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1
Detection of Coxiella burnetii in heart valve sections by fluorescence in situ hybridization.通过荧光原位杂交技术检测心脏瓣膜切片中的伯氏考克斯体。
J Med Microbiol. 2018 Apr;67(4):537-542. doi: 10.1099/jmm.0.000704. Epub 2018 Feb 20.
2
Bartonella henselae is usually not viable in lymph nodes of patients with cat scratch disease.汉赛巴尔通体通常在猫抓病患者的淋巴结中无法存活。
Eur J Clin Microbiol Infect Dis. 2017 Nov;36(11):2207-2213. doi: 10.1007/s10096-017-3047-z. Epub 2017 Jul 2.
3
Presence of Coxiella burnetii DNA in inflamed bovine cardiac valves.伯纳特柯克斯体DNA在发炎的牛心脏瓣膜中的存在。
BMC Vet Res. 2017 Mar 9;13(1):69. doi: 10.1186/s12917-017-0988-5.
4
From Q Fever to Coxiella burnetii Infection: a Paradigm Change.从Q热到伯氏考克斯氏体感染:范式转变
Clin Microbiol Rev. 2017 Jan;30(1):115-190. doi: 10.1128/CMR.00045-16.
5
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6
Deglycosylation of Tropheryma whipplei biofilm and discrepancies between diagnostic results during Whipple's disease progression.惠普尔嗜组织菌生物膜的去糖基化与惠普尔病进展过程中诊断结果的差异
Sci Rep. 2016 Mar 30;6:23883. doi: 10.1038/srep23883.
7
Treatment and Prophylactic Strategy for Coxiella burnetii Infection of Aneurysms and Vascular Grafts: A Retrospective Cohort Study.动脉瘤和血管移植物的伯氏考克斯体感染的治疗与预防策略:一项回顾性队列研究
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Complementarity between targeted real-time specific PCR and conventional broad-range 16S rDNA PCR in the syndrome-driven diagnosis of infectious diseases.靶向实时特异性PCR与传统广谱16S rDNA PCR在传染病综合征驱动诊断中的互补性。
Eur J Clin Microbiol Infect Dis. 2015 Mar;34(3):561-70. doi: 10.1007/s10096-014-2263-z. Epub 2014 Oct 28.
9
Chronic Q fever in the Netherlands 5 years after the start of the Q fever epidemic: results from the Dutch chronic Q fever database.荷兰Q热疫情开始5年后的慢性Q热:来自荷兰慢性Q热数据库的结果
J Clin Microbiol. 2014 May;52(5):1637-43. doi: 10.1128/JCM.03221-13. Epub 2014 Mar 5.
10
Persistence of DNA in a cured patient and positive culture in cases with low antibody levels bring into question diagnosis of Q fever endocarditis.在已治愈的患者中 DNA 的持续存在以及抗体水平较低的病例中的阳性培养结果,使 Q 热心内膜炎的诊断受到质疑。
J Clin Microbiol. 2013 Sep;51(9):3012-7. doi: 10.1128/JCM.00812-13. Epub 2013 Jul 12.

荧光原位杂交(FISH)和基于肽核酸探针的 FISH 诊断 Q 热心内膜炎和血管感染。

Fluorescence Hybridization (FISH) and Peptide Nucleic Acid Probe-Based FISH for Diagnosis of Q Fever Endocarditis and Vascular Infections.

机构信息

Aix Marseille Université, IRD, AP-HM, MEPHI, IHU-Méditerranée Infection, Marseille, France.

Aix Marseille Université, IRD, AP-HM, VITROME, IHU-Méditerranée Infection, Marseille, France.

出版信息

J Clin Microbiol. 2018 Aug 27;56(9). doi: 10.1128/JCM.00542-18. Print 2018 Sep.

DOI:10.1128/JCM.00542-18
PMID:29899006
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6113452/
Abstract

Endocarditis and vascular infections are common manifestations of persistent localized infection due to , and recently, fluorescence hybridization (FISH) was proposed as an alternative tool for their diagnosis. In this study, we evaluated the efficiency of FISH in a series of valve and vascular samples infected by We tested 23 -positive valves and thrombus samples obtained from patients with Q fever endocarditis. Seven aneurysms and thrombus specimens were retrieved from patients with Q fever vascular infections. Samples were analyzed by culture, immunochemistry, and FISH with oligonucleotide and PNA probes targeting -specific 16S rRNA sequences. The immunohistochemical analysis was positive for five (17%) samples with significantly more copies of DNA than the negative ones ( = 0.02). FISH was positive for 13 (43%) samples and presented 43% and 40% sensitivity compared to that for quantitative PCR (qPCR) and culture, respectively. PNA FISH detected in 18 (60%) samples and presented 60% and 55% sensitivity compared to that for qPCR and culture, respectively. Immunohistochemistry had 38% and 28% sensitivity compared to that for FISH and PNA FISH, respectively. Samples found positive by both immunohistochemistry and PNA FISH contained significantly more copies of DNA than the negative ones ( = 0.03). Finally, PNA FISH was more sensitive than FISH (60% versus 43%, respectively) for the detection of We provide evidence that PNA FISH and FISH are important assays for the diagnosis of endocarditis and vascular infections.

摘要

心内膜炎和血管感染是由持续性局部感染引起的常见表现,最近荧光杂交(FISH)被提议作为其诊断的替代工具。在这项研究中,我们评估了 FISH 在一系列感染 的心瓣膜和血管样本中的效率。我们测试了 23 例由 Q 热心内膜炎患者获得的阳性瓣膜和血栓样本。从 Q 热血管感染患者中获得了 7 个动脉瘤和血栓标本。使用针对 -特异性 16S rRNA 序列的寡核苷酸和 PNA 探针通过培养、免疫化学和 FISH 分析样本。免疫组织化学分析对 5 个(17%)样本呈阳性,这些样本的 DNA 拷贝数明显高于阴性样本(=0.02)。FISH 对 13 个(43%)样本呈阳性,与定量 PCR(qPCR)和培养相比,其灵敏度分别为 43%和 40%。PNA FISH 在 18 个(60%)样本中检测到 ,与 qPCR 和培养相比,其灵敏度分别为 60%和 55%。免疫组织化学与 FISH 和 PNA FISH 相比,其灵敏度分别为 38%和 28%。通过免疫组织化学和 PNA FISH 均呈阳性的样本中 DNA 的拷贝数明显高于阴性样本(=0.03)。最后,PNA FISH 比 FISH 更敏感(分别为 60%和 43%),用于检测 我们提供了证据表明 PNA FISH 和 FISH 是诊断 心内膜炎和血管感染的重要检测方法。