首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Detection of Tropheryma whipplei DNA in Feces by PCR Using a Target Capture Method
【2h】

Detection of Tropheryma whipplei DNA in Feces by PCR Using a Target Capture Method

机译:利用目标捕获法通过PCR检测粪便中的惠特氏鞭毛虫DNA

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Whipple's disease is a rare multisystemic bacterial infection with variable clinical manifestations. For decades, the laboratory diagnosis was based on the demonstration of periodic acid Schiff-positive inclusions in macrophages of gastrointestinal biopsies. PCR has improved the diagnosis of Whipple's disease due to its increased sensitivity compared to histopathological analysis. To avoid invasive procedures for taking specimens, we have investigated the possibility of detecting Tropheryma whipplei DNA in feces rather than in biopsies or gastric aspirate of patients with and without Whipple's disease. Total bacterial DNA was isolated from stool specimens using Qiagen columns followed by a T. whipplei-specific hybridization step with a biotinylated capture probe and streptavidin-coated magnetic particles. The captured DNA was then amplified using the same seminested PCR targeting the 16S rRNA gene of the organism that had been applied to other specimens without capturing. For five of eight patients with Whipple's disease, duodenal biopsies and stool samples were PCR positive, whereas for the three other patients, both specimens were PCR negative. Of 84 patients without Whipple's disease, 75 tested negative in the duodenal biopsy and in the stool sample. For four, both specimens were positive. Five patients tested positive in the stool sample but not in the biopsy. However, for three of these five patients, the gastric aspirate had been PCR positive, indicating that the stool PCR result was true rather than false positive. Compared to PCR from duodenal biopsies, stool PCR has a sensitivity of 100% and a specificity of 97.3%. Additionally, 15 PCR-positive and 22 PCR-negative stool samples were extracted using the Invisorb Spin Stool DNA kit. The simplified stool extraction showed 93.3% sensitivity and 95.5% specificity compared to the target capture method. We conclude that PCR with stool specimens with either extraction method is a sensitive and specific diagnostic tool for the detection of T. whipplei DNA and one not requiring invasive sampling procedures.
机译:Whipple病是一种罕见的多系统细菌感染,具有多种临床表现。数十年来,实验室诊断一直基于胃肠道活检巨噬细胞中高碘酸席夫氏阳性包裹体的证实。与组织病理学分析相比,PCR具有更高的敏感性,因此提高了Whipple病的诊断水平。为了避免采取侵入性的方法来采集标本,我们调查了在患有和未患有Whipple病的患者中,而不是在活检或胃穿刺术中检测出Trophoyma whipplei DNA的可能性。使用Qiagen色谱柱从粪便标本中分离出总细菌DNA,然后使用生物素化捕获探针和链霉亲和素包被的磁性颗粒进行T.whipplei特异性杂交步骤。然后使用靶向该生物体的16S rRNA基因的相同半巢式PCR扩增捕获的DNA,该PCR已应用于其他标本而未捕获。对于八名Whipple病患者中的五名,十二指肠活检和粪便样本均为PCR阳性,而对于其他三名患者,两份样本均为PCR阴性。在84名无Whipple病的患者中,有75名在十二指肠活检和粪便样本中呈阴性。对于四个样本,两个样本均为阳性。五名患者的粪便样本呈阳性,但活检未呈阳性。但是,在这五名患者中的三名中,胃抽吸物已呈PCR阳性,表明粪便PCR结果为真而不是假阳性。与十二指肠活检的PCR相比,粪便PCR的敏感性为100%,特异性为97.3%。此外,使用Invisorb Spin Stool DNA试剂盒提取了15个PCR阳性和22个PCR阴性的粪便样品。与目标捕获方法相比,简化的粪便提取显示出93.3%的敏感性和95.5%的特异性。我们得出的结论是,用任一种提取方法对粪便标本进行PCR是检测T.whipplei DNA的灵敏且特异的诊断工具,并且不需要侵入性采样程序。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号