Peng Yifan, Tang Jifeng, Xie Jiaqin
Genetic Engineering Research Center, School of Life Sciences, Chongqing University, Chongqing 401331, China.
Chongqing Engineering Research Center for Fungal Insecticides/Key Laboratory of Gene Function and Regulation Technology under Chongqing Municipal Education Commission, Chongqing 401331, China.
Insects. 2020 Feb 24;11(2):139. doi: 10.3390/insects11020139.
is one of the major pests of rice and results in substantial yield loss every year. Our previous study found that the entomopathogenic fungus showed effective potential for controlling this pest. However, the mechanisms underlying infection of are not well known. In the present study, we further examined the transcriptome of at 4 h, 8 h, 16 h, and 24 h after infection by Illumina deep sequencing. In total, 174.17 Gb of data was collected after sequencing, from which 23,398 unigenes were annotated by various databases, including 3694 newly annotated genes. The results showed that there were 246 vs 75, 275 vs 586, 378 vs 1055, and 638 vs 182 up- and downregulated differentially expressed genes (DEGs) at 4 h, 8 h, 16 h, and 24 h after infection, respectively. The biological functions and associated metabolic processes of these genes were determined with the Clusters of Orthologous Groups (COG), Gene Ontology (GO), and Kyoto Encyclopedia of Genes and Genomes (KEGG) databases. The DEGs data were verified using RT-qPCR. These results indicated that the DEGs during the initial fungal infection appropriately reflected the time course of the response to the fungal infection. Taken together, the results of this study provide new insights into the molecular mechanisms underlying the insect host response to fungal infection, especially during the initial stage of infection, and may improve the potential control strategies for .
是水稻的主要害虫之一,每年都会导致大量产量损失。我们之前的研究发现,昆虫病原真菌在控制这种害虫方面显示出有效的潜力。然而,其感染的潜在机制尚不清楚。在本研究中,我们通过Illumina深度测序进一步检测了感染后4小时、8小时、16小时和24小时的转录组。测序后共收集了174.17 Gb的数据,其中23,398个单基因通过各种数据库进行了注释,包括3694个新注释的基因。结果表明,感染后4小时、8小时、16小时和24小时分别有246对75、275对586、378对1055和638对182个上调和下调差异表达基因(DEG)。利用直系同源基因簇(COG)、基因本体论(GO)和京都基因与基因组百科全书(KEGG)数据库确定了这些基因的生物学功能和相关代谢过程。通过RT-qPCR验证了DEG数据。这些结果表明,在真菌感染初期的DEG适当地反映了对真菌感染反应的时间进程。综上所述,本研究结果为昆虫宿主对真菌感染的分子机制提供了新的见解,特别是在感染初期,并可能改进对的潜在控制策略。