NIH Funded Norovirus Projects


Human norovirus is the leading cause of acute gastroenteritis globally causing up to 200,000 deaths per year. However, there are no antiviral drugs or vaccines. We use the closely related mouse or murine norovirus (MNV) as a model system to understand how human norovirus causes infection and disease.

$641,093

2021: Project Number 5R01AI148467-02

The role of tuft cells in norovirus pathogenesis

Craig Brian Wilen, Yale University


Human noroviruses (HNoVs) are medically important non-enveloped positive-sense RNA viruses that cause gastroenteritis. This revised proposal leverages the recent discovery of CD300lf as a receptor for murine NoV (MNoV, Science 2016 353:933) to define mechanisms of NoV pathogenesis, persistence and intestinal immunity.

$699,874

2021: Project Number 5R01AI127552-05

Role of CD300 Family in Norovirus Tropism, Persistence, and Immunity

Megan T. Baldridge, Washington University


This K24 proposal builds upon a decade of clinical and epidemiologic research on childhood gastroenteritis in Nicaragua by the candidate, Sylvia Becker-Dreps, MD, MPH. As a natural extension of Dr. Becker-Dreps' previous work on understanding reduced rotavirus vaccine effectiveness in resource-constrained settings, the current proposal expands Dr. Becker-Dreps' skillsets to allow her to contribute to the development of an effective pediatric norovirus vaccine.

$168,497

2021: Project Number 5K24AI141744-03

The Development of Norovirus Immunity in Early Childhood and Implications for Norovirus Vaccines

Sylvia Irene Becker-Dreps, University of North Carolina Chapel Hill


The purpose of this proposal is to determine the breadth of T-cell responses to norovirus, as well as the stability of norovirus epitopes in circulating viruses. By classifying T-cells responses to norovirus, we hope to enable clinical trials of adoptive T-cell immunotherapy for chronic norovirus infections in immunocompromised hosts, and also to aid in future design of norovirus vaccines.

$89,250

2020: Project Number 1R03AI153917-01

Characterization of the T-cell Response to Human Norovirus Infection

Michael Daniel Keller, Children’s Research Institute


We continued an epidemiological investigation of noroviruses in immunocompromised patients enrolled in research protocols at the NIH Clinical Research Center. A multiplex assay for the detection of bacterial, viral, and parasitic gastrointestinal pathogens became available for use in the Clinical Center near the end of 2015. In collaboration with epidemiologists in NIAID we explored the relative contribution of viral pathogens to diarrheal illness since its employment.

$1,871,553

2020: Project Number 1ZIAAI000897-20

Noroviruses and Epidemic Gastroenteritis

Kim Y. Green, National Institute of Allergy and Infectious Diseases


Human noroviruses (HuNoV) are the major cause of acute non-bacterial, epidemic gastroenteritis, resulting in ~200,000 deaths/year, mostly in infant, elderly and immunosuppressed groups. HuNoV vaccines are under development but the results are mixed, in part reflecting antigenic seniority, virus diversity and escape.

$739,405

2021: Project Number 5R01AI148260-02

Antibody Landscape following Human Norovirus Infection and Vaccination

Ralph S. Baric, University of North Carolina Chapel Hill


Animal viruses share two important features; a) an efficient system for delivering their genome to the target cell usually involving an activation process in the virion and b) a means of interacting with the adaptive immune system of the host. The structural and biophysical studies detailed here will show how the noroviruses have evolved capsids that perform both functions.

$559,337

2020: Project Number 5R01AI141465-02

The role of structural plasticity in the norovirus capsid

Thomas James Smith, University of Texas Galveston


Narrative Human norovirus and Clostridium difficile are the leading causes of acute gastroenteritis with significant morbidity and mortality. To date there is still no single vaccine available on the market. The goal of this project is to develop a novel oral passive immunoprophylactic strategy to prevent the infections and diseases associated with the two pathogens.

$647,849

2020: Project Number 1R01AI148357-01

Preventing norovirus and Clostridium difficile gastroenteritis by engineered probiotic yeast Saccharomyces boulardii secreting multi-specific single-domain antibodies

Hanping Feng, Lijuan Yuan, University of Maryland


Experimental Drugs in Culture

Direct acting nucleoside analogs RNA-dependent RNA polymerase inhibitors:

  • Favipiravir  (mutagenic nucleoside targets viral RNA)

  • 2′-C-methylcytidine (2′-C-MeC)

  • 2′-F-2′-C-MeC

  • B-D-N(4)-hydroxycytidine (NHC)

  • CTP or 5-nitrocytidine triphosphate

  • uridine analogues

Non-nucleoside RNA-dependent RNA polymerase inhibitors:

  • Suramin

  • pyridoxal-50-phosphate-6-(20-naphthylazo-60-nitro-40,80-disulfonate) tetrasodium salt

 

Protease Inhibitors:

  • viral 3C-like, chymotrypsin-like, cysteine protease

Other compounds:

  • (E)-2-styrylchromones

  • nitazoxanide (NTZ) (Alinia®, Romark Laboratories, LC)

Animal Models

Mouse Model:

A mouse model supporting human NoV has been recently developed but, while representing a substantial breakthrough for the field, exhibits low virus production and little, if any, pathology.

(Taube et al., 2013)

Gnotobiotic Pig Model:

A gnotobiotic pig model of human NV infection has been established for several years but not widely exploited, presumably due to larger animal size and expense (Cheetham et al., 2006). However, the pig model does support high yields of virus shedding, significant pathology, and disease comparable to humans, which are amenable to quantification.

Mouse Model:

A mouse model of Mouse NoV infection utilizing interferon receptor deficient mice has been shown to exhibit modest, but quantifiable, GI symptoms, as well as high yields of virus.

(Rocha-Pereira et al., 2013).