Department of Microbiology, Faculty of Veterinary Medicine, Selçuk University, Campus, 42 075, Konya, Turkey.
Theriogenology. 2010 Sep 1;74(4):658-62. doi: 10.1016/j.theriogenology.2010.03.023. Epub 2010 May 7.
The aim of this study was to standardize and evaluate a PCR assay for the detection of Brucella canis (B. canis) in lymph node samples of naturally infected dogs. The performance of the PCR was compared with the results of bacteriological culture as reference method. Forty-eight inguinal lymph node samples were collected from 48 dogs (18 males and 30 females) that died in the city's pound in the years 2007-2008 and were examined by microbiological culture and the PCR assay. B. canis was isolated from 4 (8.3%) of 48 lymph node samples. Forty-four (91.7%) of the samples were bacteriological culture negative. B. canis DNA was directly detected from all culture positive lymph node samples (n = 4) by PCR. All of the culture negative samples were confirmed as negative by PCR. When the culture method was used as a gold standard, sensitivity and specificity of the PCR assay were found to be 100%. The limit of PCR detection of B. canis DNA was 1.4 x 10(1) CFU/g at least. In conclusion, the PCR assay has been shown to have a diagnostic performance equal to bacteriological culture for detection of B. canis. By a non-hazardous protocol for laboratory workers, the assay can be performed in one day.
本研究旨在标准化和评估用于检测自然感染犬布鲁氏菌(B. canis)的 PCR 检测方法。将 PCR 检测结果与细菌培养作为参考方法进行比较。从 2007 年至 2008 年死于城市收容所的 48 只狗(18 只雄性和 30 只雌性)的腹股沟淋巴结样本中采集了 48 个样本,通过微生物培养和 PCR 检测进行了检查。从 48 个淋巴结样本中分离出 4 个(8.3%)B. canis。44 个(91.7%)样本细菌培养阴性。PCR 可直接从所有培养阳性的淋巴结样本(n = 4)中检测到 B. canis DNA。所有培养阴性的样本均通过 PCR 确认为阴性。当培养方法用作金标准时,PCR 检测的敏感性和特异性均为 100%。PCR 检测 B. canis DNA 的检测限至少为 1.4 x 10(1) CFU/g。总之,PCR 检测在检测 B. canis 方面的诊断性能与细菌培养相当。通过对实验室工作人员无危害的方案,该检测可在一天内完成。