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一种用于鉴定、和的分子信标实时聚合酶链反应分析方法。

A molecular beacon real-time polymerase chain reaction assay for the identification of , , and .

作者信息

Anderson Scott D, Gleason Cynthia A

机构信息

Department of Plant Pathology, Washington State University, Pullman, WA, United States.

出版信息

Front Plant Sci. 2023 Feb 22;14:1096239. doi: 10.3389/fpls.2023.1096239. eCollection 2023.

Abstract

Root-knot nematodes ( spp.) are major pests of many important crops around the world. In the Northwestern region of the United States of America (USA), causes economic losses in potatoes because the nematodes can infect the tubers, which leads to potato galling and reductions in marketable yield. is a quarantine pathogen in certain potato export markets, and there is little industry tolerance for the presence of this nematode. Recently, two species that are not known to be present in agricultural fields in the USA were detected on golf turfgrasses in California and Washington. These species, and , are morphologically similar to and can infect potatoes and cause tuber damage. Their detection in the USA means that they could potentially infest potato fields and become a problem in potato production. Additionally, is a regulated plant pest in the USA, which makes the correct identification of potato-infecting root-knot nematodes important. Previously, there was no single-tube assay that could determine whether , , and/or were present in a sample. Thus, a molecular beacon real-time PCR assay which can reliably detect , , or from crude nematode extracts was designed and characterized.

摘要

根结线虫(Meloidogyne spp.)是全球许多重要农作物的主要害虫。在美国西北部地区,Meloidogyne chitwoodi会给马铃薯造成经济损失,因为这种线虫会感染块茎,导致马铃薯形成虫瘿并使可销售产量降低。Meloidogyne chitwoodi在某些马铃薯出口市场属于检疫性病原菌,该行业对这种线虫的存在几乎没有容忍度。最近,在美国加利福尼亚州和华盛顿州的高尔夫草坪草上检测到两种在美国农田中尚未发现的Meloidogyne属物种。这两个物种,Meloidogyne fallax和Meloidogyne enterolobii,在形态上与Meloidogyne chitwoodi相似,并且能够感染马铃薯并造成块茎损伤。它们在美国被检测到意味着它们有可能侵染马铃薯田并成为马铃薯生产中的一个问题。此外,Meloidogyne chitwoodi在美国是一种受管制的植物害虫,这使得正确鉴定侵染马铃薯的根结线虫变得很重要。以前,没有一种单管检测方法能够确定样品中是否存在Meloidogyne chitwoodi、Meloidogyne fallax和/或Meloidogyne enterolobii。因此,设计并鉴定了一种能够从粗制线虫提取物中可靠地检测Meloidogyne chitwoodi、Meloidogyne fallax或Meloidogyne enterolobii的分子信标实时PCR检测方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3e2/9994647/618d2bc39fb8/fpls-14-1096239-g001.jpg

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