Can Use of Viral Load Improve Norovirus Clinical Diagnosis and Disease Attribution?

Author:

Shioda Kayoko1,Barclay Leslie1,Becker-Dreps Sylvia2,Bucardo-Rivera Filemon3,Cooper Philip J4,Payne Daniel C1,Vinjé Jan1,Lopman Benjamin A15

Affiliation:

1. Division of Viral Diseases, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia

2. School of Medicine, University of North Carolina at Chapel Hill

3. Department of Microbiology, National Autonomous University of León, Nicaragua

4. Facultad de Ciencias Médicas, de la Salud y de la Vida, Universidad Internacional del Ecuador Quito; Institute of Infection and Immunity, St George’s University of London, United Kingdom

5. Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, Georgia

Abstract

Abstract Background Real-time reverse-transcriptase polymerase chain reaction (RT-PCR) is the state-of-the-art diagnostic for norovirus. Cycle threshold (Ct), an indicator of viral load, may be associated with symptomatic disease as well as demographic and outbreak characteristics. Methods Data on (1) outbreak and sporadic cases and (2) asymptomatic controls in the United States and Latin America were analyzed. With multivariate regression models, we assessed relationships between various factors and Ct values, and we calculated odds ratios (ORs) for the presence of symptoms and attributable fractions of norovirus. Receiver-operating characteristic analysis was performed to define an optimal Ct cutoff to identify disease-causing infections. Results Cycle threshold values were lower (ie, higher viral loads) among symptomatic cases (model-adjusted mean ± standard error: 25.3 ± 1.2) compared with asymptomatic controls (28.5 ± 1.4). Cycle threshold values were significantly different across age groups, norovirus genogroups, timing of specimen collection, outbreak settings, and transmission modes. Genogroup II (GII) Ct values were associated with presence of symptoms (OR = 1.1), allowing us to estimate that 16% of diarrheal disease was attributable to norovirus. The optimized Ct cutoff led to poor sensitivity and specificity for genogroup I and GII. Conclusions Cycle threshold values were associated with host, pathogen, and outbreak factors. Cycle threshold values may not effectively distinguish disease-causing infection for individual patients, but they are useful for epidemiological studies aiming to attribute disease.

Funder

Centers for Disease Control and Prevention

Oak Ridge Institute for Science and Education

Wellcome Trust

Thrasher Research Fund

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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