,从六个 PDV 基因家族中鉴定出了 19 个独特的序列,包括 ankyrin、CrV1 蛋白、cystatin、早期表达(EP)蛋白、凝集素和蛋白酪氨酸磷酸酶。

结论

本研究支持我们的假设,即寄生作用影响宿主斜纹夜蛾的脂肪体和血细胞基因的表达。一般认为,宿主代谢和免疫的操纵有利于寄生蜂后代的发育和出现。公认的有益机制包括寄生相关毒力因子(如毒液和多粒包埋病毒)对宿主组织(如细胞损伤)的直接影响,以及这些因子更深入地影响基因表达的能力。我们推断,昆虫寄生蜂通常会操纵它们的环境,即宿主内部环境。

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