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dc.contributor.authorBudnick, James A.
dc.contributor.authorSheehan, Lauren M.
dc.contributor.authorColquhoun, Jennifer M.
dc.contributor.authorDunman, Paul M.
dc.contributor.authorRoop, Martin, Jr.
dc.contributor.authorWalker, Graham C.
dc.date.accessioned2018-07-27T17:22:53Z
dc.date.available2018-07-27T17:22:53Z
dc.date.issued2018-04
dc.identifier.issn0021-9193
dc.identifier.issn1098-5530
dc.identifier.urihttp://hdl.handle.net/1721.1/117161
dc.description.abstractThe endoribonuclease YbeY is one of the most well conserved proteins across the kingdoms of life. In the present study, we demonstrate that YbeY in Brucella abortus is linked to a variety of important activities, including proper cellular morphology, mRNA transcript levels, and virulence. Deletion of ybeY in B. abortus led to a small colony phenotype when the bacteria were grown on agar medium, as well as significant aberrations in the morphology of the bacterial cell as evidenced by electron microscopy. Additionally, compared to the parental strain, the ΔybeY strain was significantly attenuated in both macrophage and mouse models of infection. The ΔybeY strain also showed increased sensitivities to several in vitro applied stressors, including bile acid, hydrogen peroxide, SDS, and paraquat. Transcriptomic analysis revealed that a multitude of mRNA transcripts are dysregulated in the ΔybeY strain, and many of the identified mRNAs encode proteins involved in metabolism, nutrient transport, transcriptional regulation, and flagellum synthesis. We subsequently constructed gene deletion strains of the most highly dysregulated systems, and several of the YbeY-linked gene deletion strains exhibited defects in the ability of the bacteria to survive and replicate in primary murine macrophages. Altogether, these data establish a clear role for YbeY in the biology and virulence of Brucella, and moreover, this work further illuminates the highly varied roles of this widely conserved endoribonuclease in bacteria. Importance Brucella spp. are highly efficient bacterial pathogens of animals and humans, causing significant morbidity and economic loss worldwide, and relapse of disease often occurs following antibiotic treatment of human brucellosis. As such, novel therapeutic strategies to combat Brucella infections are needed. Ribonucleases in the brucellae are understudied, and these enzymes represent elements that may be potential targets for future treatment approaches. The present work demonstrates the importance of the endoribonuclease YbeY for cellular morphology, efficient control of mRNA levels, and virulence in B. abortus. Overall, this study advances our understanding of the critical roles of YbeY in the pathogenesis of the intracellular brucellae and expands our understanding of this highly conserved ribonuclease.en_US
dc.description.sponsorshipNational Institute of General Medical Sciences (U.S.) (Grant GM31030)en_US
dc.language.isoen_US
dc.publisherAmerican Society for Microbiologyen_US
dc.relation.isversionofhttp://dx.doi.org/10.1128/JB.00105-18en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourceProf. Walker via Courtney Crummetten_US
dc.titleThe endoribonuclease YbeY is linked to proper cellular morphology and virulence in 2 Brucella abortusen_US
dc.typeArticleen_US
dc.identifier.citationBudnick, James A., et al. “Endoribonuclease YbeY Is Linked to Proper Cellular Morphology and Virulence in Brucella Abortus.” Journal of Bacteriology, edited by Victor J. DiRita, vol. 200, no. 12, Apr. 2018.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.approverWalker Gen_US
dc.contributor.mitauthorWalker, Graham C.
dc.relation.journalJournal of Bacteriologyen_US
dc.eprint.versionOriginal manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/NonPeerRevieweden_US
dspace.orderedauthorsBudnick, James A.; Sheehan, Lauren M.; Colquhoun, Jennifer M.; Dunman, Paul M.; Walker, Graham C.; Roop, Martin; Caswell, Clayton C.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0001-7243-8261
mit.licenseOPEN_ACCESS_POLICYen_US


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