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Bovine mammary cellular immune responses to Staphylococcus aureus

dc.contributor.advisorPotter, Andrewen_US
dc.contributor.advisorPerez-Casal, Joseen_US
dc.contributor.committeeMemberBarkema, Hermanen_US
dc.contributor.committeeMemberBabiuk, Lorneen_US
dc.contributor.committeeMemberBuchanan, Fionaen_US
dc.contributor.committeeMemberGriebel, Philipen_US
dc.creatorLuby, Christopher Daviden_US
dc.date.accessioned2011-01-17T07:26:44Zen_US
dc.date.accessioned2013-01-04T04:24:05Z
dc.date.available2012-01-17T08:00:00Zen_US
dc.date.available2013-01-04T04:24:05Z
dc.date.created2010-09en_US
dc.date.issued2010-09-01en_US
dc.date.submittedSeptember 2010en_US
dc.description.abstractMastitis is a syndrome manifested by mammary gland inflammation which is thought to cause between $300 and $400 million in annual losses to the Canadian Dairy Industry. Studies have indicated that S. aureus may cause the production of anti-inflammatory cytokines which may enhance its survival within the bovine mammary gland. However, other studies have reported differing results following S. aureus intramammary infection (IMI). This thesis tested the hypothesis that S. aureus generated anti-inflammatory cytokine responses at the site of infection. In the first objective, different S. aureus isolates were screened for their effects on cytokine production (IFN-γ, TNF-α, IL-4 and IL-10) by bovine peripheral blood mononuclear cells (PBMCs) in vitro. Nine S. aureus isolates were co-cultured with PBMCs from lactating dairy cattle. Cattle used in the study had recall immune responses to S. aureus. The majority (6/9) of S. aureus isolates had minor effectors on cytokine production. The three remaining isolates generated large cytokine responses with both pro-inflammatory (IFN-γ and TNF-α) and anti-inflammatory (IL-4 and IL-10) characteristics. Two of these three isolates were tested in vivo by experimentally infecting lactating ewes. Cytokine production was characterized in the teat end, the mammary parenchyma and the supramammary lymph nodes (SMLNs). One isolate generated anti-inflammatory responses in vivo (IL-4 and IL-10) whilst the other generated both pro-inflammatory (IFN-γ) and anti-inflammatory (IL-10) responses in vivo. Given that some studies have suggested a role of staphylococcal enterotoxin C (sec) in the generation of anti-inflammatory responses, the role of sec was also investigated using bovine PBMCs. When purified SEC protein was co-cultured with PBMCs from beef steers, anti-inflammatory cytokines were produced. However, a S. aureus strain which was transformed for the sec gene did not affect cytokine production when co-cultured with PBMCs from lactating dairy cattle. The results of this thesis suggest that S. aureus infection can cause anti-inflammatory cytokine production but the response depends on the isolate causing the infection. Furthermore, the role of sec appears to be minimal.en_US
dc.identifier.urihttp://hdl.handle.net/10388/etd-01172011-072644en_US
dc.language.isoen_USen_US
dc.subjectBovineen_US
dc.subjectStaphylococcus aureusen_US
dc.subjectMastitisen_US
dc.subjectImmuneen_US
dc.titleBovine mammary cellular immune responses to Staphylococcus aureusen_US
dc.type.genreThesisen_US
dc.type.materialtexten_US
thesis.degree.departmentVeterinary Microbiologyen_US
thesis.degree.disciplineVeterinary Microbiologyen_US
thesis.degree.grantorUniversity of Saskatchewanen_US
thesis.degree.levelDoctoralen_US
thesis.degree.nameDoctor of Philosophy (Ph.D.)en_US

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