de Haro Luis A, Dumón Analía D, Mattio María F, Argüello Caro Evangelina Beatriz, Llauger Gabriela, Zavallo Diego, Blanc Hervé, Mongelli Vanesa C, Truol Graciela, Saleh María-Carla, Asurmendi Sebastián, Del Vas Mariana
Instituto de Biotecnología, Instituto Nacional de Tecnología Agropecuaria, HurlinghamBuenos Aires, Argentina.
Consejo Nacional de Investigaciones Científicas y TécnicasBuenos Aires, Argentina.
Front Plant Sci. 2017 May 10;8:766. doi: 10.3389/fpls.2017.00766. eCollection 2017.
Plant reoviruses are able to multiply in gramineae plants and delphacid vectors encountering different defense strategies with unique features. This study aims to comparatively assess alterations of small RNA (sRNA) populations in both hosts upon virus infection. For this purpose, we characterized the sRNA profiles of wheat and planthopper vectors infected by Mal de Río Cuarto virus (MRCV, ) and quantified virus genome segments by quantitative reverse transcription PCR We provide evidence that plant and insect silencing machineries differentially recognize the viral genome, thus giving rise to distinct profiles of virus-derived small interfering RNAs (vsiRNAs). In plants, most of the virus genome segments were targeted preferentially within their upstream sequences and vsiRNAs mapped with higher density to the smaller genome segments than to the medium or larger ones. This tendency, however, was not observed in insects. In both hosts, vsiRNAs were equally derived from sense and antisense RNA strands and the differences in vsiRNAs accumulation did not correlate with mRNAs accumulation. We also established that the piwi-interacting RNA (piRNA) pathway was active in the delphacid vector but, contrary to what is observed in virus-infected mosquitoes, virus-specific piRNAs were not detected. This work contributes to the understanding of the silencing response in insect and plant hosts.
植物呼肠孤病毒能够在禾本科植物和飞虱载体中繁殖,它们会遇到具有独特特征的不同防御策略。本研究旨在比较评估病毒感染后两种宿主中小RNA(sRNA)群体的变化。为此,我们对受里奥斯夸尔托病毒(MRCV)感染的小麦和飞虱载体的sRNA谱进行了表征,并通过定量逆转录PCR对病毒基因组片段进行了定量。我们提供的证据表明,植物和昆虫的沉默机制对病毒基因组的识别存在差异,从而产生了不同的病毒衍生小干扰RNA(vsiRNA)谱。在植物中,大多数病毒基因组片段在其上游序列内被优先靶向,并且vsiRNA在较小的基因组片段上的定位密度高于中等或较大的片段。然而,在昆虫中未观察到这种趋势。在两种宿主中,vsiRNA同样来自正义和反义RNA链,并且vsiRNA积累的差异与mRNA积累无关。我们还确定,piwi相互作用RNA(piRNA)途径在飞虱载体中是活跃的,但与在病毒感染的蚊子中观察到的情况相反,未检测到病毒特异性piRNA。这项工作有助于理解昆虫和植物宿主中的沉默反应。