Wiggins Monique C, Woolums Amelia R, Sanchez Susan, Hurley David J, Cole Dana J, Ensley Douglas T, Pence Mel E
Department of Infectious Disease, College of Veterinary Medicine, University of Georgia, Athens, GA 30602, USA.
J Am Vet Med Assoc. 2007 May 15;230(10):1514-8. doi: 10.2460/javma.230.10.1514.
To characterize the prevalence of Mycoplasma bovis infection in backgrounding and stocker cattle operations and compare bacteriologic culture with PCR assay for detection of M bovis.
Prospective descriptive study.
432 calves, 3 to 9 months old, from 9 operations.
2 nasal swab specimens were collected from each calf. Swab specimens were evaluated via bacteriologic culture and PCR assay for organisms of the class Mollicutes and M bovis. Culture results were considered negative if no growth occurred within 21 days. Positive results were indicated by characteristic colony formation with PCR assay confirmation. Deoxyribonucleic acid was extracted from 1 swab specimen for direct PCR assay for Mollicutes and M bovis.
Of 432 calves, 374 (87%) had positive results for Mollicutes via PCR assay and 63 (15%) via culture. Seven (2%) calves had positive results for M bovis via PCR assay and 10 (2%) via culture. Prevalence of Mollicutes at the farm level ranged from 54% to 100% via PCR assay and from 0% to 59% via culture. Prevalence of M bovis at the farm level ranged from 0% to 4% via PCR assay and from 0% to 6% via culture. Calves that shed M bovis were significantly more likely to have a fever than were calves that did not shed M bovis.
M bovis was detected at a low level in recently purchased backgrounded and stocker calves in Georgia. Although slightly more infected calves were detected via culture and PCR assay together, PCR assay appeared to accurately identify M bovis at the farm level.
描述育肥牛和架子牛养殖场中牛支原体感染的流行情况,并比较细菌培养与聚合酶链反应(PCR)检测牛支原体的方法。
前瞻性描述性研究。
来自9个养殖场的432头3至9月龄犊牛。
从每头犊牛采集2份鼻拭子样本。通过细菌培养和PCR检测对拭子样本进行评估,以检测柔膜菌纲微生物和牛支原体。如果在21天内没有生长,则培养结果被视为阴性。PCR检测出现特征性菌落形成并经确认则表明为阳性结果。从1份拭子样本中提取脱氧核糖核酸用于直接PCR检测柔膜菌纲微生物和牛支原体。
432头犊牛中,通过PCR检测,374头(87%)柔膜菌纲微生物呈阳性,63头(15%)通过培养呈阳性。通过PCR检测,7头(2%)犊牛牛支原体呈阳性,10头(2%)通过培养呈阳性。在农场层面,柔膜菌纲微生物的流行率通过PCR检测为54%至100%,通过培养为0%至59%。牛支原体在农场层面的流行率通过PCR检测为0%至4%,通过培养为0%至6%。排出牛支原体的犊牛比未排出牛支原体的犊牛发烧的可能性显著更高。
在佐治亚州最近购买的育肥牛和架子牛犊牛中,检测到牛支原体感染水平较低。尽管联合使用培养和PCR检测发现的感染犊牛略多,但PCR检测似乎能在农场层面准确识别牛支原体。