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首页> 外文期刊>Journal of Clinical Microbiology >Multiplexed, Real-Time PCR for Quantitative Detection of Human Adenovirus
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Multiplexed, Real-Time PCR for Quantitative Detection of Human Adenovirus

机译:实时荧光定量PCR检测人类腺病毒

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Adenovirus infection is becoming increasingly recognized as a cause of morbidity and mortality in the immunosuppressed patient population. While early detection and quantitation of adenovirus in peripheral blood has been suggested as a means of directing and monitoring antiviral therapy in these patients, few methods have been published, particularly with respect to viral quantitation. A multiplexed real-time PCR assay was developed that can quantitatively detect a wide range of known serotypes of human adenovirus, including all of subgroups A to C. This assay was compared to a qualitative, Southern blot-based PCR assay by using 45 peripheral blood specimens from 16 patients. There was 100% concordance between the two tests in terms of qualitative results. The real-time assay detected adenovirus in patient samples at levels from <200 to 266,681 copies/ml of blood. By using control viral samples, sensitivity was demonstrated to less than 10 copies of viral genome per reaction and quantitative linearity was demonstrated from 10 to 106 copies of input viral DNA. Equivalent sensitivity and linearity were demonstrated for 15 different reference serotypes of adenovirus. Eleven other viral serotypes have complete target region sequence homology to one or more of the strains tested. No cross-reactivity was noted with other commonly isolated viral species. Sequence analysis showed no significant homology with any other human pathogens (bacterial or viral). This assay allows rapid, sensitive, and specific quantitation of adenovirus and may have a significant impact on the care of immunocompromised patients at risk for disseminated viral infection.
机译:腺病毒感染越来越被认为是免疫抑制患者人群发病和死亡的原因。虽然已经建议在外周血中早期检测和定量腺病毒作为指导和监测这些患者抗病毒治疗的一种手段,但很少有方法发表,特别是在病毒定量方面。开发了一种实时多重PCR检测方法,可以定量检测多种已知的人类腺病毒血清型,包括所有A至C亚组。通过使用45种外周血将该检测方法与基于Southern印迹的定性PCR检测方法进行了比较16位患者的标本。两次测试在定性结果上有100%的一致性。实时检测在患者样本中检测到的腺病毒水平低于200至266,681拷贝/毫升血液。通过使用对照病毒样品,证明了每个反应对少于10个拷贝的病毒基因组的敏感性,并证明了从10到10 6 个输入病毒DNA的定量线性。证明了15种不同参考血清型腺病毒的等效灵敏度和线性。其他11种病毒血清型与一种或多种测试菌株具有完全的靶区域序列同源性。没有发现与其他通常分离的病毒物种有交叉反应。序列分析显示与任何其他人类病原体(细菌或病毒)均无明显同源性。该测定法可以快速,灵敏和特异地定量检测腺病毒,并且可能对免疫风险低的易分散病毒感染患者的护理产生重大影响。

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