Stich Roger W, Byrum Beverly, Love Brenda, Theus Natalie, Barber Linda, Shulaw William P
Department of Veterinary Preventive Medicine, The Ohio State University, 1900 Coffey Rd., Columbus, OH 43210-1092, USA.
J Microbiol Methods. 2004 Feb;56(2):267-75. doi: 10.1016/j.mimet.2003.10.013.
Cultivation of Mycobacterium avium subsp. paratuberculosis (M. paratuberculosis) from feces remains the most reliable method to detect infected animals. The purpose of this study was to evaluate a broth-based automated system used for cultivation of mycobacteria such as M. tuberculosis from human hosts, for the detection of M. paratuberculosis in bovine feces. Bovine feces was spiked with tenfold serial dilutions of M. paratuberculosis (5x10(5) to 5x10(-1) organisms), then processed with a double-centrifugation technique that included disinfection prior to inoculation into broth tubes. The same pathogen dilution series was also inoculated directly into broth and broth with uninfected processed feces. All of the system signal-positive bottles were identified within 30 days, with the highest concentration of M. paratuberculosis detected by the system in as few as 8 days. The presence of the pathogen was confirmed with acid-fast staining and an IS900-based PCR assay when growth of M. paratuberculosis was indicated by the system. However, some of the signal-negative cultures inoculated with the equivalent of 0.5 organisms tested PCR-positive 56 days post-inoculation, indicating that longer culture periods may lead to detection of small quantities of the organisms. Additionally, it was indicated that the processing step had a detrimental effect on detection of the organism. Comparison of the broth- and Herrold's egg yolk medium (HEYM) solid media-based culture methods with defined check test specimens corroborated the experimental evaluation of this system, indicating that broth-based detection could provide a more rapid assay for M. paratuberculosis. These results suggest that this automated system could be used to detect this organism in bovine feces, but that new approaches to processing the feces for culture should be explored.
从粪便中培养副结核分枝杆菌(M. paratuberculosis)仍然是检测受感染动物最可靠的方法。本研究的目的是评估一种基于肉汤的自动化系统,该系统用于培养来自人类宿主的结核分枝杆菌等分枝杆菌,以检测牛粪便中的副结核分枝杆菌。将副结核分枝杆菌的十倍系列稀释液(5×10⁵至5×10⁻¹个菌体)加入牛粪便中,然后采用双重离心技术进行处理,该技术包括在接种到肉汤管之前进行消毒。相同的病原体稀释系列也直接接种到肉汤以及含有未感染处理粪便的肉汤中。所有系统信号阳性的瓶子在30天内被鉴定出来,该系统检测到的副结核分枝杆菌最高浓度在短短8天内即可检测到。当系统显示副结核分枝杆菌生长时,通过抗酸染色和基于IS900的PCR检测法确认病原体的存在。然而,一些接种了相当于0.5个菌体的信号阴性培养物在接种后56天PCR检测呈阳性,这表明更长的培养时间可能导致检测到少量的菌体。此外,结果表明处理步骤对该菌体的检测有不利影响。用确定的对照测试样本对基于肉汤和赫罗尔德蛋黄培养基(HEYM)固体培养基的培养方法进行比较,证实了该系统的实验评估结果,表明基于肉汤的检测可为副结核分枝杆菌提供更快速的检测方法。这些结果表明,该自动化系统可用于检测牛粪便中的这种菌体,但应探索新的粪便处理方法用于培养。