Clinical severity of enteric viruses detected using a quantitative molecular assay compared to conventional assays in the Global Enteric Multicenter Study

Jordan Cates, Helen Powell, James Platts-Mills, Dilruba Nasrin, Sandra Panchalingam, Samba O Sow, Awa Traore, Dipika Sur, Thandavarayan Ramamurthy, Anita K M Zaidi, Furqan Kabir, Abu S G Faruque, Dilruba Ahmed, Robert F Breiman, Richard Omore, John Benjamin Ochieng, M Jahangir Hossain, Martin Antonio, Inácio Mandomando, Delfino Vubil, James P Nataro, Myron M Levine, Umesh D Parashar, Karen L Kotloff, Jacqueline E Tate
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Abstract

Background Quantitative molecular assays are increasingly used for detection of enteric viruses. Methods We compared the clinical severity using modified Vesikari score (mVS) of enteric viruses detected by conventional assays (enzyme immunoassays [EIA] for rotavirus and adenovirus 40/41 and conventional polymerase chain reaction for astrovirus, sapovirus, and norovirus) and a quantitative molecular assay (TaqMan Array Card [TAC]) among children aged 0-59 months in the Global Enteric Multicenter Study. For rotavirus and adenovirus 40/41, we compared severity between EIA-positive and TAC-positive cases assigned etiologies using different cycle threshold (CT) cutoffs. Results Using conventional assays, the median (interquartile range) mVS was 10 (8, 11) for rotavirus, 9 (7, 11) for adenovirus 40/41, 8 (6, 10) for astrovirus, sapovirus, and norovirus GII, and 7 (6, 9) for norovirus GI. Compared to rotavirus EIA-positive cases, the median mVS was 2 and 3 points lower for EIA-negative/TAC-positive cases with CT<32.6 and 32.6≤CT<35, respectively (p-value<.0001). Adenovirus 40/41 EIA-positive and EIA-negative/TAC-positive cases were similar, regardless of CT cutoff. Conclusions Quantitative molecular assays compared to conventional assays, such as EIA, may influence severity of identified cases, especially for rotavirus. Cutoffs to assign etiology for quantitative assays should be considered in the design and interpretation of enteric virus studies.
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全球肠道疾病多中心研究中使用定量分子测定法检测到的肠道病毒的临床严重性与传统测定法的比较
背景 分子定量检测法越来越多地被用于检测肠道病毒。方法 在全球肠道疾病多中心研究(Global Enteric Multicenter Study)中,我们使用改良维西卡里评分(mVS)比较了传统检测方法(轮状病毒和腺病毒 40/41 的酶免疫测定 [EIA],以及星状病毒、沙波病毒和诺沃克病毒的传统聚合酶链反应)和定量分子检测方法(TaqMan Array Card [TAC])检测到的 0-59 个月儿童肠道病毒的临床严重程度。对于轮状病毒和腺病毒 40/41,我们比较了 EIA 阳性病例和 TAC 阳性病例的严重程度,并采用不同的周期阈值 (CT) 截止值来确定病因。结果 使用传统检测方法,轮状病毒的 mVS 中位数(四分位数间距)为 10(8,11),腺病毒 40/41 为 9(7,11),星状病毒、沙波病毒和诺如病毒 GII 为 8(6,10),诺如病毒 GI 为 7(6,9)。与轮状病毒 EIA 阳性病例相比,EIA 阴性/TAC 阳性病例的 mVS 中位数分别低 2 点和 3 点,CT<32.6 和 32.6≤CT<35 (p 值<.0001)。腺病毒 40/41 EIA 阳性和 EIA 阴性/TAC 阳性病例的情况相似,与 CT 临界值无关。结论 定量分子检测与传统检测(如 EIA)相比,可能会影响已发现病例的严重程度,尤其是轮状病毒。在设计和解释肠道病毒研究时,应考虑为定量检测指定病因的临界值。
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