Multiplex PCR for the early detection of fumonisin producing Fusarium verticillioides

被引:11
作者
Nagaraj, Deepa [1 ]
Adkar-Purushothama, Charith Raj [2 ]
Yanjarappa, Sreenivasa Marikunte [1 ]
机构
[1] Univ Mysore, Dept Studies Microbiol, Mol Mycol Lab, Mysore 570006, Karnataka, India
[2] Univ Sherbrooke, RNA Grp Grp ARN, Dept Biochim, Fac Med Sci Sante, Pavillon Rech Appl Canc,3201 Rue Jean Mignault, Sherbrooke, PQ J1E 4K8, Canada
关键词
Fusarium; Cereals; Maize; Paddy; Sorghum; Spiking; Mycotoxin; ASSAY;
D O I
10.1016/j.fbio.2016.01.001
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
In the present study, fumonisin producing Fusarium verticillioides was specifically detected in pure cultures, cereal samples and plant materials by multiplex PCR using one forward VERTF-1 and two reverse primers VERTR and VERTF-2. A total of 326 Fusarium isolates were obtained from maize, sorghum, paddy wheat and pearl millet samples collected from different districts of Karnataka, India. All Fusarium species were subjected to single round of PCR with species specific and fumonisin specific primers which recorded 59.50% of F. verticillioides and 53.98% of fumonisin producing F. verticillioides. Maize samples recorded highest frequency 34.42% of fumonisin producing F. verticillioides followed by paddy 28.57% and sorghum 16.66%. Sensitivity of multiplex PCR experiment was conducted by whole grain experiment of the collected cereals, roots and leaves of the cereal samples by diluting the DNA 10 to 100 times in which 1:50, 1:75 and 1:100 diluted samples recorded positive. The developed multiplex PCR assay provided a powerful tool for the accurate detection, identification and discrimination of potential fumonisin producing E verticillioides strains among the population. The present study is the first report of developing the multiplex PCR method for early detection of fumonisin producing E verticillioides from cereal samples, pure cultures and plant parts. (c) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:84 / 88
页数:5
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