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Quantifying Human Norovirus Virus-like Particles Binding to Commensal Bacteria Using Flow Cytometry
Published on: April 29, 2020
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Human Norovirus Triggers Primary B Cell Immune Activation In Vitro
Carmen Mirabelli1, Melissa K Jones2,3, Vivienne L Young4
1Department of Microbiology and Immunology, University of Michigan, Ann Arbor, Michigan, USA.
Mbio
|April 11, 2022
Summary
Human norovirus (HNoV) infects primary B cells, impacting immune responses. The NS1 protein may alter B cell activation and metabolism, potentially affecting viral pathogenesis and immunity.
Area of Science:
- Immunology
- Virology
- Gastroenterology
Background:
- Human norovirus (HNoV) causes significant global health and economic burdens, with individuals experiencing multiple infections due to a lack of lasting immunity.
- Understanding HNoV's interaction with the immune system, particularly B cells, is crucial for developing effective interventions and vaccines.
Purpose of the Study:
- To investigate the susceptibility of primary human B cells to HNoV infection.
- To determine the functional impact of HNoV infection on B cell subsets and activation.
- To explore the role of the HNoV NS1 protein in modulating B cell responses.
Main Methods:
- Primary human B cells were isolated from blood, spleen, and lymph node specimens.
- Cells were infected with HNoV and analyzed for viral RNA yield using RT-qPCR.
- B cell subsets were characterized by flow cytometry, and responses to HNoV virus-like particles and NS1 protein were assessed.
Main Results:
- HNoV RNA yield increased significantly in 50-60% of primary B cell donors.
- Infection altered the distribution of B cell subsets.
- The NS1 protein induced B cell activation and metabolic changes in vitro.
Conclusions:
- Primary human B cells are susceptible to HNoV infection.
- The HNoV NS1 protein can modulate B cell activation and metabolism, suggesting a mechanism for immune evasion and impacting pathogenesis.
- These findings have implications for understanding HNoV's recurrent nature and developing therapeutic strategies.
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