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A Rapid PCR-LAMP Assay for the Early Detection of Lasiodiplodia theobromae from Basal Stem Rot-Infected Passion Fruit Plants

文献类型： 外文期刊

作者： Liu, Ying 1 ; Rasheed, Usman 1 ; Shan, Bin 1 ; Lu, Qinyu 1 ; Chen, Shimiao 1 ; Meng, Kaikai 1 ; Qin, Aiying 3 ; Mo, Ganhui 1 ;

作者机构： 1.Guangxi Acad Agr Sci, Guangxi Subtrop Crops Res Inst, Nanning 530001, Guangxi, Peoples R China

2.Minist Agr & Rural Affairs, Guangxi Subtrop Crops Res Inst, Guangxi Key Lab Qual & Safety Control Subtrop Frui, Key Lab Qual & Safety Control Subtrop Fruit & Vege, Nanning 530001, Peoples R China

3.Guangxi Vocat & Tech Coll, Nanning 530226, Guangxi, Peoples R China

关键词： Passion fruit; Basal stem rot; Loop-mediated isothermal amplification; Hydroxy naphthol blue; Phytopathogen detection; Lasiodiplodia theobromae

期刊名称：MOLECULAR BIOTECHNOLOGY （ 影响因子：2.5； 五年影响因子：2.7 ）

ISSN： 1073-6085

年卷期： 2025 年

页码：

收录情况： SCI

摘要： Lasiodiplodia theobromae is an emerging threat and the main pathogenic fungi associated with basal stem rot of passion fruit in Guangxi Zhuang Autonomous Region, China. Current pathogen identification protocols are labor-intensive and time-consuming, emphasizing the need for more efficient methods to enable precise surveillance of L. theobromae for early detection and warning. The present study sought to develop a rapid colorimetric LAMP assay for early detection and surveillance of L. theobromae in passion fruit plants. For that, amplifications of ITS locus were performed on fungal genomic DNA using conventional PCR, with the specific primer pair ITS1 and ITS4. The hydroxy naphthol blue (HNB)-dependent colorimetric LAMP assay was then optimized by varying primer sets, inner primers concentration, reaction temperatures and incubation time. A microbial lysis buffer was employed to extract genomic DNA from stems infected with L. theobromae. The prime LAMP primer set targeting the ITS region of L. theobromae was designed and an HNB based colorimetric LAMP assay was optimized. Various optimization parameters were evaluated, with the optimal conditions determined as 1.6 mu M of each FIB and BIP, 0.2 mu M of each F3 and B3, and incubation at 65 degrees C for 40 min. This ITS-based LAMP assay could effectively distinguish L. theobromae from less dominant pathogens in passion fruits with a detection limit of 3 pg for ITS locus amplicons. Our proposed method utilizing a microbial lysis buffer enables rapid and cost-effective detection of L. theobromae DNA in early-infected passion fruit plants, eliminating the need for microbial cultivation and DNA purification.

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