Department of Plant Pathology, Stellenbosch University, Stellenbosch, Western Cape, South Africa.
PLoS One. 2020 Jul 20;15(7):e0236110. doi: 10.1371/journal.pone.0236110. eCollection 2020.
Banana is an important food crop and source of income in Africa. Sustainable production of banana, however, is at risk because of pests and diseases such as Fusarium wilt, caused by the soil-borne fungus Fusarium oxysporum f. sp. cubense (Foc). Foc can be disseminated from infested to disease-free fields in plant material, water and soil. Early detection of Foc using DNA technologies is thus required to accurately identify the fungus and prevent its further dissemination with plants, soil and water. In this study, quantitative (q)PCR assays were developed for the detection of Foc Lineage VI strains found in central and eastern Africa (Foc races 1 and 2), Foc TR4 (vegetative compatibility groups (VCG) 01213/16) that is present in Mozambique, and Foc STR4 (VCG 0120/15) that occurs in South Africa. A collection of 127 fungal isolates were selected for specificity testing, including endophytic Fusarium isolates from banana pseudostems, non-pathogenic F. oxysporum strains and Foc isolates representing the 24 VCGs in Foc. Primer sets that proved to be specific to Foc Lineage VI, Foc TR4 and Foc STR4 were used to produce standard curves for absolute quantification, and the qPCR assays were evaluated based on the quality of standard curves, repeatability and reproducibility, and limits of quantification (LOQ) and detection (LOD). The qPCR assays for Foc Lineage VI, TR4 and STR4 were repeatable and reproducible, with LOQ values of 10-3-10-4 ng/μL and a LOD of 10-4-10-5 ng/μL. The quantitative detection of Foc strains in Africa could reduce the time and improve the accuracy for identifying the Fusarium wilt pathogen from plants, water and soil on the continent.
香蕉是非洲重要的粮食作物和收入来源。然而,由于病虫害的威胁,香蕉的可持续生产面临风险,其中包括由土壤传播真菌尖孢镰刀菌古巴专化型(Foc)引起的枯萎病。Foc 可以通过植物材料、水和土壤传播到无病的田地。因此,需要使用 DNA 技术尽早检测 Foc,以准确识别该真菌,并防止其与植物、土壤和水一起进一步传播。在这项研究中,开发了用于检测在中非和东非发现的 Foc 谱系 VI 菌株(Foc 株系 1 和 2)、存在于莫桑比克的 Foc TR4(营养体不亲和群(VCG)01213/16)和存在于南非的 Foc STR4(VCG 0120/15)的 qPCR 检测方法。选择了 127 株真菌分离物进行特异性测试,包括来自香蕉假茎的内生镰刀菌分离物、非致病性 F. oxysporum 菌株以及代表 Foc 中 24 个 VCG 的 Foc 分离物。被证明对 Foc 谱系 VI、Foc TR4 和 Foc STR4 具有特异性的引物对用于产生绝对定量的标准曲线,并且根据标准曲线的质量、重复性和再现性以及定量限(LOQ)和检测限(LOD)对 qPCR 检测方法进行了评估。Foc 谱系 VI、TR4 和 STR4 的 qPCR 检测方法具有重复性和再现性,LOQ 值为 10-3-10-4 ng/μL,LOD 值为 10-4-10-5 ng/μL。在非洲对 Foc 菌株进行定量检测,可以减少识别非洲植物、水和土壤中枯萎病病原体的时间,并提高准确性。