Department of Bacteriology, Mycology, and Immunology, Faculty of Veterinary Medicine, University of Sadat City, Sadat City, Menoufia, 32897, Egypt.
Department of Molecular Biology, Genetic Engineering, and Biotechnology Research Institute, University of Sadat City, Sadat City, Menoufia, Egypt.
BMC Microbiol. 2022 Jun 11;22(1):154. doi: 10.1186/s12866-022-02568-0.
Mycobacterium bovis notoriously causes detrimental infections in bovines and humans. In this study, 1500 buffaloes and 2200 cattle were tested by single intradermal comparative cervical tuberculin test and compared with the detection rates of M. bovis isolation, real-time and simplex PCR, and flow Cytometry.
The tuberculin test is the reference test in Egypt, the positive rate was 54/3700 (1.5%) composed of 18/1500 (1.2%) buffaloes and 36/2200 (1.6%) cattle which were mandatorily slaughtered under the Egyptian legislation, after postmortem examination the non-visible-lesion proportion was 39/54 (72.2%) which surpassed the visible-lesion rate 15/54 (27.8%) with (p < 0.0001). The samples from each case were pooled into one sample representing the case, and the isolation rate of M. bovis was 25/54 (46.3%). Real-time PCR using atpE was positive for mycobacteria on the genus level in 18/18 (100%) and 5/5 (100%) of tissue samples and isolates, respectively; simplex PCR detected M. bovis in 44/54 (81.5%) and 25/25 (100%) of tissue samples and isolates, respectively. Flow Cytometry evaluation of the CD4, CD8, WC1δγ, and CD2 cell phenotypes showed increased counts in the tuberculin-positive cases compared with negative cases (p < 0.0001), and these phenotypes in the tuberculin-positive cases increased after antigen stimulation than in the negative cases (p < 0.0001). Detection rates of PCR techniques and flow Cytometry exceeded that of bacterial isolation (p < 0.0001) and exhibited a strong correlation.
The skin test suffers from interference from non-tuberculous mycobacteria able to cause false-positive reactions in cattle and other species. Real-time PCR using atpE, conventional PCR targeting RDs, and flow Cytometry are rapid and accurate methods that correlate with the isolation and can be promising for detection and confirmation of infected live and slaughtered cases.
牛分枝杆菌在牛和人类中引起严重感染,臭名昭著。在这项研究中,采用单点皮内比较颈结核菌素试验对 1500 头水牛和 2200 头牛进行了检测,并与牛分枝杆菌分离物的检测率、实时和单重 PCR 以及流式细胞术进行了比较。
结核菌素试验是埃及的参考试验,阳性率为 54/3700(1.5%),其中 18/1500(1.2%)为水牛,36/2200(1.6%)为牛,根据埃及法规,这些动物必须被强制宰杀,尸检后发现无可见病变的比例为 39/54(72.2%),超过了有可见病变的比例 15/54(27.8%)(p<0.0001)。每个病例的样本都汇集到一个样本中代表该病例,牛分枝杆菌的分离率为 25/54(46.3%)。使用 atpE 的实时 PCR 对组织样本和分离物中的属水平分枝杆菌呈阳性,分别为 18/18(100%)和 5/5(100%);单重 PCR 分别检测到 44/54(81.5%)和 25/25(100%)的组织样本和分离物中的牛分枝杆菌。流式细胞术对 CD4、CD8、WC1δγ 和 CD2 细胞表型的评估显示,与阴性病例相比,结核菌素阳性病例的计数增加(p<0.0001),并且在抗原刺激后,阳性病例的这些表型比阴性病例增加(p<0.0001)。PCR 技术和流式细胞术的检测率均高于细菌分离率(p<0.0001),且相关性较强。
皮肤试验受到非结核分枝杆菌的干扰,这些分枝杆菌能够在牛和其他物种中引起假阳性反应。使用 atpE 的实时 PCR、针对 RDs 的常规 PCR 和流式细胞术是快速准确的方法,与分离物相关,可用于检测和确认受感染的活牛和屠宰牛。