Dear colleagues,

My co-authors and I are very happy to share our recent publication on the

*Cellular Prion Protein Expression in the Brain Tissue from Brucella
ceti-Infected Striped Dolphins ( Stenella coeruleoalba)*

You will find the open access publication here:
https://www.mdpi.com/2076-2615/12/10/1304


*Angelucci CB, Giacominelli-Stuffler R, Baffoni M, Di Francesco CE, Di
Francesco G, Di Renzo L, Tittarelli M, Petrella A, Grattarola C, Mazzariol
S, Sierra E, Fernández A, Di Guardo G. Cellular Prion Protein Expression in
the Brain Tissue from Brucella ceti-Infected Striped Dolphins (Stenella
coeruleoalba). Animals. 2022 May 19;12(10):1304.*



*Abstract*


*Brucella 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.




Regards



Sandro Mazzariol
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