Bmo-miR-6498-5p suppresses Bombyx mori nucleopolyhedrovirus infection by down-regulating BmPLPP2 to modulate pyridoxal phosphate content in B. mori

IF 2.3 2区 农林科学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Hui-Hua Cao, Wei-Wei Kong, Xi-Ya Chen, Sadaf Ayaz, Cai-Ping Hou, Yi-Sheng Wang, Shi-Huo Liu, Jia-ping Xu
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引用次数: 0

Abstract

The RNA interference pathway mediated by microRNAs (miRNAs) is one of the methods to defend against viruses in insects. Recent studies showed that miRNAs participate in viral infection by binding to target genes to regulate their expression. Here, we found that the Bombyx mori miRNA, miR-6498-5p was down-regulated, whereas its predicted target gene pyridoxal phosphate phosphatase PHOSPHO2 (BmPLPP2) was up-regulated upon Bombyx mori nucleopolyhedrovirus (BmNPV) infection. Both in vivo and in vitro experiments showed that miR-6498-5p targets BmPLPP2 and suppresses its expression. Furthermore, we found miR-6498-5p inhibits BmNPV genomic DNA (gDNA) replication, whereas BmPLPP2 promotes BmNPV gDNA replication. As a pyridoxal phosphate (PLP) phosphatase (PLPP), the overexpression of BmPLPP2 results in a reduction of PLP content, whereas the knockdown of BmPLPP2 leads to an increase in PLP content. In addition, exogenous PLP suppresses the replication of BmNPV gDNA; in contrast, the PLP inhibitor 4-deoxypyridoxine facilitates BmNPV gDNA replication. Taken together, we concluded that miR-6498-5p has a potential anti-BmNPV role by down-regulating BmPLPP2 to modulate PLP content, but BmNPV induces miR-6498-5p down-regulation to promote its proliferation. Our findings provide valuable insights into the role of host miRNA in B. mori–BmNPV interaction. Furthermore, the identification of the antiviral molecule PLP offers a novel perspective on strategies for preventing and managing viral infection in sericulture.

Abstract Image

Abstract Image

Bmo-miR-6498-5p通过下调BmPLPP2来调节磷酸吡哆醛含量,从而抑制森蚕核多角体病毒感染。
由微小核糖核酸(miRNA)介导的 RNA 干扰途径是昆虫抵御病毒的方法之一。最近的研究表明,miRNA 通过与靶基因结合来调控靶基因的表达,从而参与病毒感染。在这里,我们发现在感染森蝽核型多角体病毒(BmNPV)后,森蝽miRNA miR-6498-5p被下调,而其预测的靶基因吡哆醛磷酸酶PHOSPHO2(BmPLPP2)被上调。体内和体外实验均表明,miR-6498-5p 以 BmPLPP2 为靶标并抑制其表达。此外,我们还发现 miR-6498-5p 能抑制 BmNPV 基因组 DNA(gDNA)的复制,而 BmPLPP2 能促进 BmNPV gDNA 的复制。作为一种磷酸吡哆醛(PLP)磷酸酶(PLPP),过表达 BmPLPP2 会导致 PLP 含量减少,而敲除 BmPLPP2 则会导致 PLP 含量增加。此外,外源 PLP 可抑制 BmNPV gDNA 的复制;相反,PLP 抑制剂 4-脱氧吡哆醇可促进 BmNPV gDNA 的复制。综上所述,我们得出结论:miR-6498-5p 通过下调 BmPLPP2 来调节 PLP 含量,从而具有潜在的抗 BmNPV 作用,但 BmNPV 会诱导 miR-6498-5p 下调,以促进其增殖。我们的研究结果为了解宿主 miRNA 在 B. mori-BmNPV 相互作用中的作用提供了有价值的见解。此外,抗病毒分子 PLP 的鉴定为预防和管理养蚕病毒感染的策略提供了新的视角。
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来源期刊
Insect Molecular Biology
Insect Molecular Biology 生物-昆虫学
CiteScore
4.80
自引率
3.80%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Insect Molecular Biology has been dedicated to providing researchers with the opportunity to publish high quality original research on topics broadly related to insect molecular biology since 1992. IMB is particularly interested in publishing research in insect genomics/genes and proteomics/proteins. This includes research related to: • insect gene structure • control of gene expression • localisation and function/activity of proteins • interactions of proteins and ligands/substrates • effect of mutations on gene/protein function • evolution of insect genes/genomes, especially where principles relevant to insects in general are established • molecular population genetics where data are used to identify genes (or regions of genomes) involved in specific adaptations • gene mapping using molecular tools • molecular interactions of insects with microorganisms including Wolbachia, symbionts and viruses or other pathogens transmitted by insects Papers can include large data sets e.g.from micro-array or proteomic experiments or analyses of genome sequences done in silico (subject to the data being placed in the context of hypothesis testing).
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