| Literature DB >> 27281703 |
Giulia Tebaldi1, Sarah Jacca1, Barbara Montanini2, Emanuele Capra3, Alfonso Rosamilia1, Arianna Sala1, Alessandra Stella3, Bianca Castiglioni3, Simone Ottonello2, Gaetano Donofrio4.
Abstract
Viral infections can cause genital tract disorders (including abortion) in cows, and bovine herpesvirus 4 (BoHV-4) is often present in endometritis-affected animals. A major problem with cattle uterine viral infections in general, and BoHV-4 in particular, is our limited understanding of the pathogenic role(s) that these infections play in the endometrium. A similar lack of knowledge holds for the molecular mechanisms utilized, and the host cell pathways affected, by BoHV-4. To begin to fill these gaps, we set up optimized conditions for BoHV-4 infection of a pure population of bovine endometrial stromal cells (BESCs) to be used as source material for RNA sequencing-based transcriptome profiling. Many genes were found to be upregulated (417) or downregulated (181) after BoHV-4 infection. As revealed by enrichment functional analysis on differentially expressed genes, BoHV-4 infection affects various pathways related to cell proliferation and cell surface integrity, at least three of which were centered on upregulation of matrix metalloproteinase 1 (MMP1) and interleukin 8 (IL8). This was confirmed by reverse transcription PCR, real-time PCR, Western-immunoblot analysis, and a luciferase assay with a bovine MMP1-specific promoter reporter construct. Further, it was found that MMP1 transcription was upregulated by the BoHV-4 transactivator IE2/RTA, leading to abnormally high metalloproteinase tissue levels, potentially leading to defective endometrium healing and unresolved inflammation. Based on these findings, we propose a new model for BoHV-4 action centered on IE2-mediated MMP1 upregulation and novel therapeutic interventions based on IFN gamma-mediated MMP1 downregulation.Entities:
Keywords: MMPs; bovine endometrial stromal cells; bovine herpesvirus 4; postpartum metritis; transcriptome profiling
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Year: 2016 PMID: 27281703 DOI: 10.1095/biolreprod.116.139097
Source DB: PubMed Journal: Biol Reprod ISSN: 0006-3363 Impact factor: 4.285