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Clinical Severity of Enteric Viruses Detected Using a Quantitative Molecular Assay Compared With Conventional Assays in the Global Enteric Multicenter Study

札幌病毒 轮状病毒 星状病毒 诺如病毒 病毒学 实时聚合酶链反应 生物 病毒 医学 生物化学 基因
作者
Jordan Cates,Helen Powell,James A Platts-Mills,Dilruba Nasrin,Sandra Panchalingam,Samba O. Sow,Awa Traoré,Dipika Sur,Thandavarayan Ramamurthy,Anita K. M. Zaidi,Furqan Kabir,Abu Syed Golam Faruque,Dilruba Ahmed,Robert F. Breiman,Richard Omore,John B. Ochieng,M Jahangir Hossain,Martín Antonio,Inácio Mandomando,Delfino Vubil,James P. Nataro,Myron M. Levine,Umesh D. Parashar,Karen L. Kotloff,Jacqueline E. Tate
出处
期刊:The Journal of Infectious Diseases [Oxford University Press]
卷期号:230 (5): 1157-1166
标识
DOI:10.1093/infdis/jiae201
摘要

Abstract Background Quantitative molecular assays are increasingly used for detection of enteric viruses. Methods We compared the clinical severity using the modified Vesikari score (mVS) of enteric viruses detected by conventional assays (enzyme immunoassays [EIAs] 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 mVS (interquartile range) 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 with rotavirus EIA-positive cases, the median mVS was 2 and 3 points lower for EIA-negative/TAC-positive cases with Ct <32.6 or Ct ≥32.6 and <35, respectively (P < .001). Adenovirus 40/41 EIA-positive and EIA-negative/TAC-positive cases were similar, regardless of Ct cutoff. Conclusions Quantitative molecular assays compared with conventional assays, such as EIA, may influence the 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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