Skip to main content
ARS Home » Midwest Area » Ames, Iowa » National Animal Disease Center » Virus and Prion Research » Research » Publications at this Location » Publication #147795
Title: GENE EXPRESSION CHANGES IN BVDV2-INFECTED MDBK CELLS

Author
item Neill, John
item Ridpath, Julia

Submitted to: Biologicals
Publication Type: Book / Chapter
Publication Acceptance Date: 1/15/2003
Publication Date: 6/1/2003
Citation: Neill, J.D., Ridpath, J.F. Gene expression changes in BVDV2-infected MDBK cells. Biologicals. 2003. v. 31. p. 97-102.

Interpretive Summary:

Technical Abstract: Bovine viral diarrhea viruses (BVDV) are ubiquitous viral pathogens of cattle. These viruses exist as one of two biotypes, cytopathic and noncytopathic, based on the ability to induce cytopathic effect in cell culture. The noncytopathic biotypes are able to establish nonapparent, persistent infections in both cell culture and in bovine fetuses of less than 150 days gestation. Interactions with the host cell and the mechanism by which viral tolerance is established are unknown. To examine the changes in gene expression that occur following infection of host cells with BVDV, serial analysis of gene expression (SAGE), a global gene expression technology was used. SAGE, a global, sequence-based technology, allows quantitation of virtually every transcript in a cell type without prior sequence information. Transcript expression levels and identities are determined by sequencing of libraries composed of concatamers of 14 base DNA fragments (tags) derived from the 3' end of each cellular mRNA transcript. Comparison of data obtained from noninfected and BVDV2-infected cell libraries revealed changes in gene expression associated with distinct biochemical pathways or functions. Isotypes of both tubulins were down-regulated, indicating possible dysfunction in cell division and other functions were microtubules play a major role. Expression of genes encoding proteins involved in energy metabolism were expressed at essentially equivalent levels in both infected and noninfected cells. Genes encoding proteins involved in protein translation and post-translational modifications, functions necessary for viral replication, were generally up-regulated. These data indicate that following infection with BVDV, changes in gene expression occur that are beneficial for virus replication while having only minor changes in energy metabolism.