Article citationsMore>>

B. Scherm, M. Palomba, D. Serra, A. Marcello and Q. Migheli, “Detection of Transcripts of the Aflatoxin Genes Afld, Aflo, and Aflp by Reverse Transcription-Polymerase Chain Reaction Allows Differentiation of Aflatoxin-Producing and Non-Producing Isolates of Aspergillus Flavus and Aspergillus parasiticus,” International Journal of FoodMicrobiology, Vol. 98, No. 2, 2005, pp. 201-210.

has been cited by the following article:

• TITLE: A Novel Non Radioactive PCR-DNA Probe for the Detection of Aflatoxin Producing Aspergillus Species from Major Food Crops Grown in India

  AUTHORS: S. R. Priyanka, M. Venkata Ramana, K. Balakrishna, H. S. Murali, H. V. Batra

  KEYWORDS: AFB1-Aflatoxin B1; HPLC-High Performance Liquid Chromatography; NOR-1; Norsolorinic Acid Synthase; PCR-Polymerase Chain Reaction

  JOURNAL NAME: Advances in Microbiology, Vol.2 No.4, December 28, 2012

  ABSTRACT: In the present study, a novel non radioactive digoxigenen labelled PCR-DNA probe was developed targeting nor-1 gene to assess the contamination of aflatoxigenic Aspergillus species in food grain samples from Southern parts of India. The sensitivity of developed PCR-DNA probe was determined to be 10 pg of genomic DNA and 1 pg of purified PCR product. The specificity of the DNA probe was validated by testing against an array of Aspergillus, Fusarium and Penicillium spp. A total of 89 Aspergillus isolates were recovered from 152 grain samples of maize, paddy, and groundnut. Among them, maize had the highest (90%) incidence of toxigenic Aspergillus species. When developed PCR-DNA probe was evaluated onto pure cultures of toxigenic and nontoxigenic Aspergillus species, 60 samples were positive for the nor-1 gene probe. DNA probe results unequivocally matched with the HPLC analysis. In conclusion, the novel PCR-DNA probe developed in this study may find its application in rapid detection of aflatoxin-producing Aspergillus isolates from contaminated cereal grains.