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首页> 外文期刊>Journal of Clinical Microbiology >Systematic Evaluation of Different Nucleic Acid Amplification Assays for Cytomegalovirus Detection: Feasibility of Blood Donor Screening
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Systematic Evaluation of Different Nucleic Acid Amplification Assays for Cytomegalovirus Detection: Feasibility of Blood Donor Screening

机译:巨细胞病毒检测的不同核酸扩增检测的系统评价:献血者筛查的可行性

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Acute primary cytomegalovirus (CMV) infections, which commonly occur asymptomatically among blood donors, represent a significant risk for serious morbidity in immunocompromised patients (a major group of transfusion recipients). We implemented a routine CMV pool screening procedure for plasma for the identification of CMV DNA-positive donors, and we evaluated the sensitivities and performance of different CMV DNA amplification systems. Minipools (MPs) of samples from 18,405 individual donors (54,451 donations) were screened for CMV DNA using the RealStar CMV PCR assay (Altona Diagnostic Technologies), with a minimum detection limit of 11.14 IU/ml. DNA was extracted with a high-volume protocol (4.8 ml, Chemagic Viral 5K kit; PerkinElmer) for blood donor pool screening (MP-nucleic acid testing [NAT]) and with the Nuclisens easyMAG system (0.5 ml; bioMérieux) for individual donation (ID)-NAT. In total, six CMV DNA-positive donors (0.03%) were identified by routine CMV screening, with DNA concentrations ranging from 4.35 × 102 to 4.30 × 103 IU/ml. Five donors already showed seroconversion and detectable IgA, IgM, and/or IgG antibody titers (IgA+/IgM+/IgG? or IgA+/IgM+/IgG+), and one donor showed no CMV-specific antibodies. Comparison of three commercial assays, i.e., the RealStar CMV PCR kit, the Sentosa SA CMV quantitative PCR kit (Vela Diagnostics), and the CMV R-gene PCR kit (bioMérieux), for MP-NAT and ID-NAT showed comparably good analytical sensitivities, ranging from 10.23 to 11.14 IU/ml (MP-NAT) or from 37.66 to 57.94 IU/ml (ID-NAT). The clinical relevance of transfusion-associated CMV infections requires further investigation, and the evaluated methods present powerful basic tools providing sensitive possibilities for viral testing. The application of CMV MP-NAT facilitated the identification of one donor with a window-phase donation during acute primary CMV infection.
机译:急性原发性巨细胞病毒(CMV)感染通常无症状地出现在献血者中,在免疫功能低下的患者(主要输血群体)中,存在严重发病的重大风险。我们实施了常规的血浆CMV池筛选程序,以鉴定CMV DNA阳性供体,并评估了不同CMV DNA扩增系统的敏感性和性能。使用RealStar CMV PCR测定法(Altona Diagnostic Technologies),对来自18,405个个体供体(54,451个捐赠)的样品的微型培养液(MP)进行了CMV DNA筛选,最低检测限为11.14 IU / ml。用大体积实验方案(4.8 ml,Chemagic Viral 5K试剂盒; PerkinElmer)提取DNA用于献血者池筛查(MP核酸测试[NAT]),并使用Nuclisens easyMAG系统(0.5 ml;bioMérieux)进行个人捐献。 (ID)-NAT。常规CMV筛查共鉴定出6个CMV DNA阳性供体(0.03%),DNA浓度范围为4.35×10 2 至4.30×10 3 IU /毫升五名供体已经显示出血清转化和可检测的IgA,IgM和/或IgG抗体滴度(IgA + / IgM + / IgG ?或IgA < sup> + / IgM + / IgG + ),一位供体未显示CMV特异性抗体。比较三种商业化检测方法,即RealStar CMV PCR试剂盒,Sentosa SA CMV定量PCR试剂盒(Vela Diagnostics)和CMV R基因PCR试剂盒(bioMérieux),它们对MP-NAT和ID-NAT的分析效果相当好敏感度范围为10.23至11.14 IU / ml(MP-NAT)或37.66至57.94 IU / ml(ID-NAT)。与输血相关的CMV感染的临床相关性需要进一步研究,并且所评估的方法提供了强大的基本工具,为病毒检测提供了敏感的可能性。 CMV MP-NAT的应用有助于在急性原发性CMV感染期间以窗口期捐赠的方式鉴定一名供体。

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