Molecular study of the prevalence of brucella abortus and brucella melitensis in the blood and lymph node samples of slaughtered camels by polymerase chain reaction (PCR) in Iran

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Abstract

Brucellosis is a zoonotic disease which is characterized by reduced fertility and abortion in several species of animals, as well as humans. Camel brucellosis is caused by Brucella abortus and Brucella melitensis. To overcome the limitations posed by other techniques such as culture and serology, a sensitive technique (PCR) was employed for the detection of brucellosis in 123 camels. Findings from this PCR study indicated a total of 11.38% of blood samples as positive for Brucella spp. and 13.01% of the lymph node samples were positive for Brucella spp. In this study, 5 out of 123 (4.065%) and 3 out of 123 (2.439%) camel blood samples were positive for B. abortus and B. melitensis, respectively. Also, 4 out of 123 (3.252%) and 2 out of 123 (1.626%) camel lymph node samples were positive for B. abortus and B. melitensis, respectively. Young camels were the most commonly infected age group, while adult camels were the less often infected age group. Also, higher prevalence of brucellosis was observed in female camels. These results have indicated that PCR is a sensitive technique which could be used as a confi rmatory test for the detection of brucellosis in live camels, at the same time with the lowest risk of infection of laboratory personnel. The obtained results suggest that control and eradication programs for Brucella spp. infection seem to be necessary in camels. Our fi ndings support the power of PCR test for Brucella spp. detection in the blood and lymph node samples and it could be easily used for routine diagnosis.

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Khamesipour, F., Rahimi, E., Shakerian, A., Doosti, A., & Momtaz, H. (2014). Molecular study of the prevalence of brucella abortus and brucella melitensis in the blood and lymph node samples of slaughtered camels by polymerase chain reaction (PCR) in Iran. Acta Veterinaria, 64(2), 245–256. https://doi.org/10.2478/acve-2014-0023

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