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基于 RNA 干扰的抗唾液腺肥大病毒免疫反应在白纹伊蚊中的研究。

RNA interference-based antiviral immune response against the salivary gland hypertrophy virus in Glossina pallidipes.

机构信息

Insect Pest Control Laboratory, Joint FAO/IAEA Programme of Nuclear Techniques in Food and Agriculture, International Atomic Energy Agency, Vienna International Centre, P.O. Box 100, 1400, Vienna, Austria.

Laboratory of Virology, Wageningen University, 6708, PB, Wageningen, The Netherlands.

出版信息

BMC Microbiol. 2018 Nov 23;18(Suppl 1):170. doi: 10.1186/s12866-018-1298-1.

Abstract

BACKGROUND

Glossina pallidipes salivary gland hypertrophy virus (GpSGHV; Hytrosaviridae) is a non-occluded dsDNA virus that specifically infects the adult stages of the hematophagous tsetse flies (Glossina species, Diptera: Glossinidae). GpSGHV infections are usually asymptomatic, but unknown factors can result to a switch to acute symptomatic infection, which is characterized by the salivary gland hypertrophy (SGH) syndrome associated with decreased fecundity that can ultimately lead to a colony collapse. It is uncertain how GpSGHV is maintained amongst Glossina spp. populations but RNA interference (RNAi) machinery, a conserved antiviral defense in insects, is hypothesized to be amongst the host's mechanisms to maintain the GpSGHV in asymptomatic (persistent or latent) infection state. Here, we investigated the involvement of RNAi during GpSGHV infections by comparing the expression of three key RNAi machinery genes, Dicer (DCR), Argonaute (AGO) and Drosha, in artificially virus injected, asymptomatic and symptomatic infected G. pallidipes flies compared to PBS injected (controls) individuals. We further assessed the impact of AGO2 knockdown on virus infection by RT-qPCR quantification of four selected GpSGHV genes, i.e. odv-e66, dnapol, maltodextrin glycosyltransferase (a tegument gene) and SGHV091 (a capsid gene).

RESULTS

We show that in response to hemocoelic injections of GpSGHV into G. pallidipes flies, increased virus replication was accompanied by significant upregulation of the expression of three RNAi key genes; AGO1, AGO2 and DCR2, and a moderate increase in the expression of Drosha post injection compared to the PBS-injected controls. Furthermore, compared to asymptomatically infected individuals, symptomatic flies showed significant downregulation of AGO1, AGO2 and Drosha, but a moderate increase in the expression of DCR2. Compared to the controls, knockdown of AGO2 did not have a significant impact on virus infection in the flies as evidenced by unaltered transcript levels of the selected GpSGHV genes.

CONCLUSION

The upregulation of the expression of the RNAi genes implicate involvement of this machinery in controlling GpSGHV infections and the establishment of symptomatic GpSGHV infections in Glossina. These findings provide a strategic foundation to understand GpSGHV infections and to control latent (asymptomatic) infections in Glossina spp. and thereby control SGHVs in insect production facilities.

摘要

背景

褐须虻唾液腺肥大病毒(GpSGHV;Hytrosaviridae)是一种非封闭的 dsDNA 病毒,专门感染吸血采采蝇(Glossina 属,双翅目:Glossinidae)的成虫阶段。GpSGHV 感染通常无症状,但未知因素可导致急性症状感染转变,其特征是唾液腺肥大(SGH)综合征与繁殖力下降有关,最终可能导致群体崩溃。目前尚不清楚 GpSGHV 如何在 Glossina spp. 种群中维持,但 RNA 干扰(RNAi)机制,昆虫中保守的抗病毒防御机制,被假设是宿主维持 GpSGHV 无症状(持续或潜伏)感染状态的机制之一。在这里,我们通过比较人工注射病毒、无症状和有症状感染的 G. pallidipes 苍蝇与 PBS 注射(对照)个体之间三种关键 RNAi 机制基因(Dicer(DCR)、Argonaute(AGO)和 Drosha)的表达,研究了 RNAi 在 GpSGHV 感染中的作用。我们进一步通过 RT-qPCR 定量分析了四个选定的 GpSGHV 基因(odv-e66、dnapol、麦芽糖糊精糖基转移酶(外壳蛋白基因)和 SGHV091)来评估 AGO2 敲低对病毒感染的影响。

结果

我们表明,在将 GpSGHV 注入 G. pallidipes 苍蝇的血腔后,病毒复制增加伴随着三种 RNAi 关键基因 AGO1、AGO2 和 DCR2 的表达显著上调,与 PBS 注射对照相比,注射后 Drosha 的表达也适度增加。此外,与无症状感染个体相比,有症状的苍蝇显示出 AGO1、AGO2 和 Drosha 的显著下调,但 DCR2 的表达适度增加。与对照相比,AGO2 的敲低对苍蝇中的病毒感染没有显著影响,因为所选 GpSGHV 基因的转录水平没有改变。

结论

RNAi 基因表达的上调表明该机制参与了 GpSGHV 感染的控制和 Glossina 中症状性 GpSGHV 感染的建立。这些发现为理解 GpSGHV 感染和控制 Glossina spp. 中的潜伏(无症状)感染提供了战略基础,从而控制昆虫生产设施中的 SGHVs。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c45c/6251114/f9e1045b67f5/12866_2018_1298_Fig1_HTML.jpg

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