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通过三次巢式扩增检测免疫功能正常和免疫功能低下患者临床样本(包括外周血)中的亨氏巴尔通体DNA。

Detection of Bartonella henselae DNA in clinical samples including peripheral blood of immune competent and immune compromised patients by three nested amplifications.

作者信息

Kawasato Karina Hatamoto, de Oliveira Léa Campos, Velho Paulo Eduardo Neves Ferreira, Yamamoto Lidia, Del Negro Gilda Maria Barbaro, Okay Thelma Suely

机构信息

Children's Institute, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.

出版信息

Rev Inst Med Trop Sao Paulo. 2013 Jan-Feb;55(1):1-6. doi: 10.1590/s0036-46652013000100001.

Abstract

Bacteria of the genus Bartonella are emerging pathogens detected in lymph node biopsies and aspirates probably caused by increased concentration of bacteria. Twenty-three samples of 18 patients with clinical, laboratory and/or epidemiological data suggesting bartonellosis were subjected to three nested amplifications targeting a fragment of the 60-kDa heat shock protein (HSP), the internal transcribed spacer 16S-23S rRNA (ITS) and the cell division (FtsZ) of Bartonella henselae, in order to improve detection in clinical samples. In the first amplification 01, 04 and 05 samples, were positive by HSP (4.3%), FtsZ (17.4%) and ITS (21.7%), respectively. After the second round six positive samples were identified by nested-HSP (26%), eight by nested-ITS (34.8%) and 18 by nested-FtsZ (78.2%), corresponding to 10 peripheral blood samples, five lymph node biopsies, two skin biopsies and one lymph node aspirate. The nested-FtsZ was more sensitive than nested-HSP and nested-ITS (p < 0.0001), enabling the detection of Bartonella henselae DNA in 15 of 18 patients (83.3%). In this study, three nested-PCR that should be specific for Bartonella henselae amplification were developed, but only the nested-FtsZ did not amplify DNA from Bartonella quintana. We conclude that nested amplifications increased detection of B. henselae DNA, and that the nested-FtsZ was the most sensitive and the only specific to B. henselae in different biological samples. As all samples detected by nested-HSP and nested-ITS, were also by nested-FtsZ, we infer that in our series infections were caused by Bartonella henselae. The high number of positive blood samples draws attention to the use of this biological material in the investigation of bartonellosis, regardless of the immune status of patients. This fact is important in the case of critically ill patients and young children to avoid more invasive procedures such as lymph nodes biopsies and aspirates.

摘要

巴尔通体属细菌是在淋巴结活检和穿刺物中检测到的新兴病原体,可能是由于细菌浓度增加所致。对18例具有临床、实验室和/或流行病学数据提示巴尔通体病的患者的23份样本进行了三次巢式扩增,靶向60 kDa热休克蛋白(HSP)片段、16S - 23S核糖体RNA内部转录间隔区(ITS)以及亨氏巴尔通体的细胞分裂蛋白(FtsZ),以提高临床样本中的检测率。在第一次扩增中,分别有01、04和05份样本通过HSP(4.3%)、FtsZ(17.4%)和ITS(21.7%)检测呈阳性。第二轮后,通过巢式 - HSP鉴定出6份阳性样本(26%),通过巢式 - ITS鉴定出8份阳性样本(34.8%),通过巢式 - FtsZ鉴定出18份阳性样本(78.2%),分别对应10份外周血样本、5份淋巴结活检样本、2份皮肤活检样本和1份淋巴结穿刺物。巢式 - FtsZ比巢式 - HSP和巢式 - ITS更敏感(p < 0.0001),能够在18例患者中的15例(83.3%)检测到亨氏巴尔通体DNA。在本研究中,开发了三种应特异性用于亨氏巴尔通体扩增的巢式PCR,但只有巢式 - FtsZ未扩增五日热巴尔通体的DNA。我们得出结论,巢式扩增增加了亨氏巴尔通体DNA的检测率,并且巢式 - FtsZ在不同生物样本中是最敏感且唯一特异性针对亨氏巴尔通体的。由于通过巢式 - HSP和巢式 - ITS检测到的所有样本也都通过巢式 - FtsZ检测到,我们推断在我们的系列研究中感染是由亨氏巴尔通体引起的。大量阳性血液样本促使人们关注在巴尔通体病调查中使用这种生物材料,无论患者的免疫状态如何。这一事实在重症患者和幼儿的情况下很重要,以避免更具侵入性的程序,如淋巴结活检和穿刺。

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