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用于检测和鉴定引起香蕉巴拿马病的所有序列的 PCR 诊断检测方法的验证。

Validation of PCR Diagnostic Assays for Detection and Identification of All Sequevars Causing Moko Disease in Banana.

机构信息

Centre for Horticultural Science, Queensland Alliance for Agriculture and Food Innovation, The University of Queensland, Brisbane, Australia.

Centre for Agricultural Sciences, Federal University of Alagoas, Maceió, Brazil.

出版信息

Phytopathology. 2024 Nov;114(11):2375-2384. doi: 10.1094/PHYTO-06-24-0190-R. Epub 2024 Nov 23.

DOI:10.1094/PHYTO-06-24-0190-R
PMID:39145736
Abstract

Moko disease in banana is a bacterial wilt caused by strains within sensu stricto. The disease is endemic to Central and South America but has spread to the Philippines and peninsular Malaysia. Detecting new incursions early in Moko-free banana production regions is of utmost importance for containment and eradication, as Moko management significantly increases costs in banana production. Molecular studies have supported the classification of sensu stricto into phylotypes IIA, IIB, and IIC, each comprising various sequevars based on nucleotide divergence of a partial sequence within the endoglucanase gene. Moko disease in banana is caused by strains classified as sequevars 6, 24, 41, and 53 within phylotype IIA and sequevars 3, 4, and 25 within phylotype IIB. To ensure accurate diagnostic assays are available to detect all Moko sequevars, we systematically validated previously published assays for Moko diagnostics. To be able to identify all sequevars, including the latest described sequevars, namely IIB-25, IIA-41, and IIA-53, we developed and validated two novel assays using genome-wide association studies on over 100 genomes of sensu stricto. Validations using 196 bacterial isolates confirmed that a previous multiplex PCR-based assay targeting sequevars IIB-3, IIB-4, IIA-6, and IIA-24 and our two novel assays targeting sequevars IIB-25, IIA-41, and IIA-53 were specific, reproducible, and accurate for Moko diagnostics.

摘要

香蕉巴拿马病是一种细菌性萎蔫病,由严格意义上的 菌株引起。该疾病流行于中美洲和南美洲,但已传播到菲律宾和马来半岛。在无巴拿马病的香蕉生产地区,早期发现新的疫情对控制和根除至关重要,因为巴拿马病管理会显著增加香蕉生产的成本。分子研究支持将严格意义上的 分为 phylotypes IIA、IIB 和 IIC,每个 phylotype 又由基于内切葡聚糖酶基因部分序列核苷酸差异的各种 sequevars 组成。香蕉巴拿马病是由归类为 phylotype IIA 的 sequevars 6、24、41 和 53 和 phylotype IIB 的 sequevars 3、4 和 25 的菌株引起的。为确保有准确的诊断检测方法可用于检测所有巴拿马病 sequevars,我们系统地验证了先前发表的用于巴拿马病诊断的检测方法。为了能够识别所有的 sequevars,包括最新描述的 sequevars IIB-25、IIA-41 和 IIA-53,我们使用超过 100 个严格意义上的 基因组的全基因组关联研究开发并验证了两种新的检测方法。使用 196 个细菌分离株进行验证证实,先前针对 sequevars IIB-3、IIB-4、IIA-6 和 IIA-24 的基于多重 PCR 的检测方法和我们针对 sequevars IIB-25、IIA-41 和 IIA-53 的两种新检测方法具有特异性、可重复性和准确性,可用于巴拿马病诊断。

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