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  • 1
    Publication Date: 2003-03-08
    Description: Norwalk-like caliciviruses (Noroviruses) cause over 90% of nonbacterial epidemic gastroenteritis worldwide, but the pathogenesis of norovirus infection is poorly understood because these viruses do not grow in cultured cells and there is no small animal model. Here, we report a previously unknown murine norovirus. Analysis of Murine Norovirus 1 infection revealed that signal transducer and activator of transcription 1-dependent innate immunity, but not T and B cell-dependent adaptive immunity, is essential for norovirus resistance. The identification of host molecules essential for murine norovirus resistance may provide targets for prevention or control of an important human disease.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Karst, Stephanie M -- Wobus, Christiane E -- Lay, Margarita -- Davidson, John -- Virgin, Herbert W 4th -- R01 AI49286/AI/NIAID NIH HHS/ -- T32-CA09547/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 2003 Mar 7;299(5612):1575-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/12624267" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; B-Lymphocytes/immunology ; Brain/virology ; Caliciviridae Infections/*immunology ; DNA-Binding Proteins/genetics/*physiology ; Genes, RAG-1 ; Genome, Viral ; Homeodomain Proteins/physiology ; *Immunity, Innate ; Immunocompromised Host ; Intestines/virology ; Liver/virology ; Membrane Proteins ; Mice ; Mutation ; Norovirus/classification/*immunology/*isolation & purification/pathogenicity ; Phylogeny ; RNA, Viral/analysis ; Receptor, Interferon alpha-beta ; Receptors, Interferon/genetics/physiology ; STAT1 Transcription Factor ; Spleen/virology ; T-Lymphocytes/immunology ; Trans-Activators/genetics/*physiology ; Virulence
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2014-11-08
    Description: The cell tropism of human noroviruses and the development of an in vitro infection model remain elusive. Although susceptibility to individual human norovirus strains correlates with an individual's histo-blood group antigen (HBGA) profile, the biological basis of this restriction is unknown. We demonstrate that human and mouse noroviruses infected B cells in vitro and likely in vivo. Human norovirus infection of B cells required the presence of HBGA-expressing enteric bacteria. Furthermore, mouse norovirus replication was reduced in vivo when the intestinal microbiota was depleted by means of oral antibiotic administration. Thus, we have identified B cells as a cellular target of noroviruses and enteric bacteria as a stimulatory factor for norovirus infection, leading to the development of an in vitro infection model for human noroviruses.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4401463/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4401463/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Jones, Melissa K -- Watanabe, Makiko -- Zhu, Shu -- Graves, Christina L -- Keyes, Lisa R -- Grau, Katrina R -- Gonzalez-Hernandez, Mariam B -- Iovine, Nicole M -- Wobus, Christiane E -- Vinje, Jan -- Tibbetts, Scott A -- Wallet, Shannon M -- Karst, Stephanie M -- R01 AI080611/AI/NIAID NIH HHS/ -- R21 AI103961/AI/NIAID NIH HHS/ -- T90 DE021990/DE/NIDCR NIH HHS/ -- T90 DE021990-02/DE/NIDCR NIH HHS/ -- New York, N.Y. -- Science. 2014 Nov 7;346(6210):755-9. doi: 10.1126/science.1257147.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Genetics and Microbiology, Emerging Pathogens Institute, College of Medicine, University of Florida, Gainesville, FL, USA. ; Department of Oral Biology, College of Dentistry, University of Florida, Gainesville, FL, USA. Department of Periodontology, College of Dentistry, University of Florida, Gainesville, FL, USA. ; Department of Microbiology and Immunology, University of Michigan, Ann Arbor, MI, USA. ; Department of Medicine, Division of Infectious Diseases, University of Florida, Gainesville, FL, USA. ; Division of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA. ; Department of Molecular Genetics and Microbiology, Emerging Pathogens Institute, College of Medicine, University of Florida, Gainesville, FL, USA. skarst@ufl.edu.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25378626" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Anti-Bacterial Agents/pharmacology ; B-Lymphocytes/immunology/*virology ; Caliciviridae Infections/*immunology/microbiology/virology ; Cell Line ; Enterobacteriaceae/drug effects/*physiology ; Gastroenteritis/*immunology/microbiology/virology ; Genome, Viral/genetics/physiology ; Homeodomain Proteins/genetics ; Humans ; Intestines/immunology/*microbiology ; Mice ; Mice, Mutant Strains ; Norovirus/*physiology ; Peyer's Patches/immunology/virology ; *Virus Replication
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
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