Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/120511
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dc.contributor.authorAngelucci, CBen_US
dc.contributor.authorGiacominelli-Stuffler, Ren_US
dc.contributor.authorBaffoni, Men_US
dc.contributor.authorDi Francesco, CEen_US
dc.contributor.authorDi Francesco, Gen_US
dc.contributor.authorDi Renzo, Len_US
dc.contributor.authorTittarelli, Men_US
dc.contributor.authorPetrella, Aen_US
dc.contributor.authorGrattarola, Cen_US
dc.contributor.authorMazzariol, Sen_US
dc.contributor.authorSierra Pulpillo, Eva Maríaen_US
dc.contributor.authorFernández Rodríguez, Antonio Jesúsen_US
dc.contributor.authorDi Guardo, Gen_US
dc.date.accessioned2023-02-16T09:15:03Z-
dc.date.available2023-02-16T09:15:03Z-
dc.date.issued2022en_US
dc.identifier.issn2076-2615en_US
dc.identifier.urihttp://hdl.handle.net/10553/120511-
dc.description.abstractBrucella ceti, a zoonotic pathogen of major concern to cetacean health and conservation, is responsible for severe meningo-encephalitic/myelitic lesions in striped dolphins (Stenella coeruleoalba), often leading to their stranding and death. This study investigated, for the first time, the cellular prion protein (PrPc) expression in the brain tissue from B. ceti-infected, neurobrucellosis-affected striped dolphins. Seven B. ceti-infected, neurobrucellosis-affected striped dolphins, found stranded along the Italian coastline (6) and in the Canary Islands (1), were investigated, along with five B. ceti-uninfected striped dolphins from the coast of Italy, carrying no brain lesions, which served as negative controls. Western Blot (WB) and immunohistochemistry (IHC) with an anti-PrP murine monoclonal antibody were carried out on the brain parenchyma of these dolphins. While PrPc IHC yielded inconclusive results, a clear-cut PrPc expression of different intensity was found by means of WB analyses in the brain tissue of all the seven herein investigated, B. ceti-infected and neurobrucellosis-affected cetacean specimens, with two dolphins stranded along the Italian coastline and one dolphin beached in Canary Islands also exhibiting a statistically significant increase in cerebral PrPc expression as compared to the five Brucella spp.-negative control specimens. The significantly increased PrPc expression found in three out of seven B. ceti-infected, neurobrucellosis-affected striped dolphins does not allow us to draw any firm conclusion(s) about the putative role of PrPc as a host cell receptor for B. ceti. Should this be the case, an upregulation of PrPc mRNA in the brain tissue of neurobrucellosis-affected striped dolphins could be hypothesized during the different stages of B. ceti infection, as previously shown in murine bone marrow cells challenged with Escherichia coli. Noteworthy, the inflammatory infiltrates seen in the brain and in the cervico-thoracic spinal cord segments from the herein investigated, B. ceti-infected and neurobrucellosis-affected striped dolphins were densely populated by macrophage/histiocyte cells, often harboring Brucella spp. antigen in their cytoplasm, similarly to what was reported in macrophages from mice experimentally challenged with B. abortus. Notwithstanding the above, much more work is needed in order to properly assess the role of PrPc, if any, as a host cell receptor for B. ceti in striped dolphins.en_US
dc.languageengen_US
dc.relation.ispartofAnimalsen_US
dc.sourceAnimals [EISSN 2076-2615], v. 12 (10), 1304, (Mayo 2022)en_US
dc.subject310907 Patologíaen_US
dc.subject320507 Neurologíaen_US
dc.subject.otherBrucella cetien_US
dc.subject.otherCellular prion proteinen_US
dc.subject.otherStriped dolphinen_US
dc.subject.otherStenella coeruloeoalbaen_US
dc.subject.otherBrainen_US
dc.subject.otherNeurobrucellosisen_US
dc.subject.otherPathogenesisen_US
dc.subject.otherInfectionen_US
dc.titleCellular Prion Protein Expression in the Brain Tissue from Brucella ceti-Infected Striped Dolphins (Stenella coeruleoalba)en_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.typeArticleen_US
dc.identifier.doi10.3390/ani12101304en_US
dc.identifier.scopus2-s2.0-85130223396-
dc.identifier.isiWOS:000801690100001-
dc.contributor.orcid#NODATA#-
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dc.identifier.issue10-
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.description.notasThis article belongs to the Special Issue Frontiers in Marine Mammal Health and Immunityen_US
dc.description.numberofpages12en_US
dc.utils.revisionen_US
dc.date.coverdateMayo, 2022en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-VETen_US
dc.description.sjr0,684
dc.description.jcr3,0
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
dc.description.miaricds10,5
item.fulltextCon texto completo-
item.grantfulltextopen-
crisitem.author.deptGIR IUSA-ONEHEALTH 3: Histología y Patología Veterinaria y Forense (Terrestre y Marina)-
crisitem.author.deptIU de Sanidad Animal y Seguridad Alimentaria-
crisitem.author.deptDepartamento de Morfología-
crisitem.author.deptGIR IUSA-ONEHEALTH 3: Histología y Patología Veterinaria y Forense (Terrestre y Marina)-
crisitem.author.deptIU de Sanidad Animal y Seguridad Alimentaria-
crisitem.author.deptDepartamento de Morfología-
crisitem.author.orcid0000-0003-3749-8845-
crisitem.author.orcid0000-0001-5281-0521-
crisitem.author.parentorgIU de Sanidad Animal y Seguridad Alimentaria-
crisitem.author.parentorgIU de Sanidad Animal y Seguridad Alimentaria-
crisitem.author.fullNameSierra Pulpillo, Eva María-
crisitem.author.fullNameFernández Rodríguez, Antonio Jesús-
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