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African Journal of Biotechnology

     
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  Afr. J. Biotechnol.

  Vol. 8 No. 24

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  Search Pubmed for articles by:

  Maiwore J
  Mbofung CMF

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African Journal of Biotechnology Vol. 8 (24), pp. 7156-7163, 15 December 2009

ISSN 1684-5315  © 2009 Academic Journals  

 

 

Full Length Research Paper

 

Comparison of bacterial communities of tilapia fish from Cameroon and Vietnam using PCR-DGGE (polymerase chain reaction-denaturing gradient gel electrophoresis)

 

J. Maiwore1, N. L. Tatsadjieu2*, D. Montet3, G. Loiseau3 and C. M. F. Mbofung1

 

1Department of Food Science and Nutrition, National Advanced School of Agro-Industrial Sciences, University of Ngaoundere, P.O. Box 454, Ngaoundere, Cameroon.

2Laboratory of Microbiology, IUT, University of Ngaoundere, P. O. Box 454, Ngaoundere, Cameroon.

3UMR 95 Qualisud, CIRAD, TA B-95/16, 73, rue Jean-François Breton, 34398 Montpellier cedex 5, France.

 

*Corresponding author. E-mail: tatsadjieu@yahoo.fr. Tel: + (237) 99 52 37 27.

 

Accepted 13 November, 2009

 

   Abstract

 

Fishes in general and tilapia in particular are traded all over the world. However, it is difficult to find out their exact geographical location. One of the techniques used in the traceability of fish and its by-products consist in analysing in a global way the whole viable and non viable bacterial communities. For this purpose, the molecular technique employing the bacterial 16S DNA banding profiles generated by PCR-DGGE (polymerase chain reaction-Denaturing gradient gel electrophoresis) was used to evaluate the differences between the bacterial profiles of fishes from Vietnam (An Giang, south province) and those of Cameroon (Yagoua, Maga, Lagdo). The different PCR-DGGE 16S rDNA banding profiles obtained were analysed and results showed that there were specific bands for each geographical location though some bands common to Cameroon and Vietnam were observed. This method could be used as a rapid analytical traceability tool for fish products and could be considered as a provider of a unique biological bar code.

 

Key words:  Traceability, PCR-DGGE, bacterial community.

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