Yasuhara-Bell Jarred, Rivera Yazmín
Plant Pathogen Confirmatory Diagnostics Laboratory (PPCDL), Science and Technology (S&T), Plant Protection and Quarantine (PPQ), Animal and Plant Health Inspection Service (APHIS), United States Department of Agriculture (USDA), Laurel, MD 20708, USA.
Microorganisms. 2025 Apr 17;13(4):929. doi: 10.3390/microorganisms13040929.
' Phytoplasma prunorum' has been associated with severe disease in spp., which are commodities of economic importance in the USA. The introduction and establishment of ' P. prunorum' in the USA could result in huge economic losses, thus creating a need for validated diagnostic tools, which are the cornerstone of successful surveillance, quarantine, and eradication measures. Whole-genome comparisons led to the identification of a diagnostic marker gene specific to ' P. prunorum' (PE639). The PE639 assay was duplexed with an 18S rDNA plant internal control and compared to modified 23S (phytoplasmas) and (' P. mali') assays. The PE639 assay produced congruent results to 23S and assays for all metrics, demonstrating high linearity, repeatability, intermediate precision, and reproducibility. The limit of detection was comparable for all assays tested, and all demonstrated 100% analytical specificity, selectivity, and diagnostic specificity for their respective target species. Assays metrics were consistent across two platforms, the ABI QuantStudio™ 5 and Bio-Rad CFX96™ OPUS. A synthetic gBlocks™ control was designed and validated to work with all assays, as well as conventional PCR assays targeting 16S rDNA and genes. These validated assays and synthetic control represent beneficial tools that support efforts to protect USA agriculture and facilitate safe trade.
“李属植原体”与多种李属植物的严重病害有关,这些植物在美国是具有重要经济价值的商品。“李属植原体”在美国的引入和定殖可能导致巨大的经济损失,因此需要经过验证的诊断工具,这是成功开展监测、检疫和根除措施的基石。全基因组比较导致鉴定出一种“李属植原体”特有的诊断标记基因(PE639)。PE639检测法与18S rDNA植物内对照进行了双重检测,并与改良的23S(植原体)检测法和“苹果植原体”检测法进行了比较。PE639检测法在所有指标上与23S检测法和“苹果植原体”检测法的结果一致,显示出高线性、可重复性、中间精密度和再现性。所有测试检测法的检测限相当,并且所有检测法对各自的目标物种均显示出100%的分析特异性、选择性和诊断特异性。检测指标在两个平台(ABI QuantStudio™ 5和Bio-Rad CFX96™ OPUS)上是一致的。设计并验证了一种合成gBlocks™对照,使其可用于所有检测法以及针对16S rDNA和相关基因的常规PCR检测法。这些经过验证的检测法和合成对照是有益的工具,有助于保护美国农业并促进安全贸易。