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测序草莓种质资源揭示了新的病毒遗传多样性和新的 RT-qPCR 检测方法的基础。

Sequencing a Strawberry Germplasm Collection Reveals New Viral Genetic Diversity and the Basis for New RT-qPCR Assays.

机构信息

Department of Plant Pathology, University of California-Davis, Davis, CA 95616, USA.

School of Engineering and Sciences, Tecnologico de Monterrey, Campus Queretaro, Queretaro 76130, Mexico.

出版信息

Viruses. 2021 Jul 24;13(8):1442. doi: 10.3390/v13081442.

Abstract

Viruses are considered of major importance in strawberry ( × Duchesne) production given their negative impact on plant vigor and growth. Strawberry accessions from the National Clonal Germplasm Repository were screened for viruses using high throughput sequencing (HTS). Analyses of sequence information from 45 plants identified multiple variants of 14 known viruses, comprising strawberry mottle virus (SMoV), beet pseudo yellows virus (BPYV), strawberry pallidosis-associated virus (SPaV), tomato ringspot virus (ToRSV), strawberry mild yellow edge virus (SMYEV), strawberry vein banding virus (SVBV), strawberry crinkle virus (SCV), strawberry polerovirus 1 (SPV-1), apple mosaic virus (ApMV), strawberry chlorotic fleck virus (SCFaV), strawberry crinivirus 4 (SCrV-4), strawberry crinivirus 3 (SCrV-3), Fragaria chiloensis latent virus (FClLV) and Fragaria chiloensis cryptic virus (FCCV). Genetic diversity of sequenced virus isolates was investigated via sequence homology analysis, and partial-genome sequences were deposited into GenBank. To confirm the HTS results and expand the detection of strawberry viruses, new reverse transcription quantitative PCR (RT-qPCR) assays were designed for the above-listed viruses. Further in silico and in vitro validation of the new diagnostic assays indicated high efficiency and reliability. Thus, the occurrence of different viruses, including divergent variants, among the strawberries was verified. This is the first viral metagenomic survey in strawberry, additionally, this study describes the design and validation of multiple RT-qPCR assays for strawberry viruses, which represent important detection tools for clean plant programs.

摘要

鉴于病毒对植物活力和生长的负面影响,它们在草莓( × Duchesne)生产中被认为具有重要意义。国家无性系种质资源库的草莓品种通过高通量测序(HTS)筛选病毒。对 45 株植物的序列信息进行分析,鉴定出 14 种已知病毒的多个变体,包括草莓斑驳病毒(SMoV)、甜菜伪黄化病毒(BPYV)、草莓苍白症相关病毒(SPaV)、番茄环斑病毒(ToRSV)、草莓轻度黄边病毒(SMYEV)、草莓脉带病毒(SVBV)、草莓皱缩病毒(SCV)、草莓潜隐病毒 1(SPV-1)、苹果花叶病毒(ApMV)、草莓黄化斑点病毒(SCFaV)、草莓卷叶病毒 4(SCrV-4)、草莓卷叶病毒 3(SCrV-3)、智利草莓潜隐病毒(FClLV)和智利草莓隐潜病毒(FCCV)。通过序列同源性分析研究了测序病毒分离物的遗传多样性,并将部分基因组序列存入 GenBank。为了确认 HTS 结果并扩大草莓病毒的检测范围,针对上述病毒设计了新的反转录定量 PCR(RT-qPCR)检测方法。新诊断检测方法的计算机模拟和体外验证表明其具有高效性和可靠性。因此,验证了不同病毒(包括不同变体)在草莓中的存在。这是对草莓进行的第一次病毒宏基因组调查,此外,本研究还描述了用于草莓病毒的多种 RT-qPCR 检测方法的设计和验证,这些方法是清洁植物计划的重要检测工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abdd/8402890/3de2f93bd9e9/viruses-13-01442-g001.jpg

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