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印度克罗恩病患者肠道活检组织中未检测到鸟分枝杆菌副结核亚种特异性IS900序列。

Absence of Mycobacterium avium ss paratuberculosis-specific IS900 sequence in intestinal biopsy tissues of Indian patients with Crohn's disease.

作者信息

Sasikala Mitnala, Reddy D Nageshwar, Pratap Nitesh, Sharma Sanjeev Kumar, Balkumar P Reddy, Sekaran Anuradha, Banerjee Rupa, Reddy D Bhaskara

机构信息

Asian Health Care Foundation, Somajiguda, Hyderabad, 500 082, India.

出版信息

Indian J Gastroenterol. 2009 Sep-Oct;28(5):169-74. doi: 10.1007/s12664-009-0068-2. Epub 2010 Jan 27.

Abstract

BACKGROUND AND OBJECTIVE

The role of Mycobacterium avium ss paratuberculosis (MAP) in the etiopathology of Crohn's disease (CD) remains controversial, because of conflicting reports demonstrating the presence of MAP-specific insertion sequence from intestinal biopsy tissues of patients clinically diagnosed for the disease. The present study was carried out to investigate the presence of MAP DNA in the intestinal tissues of CD patients to ascertain the relevance of MAP in Indian patients with CD.

METHODS

Patients diagnosed as CD at our institute were recruited. Healthy individuals without inflammatory bowel disease served as controls. Mucosal biopsy specimens were collected from ileum and colon in duplicates and subjected to histopathological examination and polymerase chain reaction (PCR) amplification. Total DNA (81 CD patients, 85 healthy individuals) and total RNA (12 CD patients, 12 healthy individuals) isolated from tissue specimens was used for amplification of MAP-specific IS900 by nested PCR.

RESULTS

MAP-specific IS900 DNA and RNA could not be detected by nested PCR in the intestinal tissues of any patient with CD.

CONCLUSION

Our results do not support the etiological role of MAP in the pathogenesis of CD in Indian patients.

摘要

背景与目的

鸟分枝杆菌副结核亚种(MAP)在克罗恩病(CD)病因学中的作用仍存在争议,因为有相互矛盾的报道显示,在临床诊断为该病的患者肠道活检组织中存在MAP特异性插入序列。本研究旨在调查CD患者肠道组织中MAP DNA的存在情况,以确定MAP在印度CD患者中的相关性。

方法

招募在我院诊断为CD的患者。无炎症性肠病的健康个体作为对照。从回肠和结肠采集黏膜活检标本一式两份,进行组织病理学检查和聚合酶链反应(PCR)扩增。从组织标本中分离的总DNA(81例CD患者,85例健康个体)和总RNA(12例CD患者,12例健康个体)用于通过巢式PCR扩增MAP特异性IS900。

结果

通过巢式PCR在任何CD患者的肠道组织中均未检测到MAP特异性IS900 DNA和RNA。

结论

我们的结果不支持MAP在印度患者CD发病机制中的病因学作用。

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