Xi Yu, Xing Longsheng, Wennmann Jörg T, Fan Jiangbin, Li Zaiyuan, Wu Qiang, Lu Sha, Liu Bo, Guo Jianyang, Qiao Xi, Huang Cong, Qian Wanqiang, Jehle Johannes A, Wan Fanghao
Shenzhen Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Genome Analysis Laboratory of the Ministry of Agriculture, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, 518120, China; Julius Kühn Institute (JKI) - Federal Research Centre for Cultivated Plants, Institute for Biological Control, Heinrichstraße 243, 64287, Darmstadt, Germany.
Shenzhen Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Genome Analysis Laboratory of the Ministry of Agriculture, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, 518120, China.
Virology. 2021 Jun;558:110-118. doi: 10.1016/j.virol.2021.02.015. Epub 2021 Mar 12.
The Cydia pomonella granulovirus (CpGV) has been used as a biological control agent of codling moth (Cydia pomonella), a severe global pest on pome fruit. Despite the economic importance, our knowledge of its molecular biology is still limited and a detailed picture of its gene expression is still missing. Here, we sequenced the transcriptome of codling moth larvae infected with the Mexican isolate CpGV-M and analyzed the expression of viral genes at 12, 48, and 96 h post infection (hpi). The results showed that two genes (p6.9 and pp31/39K) related to DNA binding of virus production, were highly expressed at 48 and 96 hpi. From 48 to 96 hpi, the expression of genes associated with virus replication and dissemination decreased, whereas the expression of genes related to infectious virion production and per os infectivity increased. This study provides a comprehensive view of CpGV gene expression patterns in host larvae.
苹果蠹蛾颗粒体病毒(CpGV)已被用作苹果蠹蛾(Cydia pomonella)的生物防治剂,苹果蠹蛾是一种严重危害全球梨果类水果的害虫。尽管其具有经济重要性,但我们对其分子生物学的了解仍然有限,并且其基因表达的详细情况仍不清楚。在此,我们对感染墨西哥分离株CpGV-M的苹果蠹蛾幼虫的转录组进行了测序,并分析了感染后12、48和96小时(hpi)病毒基因的表达情况。结果表明,与病毒产生的DNA结合相关的两个基因(p6.9和pp31/39K)在48和96 hpi时高表达。从48到96 hpi,与病毒复制和传播相关的基因表达下降,而与感染性病毒粒子产生和经口感染性相关的基因表达增加。本研究提供了宿主幼虫中CpGV基因表达模式的全面视图。