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Detection of Brucella spp. in Milk from Seronegative Cows by Real-Time Polymerase Chain Reaction in the Region of Batna, Algeria


Affiliations
1 Department of Veterinary Science, Institute of Veterinary and Agronomic Sciences, University of Batna 1, Batna, Algeria
2 Research Laboratory HASAQ, High National Veterinary School, Algiers, Algeria
3 Laboratory of Molecular Biology and Microbiology of Constantine Biotechnology Research Center, Constantine, Algeria
 

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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  • Detection of Brucella spp. in Milk from Seronegative Cows by Real-Time Polymerase Chain Reaction in the Region of Batna, Algeria

Abstract Views: 126  |  PDF Views: 0

Authors

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

Abstract


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.