Developing a Non-aureus Staphylococcus Intramammary Probiotic as a Preventative Measure for Bovine Mastitis

dc.contributor.advisorDe Buck, Jeroen
dc.contributor.authorVu, Dennis
dc.contributor.committeememberStorey, Douglas
dc.contributor.committeememberBarkema, Herman
dc.date2023-11
dc.date.accessioned2023-05-24T16:29:15Z
dc.date.available2023-05-24T16:29:15Z
dc.date.issued2023-05-11
dc.description.abstractBovine mastitis is the most common and economically important disease affecting the dairy industry. Intramammary infection (IMI) with Staphylococcus aureus is the leading cause of contagious mastitis. Interestingly, non-aureus staphylococci (NAS) are frequently found in cows with subclinical mastitis, but with a severity less than with S. aureus. Antibiotics are the main method for preventing and treating mastitis. Misuse and overuse of antibiotics have resulted in the emergence of antimicrobial-resistant bacteria, and thus, alternative treatments are required. Bacteriocins, antimicrobial peptides produced by bacteria, are a promising alternative. We hypothesized that by creating a NAS probiotic through genetically engineering a bacteriocin gene cluster into its genome, it will be able to inhibit S. aureus and prevent mastitis. To achieve this, we needed to find a persistent and non-inflammatory NAS strain that can colonize cow mammary glands by using an experimental mammary infusion model. After finding a persistent and non-inflammatory NAS, we will perform a bacteriocin gene cluster knock-in using allelic replacement. Finally, the probiotic will then be characterized through gene expression and killing assays. This thesis aimed to create an alternative treatment to prevent the growth of mastitis pathogens during the dry period. Ultimately, this will lower the usage of antibiotics and give us another preventative tool against mastitis. We identified S. warneri 2993 as the most persistent and non-inflammatory NAS but unfortunately, we were not able to perform our bacteriocin gene knock-in. Instead, we recommend future studies to re-attempt this gene knock-in but with a different bacteriocin gene cluster for an increased likelihood of success. The probiotic will then need testing in ¬in vivo¬ IMI experiments in mice and then in cows following the protocols we have designed.
dc.identifier.citationVu, D. (2023). Developing a non-aureus staphylococcus intramammary probiotic as a preventative measure for bovine mastitis (Master's thesis, University of Calgary, Calgary, Canada). Retrieved from https://prism.ucalgary.ca.
dc.identifier.urihttps://hdl.handle.net/1880/116571
dc.identifier.urihttps://dx.doi.org/10.11575/PRISM/dspace/41414
dc.language.isoen
dc.publisher.facultyGraduate Studies
dc.publisher.institutionUniversity of Calgary
dc.rightsUniversity of Calgary graduate students retain copyright ownership and moral rights for their thesis. You may use this material in any way that is permitted by the Copyright Act or through licensing that has been assigned to the document. For uses that are not allowable under copyright legislation or licensing, you are required to seek permission.
dc.subjectMastitis
dc.subjectProbiotic
dc.subjectBovine
dc.subjectNon-aureus Staphylococcus
dc.subjectGenetic Manipulation
dc.subjectTransformation
dc.subjectAllelic Replacement
dc.subject.classificationMicrobiology
dc.subject.classificationVeterinary Science
dc.titleDeveloping a Non-aureus Staphylococcus Intramammary Probiotic as a Preventative Measure for Bovine Mastitis
dc.typemaster thesis
thesis.degree.disciplineVeterinary Medical Sciences
thesis.degree.grantorUniversity of Calgary
thesis.degree.nameMaster of Science (MSc)
ucalgary.thesis.accesssetbystudentI do not require a thesis withhold – my thesis will have open access and can be viewed and downloaded publicly as soon as possible.
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