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首页> 外文期刊>Journal of Clinical Microbiology >Evaluation of an enzyme-linked immunosorbent assay for the detection of herpes simplex virus antigen.
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Evaluation of an enzyme-linked immunosorbent assay for the detection of herpes simplex virus antigen.

机译:评估酶联免疫吸附法检测单纯疱疹病毒抗原的能力。

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摘要

An enzyme-linked immunosorbent assay (ELISA) kit for herpes simplex virus developed by Ortho Diagnostic Systems, Inc., was evaluated. In phase I experiments, 263 clinical specimens from genital lesions were extracted into serum-free medium and then tested by ELISA for herpes simplex virus antigen. The results were compared with those obtained by conventional viral culture. Of 83 specimens, 65 were positive by ELISA (sensitivity, 78.3%). In phase II experiments, 249 clinical specimens were tested for herpes simplex virus antigen in direct specimen and in cell cultures (MRC-5 and rabbit kidney) incubated for 2, 4, and 7 days. Of 63 specimens, 40 were positive by ELISA in the direct specimen (sensitivity, 63.5%), and by 7 days incubation, 100% of the cultures positive by viral cell culture were also positive by ELISA. The ELISA was reproducible, and when both the direct detection and amplification culture were used, the sensitivity of ELISA paralleled the diagnosis of herpes simplex virus infections by viral cytopathic effect.
机译:评估了由Ortho Diagnostic Systems,Inc.开发的用于单纯疱疹病毒的酶联免疫吸附测定(ELISA)试剂盒。在第一阶段实验中,将263个来自生殖器病变的临床标本提取到无血清培养基中,然后通过ELISA检测单纯疱疹病毒抗原。将结果与通过常规病毒培养获得的结果进行比较。在83个样本中,有65个通过ELISA呈阳性(敏感性,78.3%)。在II期实验中,测试了249个临床标本,分别在直接标本和细胞培养物中(MRC-5和兔肾)培养了2、4和7天的单纯疱疹病毒抗原。在63个样本中,有40个在直接样本中通过ELISA呈阳性(敏感性为63.5%),并且在孵育7天后,通过病毒细胞培养呈阳性的培养物100%也通过ELISA呈阳性。 ELISA具有可重复性,当同时使用直接检测法和扩增培养法时,ELISA的灵敏度与病毒性细胞病变效应对单纯疱疹病毒感染的诊断平行。

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