Norovirus in symptomatic and asymptomatic individuals: cytokines and viral shedding
Corresponding Author
K. L. Newman
Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA, USA
Medical Scientist Training Program, Emory University School of Medicine, Atlanta, GA, USA
Correspondence: K. L. Newman, Department of Epidemiology, Rollins School of Public Health, Emory University, 1518 Clifton Road, NE, Atlanta, GA 30322, USA. E-mail: [email protected]Search for more papers by this authorC. L. Moe
Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA, USA
Hubert Department of Global Health, Rollins School of Public Health, Emory University, Atlanta, GA, USA
Search for more papers by this authorA. E. Kirby
Hubert Department of Global Health, Rollins School of Public Health, Emory University, Atlanta, GA, USA
Search for more papers by this authorW. D. Flanders
Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA, USA
Search for more papers by this authorC. A. Parkos
Department of Pathology, University of Michigan Medical School, Ann Arbor, MI, USA
Search for more papers by this authorJ. S. Leon
Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA, USA
Hubert Department of Global Health, Rollins School of Public Health, Emory University, Atlanta, GA, USA
Search for more papers by this authorCorresponding Author
K. L. Newman
Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA, USA
Medical Scientist Training Program, Emory University School of Medicine, Atlanta, GA, USA
Correspondence: K. L. Newman, Department of Epidemiology, Rollins School of Public Health, Emory University, 1518 Clifton Road, NE, Atlanta, GA 30322, USA. E-mail: [email protected]Search for more papers by this authorC. L. Moe
Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA, USA
Hubert Department of Global Health, Rollins School of Public Health, Emory University, Atlanta, GA, USA
Search for more papers by this authorA. E. Kirby
Hubert Department of Global Health, Rollins School of Public Health, Emory University, Atlanta, GA, USA
Search for more papers by this authorW. D. Flanders
Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA, USA
Search for more papers by this authorC. A. Parkos
Department of Pathology, University of Michigan Medical School, Ann Arbor, MI, USA
Search for more papers by this authorJ. S. Leon
Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA, USA
Hubert Department of Global Health, Rollins School of Public Health, Emory University, Atlanta, GA, USA
Search for more papers by this authorSummary
Noroviruses (NoV) are the most common cause of epidemic gastroenteritis world-wide. NoV infections are often asymptomatic, although individuals still shed large amounts of NoV in their stool. Understanding the differences between asymptomatic and symptomatic individuals would help in elucidating mechanisms of NoV pathogenesis. Our goal was to compare the serum cytokine responses and faecal viral RNA titres of asymptomatic and symptomatic NoV-infected individuals. We tested serum samples from infected subjects (n = 26; 19 symptomatic, seven asymptomatic) from two human challenge studies of GI.1 NoV for 16 cytokines. Samples from prechallenge and days 1-4 post-challenge were tested for these cytokines. Cytokine levels were compared to stool NoV RNA titres quantified previously by reverse transcription–polymerase chain reaction (RT–qPCR). While both symptomatic and asymptomatic groups had similar patterns of cytokine responses, the symptomatic group generally exhibited a greater elevation of T helper type 1 (Th1) and Th2 cytokines and IL-8 post-challenge compared to the asymptomatic group (all P < 0·01). Daily viral RNA titre was associated positively with daily IL-6 concentration and negatively with daily IL-12p40 concentration (all P < 0·05). Symptoms were not associated significantly with daily viral RNA titre, duration of viral shedding or cumulative shedding. Symptomatic individuals, compared to asymptomatic, have greater immune system activation, as measured by serum cytokines, but they do not have greater viral burden, as measured by titre and shedding, suggesting that symptoms may be immune-mediated in NoV infection.
Supporting Information
Additional Supporting information may be found in the online version of this article at the publisher's web-site:
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cei12772-sup-0001-suppfigs.docx169.8 KB |
Fig. S1. Serum cytokine concentrations of symptomatic norovirus-infected challenge study volunteers. Prechallenge (day 0) to day 4 post-challenge, one line per subject. Fig. S2. Serum cytokine concentrations of asymptomatic norovirus-infected challenge study volunteers. Prechallenge (day 0) to day 4 post-challenge, one line per subject. Fig. S3. Viral shedding in symptomatic (top panel) and asymptomatic (bottom panel) norovirus-infected challenge study volunteers. Prechallenge (day 0) to end of follow-up, one line per subject. GEC = genomic equivalence copies. |
Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
References
- 1Ahmed SM, Hall AJ, Robinson AE et al. Global prevalence of norovirus in cases of gastroenteritis: a systematic review and meta-analysis. Lancet Infect Dis 2014; 14: 725–30.
- 2Green KY. Norovirus infection in immunocompromised hosts. Clin Microbiol Infect 2014; 20: 717–23.
- 3Gustavsson L, Andersson LM, Lindh M, Westin J. Excess mortality following community-onset norovirus enteritis in the elderly. J Hosp Infect 2011; 79: 27–31.
- 4Desai R, Hembree CD, Handel A et al. Severe outcomes are associated with genogroup 2 genotype 4 norovirus outbreaks: a systematic literature review. Clin Infect Dis 2012; 55: 189–93.
- 5Atmar RL, Opekun AR, Gilger MA et al. Norwalk virus shedding after experimental human infection. Emerg Infect Dis 2008; 14: 1553–7.
- 6Kirby AE, Shi J, Montes J, Lichtenstein M, Moe CL. Disease course and viral shedding in experimental Norwalk virus and Snow Mountain virus infection. J Med Virol 2014; 86: 2055–64.
- 7Sukhrie FH, Teunis P, Vennema H et al. Nosocomial transmission of norovirus is mainly caused by symptomatic cases. Clin Infect Dis 2012; 54: 931.
- 8Zelner JL, Lopman BA, Hall AJ, Ballesteros S, Grenfell BT. Linking time-varying symptomatology and intensity of infectiousness to patterns of norovirus transmission. PLoS One 2013; 8: e68413.
- 9Newman KL, Leon JS. Norovirus immunology: of mice and mechanisms. Eur J Immunol 2015; 45: 2742–57.
- 10Bernstein DI, Atmar RL, Lyon GM et al. Norovirus vaccine against experimental human GII.4 virus illness: a challenge study in healthy adults. J Infect Dis 2015; 211: 870–8.
- 11Atmar RL, Bernstein DI, Harro CD et al. Norovirus vaccine against experimental human Norwalk Virus illness. N Engl J Med 2011; 365: 2178–87.
- 12Newman KL, Moe CL, Kirby AE, Flanders WD, Parkos CA, Leon JS. Human norovirus infection and the acute serum cytokine response. Clin Exp Immunol 2015; 182: 195–203.
- 13Teunis PF, Sukhrie FH, Vennema H, Bogerman J, Beersma MF, Koopmans MP. Shedding of norovirus in symptomatic and asymptomatic infections. Epidemiol Infect 2015; 143: 1710–7.
- 14Leon JS, Kingsley DH, Montes JS et al. Randomized, double-blinded clinical trial for human norovirus inactivation in oysters by high hydrostatic pressure processing. Appl Environ Microbiol 2011; 77: 5476–82.
- 15Seitz SR, Leon JS, Schwab KJ et al. Norovirus infectivity in humans and persistence in water. Appl Environ Microbiol 2011; 77: 6884–8.
- 16Liu P, Hsiao HM, Jaykus LA, Moe C. Quantification of Norwalk virus inocula: comparison of endpoint titration and real-time reverse transcription–PCR methods. J Med Virol 2010; 82: 1612–16.
- 17Wong HL, Pfeiffer RM, Fears TR, Vermeulen R, Ji S, Rabkin CS. Reproducibility and correlations of multiplex cytokine levels in asymptomatic persons. Cancer Epidemiol Biomarkers Prev 2008; 17: 3450–6.
- 18Lindesmith L, Moe C, Lependu J, Frelinger JA, Treanor J, Baric RS. Cellular and humoral immunity following Snow Mountain virus challenge. J Virol 2005; 79: 2900–9.
- 19Jiang B, Snipes-Magaldi L, Dennehy P et al. Cytokines as mediators for or effectors against rotavirus disease in children. Clin Diagn Lab Immunol 2003; 10: 995–1001.
- 20Azim T, Zaki MH, Podder G et al. Rotavirus-specific subclass antibody and cytokine responses in Bangladeshi children with rotavirus diarrhoea. J Med Virol 2003; 69: 286–95.
- 21Lian JQ, Yang XF, Zhao RR et al. Expression profiles of circulating cytokines, chemokines and immune cells in patients with hepatitis B virus infection. Hepat Mon 2014; 14: e18892.
- 22Yeo AS, Azhar NA, Yeow W et al. Lack of clinical manifestations in asymptomatic dengue infection is attributed to broad down-regulation and selective up-regulation of host defence response genes. PLoS One 2014; 9: e92240.
- 23Reisinger EC, Fritzsche C, Krause R, Krejs GJ. Diarrhea caused by primarily non-gastrointestinal infections. Nat Clin Pract Gastroenterol Hepatol 2005; 2: 216–22.
- 24Wang J, Li FQ, Wei HM, Lian ZX, Sun R, Tian ZG. Respiratory influenza virus infection induces intestinal immune injury via microbiota-mediated Th17 cell-dependent inflammation. J Exp Med 2014; 211: 2397–410.
- 25Mehta SK, Crucian BE, Stowe RP et al. Reactivation of latent viruses is associated with increased plasma cytokines in astronauts. Cytokine 2013; 61: 205–9.
- 26Mumphrey SM, Changotra H, Moore TN et al. Murine norovirus 1 infection is associated with histopathological changes in immunocompetent hosts, but clinical disease is prevented by STAT1-dependent interferon responses. J Virol 2007; 81: 3251–63.
- 27Karst SM, Wobus CE, Lay M, Davidson J, Virgin HW IV. STAT1-dependent innate immunity to a Norwalk-like virus. Science 2003; 299: 1575–8.
- 28McFadden N, Bailey D, Carrara G et al. Norovirus regulation of the innate immune response and apoptosis occurs via the product of the alternative open reading frame 4. PLOS Pathog 2011; 7: e1002413.
- 29Gustavsson L, Skovbjerg S, Lindh M, Westin J, Andersson LM. Low serum levels of CCL5 are associated with longer duration of viral shedding in norovirus infection. J Clin Virol 2015; 69: 133–7.
- 30Marques RE, Guabiraba R, Russo RC, Teixeira MM. Targeting CCL5 in inflammation. Expert Opin Ther Targets 2013; 17: 1439–60.
- 31Troeger H, Loddenkemper C, Schneider T et al. Structural and functional changes of the duodenum in human norovirus infection. Gut 2009; 58: 1070–7.
- 32Souza M, Azevedo MS, Jung K, Cheetham S, Saif LJ. Pathogenesis and immune responses in gnotobiotic calves after infection with the genogroup II.4-HS66 strain of human norovirus. J Virol 2008; 82: 1777–86.
- 33Cheetham S, Souza M, Meulia T, Grimes S, Han MG, Saif LJ. Pathogenesis of a genogroup II human norovirus in gnotobiotic pigs. J Virol 2006; 80: 10372–81.
- 34Chachu KA, LoBue AD, Strong DW, Baric RS, Virgin HW. Immune mechanisms responsible for vaccination against and clearance of mucosal and lymphatic norovirus infection. PLoS Pathog 2008; 4: e1000236.
- 35Chachu KA, Strong DW, LoBue AD, Wobus CE, Baric RS, Virgin HW IV. Antibody is critical for the clearance of murine norovirus infection. J Virol 2008; 82: 6610–7.
- 36Navaneethan U, Giannella RA. Mechanisms of infectious diarrhea. Nat Clin Pract Gastroenterol Hepatol 2008; 5: 637–47.
- 37Martina BE. Dengue pathogenesis: a disease driven by the host response. Sci Prog 2014; 97: 197–214.
- 38Lindesmith L, Moe C, Marionneau S et al. Human susceptibility and resistance to Norwalk virus infection. Nat Med 2003; 9: 548–53.
- 39Saif MA, Bonney DK, Bigger B et al. Chronic norovirus infection in pediatric hematopoietic stem cell transplant recipients: a cause of prolonged intestinal failure requiring intensive nutritional support. Pediatr Transplant 2011; 15: 505–9.
- 40Lindesmith LC, Donaldson E, Leon J et al. Heterotypic humoral and cellular immune responses following Norwalk virus infection. J Virol 2010; 84: 1800–15.
- 41Baldridge MT, Nice TJ, McCune BT et al. Commensal microbes and interferon-lambda determine persistence of enteric murine norovirus infection. Science 2015; 347: 266–9.
- 42Osborne LC, Monticelli LA, Nice TJ et al. Coinfection. Virus–helminth coinfection reveals a microbiota-independent mechanism of immunomodulation. Science 2014; 345: 578–82.