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首页> 外文期刊>Tropical Animal Health and Production >Rapid detection of Corynebacterium pseudotuberculosis in clinical samples from sheep
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Rapid detection of Corynebacterium pseudotuberculosis in clinical samples from sheep

机译:绵羊临床样品中假结核棒杆菌的快速检测

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Corynebacterium pseudotuberculosis, a Gram-positive bacterium is the causative agent of caseous lymphadenitis (CLA), a chronic disease of sheep, goats and other warm blooded animals. In the present study, a total of 1,080 sheep reared under semi-intensive system on organized farms situated in the semi arid tropical region of Rajasthan, India, was clinically examined. Pus samples from superficial lymph nodes of 25 (2.31 %) adult sheep showing clinical lesions similar to CLA were collected for laboratory analyses. On the basis of morphological, cultural and biochemical characteristics 12 (48 %) bacterial isolates from pus identified it as C. pseudotuberculosis. A polymerase chain reaction (PCR) assay targeting Putative oligopeptide/dipeptide ABC transporter, nicotinamide adenine dinucleotide phosphate (NADP) oxidoreductase coenzyme F420-dependent and proline iminopeptidase (PIP) genes of C. pseudotuberculosis was developed that showed 14 pus samples as positive. All C. pseudotuberculosis isolates were also found positive for these genes in the PCR. The specificity of the PCR products was confirmed by sequencing of the amplified products that showed 98-100 % homology with published sequences available in the NCBI database. The present study shows the incidence of CLA as 2.31 %, 1.1 % and 1.29 % based on clinical, bacterial culture and direct pus PCR assay, respectively. The PCR assay was rapid, specific and as significant as bacterial culture in detecting bacteria directly in the clinical pus samples. The PCR assay developed in the study can be applied for the diagnosis and control of CLA. Furthermore, the assay can also be applied to detect C. pseudotuberculosis in various clinical samples.
机译:革兰氏阳性细菌假结核棒杆菌是干酪性淋巴结炎(CLA)的病原体,后者是绵羊,山羊和其他温血动物的慢性疾病。在本研究中,对印度拉贾斯坦邦半干旱热带地区有组织的农场在半精养系统下饲养的总共1,080只绵羊进行了临床检查。收集来自25只成年绵羊(2.31%)浅表淋巴结的脓液样本,显示出与CLA相似的临床病变,以进行实验室分析。根据形态,文化和生化特征,从脓液中分离出的12种细菌(48%)将其鉴定为假结核杆菌。针对假结核分枝杆菌的推定寡肽/二肽ABC转运蛋白,烟酰胺腺嘌呤二核苷酸磷酸(NADP)氧化还原酶辅酶F420基因和脯氨酸亚肽酶(PIP)基因进行了聚合酶链反应(PCR)分析,结果显示14例脓液样本为阳性。在PCR中也发现所有假结核梭菌分离物对这些基因都是阳性的。通过对扩增产物进行测序证实了PCR产物的特异性,所述扩增产物显示出与NCBI数据库中可获得的公开序列具有98-100%的同源性。根据临床,细菌培养和直接脓液PCR检测,本研究显示CLA的发生率分别为2.31%,1.1%和1.29%。 PCR检测快速,专一且与细菌培养一样重要,可直接在临床脓液样本中检测细菌。该研究开发的PCR检测方法可用于CLA的诊断和控制。此外,该测定法还可以用于检测各种临床样品中的假结核梭菌。

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