Development of a real-time PCR for detection of Mycoplasma bovis in bovine milk and lung samples

• Published in: Journal of veterinary diagnostic investigation 2005-11, Vol.17 (6), p.537-545
• Main Authors: Cai, H.Y, Bell-Rogers, P, Parker, L, Prescott, J.F
• Format: Article
• Language: English
• Subjects: Animals; bacterial pneumonia; Base Sequence; bovine mastitis; Cattle; Cattle Diseases - diagnosis; Cattle Diseases - microbiology; dairy cattle; disease detection; DNA Primers; Female; Lung - microbiology; lungs; Mastitis, Bovine - diagnosis; Mastitis, Bovine - microbiology; microbial genetics; milk; Milk - microbiology; milk analysis; molecular sequence data; Mycoplasma bovis; Mycoplasma bovis - genetics; Mycoplasma bovis - isolation & purification; Mycoplasma Infections - diagnosis; Mycoplasma Infections - veterinary; mycoplasmosis; new technology; nucleotide sequences; polymerase chain reaction; Polymerase Chain Reaction - methods; Polymerase Chain Reaction - veterinary; Sensitivity and Specificity; Sequence Homology, Nucleic Acid; tissue analysis
• ISSN: 1040-6387; 1943-4936
• DOI: 10.1177/104063870501700603

A real-time polymerase chain reaction (PCR) assay using hybridization probes on a LightCycler platform was developed for detection of Mycoplasma bovis from individual bovine mastitis milk and pneumonic lung tissues. The detection limit was 550 colony forming units (cfu)/ml of milk and 650 cfu/25 mg of lung tissue. A panel of bovine Mycoplasma and of other bovine-origin bacteria were tested; only M. bovis strains were positive, with a melting peak of 66.6 degrees C. Mycoplasma agalactiae PG2 was also positive and could be distinguished because it had a melting peak of 63.1 degrees C. In validation testing of clinical samples, the relative sensitivity and specificity were 100% and 99.3% for individual milks and 96.6% and 100% for the lung tissue. Using M. bovis real-time PCR, the M. bovis culture-positive milk samples were estimated to contain between 5 x 10(4) and 7.7 x 10(8) cfu/ml and the M. bovis culture-positive lungs between 1 x 10(3) and 1 x 10(9) cfu/25 mg. Isolation, confirmed with the real-time PCR and colony fluorescent antibody test, showed that at the herd level, the proportion of samples positive for M. bovis isolation in mastitis milk samples submitted to the Mastitis Laboratory, Animal Health Laboratory, University of Guelph, Ontario, Canada, was 2.4% (5/201). We conclude that this probe-based real-time PCR assay is a sensitive, specific, and rapid method to identify M. bovis infection in bovine milk and pneumonic lungs.