Rapid and Sensitive Detection of Fusarium oxysporum f. sp. cubense Tropical Race 4 Using a RPA-DETECTR Assay

Jelli Venkatesh, Joanna Jankowicz-Cieslak, Hassan Mduma, Mirta Matijevic, Adel Ali, Isabel Cristina Calle Balbin, Mauricio Soto-Suarez, Cinthya Zorrilla, Pooja Bhatnagar-Mathur
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Abstract

Early and prompt detection of banana wilt pathogen Fusarium oxysporum f. sp. cubense (Foc), tropical race 4 (Foc TR4), causing global banana crop losses is crucial to curtail the disease spread, minimize damage and implement quarantine measures. We report the first successfully developed DNA Endonuclease Targeted CRISPR Trans Reporter (DETECTR) assay for the highly sensitive and specific detection of Foc TR4, validated across several isolates. Notably, specific crRNA spacer sequences and recombinant polymerase amplification (RPA) primers designed and evaluated for the DETECTR assay exhibited exceptional sensitivity, detecting Foc TR4 with genomic DNA as low as 0.005 ng, and demonstrated a very high specificity, and reproducibility. The RPA-DETECTR assay was validated using a diverse panel of samples, including both target and non-target pathogens confirming its robustness and reliability across different types of samples, ensuring practical application under varied conditions. In terms of throughput, the RPA-DETECTR assays enabled faster detection of Foc TR4 than other molecular diagnostics including PCR, quantitative PCR (qPCR) and droplet digital PCR (ddPCR) analyses, making this assay suitable for point-of-care (POC) detection of Foc TR4, and facilitating rapid decision-making and immediate response. This rapid detection capability is crucial in restricting any potential transboundary movement as part of ongoing disease management efforts.
使用 RPA-DETECTR 分析法快速灵敏地检测 Fusarium oxysporum f. sp. cubense Tropical Race 4
香蕉枯萎病病原体 Fusarium oxysporum f. sp. cubense(Foc)热带第 4 种族(Foc TR4)造成了全球香蕉作物的损失,及早、及时地检测该病原体对于遏制病害蔓延、最大限度地减少损失和实施检疫措施至关重要。我们报告了首次成功开发的 DNA 内切酶靶向 CRISPR Trans Reporter (DETECTR) 检测方法,该方法可高灵敏、特异性地检测 Foc TR4,并在多个分离株中得到验证。值得注意的是,为 DETECTR 检测法设计和评估的特异性 crRNA spacer 序列和重组聚合酶扩增(RPA)引物表现出了极高的灵敏度,能检测出基因组 DNA 低至 0.005 ng 的 Foc TR4,并表现出极高的特异性和可重复性。RPA-DETECTR 分析法通过使用不同的样本(包括目标和非目标病原体)进行验证,证实了它在不同类型样本中的稳健性和可靠性,确保了在不同条件下的实际应用。就通量而言,RPA-DETECTR 检测法比其他分子诊断方法(包括 PCR、定量 PCR (qPCR) 和液滴数字 PCR (ddPCR) 分析)更快地检测出 Foc TR4,使该检测法适用于 Foc TR4 的护理点 (POC) 检测,有助于快速决策和立即响应。作为当前疾病管理工作的一部分,这种快速检测能力对于限制任何潜在的越境转移至关重要。
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