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多发性硬化症(MS)患者脑、血液和脑脊液中支原体特异性DNA序列缺失:一项采用聚合酶链反应(PCR)和实时聚合酶链反应(real-time PCR)的研究

Absence of Mycoplasma-specific DNA sequence in brain, blood and CSF of patients with multiple sclerosis (MS): a study by PCR and real-time PCR.

作者信息

Casserly Georgina, Barry Thomas, Tourtellotte Wallace W, Hogan Edward L

机构信息

Molecular Diagnostics Laboratory, Department of Microbiology, National University of Ireland Galway, University Road, Galway, Ireland.

出版信息

J Neurol Sci. 2007 Feb 15;253(1-2):48-52. doi: 10.1016/j.jns.2006.11.017. Epub 2007 Jan 17.

Abstract

Mycoplasmas are the smallest of the known self-replicating organisms. They lack cell walls and are associated with numerous diseases in humans and animals. We are exploring the possibility that infection by Mycoplasma may induce the inflammatory demyelinating disease of the central nervous system (CNS) that is MS. The presence of specific Mycoplasma species DNA was sought in brain, serum and cerebrospinal fluid (CSF) of patients diagnosed with multiple sclerosis (MS) and other neurological diseases (OND) including inflammatory disorders. The MS samples from patients with active and progressive MS, as well as in remission, a variety of other neurological disease controls, including inflammatory CNS diseases such as meningitis, cryptococcal meningitis and encephalitis and other neurological disorders such as migraine were also examined. Clinical samples were provided by the National Neurological Research Specimen Bank and the Human Brain and Spinal Fluid Resource Centre, Los Angeles. Analysis was carried out by conventional PCR using Mycoplasma-specific primers (McAuliffe et al., 2005) that target the 16S rDNA gene in Mycoplasma species. The Mycoplasma-specific primers could detect 102 Mycoplasma species. In this study, 30 samples of human brain and 57 pairs of serum and CSF and were examined. No Mycoplasma-specific nucleic acid sequence was detected, and the consistent observation of an endogenous gene, human serum albumin (HSA), as a positive control documented the adequacy of the method. Real-time PCR analysis of serum and CSF was done also targeting utilizing the Mycoplasma 16S rDNA gene, and this also demonstrated the lack of Mycoplasma in these samples. The presence of Mycoplasma at extraneural sites in MS patients is now being explored.

摘要

支原体是已知的能够自我复制的最小生物体。它们没有细胞壁,与人类和动物的多种疾病有关。我们正在探索支原体感染可能诱发中枢神经系统(CNS)炎性脱髓鞘疾病即多发性硬化症(MS)的可能性。在被诊断为多发性硬化症(MS)以及包括炎性疾病在内的其他神经系统疾病(OND)的患者的脑、血清和脑脊液(CSF)中寻找特定支原体物种DNA的存在。还对处于活动期和进展期的MS患者以及缓解期患者的MS样本,以及包括脑膜炎、隐球菌性脑膜炎和脑炎等炎性中枢神经系统疾病以及偏头痛等其他神经系统疾病在内的各种其他神经系统疾病对照样本进行了检测。临床样本由国家神经学研究标本库以及洛杉矶的人脑和脊髓液资源中心提供。使用针对支原体物种中16S rDNA基因的支原体特异性引物(McAuliffe等人,2005年)通过常规PCR进行分析。该支原体特异性引物能够检测102种支原体物种。在本研究中,对30份人脑样本以及57对血清和脑脊液样本进行了检测。未检测到支原体特异性核酸序列,并且作为阳性对照对一种内源性基因人血清白蛋白(HSA)的一致观察证明了该方法的充分性。还利用支原体16S rDNA基因对血清和脑脊液进行了实时PCR分析,这也证明了这些样本中不存在支原体。目前正在探索MS患者神经外部位支原体的存在情况。

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