Medical Journals

Influenza A Virus Infection of Primary Differentiated Airway Epithelial Cell Cultures Derived from Syrian Golden Hamsters.

Authors:
  • Newby Celeste M
  • Rowe Regina K
  • Pekosz Andrew

From: Department of Molecular Microbiology, Washington University in St. Louis School of Medicine, 660 S. Euclid Avenue, Campus Box 8230, St. Louis, MO 63110, USA.

Virology

  • Publish Date: Oct 2006
  • ISSN: 0042-6822
  • Volume: 354
  • Issue: 1
  • Pages: 80-90
  • Medium: Print
  • Language: English
  • Citation (JAMA): Newby Celeste M, Rowe Regina K, Pekosz Andrew, et al. Influenza A Virus Infection of Primary Differentiated Airway Epithelial Cell Cultures Derived from Syrian Golden Hamsters.. Virology Oct 2006;354:80-90

Abstract

The ability of several different influenza A virus strains to infect and replicate in primary, differentiated airway epithelial cell cultures from Syrian golden hamsters was investigated. All virus strains tested replicated equivalently in the cultures and displayed a preference for infecting nonciliated cells. This tropism correlated with the expression of both alpha2,3- and alpha2,6-linked sialic acid on the nonciliated cells. In contrast, the ciliated cells did not have detectable alpha2,6-linked sialic acid and expressed only low amounts of alpha2,3-linked sialic acid. In contrast to clinical isolates, laboratory strains of influenza A virus infected a limited number of ciliated cells at late times post-infection. The presence of alpha2,3- and alpha2,6-linked sialic acid residues on the same cell type suggests that Syrian golden hamsters and differentiated airway epithelial cell cultures derived from hamsters may provide a system for studying the reassortment of influenza A virus strains which utilize different forms of sialic acid as a primary virus receptor.

Mesh Headings (Keywords): Animals, Cells, Cultured, Cilia, Cricetinae, Epithelial Cells, Influenza A virus, Mesocricetus, N-Acetylneuraminic Acid, Plaque Assay, Receptors, Virus, Respiratory Mucosa, Virus Replication


Check for Full Text / PubMed Unique Identifier (PMID): 16876846


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.

The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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