首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Detection of microsporidia (Enterocytozoon bieneusi) in intestinal biopsy specimens from human immunodeficiency virus-infected patients by PCR.
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Detection of microsporidia (Enterocytozoon bieneusi) in intestinal biopsy specimens from human immunodeficiency virus-infected patients by PCR.

机译:通过PCR检测人免疫缺陷病毒感染患者肠道活检标本中的小孢子虫(Enterocytozoon bieneusi)。

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摘要

Intestinal microsporidiosis has been implicated as a major cause of chronic diarrhea in human immunodeficiency virus (HIV)-infected patients. So far diagnosis depends on direct visualization of the parasites by light and transmission electron microscopy. We evaluated the diagnostic value of microsporidian DNA amplification by PCR on duodenal biopsy specimens obtained from patients with and without intestinal microsporidiosis caused by Enterocytozoon bieneusi. Thirteen HIV-infected patients (all CDC stage C3) were studied. Eight patients had intestinal microsporidiosis caused by E. bieneusi (n = 6), Septata intestinalis (n = 1), and Encephalitozoon cuniculi (n = 1); microsporidioses were diagnosed by light microscopy of stool samples and confirmed by light and electron microscopy of intestinal biopsy specimens. Five patients had no microsporidia in their stool samples or in their intestinal biopsy specimens, as examined by light and electron microscopy. Additionally, DNA prepared from Toxoplasma gondii derived from mouse ascites was used as a further control. A 353-bp DNA fragment of the small-subunit rRNA gene could be amplified from all six biopsy specimens infected with E. bieneusi, and the nature of the PCR products was confirmed by Southern blot hybridization. No amplification of DNA fragments was seen by using DNA extracted from biopsy specimens with S. intestinalis or E. cuniculi infection or without microsporidian infection and with template DNA extracted from T. gondii. The results suggest that PCR testing of intestinal biopsy specimens may be a useful approach to diagnosing microsporidiosis in HIV-infected patients.
机译:肠道小孢子虫病已被认为是感染人类免疫缺陷病毒(HIV)的患者慢性腹泻的主要原因。到目前为止,诊断取决于通过光镜和透射电子显微镜对寄生虫的直接观察。我们评估了通过PCR进行的微孢子虫DNA扩增对十二指肠活检标本的诊断价值,所述十二指肠活检标本来自有或没有由小肠肠杆菌引起的肠道微孢子虫病。研究了13名HIV感染患者(全部为CDC C3期)。八例患者的肠小孢子虫病是由比氏肠球菌(n = 6),小肠脓肿(n = 1)和钩形脑病(n = 1)引起的;通过粪便样品的光学显微镜检查可诊断出微孢子菌,并通过肠道活检样品的光学和电子显微镜检查来确认。通过光学和电子显微镜检查,五名患者的粪便样本或肠活检样本中均无小孢子虫。另外,将从弓形虫源于小鼠腹水制备的DNA用作进一步的对照。小亚基rRNA基因的353 bp DNA片段可从感染了比氏大肠杆菌的所有六个活检标本中扩增,PCR产物的性质已通过Southern印迹杂交得以证实。通过使用从肠炎链球菌或cu.cuniculi感染或无小孢子虫感染的活检标本中提取的DNA以及从弓形虫中提取的模板DNA,未观察到DNA片段的扩增。结果表明,肠道活检标本的PCR检测可能是诊断HIV感染患者微孢子虫病的有用方法。

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