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印度拉贾斯坦邦西罗希山羊干酪性淋巴结炎的流行病学、细菌学及分子研究

Epidemiological, bacteriological and molecular studies on caseous lymphadenitis in Sirohi goats of Rajasthan, India.

作者信息

Kumar Jyoti, Singh Fateh, Tripathi Bhupendra Nath, Kumar Rajiv, Dixit Shivendra Kumar, Sonawane Ganesh Gangaram

机构信息

Division of Animal Health, Central Sheep and Wool Research Institute, Avikanagar, 304501, India.

出版信息

Trop Anim Health Prod. 2012 Oct;44(7):1319-22. doi: 10.1007/s11250-012-0102-8. Epub 2012 Feb 29.

Abstract

Corynebacterium pseudotuberculosis is the causative agent of caseous lymphadenitis (CL), a chronic debilitating disease of goats. In the present study, a total of 575 goats of Sirohi breed on an organized farm situated in the semi-arid tropical region of Rajasthan, India were clinically examined. Pus samples from superficial lymph nodes of 27 (4.7%) adult goats presenting clinical lesions suggestive of CL were collected for bacteriological and molecular analyses. Of these goats, 51.9% yielded C. pseudotuberculosis on the basis of morphological, cultural and biochemical characteristics. A polymerase chain reaction (PCR) assay targeting proline iminopeptidase gene specific to C. pseudotuberculosis was developed that confirmed all 14 bacterial isolates. The specificity of the PCR product was confirmed by sequencing of the 551-bp amplicon in both senses, showing 98-100% homology with published sequences. Thus, overall prevalence rate based on clinical, bacterial culture and PCR assay were found to be 4.7%, 2.4% and 2.4%, respectively. The PCR assay developed in this study was found to be specific and rapid, and could be used for confirmation of CL in goats as an alternative method to generally cumbersome, time-consuming and less reliable conventional methods.

摘要

伪结核棒状杆菌是山羊干酪性淋巴结炎(CL)的病原体,CL是一种使山羊衰弱的慢性疾病。在本研究中,对位于印度拉贾斯坦邦半干旱热带地区一个集约化养殖场的575只西罗希品种山羊进行了临床检查。从27只(4.7%)出现提示CL临床病变的成年山羊的浅表淋巴结采集脓液样本,用于细菌学和分子分析。在这些山羊中,基于形态学、培养和生化特征,51.9%的样本检出伪结核棒状杆菌。开发了一种针对伪结核棒状杆菌特异性脯氨酸亚氨基肽酶基因的聚合酶链反应(PCR)检测方法,该方法证实了所有14株细菌分离株。通过对551 bp扩增子的双向测序证实了PCR产物的特异性,与已发表序列显示出98 - 100%的同源性。因此,基于临床、细菌培养和PCR检测的总体患病率分别为4.7%、2.4%和2.4%。本研究中开发的PCR检测方法具有特异性和快速性,可作为一种替代方法用于确诊山羊的CL,以替代通常繁琐、耗时且不太可靠的传统方法。

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