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肉芽肿性卡氏肺孢子虫肺炎:支气管肺泡灌洗样本的DNA扩增研究

Granulomatous Pneumocystis carinii pneumonia: DNA amplification studies on bronchoscopic alveolar lavage samples.

作者信息

Wakefield A E, Miller R F, Guiver L A, Hopkin J M

机构信息

Department of Paediatrics, John Radcliffe Hospital, Oxford.

出版信息

J Clin Pathol. 1994 Jul;47(7):664-6. doi: 10.1136/jcp.47.7.664.

Abstract

Three HIV positive subjects presented with symptoms and radiographic changes suggestive of Pneumocystis carinii pneumonia. Methenamine silver staining of bronchoscopic alveolar lavage (BAL) fluid was negative (from one sample in one patient and two samples in the other two patients). Open lung biopsy was performed because of uncertain clinical progress and diagnosis; all three patients were found to have multiple pulmonary granulomata encasing numerous P carinii organisms. DNA amplification, using P carinii specific oligonucleotides, was performed on stored bronchoscopic BAL samples. P carinii specific amplification product was detected by ethidium bromide staining after electrophoretic separation on agarose gel in one case, and by the more sensitive technique of oligohybridisation in all three cases. In granulomatous P carinii pneumonia organisms are rarely identified in bronchoscopic alveolar lavage samples using histochemical staining, but are detectable by DNA amplification, although not at levels which can be readily distinguished from low, subclinical infection.

摘要

三名HIV阳性患者出现了提示卡氏肺孢子虫肺炎的症状和影像学改变。支气管肺泡灌洗(BAL)液的亚甲胺银染色呈阴性(一名患者的一个样本以及另外两名患者的两个样本)。由于临床进展和诊断不确定,进行了开胸肺活检;所有三名患者均发现有多个肺肉芽肿,其中包裹着大量卡氏肺孢子虫。使用卡氏肺孢子虫特异性寡核苷酸对储存的支气管镜BAL样本进行DNA扩增。在一例中,经琼脂糖凝胶电泳分离后,用溴化乙锭染色检测到卡氏肺孢子虫特异性扩增产物,在所有三例中均通过更敏感的寡杂交技术检测到。在肉芽肿性卡氏肺孢子虫肺炎中,使用组织化学染色在支气管肺泡灌洗样本中很少能鉴定出病原体,但通过DNA扩增可以检测到,尽管其水平与低水平的亚临床感染难以区分。

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Detection of Pneumocystis carinii with DNA amplification.采用DNA扩增技术检测卡氏肺孢子虫。
Lancet. 1990 Aug 25;336(8713):451-3. doi: 10.1016/0140-6736(90)92008-6.

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Detection of Pneumocystis carinii with DNA amplification.采用DNA扩增技术检测卡氏肺孢子虫。
Lancet. 1990 Aug 25;336(8713):451-3. doi: 10.1016/0140-6736(90)92008-6.

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