破坏者 Varroa 的唾液腺转录组揭示了基于 RNAi 的螨虫控制的合适目标。

IF 2.3 2区 农林科学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Insect Molecular Biology Pub Date : 2024-07-22 DOI:10.1111/imb.12945
Andrea Becchimanzi, Alfonso Cacace, Martina Parziale, Giovanna De Leva, Sergio Iacopino, Giovanni Jesu, Ilaria Di Lelio, Virgilio Stillittano, Emilio Caprio, Francesco Pennacchio
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引用次数: 0

摘要

瓦氏螨(Varroa destructor Anderson and Trueman,中生代:Varroidae)对养蜂业影响巨大,是造成蜂群损失的主要原因之一。这种体外寄生虫通过寄主皮肤上的伤口吸食蜜蜂的液体组织,导致蜜蜂体重减轻、寿命缩短,并传播病毒病原体。然而,尽管螨虫的取食策略非常重要,唾液分泌物对宿主的调节作用却鲜有研究。在此,我们通过鉴定毁灭蚁的唾液成分,研究它们对螨虫摄食和生存的功能重要性,从而填补这一空白。差异表达分析确定了 30 个唾液腺基因,这些基因编码推测的分泌蛋白,其中只有 15 个有功能注释。后者包括可能具有抗菌、抗真菌、细胞溶解、消化和免疫抑制功能的蛋白质。我们选择了转录率最高的三个基因,分别编码几丁质结合域蛋白、卡扎尔结构域丝氨酸蛋白酶抑制剂和木瓜蛋白酶样半胱氨酸蛋白酶,通过反向遗传学方法研究它们在功能上的重要性。通过 RNA 干扰(RNAi)敲除(90%-99%)一种几丁质结合域蛋白的转录本,螨虫的存活率降低了 40%-50%。这项工作拓展了我们对节肢动物外寄生虫所采取的宿主调节和营养利用策略的认识,并确定了 RNAi 的潜在靶标,为制定新的 Varroa 螨虫控制策略铺平了道路。
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The salivary gland transcriptome of Varroa destructor reveals suitable targets for RNAi-based mite control.

The mite Varroa destructor Anderson and Trueman (Mesostigmata: Varroidae) has a dramatic impact on beekeeping and is one of the main causes of honey bee colony losses. This ectoparasite feeds on honey bees' liquid tissues, through a wound created on the host integument, determining weight loss and a reduction of lifespan, as well as the transmission of viral pathogens. However, despite its importance, the mite feeding strategy and the host regulation role by the salivary secretions have been poorly explored. Here, we contribute to fill this gap by identifying the salivary components of V. destructor, to study their functional importance for mite feeding and survival. The differential expression analysis identified 30 salivary gland genes encoding putatively secreted proteins, among which only 15 were found to be functionally annotated. These latter include proteins with putative anti-bacterial, anti-fungal, cytolytic, digestive and immunosuppressive function. The three most highly transcribed genes, coding for a chitin-binding domain protein, a Kazal domain serine protease inhibitor and a papain-like cysteine protease were selected to study their functional importance by reverse genetics. Knockdown (90%-99%) by RNA interference (RNAi) of the transcript of a chitin-binding domain protein, likely interfering with the immune reaction to facilitate mite feeding, was associated with a 40%-50% decrease of mite survival. This work expands our knowledge of the host regulation and nutritional exploitation strategies adopted by ectoparasites of arthropods and allows the identification of potential targets for RNAi, paving the way towards the development of new strategies for Varroa mite control.

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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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