A Comparison of Bacteriological Culture, Serology, and Quantitative PCR for Detecting Brucellosis in Ewes with a History of Abortion

سال انتشار: 1402
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 162

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شناسه ملی سند علمی:

JR_IJVST-15-4_003

تاریخ نمایه سازی: 26 آذر 1402

چکیده مقاله:

The zoonotic disease brucellosis is a serious public health and livestock industry concern. In the present study, we used bacteriological culture, RBT, and qPCR to determine the prevalence of brucellosis in the serum and milk samples of sheep with a history of abortion. Serum and milk samples were obtained from ۱۰۰ sheep aged ۳-۵ years. In order to determine the prevalence of brucellosis, a modified RBT was performed on serum samples, Brucella was isolated from milk by bacteriological culture, and qPCR was applied to detect bacterial DNA in milk. The prevalence of brucellosis using modified RBT, bacteriological culture, and qPCR was ۳۲%, ۴۲%, and ۴۴%, respectively. By considering qPCR as the standard, modified RBT showed a sensitivity of ۹۵%, a specificity of ۱۰۰%, an accuracy of ۹۸%, a PV+ of ۱۰۰%, and a PV- of ۹۷%. The sensitivity, specificity, accuracy, PV+, and PV- for bacteriological culture were ۷۷%, ۱۰۰%, ۹۰%, ۱۰۰%, and ۸۵%, respectively. The agreement between qPCR and modified RBT was ۰.۹۵۹ (۹۵% CI: ۰.۸۹۶-۱), between qPCR and bacteriological culture was ۰.۷۹۲ (۹۵% CI: ۰.۶۶۷-۰.۸۹۷), and between modified RBT and bacteriological culture was ۰.۸۳۱ (۹۵% CI: ۰.۷۰۹-۰.۳۸). Based on the results, bacterial isolation from sheep milk is not recommended except in specific cases due to its low sensitivity, as well as its time-consuming and hazardous nature. However, the modified RBT can be used as a routine method because of its cost-effectiveness, higher sensitivity, and higher accuracy compared to bacterial isolation. Moreover, qPCR is recommended as the gold standard test for detecting brucellosis in sheep milk, especially in those with a history of abortion.

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نویسندگان

Mohammad Javad Aminzadeh

Department of Clinical Sciences, School of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran.

Hamideh Kalateh Rahmani

Department of Pathobiology, School of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran.

Khadijeh Hashemi

Division of Biotechnology, School of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran & Stem Cell Biology and Regenerative Medicine Research Group, Research Institute of Biotechnology, Ferdowsi University of Mashhad, Mashhad,

Narges Khaleghnia

Centre of Excellence in Ruminant Abortion and Neonatal Mortality, School of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran.

Mohammad Azizzadeh

Department of Clinical Sciences, School of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran.

Pezhman Mirshokraei

Department of Clinical Sciences, School of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran & Centre of Excellence in Ruminant Abortion and Neonatal Mortality, School of Veterinary Medicine, Ferdowsi University of Mashhad,

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