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通过高通量测序在金诺橘中鉴定出两种柑橘病毒的混合感染,并利用双重RT-PCR技术开发了它们的特异性检测方法。

Mixed infection of two mandariviruses identified by high-throughput sequencing in Kinnow mandarin and development of their specific detection using duplex RT-PCR.

作者信息

Kumar Rakesh, Gupta Nitika, Sharma Susheel Kumar, Kishan Gopi, Srivastava Nishant, Khan Zainul A, Kumar Ashwini, Baranwal Virendra Kumar

机构信息

Advanced Centre for Plant Virology, Division of Plant Pathology, ICAR-Indian Agricultural Research Institute, New Delhi, 110012 India.

ICAR-Indian Institute of Seed Science, Uttar Pradesh, Kushmaur, Mau, 275101 India.

出版信息

3 Biotech. 2024 Jun;14(6):170. doi: 10.1007/s13205-024-04011-9. Epub 2024 May 31.

Abstract

UNLABELLED

In the current study, high-throughput sequencing (HTS) was used to identify viruses associated with the Kinnow mandarin () plants exhibiting yellow vein clearing, mottling, and chlorosis symptoms at experimental farm of ICAR-Indian Agricultural Research Institute, New Delhi, India. During November 2022, leaf samples of symptomatic and asymptomatic Kinnow mandarin trees were collected, subjected to HTS and one of the representative symptomatic samples was subjected to leaf-dip electron microscopy (EM). In the EM results, flexuous virus particles typical of mandarivirus were observed. Ribosomal RNA was depleted from total RNA of pooled samples and RNA sequencing was done using NovaSeq 6000. Host unaligned reads were de novo assembled into contigs, which were annotated through BLASTn using database of plant viruses/viroids reference genomes (NCBI). Results of assembled contigs revealed near-complete genomes of two mandariviruses, , citrus yellow vein clearing virus (CYVCV) and citrus yellow mottle-associated virus (CiYMaV). The values of fragments per kilo base transcript length per million fragments mapped estimation indicated the dominance of CYVCV in HTS data and it was also confirmed through krona plot distribution of viruses in the pooled samples. A rapid and reliable duplex RT-PCR assay was also developed and standardized for the simultaneous detection of both CYVCV and CiYMaV in a pooled Kinnow mandarin sample. The developed duplex RT-PCR was then validated for the presence of these viruses in individual Kinnow mandarin samples. The specificity and sensitivity results confirmed that primers were highly specific to their targets and able to detect viruses up to 10 dilutions of RNA in standard and duplex RT-PCR. Therefore, the developed rapid duplex RT-PCR can be used for virus indexing and production of virus-free Kinnow mandarin plants for certification programs.

SUPPLEMENTARY INFORMATION

The online version contains supplementary material available at 10.1007/s13205-024-04011-9.

摘要

未标注

在当前研究中,高通量测序(HTS)被用于识别印度新德里ICAR-印度农业研究所在实验农场中表现出黄脉清、斑驳和黄化症状的金诺橘()植株相关的病毒。2022年11月,采集了有症状和无症状金诺橘树的叶片样本,进行高通量测序,并对其中一个有代表性的有症状样本进行叶浸电镜检查(EM)。在电镜检查结果中,观察到了典型的柑橘病毒属弯曲病毒粒子。从混合样本的总RNA中去除核糖体RNA,并使用NovaSeq 6000进行RNA测序。宿主未比对的 reads 被从头组装成重叠群,通过使用植物病毒/类病毒参考基因组数据库(NCBI)的BLASTn进行注释。组装重叠群的结果揭示了两种柑橘病毒属病毒的近乎完整基因组,即柑橘黄脉清病毒(CYVCV)和柑橘黄斑驳相关病毒(CiYMaV)。每百万映射片段中每千碱基转录本长度的片段值估计表明CYVCV在高通量测序数据中占主导地位,这也通过混合样本中病毒的科罗纳图分布得到了证实。还开发并标准化了一种快速可靠的双重RT-PCR检测方法,用于同时检测混合金诺橘样本中的CYVCV和CiYMaV。然后对开发的双重RT-PCR在单个金诺橘样本中这些病毒的存在情况进行了验证。特异性和灵敏度结果证实,引物对其靶标具有高度特异性,并且能够在标准和双重RT-PCR中检测到高达10倍稀释的RNA中的病毒。因此,开发的快速双重RT-PCR可用于病毒检测以及为认证计划生产无病毒的金诺橘植株。

补充信息

在线版本包含可在10.1007/s13205-024-04011-9获取的补充材料。

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