首页> 外文期刊>Journal of Virological Methods >Detection of human herpesviruses HHV-6, HHV-7 and HHV-8 in whole blood by real-time PCR using the new CMV, HHV-6, 7, 8 R-genetrade mark kit.
【24h】

Detection of human herpesviruses HHV-6, HHV-7 and HHV-8 in whole blood by real-time PCR using the new CMV, HHV-6, 7, 8 R-genetrade mark kit.

机译:使用新型CMV,HHV-6、7、8 R-genetrade mark试剂盒通过实时PCR检测全血中的人类疱疹病毒HHV-6,HHV-7和HHV-8。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Human herpesviruses 6 (HHV-6), 7 (HHV-7) and 8 (HHV-8) are lymphotropic herpesviruses that may cause opportunistic diseases in immunosuppressed patients such as transplant or AIDS patients. The new commercial CMV HHV-6, 7, 8 R-genetrade mark kit (Argene, Varilhes, France) for the simultaneous quantitation of HHV-6 and qualitative detection of HHV-7 and HHV-8 was evaluated using whole blood samples (respectively, n=175, 100 and 161) and using different extraction and real-time PCR platforms in two Centers A and B. In comparison with HHV-6 in-house real-time PCR the commercial kit showed agreements of 96% (n=75) and 85% (n=100) in A and B, respectively, with significant Spearman's correlation between both techniques (in A: r=0.97 [p<0.001]; in B: r=0.70 [p<0.001]). The Bland-Altman test results and prospective monitoring of patients confirmed the accuracy of these HHV-6 real-time PCR techniques. The agreement between the in-house HHV-7 PCR and commercial kit was of 86% (n=100). In comparison with in-house HHV-8 real-time PCRs, the commercial kit showed agreements of 100% (n=61) and 93.7% (n=96) in A and B, respectively. These results demonstrate that the new commercial CMV HHV-6, 7, 8 R-genetrade mark kit was an efficient and reliable tool for the diagnosis of herpesvirus 6, 7, 8 infections.
机译:人疱疹病毒6(HHV-6),7(HHV-7)和8(HHV-8)是淋巴性疱疹病毒,可能在免疫抑制的患者(例如移植或AIDS患者)中引起机会性疾病。使用全血样品分别评估了用于同时定量HHV-6和定性检测HHV-7和HHV-8的新型商用CMV HHV-6、7、8 R-genetrade试剂盒(Argene,Varilhes,France) (n = 175、100和161),并在两个中心A和B中使用不同的提取和实时PCR平台。与HHV-6内部实时PCR相比,该商业试剂盒显示出96%的一致性(n = A和B分别为75%)和85%(n = 100),两种技术之间都具有明显的Spearman相关性(A:r = 0.97 [p <0.001]; B:r = 0.70 [p <0.001])。 Bland-Altman测试结果和对患者的前瞻性监测证实了这些HHV-6实时PCR技术的准确性。内部HHV-7 PCR与市售试剂盒之间的一致性为86%(n = 100)。与内部HHV-8实时PCR相比,该商业试剂盒显示A和B的一致性分别为100%(n = 61)和93.7%(n = 96)。这些结果表明,新型的商用CMV HHV-6、7、8 R基因商标试剂盒是诊断疱疹病毒6、7、8感染的有效且可靠的工具。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号