Transcriptome microRNA profiling of bovine mammary epithelial cells challenged with Escherichia coli or Staphylococcus aureusbacteria reveals pathogen directed microRNA expression profiles

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dc.contributor.author
Jin, Weiwu
Ibeagha-Awemu, Eveline M.
Liang, Guanxiang
Beaudoin, Frédéric
Zhao, Xin
Guan, Le Luo
dc.date.accepted
2014-02-25
dc.date.accessioned
2024-01-09T14:50:31Z
dc.date.available
2024-01-09T14:50:31Z
dc.date.issued
2014-03-07
dc.date.submitted
2013-10-14
dc.description.abstract - en
Background MicroRNAs (miRNAs) can post-transcriptionally regulate gene expression and have been shown to be critical regulators to the fine-tuning of epithelial immune responses. However, the role of miRNAs in bovine responses to E. coli and S. aureus, two mastitis causing pathogens, is not well understood. Results The global expression of miRNAs in bovine mammary epithelial cells (MAC-T cells) challenged with and without heat-inactivated Staphylococcus aureus (S. aureus) or Escherichia coli (E. coli) bacteria at 0, 6, 12, 24, and 48 hr was profiled using RNA-Seq. A total of 231 known bovine miRNAs were identified with more than 10 counts per million in at least one of 13 libraries and 5 miRNAs including bta-miR-21-5p, miR-27b, miR-22-3p, miR-184 and let-7f represented more than 50% of the abundance. One hundred and thirteen novel miRNAs were also identified and more than one third of them belong to the bta-miR-2284 family. Seventeen miRNAs were significantly (P < 0.05) differentially regulated by the presence of pathogens. E. coli initiated an earlier regulation of miRNAs (6 miRNAs differentially regulated within the first 6 hrs post challenge as compared to 1 miRNA for S. aureus) while S. aureus presented a delayed response. Five differentially expressed miRNAs (bta-miR-184, miR-24-3p, miR-148, miR-486 and let-7a-5p) were unique to E. coli while four (bta-miR-2339, miR-499, miR-23a and miR-99b) were unique to S. aureus. In addition, our study revealed a temporal differential regulation of five miRNAs (bta-miR-193a-3p, miR-423-5p, miR-30b-5p, miR-29c and miR-un116) in unchallenged cells. Target gene predictions of pathogen differentially expressed miRNAs indicate a significant enrichment in gene ontology functional categories in development/cellular processes, biological regulation as well as cell growth and death. Furthermore, target genes were significantly enriched in several KEGG pathways including immune system, signal transduction, cellular process, nervous system, development and human diseases. Conclusion Using next-generation sequencing, our study identified a pathogen directed differential regulation of miRNAs in MAC-T cells with roles in immunity and development. Our study provides a further confirmation of the involvement of mammary epithelia cells in contributing to the immune response to infecting pathogens and suggests the potential of miRNAs to serve as biomarkers for diagnosis and development of control measures.
dc.identifier.citation
Jin, W., Ibeagha-Awemu, E. M., Liang, G., Beaudoin, F., Zhao, X., & Guan, L. L. (2014). Transcriptome microRNA profiling of bovine mammary epithelial cells challenged with Escherichia coli or Staphylococcus aureusbacteria reveals pathogen directed microRNA expression profiles. BMC Genomics, 15, Article 181. https://doi.org/10.1186/1471-2164-15-181
dc.identifier.doi
https://doi.org/10.1186/1471-2164-15-181
dc.identifier.issn
1471-2164
dc.identifier.uri
https://open-science.canada.ca/handle/123456789/1589
dc.language.iso
en
dc.publisher
BioMed Central Ltd.
dc.rights.openaccesslevel - en
Gold
dc.rights.openaccesslevel - fr
Or
dc.subject - en
Agriculture
dc.subject - fr
Agriculture
dc.subject.en - en
Agriculture
dc.subject.fr - fr
Agriculture
dc.title - en
Transcriptome microRNA profiling of bovine mammary epithelial cells challenged with Escherichia coli or Staphylococcus aureusbacteria reveals pathogen directed microRNA expression profiles
dc.type - en
Article
dc.type - fr
Article
local.acceptedmanuscript.articlenum
181
local.article.journaltitle
BMC Genomics
local.article.journalvolume
15
local.pagination
1-16
local.peerreview - en
Yes
local.peerreview - fr
Oui
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