Development of a one-run real-time PCR detection system for pathogens associated with bovine respiratory disease complex

• Published in: Journal of Veterinary Medical Science Vol. 79; no. 3; pp. 517 - 523
• Main Authors: KISHIMOTO, Mai, TSUCHIAKA, Shinobu, RAHPAYA, Sayed Samim, HASEBE, Ayako, OTSU, Keiko, SUGIMURA, Satoshi, KOBAYASHI, Suguru, KOMATSU, Natsumi, NAGAI, Makoto, OMATSU, Tsutomu, NAOI, Yuki, SANO, Kaori, OKAZAKI-TERASHIMA, Sachiko, OBA, Mami, KATAYAMA, Yukie, SATO, Reiichiro, ASAI, Tetsuo, MIZUTANI, Tetsuya
• Format: Journal Article
• Language: English
• Published: Japan JAPANESE SOCIETY OF VETERINARY SCIENCE 01.03.2017; Japan Science and Technology Agency; The Japanese Society of Veterinary Science
• Subjects: Adenoviruses; Animals; bovine respiratory disease complex; Bovine Respiratory Disease Complex - microbiology; Bovine Respiratory Disease Complex - virology; Coronaviridae; Coronaviruses; Deoxyribonucleic acid; diagnosis; Diarrhea; DNA; Etiology; Farms; Influenza; Parainfluenza; Pathogens; Polymerase chain reaction; Real-Time Polymerase Chain Reaction - veterinary; Reproducibility of Results; Respiratory diseases; Respiratory syncytial virus; Rhinitis; Sensitivity and Specificity; taqMan real-time PCR; Virology
• ISSN: 0916-7250; 1347-7439
• DOI: 10.1292/jvms.16-0489

Bovine respiratory disease complex (BRDC) is frequently found in cattle worldwide. The etiology of BRDC is complicated by infections with multiple pathogens, making identification of the causal pathogen difficult. Here, we developed a detection system by applying TaqMan real-time PCR (Dembo respiratory-PCR) to screen a broad range of microbes associated with BRDC in a single run. We selected 16 bovine respiratory pathogens (bovine viral diarrhea virus, bovine coronavirus, bovine parainfluenza virus 3, bovine respiratory syncytial virus, influenza D virus, bovine rhinitis A virus, bovine rhinitis B virus, bovine herpesvirus 1, bovine adenovirus 3, bovine adenovirus 7, Mannheimia haemolytica, Pasteurella multocida, Histophilus somni, Trueperella pyogenes, Mycoplasma bovis and Ureaplasma diversum) as detection targets and designed novel specific primer-probe sets for nine of them. The assay performance was assessed using standard curves from synthesized DNA. In addition, the sensitivity of the assay was evaluated by spiking solutions extracted from nasal swabs that were negative by Dembo respiratory-PCR for nucleic acids of pathogens or synthesized DNA. All primer-probe sets showed high sensitivity. In this study, a total of 40 nasal swab samples from cattle on six farms were tested by Dembo respiratory-PCR. Dembo respiratory-PCR can be applied as a screening system with wide detection targets.