Novel real‐time PCR detection assay for Brucella suis. Issue 1 (1st April 2015)

• Record Type: Journal Article
• Authors: Hänsel, C.; Mertens, K.; Elschner, M. C.; Melzer, F.
• Is Part Of: Veterinary record open. Volume 2:Issue 1(2015)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2015-04-01
• Subjects: Brucellosis -- Diagnostics -- Disease surveillance -- Food safety -- Infectious diseases -- RT‐PCR techniques; Veterinary medicine -- Periodicals; Veterinary medicine -- Research -- Periodicals; 636.08905
• DOI: 10.1136/vetreco-2014-000084
• Languages: English
• ISSNs: 2052-6113

Abstract

Abstract : Introduction: Brucella suis is the causative agent of brucellosis in suidae and is differentiated into five biovars (bv). Biovars 1 and 3 possess zoonotic potential and can infect humans, whereas biovar 2 represents the main source of brucellosis in feral and domestic pigs in Europe. Both aspects, the zoonotic threat and the economic loss, emphasize the necessity to monitor feral and domestic pig populations. Available serological or PCR based methods lack sensitivity and specificity. Results: Here a bioinformatics approach was used to identify a B. suis specific 17 bp repeat on chromosome II (BS1330_II0657 locus). This repeat is common for B. suis bv 1 to 4 and was used to develop a TaqMan probe assay. The average PCR efficiency was determined as 95% and the limit of detection as 12, 5 fg/µl of DNA, equally to 3.7 bacterial genomes. This assay has the highest sensitivity of all previously described B. suis specific PCR assays, making it possible to detect 3‐4 bacterial genomes per 1 µl of sample. The assay was tested 100% specific for B. suis and negative for other Brucella spp. and closely related non‐ Brucella species. Conclusions: This novel qPCR assay could become a rapid, inexpensive and reliable screening method for large sample pools of B. suis 1 to 4. This method will be applicable for field samples after validation.