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甘蔗对媒介传播的甘蔗黄叶病毒感染响应的转录组分析

Transcriptome Analysis of Sugarcane Response to Sugarcane Yellow Leaf Virus Infection Transmitted by the Vector .

作者信息

Shabbir Rubab, Zhaoli Lin, Yueyu Xu, Zihao Sun, Pinghua Chen

机构信息

Key Laboratory of Sugarcane Biology and Genetic Breeding, Ministry of Agriculture, National Engineering Research Center of Sugarcane, Fujian Agriculture and Forestry University, Fuzhou, China.

Key Laboratory of Ministry of Education for Genetics, Breeding and Multiple Utilization of Crops, College of Agriculture, Fujian Agriculture and Forestry University, Fuzhou, China.

出版信息

Front Plant Sci. 2022 Jun 14;13:921674. doi: 10.3389/fpls.2022.921674. eCollection 2022.

Abstract

Sugarcane yellow leaf disease severely affects sugarcane production. As a viral disease, the pathogen sugarcane yellow leaf virus can only be transmitted by aphid vectors rather than mechanical means. To understand the sugarcane responses to ScYLV infection, the corresponding transcriptomic profile of ScYLV-infected and ScYLV-free plants were analyzed with RNA-Seq technology. In this study, was used as the vector to transmit ScYLV to the susceptible sugarcane cultivar CP72-1210 and transcriptome was sequenced as well as differentially expressed genes between disease-infected and non-infected sugarcane plants were investigated. A total of 1,22,593 genes were assembled, of which 1,630 genes were differentially expressed. Among DEGs, 1,622 were upregulated and eight were downregulated that were further annotated with GO, KEGG, KOG, PFAM, SwissProt, and Nr databases. The expression levels of DEGs in the three KEGG pathways, namely endocytosis, PEX protein synthesis, and endoplasmic reticulum stress response to viral protein synthesis were observed. Interestingly, it was found that the yellow leaf virus could induce the formation of autophagosomes by LC3, promoted by ER stress, and may be related to the replication of viral RNA. We tested 63 DEGs in this research. The qRT-PCR results showed that two were downregulated and 45 were upregulated in response to the ScYLV infection. This study will not only offer an overall comprehension of sugarcane responses to ScYLV infection at the gene expression level but also increase the chances to block the transmission of ScYLV for use in further molecular biology techniques and will aid in increasing the resistance of plants against ScYLV.

摘要

甘蔗黄叶病严重影响甘蔗生产。作为一种病毒性疾病,病原体甘蔗黄叶病毒只能通过蚜虫媒介传播,而非机械传播方式。为了解甘蔗对甘蔗黄叶病毒(ScYLV)感染的反应,利用RNA测序技术分析了感染ScYLV和未感染ScYLV的植物的相应转录组图谱。在本研究中,以[具体内容缺失]为媒介将ScYLV传播至易感甘蔗品种CP72 - 1210,并对转录组进行测序,同时研究了病害感染和未感染甘蔗植株之间的差异表达基因。共组装了122593个基因,其中1630个基因差异表达。在差异表达基因中,1622个上调,8个下调,这些基因进一步用GO、KEGG、KOG、PFAM、SwissProt和Nr数据库进行注释。观察了差异表达基因在三个KEGG途径中的表达水平,即内吞作用、PEX蛋白合成以及内质网对病毒蛋白合成的应激反应。有趣的是,发现黄叶病毒可通过LC3诱导自噬体形成,内质网应激起促进作用,且可能与病毒RNA复制有关。本研究中测试了63个差异表达基因。qRT - PCR结果显示,响应ScYLV感染,2个下调,45个上调。本研究不仅将在基因表达水平上全面理解甘蔗对ScYLV感染的反应,还将增加在进一步分子生物学技术中阻断ScYLV传播的机会,并有助于提高植物对ScYLV的抗性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70b6/9237618/9e11a83b1354/fpls-13-921674-g001.jpg

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