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首页> 外文期刊>Journal of Clinical Microbiology >Diagnosing Herpesvirus Infections by Real-Time Amplification and Rapid Culture
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Diagnosing Herpesvirus Infections by Real-Time Amplification and Rapid Culture

机译:通过实时扩增和快速培养诊断疱疹病毒感染

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Procedures using real-time technique were developed to demonstrate the presence of herpes simplex virus type 1 (HSV-1) and HSV-2, varicella zoster virus (VZV), and cytomegalovirus (CMV) in miscellaneous clinical specimens. The assays were compared to rapid culture using centrifugation followed by detection with monoclonal antibodies. A total of 711 consecutive samples were collected from different patient groups. Throat swabs were obtained from transplant patients; dermal or oral specimens were collected from patients suspected for VZV or HSV infection. Genital specimens were taken from patients who attended the Clinic for Sexually Transmitted Diseases at the Dijkzigt Hospital Rotterdam presenting with symptoms of a primary genital ulcer. Nucleic acid extraction was carried out using a MagnaPure LC instrument. The amplification steps were performed on the ABI Prism 7700 sequence detection system. To monitor the process of extraction and amplification, a universal control consisting of seal herpesvirus type 1 (PhHV-1) was added to the clinical specimens. By culture 127 of 668 (19%) samples were positive for HSV-1, 72 of 668 (10.8%) specimens were positive for HSV-2, and 17 of 366 (4.6%) were positive for VZV. Using real-time amplification the numbers of positive specimens were 143 of 668 (21.4%), 97 of 668 (14.5%), and 27 of 366 (7.4%), respectively. Eighty-six specimens were tested for CMV, 12 (14.0%) were positive by culture, and 17 (19.8%) were positive by real-time PCR. The clinical data of the patients with discrepant results were reviewed thoroughly. In all cases the patients with only real-time PCR-positive results could be considered as truly infected. We concluded that the real-time amplification technique is suitable for the detection of human herpesvirus infection. It offers a semiquantitative and reliable assay with a quick result that is more sensitive than rapid culture, especially for the diagnosis of HSV-2 and VZV infections.
机译:开发了使用实时技术的程序,以证明杂项临床标本中存在1型单纯疱疹病毒(HSV-1)和HSV-2,水痘带状疱疹病毒(VZV)和巨细胞病毒(CMV)。将测定与使用离心的快速培养进行比较,然后用单克隆抗体进行检测。从不同患者组收集了总共711个连续样本。咽拭子取自移植患者;从怀疑有VZV或HSV感染的患者中收集皮肤或口腔标本。生殖器标本取自在鹿特丹迪克吉格特医院就诊的性传播疾病患者,出现原发性生殖器溃疡症状。使用MagnaPure LC仪器进行核酸提取。扩增步骤在ABI Prism 7700序列检测系统上进行。为了监测提取和扩增的过程,在临床标本中添加了由1型海豹疱疹病毒(PhHV-1)组成的通用对照。通过培养668个样本中的127个(19%)对HSV-1呈阳性,668个样本中的72个(10.8%)对HSV-2呈阳性,而366个样本中的17个(4.6%)对VZV呈阳性。使用实时扩增,阳性标本的数量分别为668个样本中的143个(21.4%),668个样本中的97个(14.5%)和366个样本中的27个(7.4%)。测试了86份标本的CMV,通过培养阳性12份(14.0%),通过实时PCR阳性17份(19.8%)。对结果不一的患者的临床资料进行了全面回顾。在所有情况下,仅具有实时PCR阳性结果的患者都可以视为真正感染。我们得出的结论是,实时扩增技术适用于检测人类疱疹病毒感染。它提供了一种半定量,可靠的测定方法,具有比快速培养更为灵敏的快速结果,尤其是对于HSV-2和VZV感染的诊断。

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