Characterization of a porcine intestinal epithelial cell line for influenza virus production

Author:

Sun Zhi1,Huber Victor C.2,McCormick Kara2,Kaushik Radhey S.31,Boon Adrianus C. M.4,Zhu Longchao1,Hause Ben51,Webby Richard J.6,Fang Ying31

Affiliation:

1. Department of Veterinary and Biomedical Sciences, South Dakota State University, Brookings, SD 57007, USA

2. Division of Basic Biomedical Sciences, Sanford School of Medicine, The University of South Dakota, Vermillion, SD 57069, USA

3. Department of Biology/Microbiology, South Dakota State University, Brookings, SD 57007, USA

4. Division of Infectious Diseases, Department of Internal Medicine, Department of Molecular Microbiology, Department of Pathology and Immunology, Washington University School of Medicine, St Louis, MO 63110, USA

5. Newport Laboratories, Worthington, MN 56187, USA

6. Department of Infectious Diseases, St Jude Children’s Research Hospital, Memphis, TN 38105, USA

Abstract

We have developed a porcine intestine epithelial cell line, designated SD-PJEC for the propagation of influenza viruses. The SD-PJEC cell line is a subclone of the IPEC-J2 cell line, which was originally derived from newborn piglet jejunum. Our results demonstrate that SD-PJEC is a cell line of epithelial origin that preferentially expresses receptors of oligosaccharides with Sia2-6Gal modification. This cell line is permissive to infection with human and swine influenza A viruses and some avian influenza viruses, but poorly support the growth of human-origin influenza B viruses. Propagation of swine-origin influenza viruses in these cells results in a rapid growth rate within the first 24 h post-infection and the titres ranged from 4 to 8 log10TCID50ml−1. The SD-PJEC cell line was further tested as a potential alternative cell line to Madin–Darby canine kidney (MDCK) cells in conjunction with 293T cells for rescue of swine-origin influenza viruses using the reverse genetics system. The recombinant viruses A/swine/North Carolina/18161/02 (H1N1) and A/swine/Texas/4199-2/98 (H3N2) were rescued with virus titres of 7 and 8.25 log10TCID50ml−1, respectively. The availability of this swine-specific cell line represents a more relevant substrate for studies and growth of swine-origin influenza viruses.

Publisher

Microbiology Society

Subject

Virology

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