Differentiated swine airway epithelial cell cultures for the investigation of influenza A virus infection and replication. Issue 2 (25th April 2012)

• Record Type: Journal Article
• Authors: Bateman, Allen C.; Karasin, Alexander I.; Olsen, Christopher W.
• Is Part Of: Influenza and other respiratory viruses. Volume 7:Issue 2(2013:Mar.)
• Page Start: 139
• Page End: 150
• Publication Date: 2012-04-25
• Subjects: Influenza -- Periodicals; Respiratory infections -- Periodicals; Virus diseases -- Periodicals; Influenza, Human -- Periodicals; Respiratory Tract Diseases -- Periodicals; Virus Diseases -- Periodicals; Grippe -- Périodiques; Appareil respiratoire -- Infections -- Périodiques; Maladies à virus -- Périodiques; 616.203
• DOI: 10.1111/j.1750-2659.2012.00371.x
• Languages: English
• ISSNs: 1750-2640

Abstract

<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p> <italic>Please cite this paper as:</italic> Bateman <italic>et al.</italic> (2013) Differentiated swine airway epithelial cell cultures for the investigation of influenza A virus infection and replication. Influenza and Other Respiratory Viruses 7(2) 139–150.</p> <p> <bold>Background </bold> Differentiated human airway epithelial cell cultures have been utilized to investigate cystic fibrosis, wound healing, and characteristics of viral infections. These cultures, grown at an air–liquid interface (ALI) in media with defined hormones and growth factors, recapitulate many aspects of the <italic>in vivo</italic> respiratory tract and allow for experimental studies at the cellular level.</p> <p> <bold>Objectives </bold> To optimize growth conditions for differentiated swine airway epithelial cultures and to use these cultures to examine influenza virus infection and replication.</p> <p> <bold>Methods </bold> Primary swine respiratory epithelial cells were grown at an air–liquid interface with varying amounts of retinoic acid and epidermal growth factor. Cells grown with optimized concentrations of these factors for 4 weeks differentiated into multilayer epithelial cell cultures resembling the lining of the swine respiratory tract. Influenza virus infection and replication were examined in these cultures.</p> <p> <bold>Results/Conclusions </bold> Retinoic acid promoted ciliogenesis, whereas epidermal growth factor controlled the thickness of the pseudoepithelium. The optimal concentrations for differentiated swine cell cultures were 1·5 ng/ml epidermal growth factor and 100 n<sc>m</sc> retinoic acid. Influenza A viruses infected and productively replicated in these cultures in the absence of exogenous trypsin, suggesting that the cultures express a protease capable of activating influenza virus hemagglutinin. Differences in virus infection and replication characteristics found previously in pigs <italic>in vivo</italic> were recapitulated in the swine cultures. This system could be a useful tool for a range of applications, including investigating influenza virus species specificity, defining cell tropism of influenza viruses in the swine respiratory epithelium, and studying other swine respiratory diseases.</p> </abstract>