Xu Wen-Feng, Yang Jia-Lin, Meng Xiang-Kun, Gu Zhi-Guang, Zhang Qi-Lin, Lin Lian-Bing
Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, China.
Kingenta Ecological Engineering Group Co., Ltd., Linyi, China.
Front Microbiol. 2021 Apr 7;12:617710. doi: 10.3389/fmicb.2021.617710. eCollection 2021.
The egg-pathogenic fungus parasitizes on nematode eggs, and thus, it is used as a good biocontrol agent against plant root-knot nematodes. However, little is known about the transcriptional response of while infecting nematode eggs. This study presents the whole transcriptome sequencing of and transcriptome-wide gene expression analysis of upon infecting the eggs of compared to non-infecting controls. A transcriptomic library of was used as reference gene set and six transcriptomic libraries of the non-infecting control and infecting eggs were constructed, respectively, comprising three biological replicates of each. A total of 1,011 differently expressed genes (DEGs) were identified in the infecting samples, including 553 up-regulated and 458 down-regulated genes compared to the non-infecting control samples. Furthermore, functional enrichment analysis exhibited that these DEGs were primarily involved in oxidative phosphorylation, oxidoreductase activity, and metabolic processes. Fifteen DEGs were randomly selected to verify the RNA sequencing results through quantitative real-time polymerase chain reaction (qPCR). The study focused on genes that were strongly expressed upon infecting eggs. These DEGs were primarily involved in detoxification, parasitic behavior, and nutritional utilization. This study contributes significantly to the understanding of the molecular mechanisms underlying the parasitic action of on nematode eggs and provides a valuable genetic resource for further research on parasitic behavior of . Notably, this study examined the transcriptomics of infecting eggs at only one time point. Since there were fungi at different stages of the infection process at that time point, the transcriptional profiles are not precisely examining one specific stage in this process.
这种卵寄生真菌寄生于线虫卵上,因此,它被用作对抗植物根结线虫的良好生物防治剂。然而,关于其感染线虫卵时的转录反应知之甚少。本研究呈现了该真菌的全转录组测序以及与未感染对照相比,其感染线虫卵时的全转录组范围的基因表达分析。使用该真菌的转录组文库作为参考基因集,分别构建了未感染对照和感染线虫卵的该真菌的六个转录组文库,每个文库包含三个生物学重复。在感染样本中总共鉴定出1011个差异表达基因(DEG),与未感染对照样本相比,其中包括553个上调基因和458个下调基因。此外,功能富集分析表明这些DEG主要参与氧化磷酸化、氧化还原酶活性和代谢过程。随机选择15个DEG通过定量实时聚合酶链反应(qPCR)验证RNA测序结果。该研究聚焦于感染线虫卵时强烈表达的基因。这些DEG主要参与解毒、寄生行为和营养利用。本研究对理解该真菌对线虫卵寄生作用的分子机制有显著贡献,并为该真菌寄生行为的进一步研究提供了宝贵的遗传资源。值得注意的是,本研究仅在一个时间点检测了该真菌感染线虫卵的转录组学。由于在那个时间点存在处于感染过程不同阶段的真菌,转录谱并未精确检测该过程中的一个特定阶段。