article information

Zahedan Journal of Research in Medical Sciences: Vol.15, issue 12; e4325
published online: February 12, 2013
article type: Research Article
received: November 27, 2012
accepted: January 09, 2013

Comparison of Culture and Multiplex PCR Technique for Detection of Brucella abortus and Brucella melitensis from Human Blood Samples

authors:

avatar Reza Mirnejad 1 , avatar Ali Reza Vahdati 2 , avatar Ali Ahmadi 1 , avatar Seied Mojtaba Mortazavi 3 , avatar Vahhab Piranfar 4 , *

Molecular Biology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran
Institute of Evolutionary Biology and Environmental Studies, University of Zurich, Zurich, Switzerland
Health Station, Kerman University of Medical Sciences, Kerman, Iran
Department of Microbiology, Tonekabon Branch, Islamic Azad University of Tonekabon, Tonekabon, Iran

how to cite: Mirnejad R, Vahdati A R, Ahmadi A, Mortazavi S M, Piranfar V. Comparison of Culture and Multiplex PCR Technique for Detection of Brucella abortus and Brucella melitensis from Human Blood Samples. Zahedan J Res Med Sci. 2013;15(12):e4325.

Abstract

Background: To compare culture methods with multiplex PCR technique for identification of Brucella abortus and Brucella melitensis from suspicious patients with clinical history of brucellosis and positive serological test (Rose Bengal test and serum agglutination test).
Materials and Methods: In this study, 160 blood samples from patients suspected of Brucellosis with high serum titers of 1/80 were studied. All samples were cultured in Brucella-specific media. Brucella species were identified by using microbiological methods. DNA was extracted with Phenol-chloroform DNA extraction method. IS711 was amplified simultaneously using three specific primers and obtained patterns were analyzed.
Results: From 160 samples, 47.5% (76) were culture positive cases from which 43 cases were B. melitensis and 33 were B. abortus With the PCR technique 108 were detected positive from which 45.3% were B. abortus and 54.6% were B. melitensis. It should be noted that all 76 samples with positive culture were also identified by PCR.
Conclusion: Generally, use of the molecular technique multiplex PCR in addition to increased speed and accuracy and less false results than bacterial culture method, is able to identify different species of brucella. This will facilitate the treatment process.

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