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dc.creatorRossetti, Carlos A.
dc.creatorDrake, Kenneth L.
dc.creatorSiddavatam, Prasad
dc.creatorLawhon, Sara D.
dc.creatorNunes, Jairo E.
dc.creatorGull, Tamara
dc.creatorKhare, Sangeeta
dc.creatorEverts, Robin E.
dc.creatorLewin, Harris A.
dc.creatorAdams, Leslie Garry
dc.date.accessioned2014-02-27T21:37:18Z
dc.date.available2014-02-27T21:37:18Z
dc.date.issued2013-12-09
dc.identifier.citationRossetti CA, Drake KL, Siddavatam P, Lawhon SD, Nunes JES, et al. (2013) Systems Biology Analysis of Brucella Infected Peyer’s Patch Reveals Rapid Invasion with Modest Transient Perturbations of the Host Transcriptome. PLoS ONE 8(12): e81719. doi:10.1371/journal.pone.0081719en_US
dc.identifier.urihttp://dx.doi.org/10.1371/journal.pone.0081719
dc.identifier.urihttp://hdl.handle.net/1969.1/151490
dc.description.abstractBrucella melitensis causes the most severe and acute symptoms of all Brucella species in human beings and infects hosts primarily through the oral route. The epithelium covering domed villi of jejunal-ileal Peyer’s patches is an important site of entry for several pathogens, including Brucella. Here, we use the calf ligated ileal loop model to study temporal in vivo Brucella-infected host molecular and morphological responses. Our results document Brucella bacteremia occurring within 30 min after intraluminal inoculation of the ileum without histopathologic traces of lesions. Based on a system biology Dynamic Bayesian Network modeling approach (DBN) of microarray data, a very early transient perturbation of the host enteric transcriptome was associated with the initial host response to Brucella contact that is rapidly averted allowing invasion and dissemination. A detailed analysis revealed active expression of Syndecan 2, Integrin alpha L and Integrin beta 2 genes, which may favor initial Brucella adhesion. Also, two intestinal barrier-related pathways (Tight Junction and Trefoil Factors Initiated Mucosal Healing) were significantly repressed in the early stage of infection, suggesting subversion of mucosal epithelial barrier function to facilitate Brucella transepithelial migration. Simultaneously, the strong activation of the innate immune response pathways would suggest that the host mounts an appropriate protective immune response; however, the expression of the two key genes that encode innate immunity anti-Brucella cytokines such as TNF-a and IL12p40 were not significantly changed throughout the study. Furthermore, the defective expression of Toll-Like Receptor Signaling pathways may partially explain the lack of proinflammatory cytokine production and consequently the absence of morphologically detectable inflammation at the site of infection. Cumulatively, our results indicate that the in vivo pathogenesis of the early infectious process of Brucella is primarily accomplished by compromising the mucosal immune barrier and subverting critical immune response mechanisms.en_US
dc.description.sponsorshipThe open access fee for this work was funded through the Texas A&M University Open Access to Knowledge (OAK) Fund.en_US
dc.language.isoen_USen_US
dc.publisherPLoSen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.titleSystems Biology Analysis of Brucella Infected Peyers Patch Reveals Rapid Invasion with Modest Transient Perturbations of the Host Transcriptomeen_US
dc.typeArticleen_US
local.departmentVeterinary Pathobiologyen_US
dc.rights.requestablefalseen_US


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Attribution 3.0 United States
Except where otherwise noted, this item's license is described as Attribution 3.0 United States