Chikh-Ali Mohamad, Daniel Jeremy, Usman Aslam Hafiz Muhammad, Agindotan Bright, Charkowski Amy
San Luis Valley Research Center, Colorado State University, Fort Collins, CO 81125, U.S.A.
Department of Agricultural Biology, Colorado State University, Fort Collins, CO 80523, U.S.A.
Plant Dis. 2025 Jun;109(6):1354-1358. doi: 10.1094/PDIS-11-24-2288-RE. Epub 2025 Jun 19.
Potato is an important sector to the U.S. economy, and it created more than $100 billion in economic activity in 2021. The United States exports fresh potatoes to several countries. In certain cases, fresh potato shipments from the United States to the international market requires the crop to be free of potato mop-top virus (PMTV). This increased the need to provide potato growers with an optional, reliable, and large-scale detection method of PMTV, especially in asymptomatic tubers. We developed a duplex immunocapture reverse-transcription quantitative PCR (IC-RT-qPCR) for the large-scale detection of PMTV in dormant tubers. The IC step eliminates the need for RNA extraction kits, making this assay appropriate for large-scale tuber testing. To enhance the reliability of the current assay and reduce the chance of false negatives, a duplex format was used by deploying two primer-probe sets, including a previously reported primer-probe set targeting the RNA-CP and a newly designed primer-probe set targeting a conserved region of RNA-TGB of PMTV genome. We also determined that peels from the stem end of the tubers were more likely to test positive for PMTV than bud end peels or lateral tuber cores. The duplex IC-RT-qPCR will provide a reliable and sensitive tool for the large-scale detection of PMTV in dormant tubers and will help safeguard potato movement in the United States and internationally.
马铃薯对美国经济而言是一个重要领域,2021年其创造了超过1000亿美元的经济活动。美国向多个国家出口新鲜马铃薯。在某些情况下,从美国运往国际市场的新鲜马铃薯需要作物不含马铃薯帚顶病毒(PMTV)。这就更需要为马铃薯种植者提供一种可选、可靠且大规模的PMTV检测方法,尤其是针对无症状块茎。我们开发了一种用于在休眠块茎中大规模检测PMTV的双重免疫捕获逆转录定量PCR(IC-RT-qPCR)方法。免疫捕获步骤无需使用RNA提取试剂盒,使得该检测方法适用于大规模块茎检测。为提高当前检测方法的可靠性并减少假阴性的可能性,采用了双重检测形式,部署了两组引物-探针,包括先前报道的靶向RNA-CP的引物-探针组和新设计的靶向PMTV基因组RNA-TGB保守区域的引物-探针组。我们还确定,块茎茎端的外皮比芽端外皮或块茎侧面中心更有可能检测出PMTV呈阳性。双重IC-RT-qPCR将为在休眠块茎中大规模检测PMTV提供一种可靠且灵敏的工具,并有助于保障美国国内及国际马铃薯的流通。