Centre for Horticultural Science, Queensland Alliance for Agriculture and Food Innovation, The University of Queensland, Brisbane, QLD 4072, Australia.
Research Center for Biotechnology, Universitas Gadjah Mada, Yogyakarta 55281, Indonesia.
Plant Dis. 2022 Mar;106(3):947-959. doi: 10.1094/PDIS-07-21-1436-RE. Epub 2022 Mar 10.
Blood disease in bananas caused by subsp. is a bacterial wilt disease that causes major yield losses of banana in Indonesia and peninsular Malaysia. The disease has significantly increased its geographic distribution in the past decade. Diagnostic methods are an important component of disease management in vegetatively propagated crops such as banana to constrain incursions of plant pathogens. Therefore, the objectives of this study were (i) to design and rigorously validate a novel banana Blood disease (BBD) real-time PCR assay with a high level of specificity and sensitivity of detection and (ii) to validate published PCR-based diagnostic methods targeting the intergenic region in the megaplasmid ("121 assay" with primer set 121) or the phage tail protein-coding sequence in the bacterial chromosome ("Kubota assay" and "BDB2400 assay" with primer set BDB2400). Assay validation included 339 samples (174 Blood disease bacteria, 51 bacteria associated with banana plants, 51 members of the species complex, and 63 samples from symptomatic and healthy plant material). Validation parameters were analytical specificity (inclusivity and exclusivity), selectivity, limit of detection, accuracy, and ruggedness. The 121 assay and our newly developed BBD real-time PCR assay detected all subsp. strains with no cross-specificity during validation. Two different PCR assays using the primer set BDB2400 lacked specificity and selectivity. This study reveals that our novel BBD real-time PCR assay and the conventional PCR 121 assay are reliable methods for Blood disease diagnostics, as they comply with all tested validation parameters.
香蕉细菌性枯萎病由 subsp. 引起,是一种细菌性枯萎病,会导致印度尼西亚和马来半岛的香蕉产量大幅下降。在过去十年中,这种疾病的地理分布显著扩大。诊断方法是香蕉等营养繁殖作物病害管理的重要组成部分,可限制植物病原体的入侵。因此,本研究的目的是:(i) 设计并严格验证一种新型香蕉细菌性枯萎病(BBD)实时 PCR 检测方法,该方法具有高特异性和灵敏度;(ii) 验证针对巨质粒中基因间区的已发表的基于 PCR 的诊断方法(引物对 121 的“121 检测法”)或细菌染色体中噬菌体尾部蛋白编码序列(引物对 BDB2400 的“Kubota 检测法”和“BDB2400 检测法”)。检测方法验证包括 339 个样本(174 株 Blood 病细菌、51 株与香蕉植物相关的细菌、51 株 种复合体成员和 63 株来自有症状和健康植物材料的样本)。验证参数包括分析特异性(包容性和排他性)、选择性、检测限、准确性和稳健性。121 检测法和我们新开发的 BBD 实时 PCR 检测法在验证过程中均未检测到与 subsp. 菌株的交叉特异性。使用引物对 BDB2400 的两种不同 PCR 检测法缺乏特异性和选择性。本研究表明,我们新的 BBD 实时 PCR 检测法和常规的 121 检测法是 Blood 病诊断的可靠方法,因为它们符合所有测试的验证参数。