Papin James F, Vahrson Wolfgang, Dittmer Dirk P
Department of Microbiology and Immunology, The University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma 73104, USA.
J Clin Microbiol. 2004 Apr;42(4):1511-8. doi: 10.1128/JCM.42.4.1511-1518.2004.
Real-time quantitative PCR is used routinely for the high-throughput diagnosis of viral pathogens, such as West Nile virus (WNV). Rapidly evolving RNA viruses present a challenge for diagnosis because they accumulate mutations that may render them undetectable. To explore the effect of sequence variations on assay performance, we generated every possible single point mutation within the target region of the widely used TaqMan assay for WNV and found that the TaqMan assay failed to detect 47% of possible single nucleotide variations in the probe-binding site and was unable to detect any targets with more than two mutations. In response, we developed and validated a less expensive assay with the intercalating dye SYBR green. The SYBR green-based assay was as sensitive as the TaqMan assay for WNV. Importantly, it detected 100% of possible WNV target region variants. The assay developed here adds an additional layer of protection to guard against false-negative results that result from natural variations or drug-directed selection and provides a rapid means to identify such variants for subsequent detailed analysis.
实时定量聚合酶链反应(PCR)常用于对病毒病原体进行高通量诊断,如西尼罗河病毒(WNV)。快速进化的RNA病毒给诊断带来了挑战,因为它们会积累突变,可能导致无法检测到。为了探究序列变异对检测性能的影响,我们在广泛使用的WNV TaqMan检测法的靶区域内产生了每一种可能的单点突变,发现TaqMan检测法未能检测到探针结合位点中47%的可能单核苷酸变异,并且无法检测到任何有两个以上突变的靶标。作为应对措施,我们开发并验证了一种使用嵌入染料SYBR Green的成本较低的检测方法。基于SYBR Green的检测方法对WNV的敏感性与TaqMan检测法相同。重要的是,它检测到了100%的可能WNV靶区域变异体。这里开发的检测方法增加了一层额外的保护,以防止因自然变异或药物定向选择导致的假阴性结果,并提供了一种快速方法来识别此类变异体以便进行后续详细分析。