U.S. Department of Agriculture, Agricultural Research Service, U.S. Vegetable laboratory, Charleston, SC, United States of America.
Boyce Thompson Institute, Cornell University, Ithaca, New York, United States of America.
PLoS One. 2019 Mar 12;14(3):e0213149. doi: 10.1371/journal.pone.0213149. eCollection 2019.
The whitefly Bemisia tabaci MEAM1 is a notorious vector capable of transmitting many plant viruses, resulting in serious crop loss and food shortage around the world. To investigate potential sRNA-mediated regulatory mechanisms in whiteflies that are affected by virus acquisition and transmission, we conducted small RNA (sRNA) deep sequencing and performed genome-wide profiling of piwi-interacting RNAs (piRNAs) in whiteflies that were fed on tomato yellow leaf curl virus (TYLCV)-infected or non-infected tomato plants for 24, 48, and 72 h. In the present study, piRNA reads ranging from 564,395 to 1,715,652 per library were identified and shown to distribute unevenly in clusters (57 to 96 per library) on the whitefly (B. tabaci MEAM1) genome. Among them, 53 piRNA clusters were common for all treatments. Comparative analysis between libraries generated from viruliferous and non-viruliferous whiteflies identified five TYLCV-induced and 24 TYLCV-suppressed piRNA clusters. Approximately 62% of piRNAs were derived from non-coding sequences including intergenic regions, introns, and untranslated regions (UTRs). The remaining 38% were derived from coding sequences (CDS) or repeat elements. Interestingly, six protein coding genes were targeted by the TYLCV-induced piRNAs. We identified a large number of piRNAs that were distributed in clusters across the whitefly genome, with 60% being derived from non-coding regions. Comparative analysis revealed that feeding on a virus-infected host caused induction and suppression of only a small number of piRNA clusters in whiteflies. Although piRNAs primarily regulate the activity of transposable elements, our results suggest that they may have additional functions in regulating protein coding genes and in insect-virus interactions.
烟粉虱(Bemisia tabaci MEAM1)是一种臭名昭著的载体,能够传播许多植物病毒,导致全球作物损失和粮食短缺。为了研究受病毒获取和传播影响的烟粉虱中潜在的小 RNA(sRNA)介导的调控机制,我们对吸食感染和未感染番茄黄曲叶病毒(TYLCV)的番茄植株 24、48 和 72 小时的烟粉虱进行了小 RNA(sRNA)深度测序和全基因组 piwi 相互作用 RNA(piRNA)谱分析。在本研究中,每个文库中鉴定到的 piRNA 读数范围为 564395 到 1715652 条,并显示不均匀地分布在白(B. tabaci MEAM1)基因组上的聚类中(每个文库 57 到 96 个)。其中,53 个 piRNA 聚类在所有处理中都是常见的。从带毒和不带毒的烟粉虱文库之间的比较分析中,鉴定出 5 个 TYLCV 诱导和 24 个 TYLCV 抑制的 piRNA 聚类。大约 62%的 piRNAs 来自非编码序列,包括基因间区、内含子和非翻译区(UTR)。其余 38%来自编码序列(CDS)或重复元件。有趣的是,6 个蛋白编码基因被 TYLCV 诱导的 piRNAs 靶向。我们鉴定出大量分布在白(B. tabaci MEAM1)基因组聚类中的 piRNAs,其中 60%来自非编码区。比较分析表明,吸食病毒感染的宿主仅引起烟粉虱中少数 piRNA 聚类的诱导和抑制。虽然 piRNAs 主要调节转座元件的活性,但我们的结果表明它们可能在调节蛋白编码基因和昆虫-病毒相互作用方面具有额外的功能。