2019
DOI: 10.1002/ps.5293
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Differential expression of genes in greenbug (Schizaphis graminum Rondani) treated by imidacloprid and RNA interference

Abstract: BACKGROUND Insecticides act as toxins, inhibitors of digestion and deterrents, and affect the expression of many genes in insects. To assess key genes associated with the detoxification or regulation of imidacloprid in greenbug, Schizaphis graminum (Rondani), the transcriptome and digital gene expression (DGE) profile were analyzed using Illumina sequencing. RESULTS In total, 48 763 494 clean reads were obtained by sequencing. Expression profile analysis showed that 2782 unigenes were differently expressed bet… Show more

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Cited by 24 publications
(17 citation statements)
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“…Wheat ( Triticum aestivum L.) is an important food crop grown worldwide and used as a staple food in many countries 1 . The wheat aphid ( Schizaphis graminum Rondani) (Hemiptera: Aphididae) is a destructive insect pest of many cereal crops and causes severe damage by phloem sap ingestion and virus transmission 2–5 . However, efforts to control this pest by spraying crops with high doses of multiple pesticides pose serious risks to the environment and have resulted in pesticide resistance 6–8 .…”
Section: Introductionmentioning
confidence: 99%
“…Wheat ( Triticum aestivum L.) is an important food crop grown worldwide and used as a staple food in many countries 1 . The wheat aphid ( Schizaphis graminum Rondani) (Hemiptera: Aphididae) is a destructive insect pest of many cereal crops and causes severe damage by phloem sap ingestion and virus transmission 2–5 . However, efforts to control this pest by spraying crops with high doses of multiple pesticides pose serious risks to the environment and have resulted in pesticide resistance 6–8 .…”
Section: Introductionmentioning
confidence: 99%
“…At last, PCR products were purified (AMPure XP system) and library products were then ready for sequencing analysis via Illumina HiseqTM 4000 (Beijing Novogene, Beijing, China) using paired‐end technology in a single run (Zhang et al . ).…”
Section: Methodsmentioning
confidence: 97%
“…Then PCR was performed with Phusion High-Fidelity DNA polymerase, Universal PCR primers and Index (X) Primer. At last, PCR products were purified (AMPure XP system) and library products were then ready for sequencing analysis via Illumina HiseqTM 4000 (Beijing Novogene, Beijing, China) using paired-end technology in a single run (Zhang et al 2019).…”
Section: Insect Culture and Collectionmentioning
confidence: 99%
“…Total RNA, first strand cDNA synthesized, SYBR Green Master Mix (miScript SYBR Green PCR Kit, Qiagen) and qPCR procedure determined was described as previously. 33 Relative expression quantification was calculated by the 2 −∆∆Ct method. 34 U6 snRNA was used to normalize expression quantiy of miRNAs as an endogenous control.…”
Section: Quantitative Real-time Pcr (Qpcr) Validationmentioning
confidence: 99%