Open Access
Research (Published online: 26-03-2018)
17. Detection of Brucella spp. in milk from seronegative cows by real-time polymerase chain reaction in the region of Batna, Algeria
Rabehi Sabrina, Hamdi Taha Mossadak, Mamache Bakir, Meghezzi Asma and Boushaba Khaoula
Veterinary World, 11(3): 363-367

Rabehi Sabrina: Department of Veterinary Science, Institute of Veterinary and Agronomic Sciences, University of Batna 1, Batna, Algeria.
Hamdi Taha Mossadak: Research Laboratory HASAQ, High National Veterinary School, Algiers, Algeria.
Mamache Bakir: Department of Veterinary Science, Institute of Veterinary and Agronomic Sciences, University of Batna 1, Batna, Algeria.
Meghezzi Asma: Laboratory of Molecular Biology and Microbiology of Constantine Biotechnology Research Center, Constantine, Algeria.
Boushaba Khaoula: Laboratory of Molecular Biology and Microbiology of Constantine Biotechnology Research Center, Constantine, Algeria.

doi: 10.14202/vetworld.2018.363-367

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Article history: Received: 03-12-2017, Accepted: 21-02-2018, Published online: 26-03-2018

Corresponding author: Mamache Bakir


Citation: Sabrina R, Taha Mossadak H, Bakir M, Asma M, Khaoula B (2018) Detection of Brucella spp. in milk from seronegative cows by real-time polymerase chain reaction in the region of Batna, Algeria, Veterinary World, 11(3): 363-367.

Aim: The aim of this study was to detect Brucella spp. DNA in milk samples collected from seronegative cows using the real-time polymerase chain reaction (PCR) assay for diagnosis of brucellosis in seronegative dairy cows to prevent transmission of disease to humans and to reduce economic losses in animal production.

Materials and Methods: In this study, 65 milk samples were investigated for the detection of Brucella spp. The detection of the IS711 gene in all samples was done by real-time PCR assay by comparative cycle threshold method.

Results: The results show that of the 65 DNA samples tested, 2 (3.08%) were positive for Brucella infection. The mean cyclic threshold values of IS711 real-time PCR test were 37.97 and 40.48, indicating a positive reaction.

Conclusion: The results of the present study indicated that the real-time PCR appears to offer several advantages over serological tests. For this reason, the real-time PCR should be validated on representative numbers of Brucella-infected and free samples before being implemented in routine diagnosis in human and animal brucellosis for controlling this disease.

Keywords: Brucella spp., milk, real-time polymerase chain reaction, seronegative cows.


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