Singh Satnam, Gupta Mridula, Pandher Suneet, Kaur Gurmeet, Rathore Pankaj, Palli Subba Reddy
Punjab Agricultural University, Regional Station, Faridkot, Punjab, India.
Department of Entomology, University of Kentucky, Lexington, KY, United States of America.
PLoS One. 2018 Jan 12;13(1):e0191116. doi: 10.1371/journal.pone.0191116. eCollection 2018.
Amrasca biguttula biguttula (Ishida) commonly known as cotton leafhopper is a severe pest of cotton and okra. Not much is known on this insect at molecular level due to lack of genomic and transcriptomic data. To prepare for functional genomic studies in this insect, we evaluated 15 common housekeeping genes (Tub, B-Tub, EF alpha, GADPH, UbiCF, RP13, Ubiq, G3PD, VATPase, Actin, 18s, 28s, TATA, ETF, SOD and Cytolytic actin) during different developmental stages and under starvation stress. We selected early (1st and 2nd), late (3rd and 4th) stage nymphs and adults for identification of stable housekeeping genes using geNorm, NormFinder, BestKeeper and RefFinder software. Based on the different algorithms, RP13 and VATPase are identified as the most suitable reference genes for quantification of gene expression by reverse transcriptase quantitative PCR (RT-qPCR). Based on RefFinder which comprehended the results of three algorithms, RP13 in adults, Tubulin (Tub) in late nymphs, 28S in early nymph and UbiCF under starvation stress were identified as the most stable genes. We also developed methods for feeding double-stranded RNA (dsRNA) incorporated in the diet. Feeding dsRNA targeting Snf7, IAP, AQP1, and VATPase caused 56.17-77.12% knockdown of targeted genes compared to control and 16 to 48% mortality of treated insects when compared to control.
棉叶蝉(Amrasca biguttula biguttula (Ishida))通常被称为棉叶蝉,是棉花和秋葵的一种严重害虫。由于缺乏基因组和转录组数据,在分子水平上对这种昆虫的了解并不多。为了准备对这种昆虫进行功能基因组学研究,我们评估了15个常见的管家基因(Tub、B-Tub、EF alpha、GADPH、UbiCF、RP13、Ubiq、G3PD、VATPase、Actin、18s、28s、TATA、ETF、SOD和溶细胞肌动蛋白)在不同发育阶段和饥饿胁迫下的情况。我们选择了若虫早期(第1和第2龄)、晚期(第3和第4龄)以及成虫,使用geNorm、NormFinder、BestKeeper和RefFinder软件来鉴定稳定的管家基因。基于不同的算法,RP13和VATPase被确定为通过逆转录定量PCR(RT-qPCR)定量基因表达最合适的参考基因。基于综合了三种算法结果的RefFinder,成虫中的RP13、晚期若虫中的微管蛋白(Tub)、早期若虫中的28S以及饥饿胁迫下的UbiCF被确定为最稳定的基因。我们还开发了在食物中添加双链RNA(dsRNA)的喂食方法。与对照相比,喂食靶向Snf7、IAP、AQP1和VATPase的dsRNA导致靶基因敲低56.17 - 77.12%,与对照相比,处理后的昆虫死亡率为16%至48%。