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用聚合酶链反应从猫抓病患儿化脓性淋巴结中检测汉赛巴尔通体DNA

Detection of Rochalimaea henselae DNA by polymerase chain reaction from suppurative nodes of children with cat-scratch disease.

作者信息

Goral S, Anderson B, Hager C, Edwards K M

机构信息

Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN.

出版信息

Pediatr Infect Dis J. 1994 Nov;13(11):994-7. doi: 10.1097/00006454-199411000-00011.

Abstract

A polymerase chain reaction (PCR) assay was designed to amplify DNA from Rochalimaea henselae, Rochalimaea quintana and Afipia felis in the purulent material from lymph nodes in three patients with clinical cat-scratch disease (CSD) and two patients with lymphadenitis from other causes. All of the patients with CSD had positive immunofluorescent antibody serology for R. henselae, while none of the controls was positive. PCR amplification confirmed the presence of R. henselae DNA and the absence of R. quintana and A. felis DNA in the purulent material from CSD patients. PCR samples from control patients were negative. The PCR amplification of R. henselae DNA was performed quickly and with great sensitivity and specificity. It confirmed the presence of R. henselae in the CSD patients and eliminated the need for more extensive diagnostic and therapeutic procedures.

摘要

设计了一种聚合酶链反应(PCR)检测方法,用于扩增3例临床猫抓病(CSD)患者淋巴结脓性物质以及2例其他原因引起的淋巴结炎患者脓性物质中汉氏罗卡利马氏体、五日罗卡利马氏体和阿菲彼亚 felis的DNA。所有CSD患者针对汉氏罗卡利马氏体的免疫荧光抗体血清学检测均为阳性,而对照组均为阴性。PCR扩增证实CSD患者脓性物质中存在汉氏罗卡利马氏体DNA,不存在五日罗卡利马氏体和阿菲彼亚 felis DNA。对照患者的PCR样本为阴性。汉氏罗卡利马氏体DNA的PCR扩增快速,且具有很高的敏感性和特异性。它证实了CSD患者中存在汉氏罗卡利马氏体,无需进行更广泛的诊断和治疗程序。

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