Department of Pediatrics, Division of Infectious Disease, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Department of Pediatrics, Division of Quantitative Health Sciences, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
J Clin Microbiol. 2021 Jul 19;59(8):e0096421. doi: 10.1128/JCM.00964-21.
Infection with human cytomegalovirus (CMV) is common and may have grave consequences in transplant recipients and congenitally infected children. Diagnosis of CMV infection is based on detection of specific antibodies and molecular assays. The incorporation of CMV serological assays into diagnostic algorithms requires careful evaluation and interpretation. Very few serological assays measure CMV infection by a specific strain. We developed an enzyme-linked immunosorbent assay (ELISA) using CMV-encoded UL144 as the antigen. UL144 encodes three major genotypes, A, B, and C, and recombinants. The ELISA was developed with the three UL144 proteins and optimized as a multiplex assay. Sera from 55 positive and 59 negative CMV IgG, determined by the clinical microbiology laboratory, were used for evaluation and optimization. A cutoff optical density (OD) that distinguishes UL144 antibody-positive from antibody-negative sera was established. UL144 A, B, C, and combinations of these antigens were detected in sera. An assay threshold of 0.1 was established and, from a total of 303 sera, the overall sensitivity, specificity, and positive and negative predictive values of the multiplex ELISA were 86.72% (95% confidence interval [CI] 79.59% to 92.07%), 96.57% (92.69% to 98.73%), 94.40% (88.45% to 97.38%), and 91.60% (87.50% to 94.44%), respectively. The inter- and intraassay median coefficients of variation were 0.06 (interquartile range [IQR] 0.56, 0.2) and 0.171 (IQR 0.038, 0.302), respectively. No cross-reactivity was observed with HSV-positive CMV-negative sera. This ELISA gives simple and reproducible results for detection of anti-CMV UL144 IgG. It may assist in differentiating natural infection from CMV vaccines that lack UL144, and may provide an important tool for epidemiological studies of CMV strains.
人巨细胞病毒(CMV)感染很常见,在移植受者和先天性感染儿童中可能产生严重后果。CMV 感染的诊断基于特异性抗体和分子检测。将 CMV 血清学检测纳入诊断算法需要仔细评估和解释。很少有血清学检测方法可以通过特定株来检测 CMV 感染。我们使用 CMV 编码的 UL144 作为抗原开发了一种酶联免疫吸附试验(ELISA)。UL144 编码三个主要基因型 A、B 和 C 以及重组体。该 ELISA 使用三种 UL144 蛋白开发,并优化为多重检测法。用临床微生物学实验室确定的 55 份 CMV IgG 阳性和 59 份 CMV IgG 阴性血清对其进行评估和优化。建立了区分 UL144 抗体阳性和阴性血清的光密度(OD)临界值。检测到血清中存在 UL144 A、B、C 及其组合。建立了 0.1 的检测阈值,在总共 303 份血清中,多重 ELISA 的总体敏感性、特异性、阳性和阴性预测值分别为 86.72%(95%置信区间 [CI] 79.59%至 92.07%)、96.57%(92.69%至 98.73%)、94.40%(88.45%至 97.38%)和 91.60%(87.50%至 94.44%)。批内和批间的中位变异系数分别为 0.06(四分位距 [IQR] 0.56,0.2)和 0.171(IQR 0.038,0.302)。未观察到与单纯疱疹病毒(HSV)阳性但 CMV 阴性血清的交叉反应。该 ELISA 可用于检测抗 CMV UL144 IgG,结果简单且可重复。它可能有助于区分自然感染和缺乏 UL144 的 CMV 疫苗,并且可能为 CMV 株的流行病学研究提供重要工具。