4.7 Article

Identifying potential RNAi targets in grain aphid (Sitobion avenae F.) based on transcriptome profiling of its alimentary canal after feeding on wheat plants

期刊

BMC GENOMICS
卷 14, 期 -, 页码 -

出版社

BMC
DOI: 10.1186/1471-2164-14-560

关键词

Grain aphid (Sitobion avenae F.); Alimentary canal; Transcriptome profile; Double strand RNA (dsRNA); Artificial feeding assay; RNA interference (RNAi); Aphid control

资金

  1. Research Initiative on Development of Disease and Insect Resistance Transgenic Wheat Plants from the Ministry of Agriculture of China [2013ZX08002-001, 2014ZX0800201B]
  2. Natural Science Foundation of China [31171618, 31371702]
  3. Chinese State Key Laboratory for Biology of Plant Diseases and Insects [SKLOF201307]
  4. Biotechnology and Biological Sciences Research Council (BBSRC) of the UK
  5. Biotechnology and Biological Sciences Research Council [BBS/E/C/00004975, BBS/E/C/00005202] Funding Source: researchfish
  6. BBSRC [BBS/E/C/00005202, BBS/E/C/00004975] Funding Source: UKRI

向作者/读者索取更多资源

Background: The grain aphid (Sitobion avenae F.) is a major agricultural pest which causes significant yield losses of wheat in China, Europe and North America annually. Transcriptome profiling of the grain aphid alimentary canal after feeding on wheat plants could provide comprehensive gene expression information involved in feeding, ingestion and digestion. Furthermore, selection of aphid-specific RNAi target genes would be essential for utilizing a plant-mediated RNAi strategy to control aphids via a non-toxic mode of action. However, due to the tiny size of the alimentary canal and lack of genomic information on grain aphid as a whole, selection of the RNAi targets is a challenging task that as far as we are aware, has never been documented previously. Results: In this study, we performed de novo transcriptome assembly and gene expression analyses of the alimentary canals of grain aphids before and after feeding on wheat plants using Illumina RNA sequencing. The transcriptome profiling generated 30,427 unigenes with an average length of 664 bp. Furthermore, comparison of the transcriptomes of alimentary canals of pre- and post feeding grain aphids indicated that 5490 unigenes were differentially expressed, among which, diverse genes and/or pathways were identified and annotated. Based on the RPKM values of these unigenes, 16 of them that were significantly up or down-regulated upon feeding were selected for dsRNA artificial feeding assay. Of these, 5 unigenes led to higher mortality and developmental stunting in an artificial feeding assay due to the down-regulation of the target gene expression. Finally, by adding fluorescently labelled dsRNA into the artificial diet, the spread of fluorescence signal in the whole body tissues of grain aphid was observed. Conclusions: Comparison of the transcriptome profiles of the alimentary canals of pre- and post-feeding grain aphids on wheat plants provided comprehensive gene expression information that could facilitate our understanding of the molecular mechanisms underlying feeding, ingestion and digestion. Furthermore, five novel and effective potential RNAi target genes were identified in grain aphid for the first time. This finding would provide a fundamental basis for aphid control in wheat through plant mediated RNAi strategy.

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