Abstract:Rhizoctonia solani, the pathogen of potato black scurf, has been a threatening factor to potato (Solanum tuberosum) production. R. solani in the soil mainly uses the sclerotium structure as the initial source of infection for latent dormancy, and its density is positively correlated with the incidence of potato black scurf disease. In order to quickly and accurately detect the density of R. solani and sclerotia in soil, TEF3/TEF7 specific primers were designed based on the conservative region of translation elongation factor (TEF) of R. solani anastomosis group 3 (AG3). A real-time quantitative PCR (qPCR) detection system for quantification of R. solani AG3 was developed using recombinant plasmid of 191-bp amplification product as the standard, and the sensitivity of qPCR (19.5 fg/µL) was 1 000 fold higher than that of common PCR. Common PCR and qPCR tests were carried out on suspected potato moles (n=18) and diseased soil (n=41) in 4 regions. The detection rate of potato moles was 100%, but common PCR (65.85%) failed to detect all DNA in the diseased soil, while the detection rate of the diseased soil by qPCR was 97.56%. In order to determine the pathogen quantity in the early detection of diseased soil in the field, the soil with different amount of sclerotium was artificially simulated, and qPCR detection was carried out by wet-sieving method. The curve relationship between cycle threshold (Ct) and sclerotium content in soil was established. The results showed that regression equation was y=-3.982x+12.687, and correlation coefficient R2 was 0.986, showing good linear relationship, and the detection limit of artificially simulated pathogen quantity was 5×10-6 g/g soil. The detection system developed in present study could detect sclerotium density of AG3 in soil rapidly and accurately. Detection of sclerotium content of R. solani in soil before planting could provide technical support for early warning of potato black scurf.
李磊, 陈利达, 黄艺烁, 谢学文, 石延霞, 柴阿丽, 李宝聚. 马铃薯黑痣病菌实时荧光定量PCR检测体系的建立及应用[J]. 农业生物技术学报, 2021, 29(7): 1417-1425.
LI Lei CHEN Li-Da Huang Yi-Shuo XIE Xue-Wen SHI Yan-Xia CHAI A-Li LI Bao-Ju. Establishment and Application of Real-time Quantitative PCR Detection System for Black Scurf Pathogen in Potato (Solanum tuberosum). 农业生物技术学报, 2021, 29(7): 1417-1425.
[1] 曹春梅, 李文刚, 张建平, 等.2009.马铃薯黑痣病的研究现状[J].中国马铃薯, 23(3): 171-173. (Cao C M, Li W G, Zhang J P, et al.2009.Research status of potato melanosis[J].Chinese Potato, 23(3): 171-173.) [2] 陈利达, 谢学文, 石延霞, 等.2020.酸疮痂链霉菌实时荧光定量PCR检测体系的构建及应用[J].农业生物技术学报, 28(7): 1314-1321. (Chen L D, Xie X W, Shi Y X, et al.2020.Establishment and application of real-time quantitative PCR for detecting of Streptomyces acidiscabies[J].Journal of Agricultural Biotechnology, 28(7): 1314-1321.) [3] 李世东, 陈延熙.1989.Rhizoctonia solani的一种选择性培养基[J].植物病理学报, 19(3): 189-192. (Li S D, Chen Y X.1989.A selective medium of Rhizoctonia solani[J].Acta Phytopathologyica Sinica, 19(3): 189-192.) [4] 李晓妮, 徐娜娜, 于金凤.2014.中国北方马铃薯黑痣病立枯丝核菌的融合群鉴定[J].菌物学报, 33(3): 584‐593. (Li X N, Xu N N, Yu J F.2014.Anastomosis groups of Rhizoctonia solani from black scurf of potato in northern China[J].Mycosystema, 33(3): 584-593.) [5] 刘小娟, 安建华, 莫娟, 等.2019.5种杀菌剂对马铃薯黑痣病的田间防效试验[J].中国马铃薯, 33(3): 170-174. (Liu X J, An J H, Mo J, et al.2019.Control efficacy of five fungicides on potato black scurf[J].Chinese Potato, 33(3): 170-174.) [6] 吕顺, 曾莉莎, 刘文清, 等.2014.大蕉枯萎病病原菌鉴定及TEF-1α序列分析[J].植物病理学报, 44(4): 337-348. (Lv S, Zeng L S, Liu W Q, et al.2014.Iidentification and TEF-1α sequence analysis of Fusarium wilt pathogens from Dajiao[J].Acta Phytopathologyica Sinica, 44(4): 337-348.) [7] 牟明, 赵伟, 杨明秀, 等.2017.黑龙江马铃薯黑痣病菌生物学特性及菌丝融合群的鉴定[J].中国瓜菜, 30(10): 12-17. (Mu M, Zhao W, Yang M X, et al.2017.Identification of the biological characteristics and the hyphal fusion group of potato black nevus in Heilongjiang province[J].Chinese Melon and Vegetable, 30(10): 12-17.) [8] 申永铭, 郭成瑾, 王喜刚, 等.2017.土壤中立枯丝核菌AG-3菌核的荧光定量PCR快速检测[J].菌物学报, 36(10): 1383-1391. (Shen Y M, Guo C J, Wang X G, et al.2017.Rapid detection of AG-3 sclerotia of Rhizoctonia solani by fluorescence quantitative PCR[J].Mycosystema, 36(10): 1383-1391.) [9] 田晓燕, 蒙美莲, 张笑宇, 等.2011.马铃薯黑痣病菌菌丝融合群的鉴定[J].中国马铃薯, 25(5): 298-301. (Tian X Y, Meng M L, Zhang X Y, et al.2011.Identification of anastomosis groups of Rhizoctonia solani on potato plant[J].Chinese Potato, 25(5): 298-301.) [10] 王朵, 谢学文, 柴阿丽, 等.2019.甘肃省白菜死棵病病原菌鉴定及其融合群检测技术[J].中国农业科学, (16):2787-2799. (Wang D, Xie X W, Chai A L, et al.2019.Identification of the pathogen causing cabbage died in Gansu province and detection of anastomosis groups[J].Scientia Agricultura Sinica (16):2787-2799.) [11] 杨继堂, 陶亚群, 闫文凯, 等.2015.11种杀菌剂对立枯丝核菌的室内毒力测定[J].长江大学学报(自然科学版), 12(3): 1-4. (Yang J T, Tao Y Q, Yan W K, et al.2015.Determination of indoor virulence of 11 fungicides against Rhizoctonia solani in 2015[J].Journal of Changjiang University (Natural Science Edition), 12(3): 1-4.) [12] 张春艳.2014.马铃薯黑痣病菌系统发育分析及融合群快速鉴定[D].硕士学位论文, 河北农业大学, 导师: 朱杰华, 杨志辉, pp.29-30. (Zhang C Y.2014.Phylogenetic analysis of Rhizoctonia solani from potato and the rapid identification of their anastomosis groups[D].Thesis for M.S., Hebei Agricultural University, Supervisor: Zhu J H, Yang Z H, pp.60-65.) [13] Brierley J L, Hilton A J, Wale S J, et al.2016.The relative importance of seed-and soil-borne inoculum of Rhizoctonia solani, AG‐3 in causing black scurf on potato[J].Potato Research, 59(2): 181‐193. [14] Budge G E, Shaw M W, Colyer A, et al.2009.Molecular tools to investigate Rhizoctonia solani distribution in soil[J].Plant Pathology, 58(6): 1071-1080. [15] Campion C, Chatot C, Perraton B, et al.2003.Anastomosis groups, pathogenicity and sensitivity to fungicides of Rhizoctonia solani isolates collected on potato crops in France[J].European Journal of Plant Pathology, 109(9): 983-992. [16] Carling D E, Baird R E, Gitaitis R D, et al.2002.Characterization of AG-13, a newly reported anastomosis group of Rhizoctonia solani[J].Phytopathology, 92(8): 893-899. [17] Coley-Smith J R, Cooke R C, 2003.Survival and germination of fungal sclerotia[J].Annual Review of Phytopathology, 9(1): 65‐92. [18] Dubey S C, Tripathi A, Upadhyay B K, et al.2016.Development of conventional and real time PCR assay for detection and quantification of Rhizoctonia solani infecting pulse crops[J].Biologia, 71(2): 133-138. [19] Harveson R M, Watkins J E, Giesler L J, et al.2005.EC05-1894 dry bean disease profiles Ⅱ: Fungal root rot and wilt diseases[J].Employment, (32): 1613 [20] Lees A K, Cullen D W, Sullivan L, et al.2002.Development of a PCR assay for the detection and identification of Rhizoctonia solani AG-3 in potato and soil[J].Plant Pathology, 51(3): 293-302 [21] Lehtonen M J, Ahvenniemi P, Wilson P S, et al.2008.Biological diversity of Rhizoctonia solani (AG‐3) in a northern potato-cultivation environment in Finland[J].Plant Pathology, 57(1): 141-151. [22] Ritchie F, Bain R, Mcquilken M.2013.Survival of sclerotia of Rhizoctonia solani AG3 PT and effect of soil-borne inoculum density on disease development on potato[J].Journal of Phytopathology, 161(3): 180-189. [23] Salamone A L, Okubara P A.2020.Real-time PCR quantification of Rhizoctonia solani AG-3 from soil samples[J].Journal of Microbiological Methods, 172: 1-8. [24] Sneh B, Jabaji H S, Neate S M, et al.1996.Rhizoctonia species: Taxonomy, molecular biology, ecology; pathology and disease control[J].Springer Netherlands, 31(3): 37-47. [25] Thornton R, Neill T M, Hilton G, et al.2002.Detection and recovery of Rhizoctonia solani in naturally infested glasshouse soils using a combined baiting, double monoclonal antibody ELISA[J].Plant Pathology, 48(5): 627‐634. [26] Woodhall J W, Adams I P, Peters J C, et al.2013.A new quantitative real-time PCR assay for Rhizoctonia solani AG-3-PT and the detection of AGs of Rhizoctonia solani associated with potato in soil and tuber samples in Great Britain[J].European Journal of Plant Pathology, 136(2): 273-280. [27] Woodhall J W, Lees A K, Edwards S G, et al.2006.Characterization of Rhizoctonia solani from potato in Great Britain[J].Plant Pathology, 56(2): 286‐295. [28] Yanar Y, Yusuf G, Cesmeli I, et al.2005.Characterization of Rhizoctonia solani isolates from potatoes in Turkey and screening potato cultivars for resistance to AG-3 isolates[J].Phytoparasitica, 33(4): 370-376. [29] Yang S, Min F X, Wang W Z, et al.2017.Anastomosis group and pathogenicity of Rhizoctonia solani associated with stem canker and black scurf of potato in Heilongjiang province of China[J].American Journal of Potato Research, 94(2): 95-104