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利用 INABS 对发育腋芽且能通过扦插存活的作物进行 VIGS 和体外接种植物病毒的快速、简单且高效的方法。

A rapid, simple, and highly efficient method for VIGS and in vitro-inoculation of plant virus by INABS applied to crops that develop axillary buds and can survive from cuttings.

机构信息

College of Plant Protection, Henan Agricultural University, Zhengzhou, 450002, China.

Postdoctoral Research Base, Henan Institute of Science and Technology, Xinxiang, 453001, China.

出版信息

BMC Plant Biol. 2021 Nov 20;21(1):545. doi: 10.1186/s12870-021-03331-9.

Abstract

BACKGROUND

Virus-induced gene silencing (VIGS) is one of the most convenient and powerful methods of reverse genetics. In vitro-inoculation of plant virus is an important method for studying the interactions between viruses and plants. Agrobacterium-based infiltration has been widely adopted as a tool for VIGS and in vitro-inoculation of plant virus. Most agrobacterium-based infiltration methods applied to VIGS and virus inoculation have the characteristics of low transformation efficiencies, long plant growth time, large amounts of plant tissue, large test spaces, and complex preparation procedures. Therefore, a rapid, simple, economical, and highly efficient VIGS and virus inoculation method is in need. Previous studies have shown that the selection of suitable plant tissues and inoculation sites is the key to successful infection.

RESULTS

In this study, Tobacco rattle virus (TRV) mediated VIGS and Tomato yellow leaf curl virus (TYLCV) for virus inoculation were developed in tomato plants based on the agrobacterium tumefaciens-based infiltration by injection of the no-apical-bud stem section (INABS). The no-apical-bud stem section had a "Y- type" asymmetric structure and contained an axillary bud that was about 1-3 cm in length. This protocol provides high transformation (56.7%) and inoculation efficiency (68.3%), which generates VIGS transformants or diseased plants in a very short period (8 dpi). Moreover, it greatly reduces the required experimental space. This method will facilitate functional genomic studies and large-scale disease resistance screening.

CONCLUSIONS

Overall, a rapid, simple, and highly efficient method for VIGS and virus inoculation by INABS was developed in tomato. It was reasonable to believe that it can be used as a reference for the other virus inoculation methods and for the application of VIGS to other crops (such as sweet potato, potato, cassava and tobacco) that develop axillary buds and can survive from cuttings.

摘要

背景

病毒诱导的基因沉默(VIGS)是反向遗传学中最方便、最强大的方法之一。体外接种植物病毒是研究病毒与植物相互作用的重要方法。基于农杆菌的渗透已广泛应用于 VIGS 和植物病毒的体外接种。大多数基于农杆菌的渗透方法应用于 VIGS 和病毒接种,具有转化效率低、植物生长时间长、植物组织量大、试验空间大、准备程序复杂等特点。因此,需要一种快速、简单、经济、高效的 VIGS 和病毒接种方法。以前的研究表明,选择合适的植物组织和接种部位是成功感染的关键。

结果

在这项研究中,基于农杆菌介导的渗透,通过注射无顶芽茎段(INABS),在番茄植株中开发了烟草脆裂病毒(TRV)介导的 VIGS 和番茄黄曲叶病毒(TYLCV)用于病毒接种。无顶芽茎段具有“Y 型”不对称结构,包含一个约 1-3cm 长的腋芽。该方案提供了高转化(56.7%)和接种效率(68.3%),可在很短的时间(8dpi)内产生 VIGS 转化体或患病植株。此外,它大大减少了所需的实验空间。这种方法将有助于功能基因组学研究和大规模抗病性筛选。

结论

总体而言,通过 INABS 在番茄中建立了一种快速、简单、高效的 VIGS 和病毒接种方法。可以合理地认为,它可以作为其他病毒接种方法的参考,也可以作为 VIGS 应用于其他作物(如甘薯、马铃薯、木薯和烟草)的参考,这些作物会发育腋芽并可以通过扦插存活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecdb/8605592/00dcd5885bd0/12870_2021_3331_Fig1_HTML.jpg

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