Indian Journal of Animal Research

  • Chief EditorK.M.L. Pathak

  • Print ISSN 0367-6722

  • Online ISSN 0976-0555

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Indian Journal of Animal Research, volume 51 issue 4 (august 2017) : 676-678

Evaluation of a Real time polymerase chain reaction assay for the detection of aflatoxin / sterigmatocystin producing strains of Aspergillus spp.

R. Singh, T.S. Rai, N.S. Sharma, A.K. Arora, Paviter Kaur
1<p>Department of Veterinary Microbiology, COVS,&nbsp;Guru Angad Dev Veterinary and Animal Sciences University, Ludhiana-141 001, India.</p>
Cite article:- Singh R., Rai T.S., Sharma N.S., Arora A.K., Kaur Paviter (2017). Evaluation of a Real time polymerase chain reaction assay for the detectionof aflatoxin / sterigmatocystin producing strains of Aspergillus spp. . Indian Journal of Animal Research. 51(4): 676-678. doi: 10.18805/ijar.v0iOF.7263.

Aflatoxin and sterigmatocystin produced by Aspergillus flavus, A. parasiticus and A. versicolor are common mycotoxins found in food and feed stuffs. Sterigmatocystin is a direct precursor in aflatoxin biosynthesis. In the present study, Real time PCR using TaqMan probe chemistry was standardized for amplification of the aflatoxin/sterigmatocystin biosynthesis gene omt-1 of Aspergillus spp. The gene was amplified in six cultures of Aspergillus spp. isolated from 53 aflatoxin positive feed samples hence indicating their aflatoxigenic potential. Data clearly revealed that the real time PCR technique is efficient in distinguishing toxigenic strains of A. parasiticus, A. versicolor and A. flavus from other molds commonly inhabiting the feed.


  1. Bennett, J. W. and Lee, L. S. (1979). Mycotoxins their biosynthesis in fungi: aflatoxins and other bisfuranoids. J. Food Protect., 42: 805-809.

  2. Dutton, M. F. (1988). Enzymes in aflatoxin biosynthesis. Microbio. Rev., 52: 274-295.

  3. Ellis, W. O., J. P. Smith. and B. K. Simpson. 1991. Aflatoxins in food-occurrence, biosynthesis, effects on organisms, detection and methods of control. Crit. Rev. Food Sci., 30: 403-439. 

  4. Iheanacho, H. E., Dutton, M. F., Steenkamp, P. A., Steenkamp, L., Makun, H. A., Swart, A. and Mthombeni, J. Q. (2014). Real time PCR of nor-1 (aflD) gene of aflatoxin producing fungi and its correlative quantization to aflatoxin levels in South African compound feeds. J. Microbiol. Meth., 97: 63–67

  5. Kathuria, P. C., Jand, S. K. and Singh, N. (1993). Comparison of simple and rapid screening methods for the detection of aflatoxins contamination in poultry feeds. Indian Vet. J., 70: 1093-1096.

  6. Konietzny, U. and Greiner, R. (2003). The application of PCR in the detection of mycotoxigenic fungi in foods. Braz. J. Microbiol., 34: 283-300. 

  7. Moller, E. M., Bahnweg, G., Sandermann, H. and Geiger, H. (1992). A simple and efficient protocol for isolation of high molecular weight DNA from filamentous fungi, fruit bodies, and infected plant tissues. Nucleic Acids Res., 20: 6115-6116.

  8. Rodriguez, A., Rodríguez, M., Luque, M. I., Martín, A. and Cordoba, J. J. (2012). Real-time PCR assays for detection and quantification of aflatoxin-producing molds in foods. Food Microbiol., 31: 89-99.

  9. Wolf-Hall, C. E., Hanna, M. A. and Bullerman, L. B. (1999). Stability of deoxynivalenol in heat treated foods. J. Food Prot., 62: 962-964.

  10. Yu, J., Cary, J. W., Bhatnagar, D., Cleveland, T. E., Keller, N. P. and Chu, F. S. (1993). Cloning and characterization of a cDNA from Aspergillus parasiticus encoding an O-methyltransferase involved in aûatoxin biosynthesis. Appl. Env. Microbiol., 59: 3564–3571.

     

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