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dc.contributor.authorZhu, Jianguo
dc.contributor.authorLarson, Charles B.
dc.contributor.authorRamaker, Megan Ann
dc.contributor.authorQuandt, Kimberly
dc.contributor.authorWendte, Jered M.
dc.contributor.authorKu, Kimberly P.
dc.contributor.authorChen, Fang
dc.contributor.authorJourdian, George W.
dc.contributor.authorVemulapalli, Ramesh
dc.contributor.authorSchurig, Gerhardt G.
dc.contributor.authorHe, Yongqun
dc.date.accessioned2019-08-28T16:00:57Z
dc.date.available2019-08-28T16:00:57Z
dc.date.issued2011-11-25
dc.identifieroksd_zhu_characterizatio_2011
dc.identifier.citationZhu, J., Larson, C. B., Ramaker, M. A., Quandt, K., Wendte, J. M., Ku, K. P., ... He, Y. (2011). Characterization of recombinant B. abortus strain RB51SOD toward understanding the uncorrelated innate and adaptive immune responses induced by RB51SOD compared to its parent vaccine strain RB51. Frontiers in Cellular and Infection Microbiology, 1, Article 10. https://doi.org/10.3389/fcimb.2011.00010
dc.identifier.urihttps://hdl.handle.net/11244/321393
dc.description.abstractBrucella abortus is a Gram-negative, facultative intracellular pathogen for several mammals, including humans. Live attenuated B. abortus strain RB51 is currently the official vaccine used against bovine brucellosis in the United States and several other countries. Overexpression of protective B. abortus antigen Cu/Zn superoxide dismutase (SOD) in a recombinant strain of RB51 (strain RB51SOD) significantly increases its vaccine efficacy against virulent B. abortus challenge in a mouse model. An attempt has been made to better understand the mechanism of the enhanced protective immunity of RB51SOD compared to its parent strain RB51. We previously reported that RB51SOD stimulated enhanced Th1 immune response. In this study, we further found that T effector cells derived from RB51SOD-immunized mice exhibited significantly higher cytotoxic T lymphocyte activity than T effector cells derived from RB51-immunized mice against virulent B. abortus-infected target cells. Meanwhile, the macrophage responses to these two strains were also studied. Compared to RB51, RB51SOD cells had a lower survival rate in macrophages and induced lower levels of macrophage apoptosis and necrosis. The decreased survival of RB51SOD cells correlates with the higher sensitivity of RB51SOD, compared to RB51, to the bactericidal action of either Polymyxin B or sodium dodecyl sulfate (SDS). Furthermore, a physical damage to the outer membrane of RB51SOD was observed by electron microscopy. Possibly due to the physical damage, overexpressed Cu/Zn SOD in RB51SOD was found to be released into the bacterial cell culture medium. Therefore, the stronger adaptive immunity induced by RB51SOD did not correlate with the low level of innate immunity induced by RB51SOD compared to RB51. This unique and apparently contradictory profile is likely associated with the differences in outer membrane integrity and Cu/Zn SOD release.
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dc.languageen_US
dc.publisherFrontiers Media
dc.rightsThis material has been previously published. In the Oklahoma State University Library's institutional repository this version is made available through the open access principles and the terms of agreement/consent between the author(s) and the publisher. The permission policy on the use, reproduction or distribution of the material falls under fair use for educational, scholarship, and research purposes. Contact Digital Resources and Discovery Services at lib-dls@okstate.edu or 405-744-9161 for further information.
dc.titleCharacterization of recombinant B. abortus strain RB51SOD toward understanding the uncorrelated innate and adaptive immune responses induced by RB51SOD compared to its parent vaccine strain RB51
osu.filenameoksd_zhu_characterizatio_2011.pdf
dc.description.peerreviewPeer reviewed
dc.identifier.doi10.3389/fcimb.2011.00010
dc.description.departmentVeterinary Health Sciences
dc.type.genreArticle
dc.type.materialText
dc.subject.keywordsbrucella abortus strains rb51 and rb51sod
dc.subject.keywordscu/zn superoxide dismutase (cu/zn sod)
dc.subject.keywordsadaptive immunity
dc.subject.keywordscytotoxic t lymphocyte (ctl)
dc.subject.keywordsinnate immunity
dc.subject.keywordsmacrophage cell death
dc.subject.keywordsouter membrane integrity
dc.subject.keywordsprotein release


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