School of Life Sciences, Jiangsu University, Zhenjiang 212013, China.
School of Life Sciences, Jiangsu University, Zhenjiang 212013, China.
J Invertebr Pathol. 2024 Jun;204:108103. doi: 10.1016/j.jip.2024.108103. Epub 2024 Apr 5.
Bombyx mori nucleopolyhedrovirus (BmNPV) caused serious economic losses in sericulture. Analyzing the molecular mechanism of silkworms (B. mori) resistance to BmNPV is of great significance for the prevention and control of silkworm virus diseases and the biological control of agricultural lepidopteran pests. In order to clarify the defense mechanisms of silkworms against BmNPV, we constructed a near isogenic line BC8 with high resistance to BmNPV through the highly BmNPV-resistant strain NB and the highly BmNPV-susceptible strain 306. In this study, RNA-Seq technique was used to analyze the transcriptome level differences in the midgut of BC8 and 306 following BmNPV infection. A total of 1350 DEGs were identified. Clustering analysis showed that these genes could be divided into 8 clusters with different expression patterns. Functional annotations based on GO and KEGG analysis indicated that they were involved in various metabolism pathways. Finally, 32 BmNPV defense responsive genes were screened. They were involved in metabolism, reactive oxygen species (ROS), signal transduction and immune response, and insect hormones. The further verification shows that HSP70 should participate in resistance responses of anti-BmNPV. These findings have paved the way in further functional characterization of candidate genes and subsequently can be used in breeding of BmNPV resistance dominant silkworms.
家蚕核型多角体病毒(BmNPV)给蚕桑业造成了严重的经济损失。分析家蚕(B. mori)对 BmNPV 抗性的分子机制,对于蚕病毒病的防治和农业鳞翅目害虫的生物防治具有重要意义。为了阐明家蚕抵抗 BmNPV 的防御机制,我们通过高度抗 BmNPV 的品系 NB 和高度感 BmNPV 的品系 306 构建了一个近等基因系 BC8。在本研究中,我们利用 RNA-Seq 技术分析了 BC8 和 306 中肠在感染 BmNPV 后的转录组水平差异。共鉴定出 1350 个差异表达基因。聚类分析表明,这些基因可分为 8 个具有不同表达模式的簇。基于 GO 和 KEGG 分析的功能注释表明,它们参与了各种代谢途径。最后,筛选出 32 个 BmNPV 防御响应基因。它们参与代谢、活性氧(ROS)、信号转导和免疫反应以及昆虫激素。进一步的验证表明,HSP70 应该参与抗 BmNPV 的抗性反应。这些发现为候选基因的进一步功能特征分析铺平了道路,并可随后用于培育 BmNPV 抗性显性家蚕。