163 results on '"Casalone C"'
Search Results
2. First report of Salmonella 1,4,[5],12:i:- in free-ranging striped dolphins (Stenella coeruleoalba), Italy
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Grattarola, C., Gallina, S., Giorda, F., Pautasso, A., Ballardini, M., Iulini, B., Varello, K., Goria, M., Peletto, S., Masoero, L., Serracca, L., Romano, A., Dondo, A., Zoppi, S., Garibaldi, F., Scaglione, F. E., Marsili, L., Di Guardo, G., Lettini, A. A., Mignone, W., Fernandez, A., and Casalone, C.
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- 2019
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3. Integrated surveillance on tick-borne diseases in northwestern Italy
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Tomassone, L., Garcia-Vozmediano, A., Mannelli, A., Rossi, L., Pintore, M., Pautasso, A., and Casalone, C
- Published
- 2022
4. Multidisciplinary studies on a sperm whales’ mass stranding
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Sandro Mazzariol, Cinzia Centelleghe, Povinelli, M., Federico Bonsembiante, Bruno Cozzi, FEDERICA MARCER, Ferri, N., Di Francesco, G., Di Provvido, A., Di Renzo, L., Badagliacca, P., Di Guardo, G., Di Francesco, C. E., Cocumelli, C., Terracciano, G., Cersini, A., Cardeti, G., Petrella, A., Troiano, P., Beverelli, M., Garibaldi, F., Podestà, M., Marsili, L., Fossi, C., Capanni, Fabio, Mattiucci, S., Cipriani, P., Nurra, D., Rossi, R., Zaccaroni, A., Andreini, R., Rubini, S., Berto, Daniele, Beraldo Quiros, Y., Fernandez, A., Morelli, Mara, Giorda, F., Pautasso, A., Modesto, P., Biolatti, C., Mignone, W., and Casalone, C.
- Published
- 2018
5. Astroblastoma: beside being a tumor entity, an occasional phenotype of astrocytic gliomas?
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Mellai M, Piazzi A, Casalone C, Grifoni S, Melcarne A, Annovazzi L, Cassoni P, Denysenko T, Valentini MC, Cistaro A, and Schiffer D
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lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,lcsh:RC254-282 - Abstract
Marta Mellai,1 Angela Piazzi,1 Cristina Casalone,2 Silvia Grifoni,2 Antonio Melcarne,3 Laura Annovazzi,1 Paola Cassoni,4 Tetyana Denysenko,1 Maria Consuelo Valentini,5 Angelina Cistaro,6,7 Davide Schiffer1 1Neuro-Bio-Oncology Center, Policlinico di Monza Foundation/Consorzio di Neuroscienze, University of Pavia, Vercelli, Italy; 2Istituto Zooprofilattico Sperimentale del Piemonte, Liguria e Valle d'Aosta, Turin, Italy; 3Department of Neurosurgery, CTO Hospital/Città della Salute e della Scienza, Turin, Italy; 4Department of Medical Sciences, University of Turin, Turin, Italy; 5Department of Neuroradiology, CTO Hospital/Città della Salute e della Scienza, Turin, Italy; 6Positron Emission Tomography Center IRMET S.p.A, Euromedic Inc., Turin, Italy; 7Institute of Cognitive Sciences and Technologies, National Research Council, Rome, Italy Abstract: The diagnosis of astroblastoma is based on a typical histological aspect with perivascular distribution of cells sending cytoplasmic extensions to the vessels and vascular hyalinization. These criteria are useful for standardizing the identification of the tumor, but, in spite of this, there are discrepancies in the literature concerning the age distribution and the benign or malignant nature of the tumor. Three cases are discussed in this study: Case 1 was a typical high-grade astroblastoma; Case 2 was an oligodendroglioma at the first intervention and an oligoastrocytoma at the second intervention with typical perivascular arrangements in the astrocytic component; Case 3 was a gemistocytic glioma with malignant features and typical perivascular arrangements. Genetic analysis showed genetic alterations that are typical of gliomas of all malignancy grades. Using the neurosphere assay, neurospheres and adherent cells were found to have developed in Case 1, while adherent cells only developed in Case 2, in line with the stemness potential of the tumors. The cases are discussed in relation to their diagnostic assessment as astroblastoma, and it is hypothesized that the typical perivascular distribution of cells may not indicate a separate and unique tumor entity, but may be a peculiarity that can be acquired by astrocytic gliomas when an unknown cause from the tumor microenvironment influences the relationship between vessels and tumor cells. Keywords: gliomas, cell lines, histology, genetics
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- 2015
6. “One Health” approach in West Nile disease surveillance: the northwestern Italian experience
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Radaelli, M.C., primary, Verna, F., additional, Pautasso, A., additional, Bellavia, V., additional, Ballardini, M., additional, Mignone, W., additional, Masoero, L., additional, Dondo, A., additional, Orusa, R., additional, Picco, L., additional, Moschi, R., additional, Mosca, A., additional, Chianese, R., additional, Chiavacci, L., additional, and Casalone, C., additional
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- 2019
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7. Novel dolphin morbillivirus (DMV) outbreak among Mediterranean striped dolphins Stenella coeruleoalba in Italian waters
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Pautasso, A, primary, Iulini, B, additional, Grattarola, C, additional, Giorda, F, additional, Goria, M, additional, Peletto, S, additional, Masoero, L, additional, Mignone, W, additional, Varello, K, additional, Petrella, A, additional, Carbone, A, additional, Pintore, A, additional, Denurra, D, additional, Scholl, F, additional, Cersini, A, additional, Puleio, R, additional, Purpari, G, additional, Lucifora, G, additional, Fusco, G, additional, Di Guardo, G, additional, Mazzariol, S, additional, and Casalone, C, additional
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- 2019
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8. Occlusive mycotic tracheobronchitis and systemic Alphaherpesvirus coinfection in a free-living striped dolphin Stenella coeruleoalba in Italy
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Grattarola, C, primary, Giorda, F, additional, Iulini, B, additional, Pautasso, A, additional, Ballardini, M, additional, Zoppi, S, additional, Marsili, L, additional, Peletto, S, additional, Masoero, L, additional, Varello, K, additional, Garibaldi, F, additional, Scaglione, FE, additional, Di Guardo, G, additional, Dondo, A, additional, Goria, M, additional, Serracca, L, additional, Mignone, W, additional, and Casalone, C, additional
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- 2018
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9. Low fraction of the 222K PrP variant in the protease-resistant moiety of PrPres in heterozygous scrapie positive goats
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Mazza, M., Guglielmetti, Chiara, Ingravalle, Francesco, Brusadore, Sonia, Langeveld, J.P.M., Ekateriniadou, Loukia V., Andreoletti, O., Casalone, C., Acutis, P.L., Mazza, M., Guglielmetti, Chiara, Ingravalle, Francesco, Brusadore, Sonia, Langeveld, J.P.M., Ekateriniadou, Loukia V., Andreoletti, O., Casalone, C., and Acutis, P.L.
- Abstract
The presence of lysine (K) at codon 222 has been associated with resistance to classical scrapie in goats, but few scrapie cases have been identified in 222Q/K animals. To investigate the contribution of the 222K variant to PrPres formation in natural and experimental Q/K scrapie cases, we applied an immunoblotting method based on the use of two different monoclonal antibodies, F99/97.6.1 and SAF84, chosen for their different affinities to 222K and 222Q PrP variants. Our finding that PrPres seems to be formed nearly totally by the 222Q variant provides evidence that the 222K PrP variant confers resistance to conversion to PrPres formation and reinforces the view that this mutation has a protective role against classical scrapie in goats.
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- 2017
10. NOX2 in the hSOD1G93A Transgenic Swine: a preliminary overview
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Casale, Federico, DE MARCO, Giovanni, Lomartire, Annarosa, Marrali, Giuseppe, Salamone, Paolina, Fuda, Giuseppe, Berrone, E, Crociara, P, Chieppa, Mn, Corona, C, Casalone, C, Calvo, Andrea, and Chio', Adriano
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epilessia ,SLA ,sclerosi multipla ,SLA, epilessia, sclerosi multipla - Published
- 2015
11. Diets with different lipid contents do not modify the neuronal membrane lipid raft profile in a scrapie murine model
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Dall'Ara, P, Iulini, B, Botto, L, Filipe, J, Martino, P, Pintore, M, Gazzuola, P, Mazza, M, Dagrada, M, Ingravalle, F, Casalone, C, Palestini, P, Poli, G, Martino, PA, Pintore, MD, Poli, G., BOTTO, LAURA MARIA, PALESTINI, PAOLA NOVERINA ADA, Dall'Ara, P, Iulini, B, Botto, L, Filipe, J, Martino, P, Pintore, M, Gazzuola, P, Mazza, M, Dagrada, M, Ingravalle, F, Casalone, C, Palestini, P, Poli, G, Martino, PA, Pintore, MD, Poli, G., BOTTO, LAURA MARIA, and PALESTINI, PAOLA NOVERINA ADA
- Abstract
In Transmissible Spongiform Encephalopathies (TSEs), the localization of the prion protein in the neuronal membrane lipid rafts (LR) seems to play a role in sustaining the protein misfolding. Changes in membrane properties, due to altered lipid composition, affect their organization and interaction between lipids and protein therein, and consequently also membrane resident protein functionality; dietary polyunsaturated fatty acids (PUFAs), gangliosides and cholesterol seem to influence these processes. Aims In this work, the influence of administration of different feed, able to change the composition of lipid membrane, on the clinical progression of prion disease was studied. Main methods The activity of three diets (hyperlipidic with 6% fats; hypolipidic with 0.1% fats; and purified with 4% fats) was tested in CD1 mouse model experimentally infected with RML scrapie strain. Presence and distribution of typical central nervous system (CNS) lesions and deposits of PrPsc were evaluated by histopathological analysis and immunohistochemistry. Analysis of lipids was performed in homogenate and insoluble brain fraction of the neuronal membrane rich in LR. Key findings Results show that a diet with a different lipid level has not a significant role in the development of the scrapie disease. All infected mice fed with different diets died in the same time span. Histology, immunohistochemistry, and neuropathological analyses of the infected brains did not show significant differences between animals subjected to different diets. Significance Independently of the diet, the infection induced a significant modification of the lipid composition in homogenates, and a less noticeable one in insoluble brain fraction.
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- 2016
12. The entomological surveillance as a tool for the early detection of mosquito-borne diseases: the experience of Piemonte, Liguria and Valle d’Aosta (Northwestern Italy)
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Verna, F., primary, Ballardini, M., additional, Pautasso, A., additional, Radaelli, M.C., additional, Francese, D.R., additional, Mosca, A., additional, Savini, G., additional, Orusa, R., additional, Chiavacci, L., additional, and Casalone, C., additional
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- 2016
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13. Listeria monocytogenes strains from ruminant rhombencephalitis constitute a genetically homogeneous group related to human outbreak strains
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Rocha, Pr, Lomonaco, Sara, Bottero, Maria Teresa, Dalmasso, Alessandra, Dondo, A, Grattarola, C, Zuccon, F, Iulini, B, Knabel, Sj, Capucchio, Maria Teresa, and Casalone, C.
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- 2013
14. Dolphin Morbillivirus and Toxoplasma gondii coinfection in a fin whale (Balenoptera physalus)
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Mazzariol, Sandro, Marcer, Federica, Mignone, W., Serracca, L., Goria, M., Marsili, L., Di Guardo, G., and Casalone, C.
- Published
- 2012
15. SINDROME DELLA VACCA A TERRA: SISTEMA DI MONITORAGGIO CLINICO DIAGNOSTICO IN PIEMONTE
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Pautasso, A, Iulini, B, D'Angelo, Antonio, Bellino, Claudio, Dondo, A, Tursi, Massimiliano, Corrente, M, Greco, Mf, Pintore, Md, Bozzetta, E, Maurella, C, and Casalone, C.
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- 2011
16. Meningoencephalitis and Listeria monocytogenes, Toxoplasma gondii and Brucella spp. coinfection in a dolphin in Italy
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Grattarola, C, primary, Giorda, F, additional, Iulini, B, additional, Pintore, MD, additional, Pautasso, A, additional, Zoppi, S, additional, Goria, M, additional, Romano, A, additional, Peletto, S, additional, Varello, K, additional, Garibaldi, F, additional, Garofolo, G, additional, Di Francesco, CE, additional, Marsili, L, additional, Bozzetta, E, additional, Di Guardo, G, additional, Dondo, A, additional, Mignone, W, additional, and Casalone, C, additional
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- 2016
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17. Seizure Disorders in 43 Cattle
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D'Angelo, A., primary, Bellino, C., additional, Bertone, I., additional, Cagnotti, G., additional, Iulini, B., additional, Miniscalco, B., additional, Casalone, C., additional, Gianella, P., additional, and Cagnasso, A., additional
- Published
- 2015
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18. SORVEGLIANZA DELLA BSE IN ITALIA: ASPETTI NEUROPATOLOGICI IN BOVINI CLINICAMNTE SOSPETTI
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Iulini, B., Maurella, C., D'Angelo, Antonio, Avanzato, T., Florio, C. L., Bellino, Claudio, Manea, B., Gelmetti, D., MARONI PONTI, A., Caramelli, M., and Casalone, C.
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ENCEFALO ,SISTEMA DI SORVEGLIANZA ,BOVINI ,BSE - Published
- 2009
19. Modeling amyotrophic lateral sclerosis in hSOD1 transgenic swine
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Chieppa, Mn, Perota, A, Corona, C, Grindatto, A, Lagutina, I, Vallino Costassa, E, Lazzari, G, Colleoni, S, Duchi, R, Lucchini, Franco, Caramelli, M, Bendotti, C, Galli, C, Casalone, C., Lucchini, Franco (ORCID:0000-0003-0280-7062), Chieppa, Mn, Perota, A, Corona, C, Grindatto, A, Lagutina, I, Vallino Costassa, E, Lazzari, G, Colleoni, S, Duchi, R, Lucchini, Franco, Caramelli, M, Bendotti, C, Galli, C, Casalone, C., and Lucchini, Franco (ORCID:0000-0003-0280-7062)
- Abstract
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that occurs in two clinically indistinguishable forms: sporadic (SALS) and familial (FALS), the latter linked to several gene mutations, mostly inheritable in a dominant manner. Nearly 20% of FALS forms are linked to mutations in the Cu/Zn superoxide dismutase (SOD1) gene. Research on ALS relies on transgenic models and particularly on mice carrying a glycine-to-alanine conversion at the 93rd codon (G93A) of the hSOD1 gene. Although G93A transgenic mice have been widely employed in clinical trials and basic research, doubts have been recently raised from numerous reliable sources about their suitability to faithfully reproduce human disease. Besides, the scientific community has already foreseen swine as an attractive and alternative model to nonhuman primates for modeling human diseases due to closer anatomical, physiological and biochemical features of swine rather than rodents to humans. On this basis, we have produced the first swine ALS model by in vitro transfection of cultured somatic cells combined with somatic cell nuclear transfer (SCNT). To achieve this goal we developed a SOD1(G93A) (superoxide dismutase 1 mutated in Gly93-Ala) vector, capable of promoting a high and stable transgene expression in primary porcine adult male fibroblasts (PAF). After transfection, clonal selection and transgene expression level assessment, selected SOD1(G93A) PAF colonies were used as nuclei donors in SCNT procedures. SOD1(G93A) embryos were transferred in recipient sows, and pregnancies developed to term. A total of 5 piglets survived artificial hand raising and weaning and developed normally, reaching adulthood. Preliminary analysis revealed transgene integration and hSOD1(G93A) expression in swine tissues and 360° phenotypical characterization is ongoing. We believe that our SOD1(G93A) swine would provide an essential bridge between the fundamental work done in rodent models and the reality of trea
- Published
- 2014
20. Cetacean strandings in Italy: an unusual mortality event along the Tyrrhenian Sea coast in 2013
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Casalone, C, primary, Mazzariol, S, additional, Pautasso, A, additional, Di Guardo, G, additional, Di Nocera, F, additional, Lucifora, G, additional, Ligios, C, additional, Franco, A, additional, Fichi, G, additional, Cocumelli, C, additional, Cersini, A, additional, Guercio, A, additional, Puleio, R, additional, Goria, M, additional, Podestà, M, additional, Marsili, L, additional, Pavan, G, additional, Pintore, A, additional, De Carlo, E, additional, Eleni, C, additional, and Caracappa, S, additional
- Published
- 2014
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21. Amyotrophic lateral sclerosis (ALS) swine models: Production and preliminary characterization
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Grindatto, A, Perota, A, Chieppa, Mn, Costassa, Ev, Colleoni, S, Lo Faro, M, Duchi, R, Palmitessa, C, Lagutina, I, Tortarolo, M, Lazzari, G, Lucchini, Franco, Bendotti, C, Corona, C, Galli, C, Casalone, C., Lucchini, Franco (ORCID:0000-0003-0280-7062), Grindatto, A, Perota, A, Chieppa, Mn, Costassa, Ev, Colleoni, S, Lo Faro, M, Duchi, R, Palmitessa, C, Lagutina, I, Tortarolo, M, Lazzari, G, Lucchini, Franco, Bendotti, C, Corona, C, Galli, C, Casalone, C., and Lucchini, Franco (ORCID:0000-0003-0280-7062)
- Published
- 2013
22. Evaluation of the zoonotic potential of transmissible mink encephalopathy
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Comoy, E. E., Mikol, J., Ruchoux, M. M., Durand, Valerie, Luccantoni-Freire, S., Dehen, C., Correia, Evelyne, Casalone, C., Richt, Jürgen A., Greenlee, J. J., Torres, J. M., Brown, Paul A., Deslys, J. P., Comoy, E. E., Mikol, J., Ruchoux, M. M., Durand, Valerie, Luccantoni-Freire, S., Dehen, C., Correia, Evelyne, Casalone, C., Richt, Jürgen A., Greenlee, J. J., Torres, J. M., Brown, Paul A., and Deslys, J. P.
- Abstract
Successful transmission of Transmissible Mink Encephalopathy (TME) to cattle supports the bovine hypothesis for the still controversial origin of TME outbreaks. Human and primate susceptibility to classical Bovine Spongiform Encephalopathy (c-BSE) and the transmissibility of L-type BSE to macaques indicate a low cattle-to-primate species barrier. We therefore evaluated the zoonotic potential of cattle-adapted TME. In less than two years, this strain induced in cynomolgus macaques a neurological disease similar to L-BSE but distinct from c-BSE. TME derived from another donor species (raccoon) induced a similar disease with even shorter incubation periods. L-BSE and cattle-adapted TME were also transmissible to transgenic mice expressing human prion protein (PrP). Secondary transmissions to transgenic mice expressing bovine PrP maintained the features of the three tested bovine strains (cattle TME, c-BSE and L-BSE) regardless of intermediate host. Thus, TME is the third animal prion strain transmissible to both macaques and humanized transgenic mice, suggesting zoonotic potentials that should be considered in the risk analysis of animal prion diseases for human health. Moreover, the similarities between TME and L-BSE are highly suggestive of a link between these strains, and therefore the possible presence of L-BSE for many decades prior to its identification in USA and Europe. © 2013 by the authors; licensee MDPI, Basel, Switzerland.
- Published
- 2013
23. Generation of pre-implantation pig SCNT embryos harboring the amyotrophic lateral sclerosis related hSOD1G93A gene
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Chieppa, Mn, Perota, A, Lagutina, I, Costassa, Ev, Grindatto, A, Palmitessa, C, Corbellini, D, Tortarolo, M, Colleoni, S, Duchi, R, Lazzari, G, Corona, C, Lucchini, Franco, Bendotti, C, Galli, C, Casalone, C., Lucchini, Franco (ORCID:0000-0003-0280-7062), Chieppa, Mn, Perota, A, Lagutina, I, Costassa, Ev, Grindatto, A, Palmitessa, C, Corbellini, D, Tortarolo, M, Colleoni, S, Duchi, R, Lazzari, G, Corona, C, Lucchini, Franco, Bendotti, C, Galli, C, Casalone, C., and Lucchini, Franco (ORCID:0000-0003-0280-7062)
- Published
- 2012
24. EU-Approved Rapid Tests for Bovine Spongform Encephalopathy Detect Atypical Forms: A Study for Their Sensitivities
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Meloni, D., Davidse, A., Langeveld, J.P.M., varello, K., Casalone, C., Corona, C., Balkema-Buschmann, A., Groschup, M., Ingravalle, F., Bozzetta, E., Meloni, D., Davidse, A., Langeveld, J.P.M., varello, K., Casalone, C., Corona, C., Balkema-Buschmann, A., Groschup, M., Ingravalle, F., and Bozzetta, E.
- Abstract
Since 2004 it become clear that atypical bovine spongiform encephalopthies (BSEs) exist in cattle. Whenever their detection has relied on active surveillance plans implemented in Europe since 2001 by rapid tests, the overall and inter-laboratory performance of these diagnostic systems in the detection of the atypical strains has not been studied thoroughly to date. To fill this gap, the present study reports on the analytical sensitivity of the EU-approved rapid tests for atypical L-and H-type and classical BSE in parallel. Each test was challenged with two dilution series, one created from a positive pool of the three BSE forms according to the EURL standard method of homogenate preparation (50% w/v) and the other as per the test kit manufacturer's instructions. Multilevel logistic models and simple logistic models with the rapid test as the only covariate were fitted for each BSE form analyzed as directed by the test manufacturer's dilution protocol. The same schemes, but excluding the BSE type, were then applied to compare test performance under the manufacturer's versus the water protocol. The IDEXX HerdChek (R) BSE-scrapie short protocol test showed the highest sensitivity for all BSE forms. The IDEXX (R) HerdChek BSE-scrapie ultra short protocol, the Prionics (R) - Check WESTERN and the AJ Roboscreen (R) BetaPrion tests showed similar sensitivities, followed by the Roche (R) PrionScreen, the Bio-Rad (R) TeSeE (TM) SAP and the Prionics (R) - Check PrioSTRIP in descending order of analytical sensitivity. Despite these differences, the limit of detection of all seven rapid tests against the different classes of material set within a 2 log(10) range of the best-performing test, thus meeting the European Food Safety Authority requirement for BSE surveillance purposes. These findings indicate that not many atypical cases would have been missed surveillance since 2001 which is important for further epidemiological interpretations of the sporadic character of atypical
- Published
- 2012
25. Creation of a ubiquitous vector for expression oh hSOD1G93Ain pig
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Chieppa, Mn, Perota, A, Brunetti, D, Porcario, C, Tortarolo, M, Lazzari, G, Bendotti, C, Corona, C, Lucchini, Franco, Casalone, C, Galli, C., Lucchini, Franco (ORCID:0000-0003-0280-7062), Chieppa, Mn, Perota, A, Brunetti, D, Porcario, C, Tortarolo, M, Lazzari, G, Bendotti, C, Corona, C, Lucchini, Franco, Casalone, C, Galli, C., and Lucchini, Franco (ORCID:0000-0003-0280-7062)
- Abstract
Amyotrophic Lateral Sclerosis (ALS) is a lethal neurodegenerative disease that may occur in two forms: sporadic and familial, the latter linked to a mutation in the Cu/Zn superoxide dismutase (SOD1) gene. Rodents expressing the human mutated form of SOD1 (hSOD1G93A) fail to faithfully reproduce the biology of the disease. Moreover, results of drug tests in mice have never been translated into humans. Aim of this work is to create a novel model for ALS, closer related to man, by overexpressing the hSOD1G93A cDNA in pig. We have previously developed an ubiquitous EGFP expression vector, driven by the pCAGGS hybrid promoter (CMV-IE enhancer ? chicken beta actin promoter) that maintains high level of expression through the next generation of pigs (Brunetti et al. 2008). We created a Destination Vector (pMGMARneoP-OrfA) inserting the Conversion cassette (OrfA) of Multisite Gateway system (Invitrogen) into the ubiquitous expression vector. This vector had the pCAGGS promoter inserted between two insulators (MAR of chicken lysozyme gene) to prevent different silencing effects (positional or copy number effects). On the same structure there is a floxed PGK-neo cassette to select the transfected clones but keeping the possibility to remove the selection cassette using the Cre recombinase. We initially inserted the hSOD1G93A cDNA into the Entry clone of Gateway system obtaining the pENTRL1L2-hSODG93A. The SalI-BamHI fragment of this construct was removed and the resulting pENTRL1L2-hSODG93AdelSB was verified by sequencing before using it in a LR exchange reaction with the Destination Vector pMG MARneoP-OrfA mediated by the LR Clonase. The obtained exchange reaction was used to transform chemically competent E.coli cells (One Shot Mach1-Invitrogen) and the resulting pMGMARneoP-CXhSODG93A vector was purified and analyzed by different restriction enzymes and confirmed by sequencing. Specific PCR reaction and DIGlabelled probe have been developed and validated. The linearized exp
- Published
- 2010
26. Variability in disease phenotypes within a single PRNP genotype suggests the existence of multiple natural sheep scarpie strains within Europe
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González, L., Sisó, S., Monleón, E., Casalone, C., van Keulen, L.J.M., Balkema-Buschmann, A., Ortiz-Peláez, A., Lulini, B., Langeveld, J.P.M., Hoffmann, C., Badiola, J.J., Jeffrey, M., Acín, C., González, L., Sisó, S., Monleón, E., Casalone, C., van Keulen, L.J.M., Balkema-Buschmann, A., Ortiz-Peláez, A., Lulini, B., Langeveld, J.P.M., Hoffmann, C., Badiola, J.J., Jeffrey, M., and Acín, C.
- Abstract
Variability of pathological phenotypes within classical sheep scrapie cases has been reported for some time, but in many instances it has been attributed to differences in the PRNP genotype of the host. To address this issue we have examined by immunohistochemistry (IHC) and Western blotting (WB) for the disease-associated form of the prion protein (PrPd), the brains of 23 sheep from five European countries, all of which were of the same ARQ/ARQ genotype. As a result of IHC examinations, sheep were distributed into five groups with different phenotypes and the groups were the same regardless of the scoring method used, ‘long’ or ‘short’ PrPd profiling. The groups made did not respond to the geographical origin of the cases and did not correlate with the vacuolar lesion profiles, which showed a high individual variability. Discriminatory IHC and WB methods coincided to detect a ‘CH1641-like’ case but otherwise correlated poorly in the classification of disease phenotypes. No other polymorphisms of the PRNP gene were found that could account for the pathological differences, except perhaps for a sheep from Spain with a mutation at codon 103 and a unique pathological phenotype. Preliminary evidence indicates that those different IHC phenotypes correlate with distinct biological properties on bioassay, suggesting that they are indicative of strain diversity. We therefore conclude that natural scrapie strains exist and that they can be revealed by detailed pathological examinations, which can be harmonized between laboratories to produce comparable results.
- Published
- 2010
27. Molecular discrimination of atypical bovine spongiform encephalopathy strains from a geographical region spanning a wide area in Europe
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Jacobs, J.G., Langeveld, J.P.M., Biacabe, A.G., Acutis, P.L., Polak, M.P., Gavier-Widen, D., Buschmann, A., Caramelli, M., Casalone, C., Mazza, M., Groschup, M., Erkens, J.H.F., Davidse, A., van Zijderveld, F.G., Baron, T., Jacobs, J.G., Langeveld, J.P.M., Biacabe, A.G., Acutis, P.L., Polak, M.P., Gavier-Widen, D., Buschmann, A., Caramelli, M., Casalone, C., Mazza, M., Groschup, M., Erkens, J.H.F., Davidse, A., van Zijderveld, F.G., and Baron, T.
- Abstract
Transmissible spongiform encephalopathy strains can be differentiated by their behavior in bioassays and by molecular analyses of the disease-associated prion protein (PrP) in a posttranslationally transformed conformation (PrPSc). Until recently, isolates from cases of bovine spongiform encephalopathy (BSE) appeared to be very homogeneous. However, a limited number of atypical BSE isolates have recently been identified upon analyses of the disease-associated proteinase K (PK) resistance-associated moiety of PrPSc (Prp(res)), suggesting the existence of at least two additional BSE PrPres variants. These are defined here as the H type and the L type, according to the higher and lower positions of the nonglycosylated PrPres band in Western blots, respectively, compared to the position of the band in classical BSE (C-type) isolates. These molecular Prpres variants, which originated from six different European countries, were investigated together. In addition to the migration properties and glycosylation profiles (glycoprofiles), the H- and L-type isolates exhibited enhanced PK sensitivities at pH 8 compared to those of the C-type isolates. Moreover, H-type BSE isolates exhibited differences in the binding of antibodies specific for N- and more C-terminal PrP regions and principally contained two aglycosylated PrPres moieties which can both be glycosylated and which is thus indicative of the existence of two PrPres, populations or intermediate cleavage sites. These properties appear to be consistent within each BSE type and independent of the geographical origin, suggesting the existence of different BSE strains in cattle. The choice of three antibodies and the application of two pHs during the digestion of brain homogenates provide practical and diverse tools for the discriminative detection of these three molecular BSE types and might assist with the recognition of other variants.
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- 2007
28. Identification of prion protein gene polymorphisms in goats from Italian scrapie outbreaks
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Acutis, P.L., Bossers, A., Priem, J., Riina, M.V., Peletto, S., Mazza, M., Casalone, C., Forloni, G., Ru, G., Caramelli, M., Acutis, P.L., Bossers, A., Priem, J., Riina, M.V., Peletto, S., Mazza, M., Casalone, C., Forloni, G., Ru, G., and Caramelli, M.
- Abstract
Susceptibility to scrapie in sheep is influenced by polymorphisms of the prion protein (PrP) gene, whereas no strong association between genetics and scrapie has yet been determined in goats due to the limited number of studies on these animals. In this case¿control study on 177 goats from six Italian scrapie outbreaks, the association between PrP alleles and the occurrence of scrapie was studied. Three silent mutations and 11 PrP polymorphisms were identified, of which two polymorphisms (L133Q and M137I) and one silent mutation (T202T) have not been reported previously. Twelve alleles were determined by cloning. Statistical analysis suggested a possible protective role against scrapie for the glutamine to lysine mutation at codon 222
- Published
- 2006
29. Variability in disease phenotypes within a single PRNP genotype suggests the existence of multiple natural sheep scrapie strains within Europe
- Author
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Gonzalez, L., primary, Siso, S., additional, Monleon, E., additional, Casalone, C., additional, van Keulen, L. J. M., additional, Balkema-Buschmann, A., additional, Ortiz-Pelaez, A., additional, Iulini, B., additional, Langeveld, J. P. M., additional, Hoffmann, C., additional, Badiola, J. J., additional, Jeffrey, M., additional, and Acin, C., additional
- Published
- 2010
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30. Cerebral Toxoplasmosis in Striped Dolphins (Stenella coeruleoalba) Stranded Along the Ligurian Sea Coast of Italy
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Di Guardo, G., primary, Proietto, U., additional, Di Francesco, C. E., additional, Marsilio, F., additional, Zaccaroni, A., additional, Scaravelli, D., additional, Mignone, W., additional, Garibaldi, F., additional, Kennedy, S., additional, Forster, F., additional, Iulini, B., additional, Bozzetta, E., additional, and Casalone, C., additional
- Published
- 2009
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31. Histidine at codon 154 of the prion protein gene is a risk factor for Nor98 scrapie in goats
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Colussi, S., primary, Vaccari, G., additional, Maurella, C., additional, Bona, C., additional, Lorenzetti, R., additional, Troiano, P., additional, Casalinuovo, F., additional, Di Sarno, A., additional, Maniaci, M. G., additional, Zuccon, F., additional, Nonno, R., additional, Casalone, C., additional, Mazza, M., additional, Ru, G., additional, Caramelli, M., additional, Agrimi, U., additional, and Acutis, P. L., additional
- Published
- 2008
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32. Neuropathology of Italian Cats in Feline Spongiform Encephalopathy Surveillance
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Iulini, B., primary, Cantile, C., additional, Mandara, M. T., additional, Maurella, C., additional, Loria, G. R., additional, Castagnaro, M., additional, Salvadori, C., additional, Porcario, C., additional, Corona, C., additional, Perazzini, A. Z., additional, Maroni, A., additional, Caramelli, M., additional, and Casalone, C., additional
- Published
- 2008
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33. A Histopathologic and Immunohistochemical Review of Archived UK Caprine Scrapie Cases
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Dustan, B. H., primary, Spencer, Y. I., additional, Casalone, C., additional, Brownlie, J., additional, and Simmons, M. M., additional
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- 2008
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34. A Bovine Prion Acquires an Epidemic Bovine Spongiform Encephalopathy Strain-Like Phenotype on Interspecies Transmission
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Beringue, V., primary, Andreoletti, O., additional, Le Dur, A., additional, Essalmani, R., additional, Vilotte, J.-L., additional, Lacroux, C., additional, Reine, F., additional, Herzog, L., additional, Biacabe, A.-G., additional, Baron, T., additional, Caramelli, M., additional, Casalone, C., additional, and Laude, H., additional
- Published
- 2007
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35. Identification of prion protein gene polymorphisms in goats from Italian scrapie outbreaks
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Acutis, P. L., primary, Bossers, A., additional, Priem, J., additional, Riina, M. V., additional, Peletto, S., additional, Mazza, M., additional, Casalone, C., additional, Forloni, G., additional, Ru, G., additional, and Caramelli, M., additional
- Published
- 2006
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36. Necrosis of hippocampus and piriform lobe: Clinical and neuropathological findings in two italian cats
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Brini, E., primary, Gandini, G., additional, Crescio, I., additional, Fatzer, R., additional, and Casalone, C., additional
- Published
- 2004
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37. BSE Surveillance in Italy: Neuropathological Findings in Cattle in the Frame of the Passive Surveillance Programme
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Bozzetta, E., primary, Caramelli, M., additional, Casalone, C., additional, Acutis, P. L., additional, and Ru, G., additional
- Published
- 2003
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38. Cerebral Toxoplasmosis in Striped Dolphins (Stenella coeruleoalba) Stranded Along the Ligurian Sea Coast of Italy.
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Di Guardo, G., Proietto, U., Di Francesco', C. E., Marsilio, F., Zaccaroni, A., Scaravelli, D., Mignone, W., Garibaldi, F., Kennedy, S., Forster, F., Iulini, B., Bozzetta, E., and Casalone, C.
- Subjects
STRIPED dolphin ,MAMMAL diseases ,TOXOPLASMOSIS in animals ,CEREBRAL toxoplasmosis - Abstract
The article presents the result of examinations on striped dolphins (stenella coeruleoalba) for cerebral toxoplasmosis stranded in the Ligurian sea coast in Italy. The authors reveal that severe, nonsuppurative meningoencephalitis was detected in 4 striped dolphins. They mention that other findings included severe bronchointerstitial pneumonia and pulmonary atelectasis, consolidation and emphysema.
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- 2010
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39. Transmission of atypical bovine prions to mice transgenic for human prion protein.
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Béringue V, Herzog L, Reine F, Le-Dur A, Casalone C, Vilotte JL, Laude H, Béringue, Vincent, Herzog, Laëtitia, Reine, Fabienne, Le Dur, Annick, Casalone, Cristina, Vilotte, Jean-Luc, and Laude, Hubert
- Abstract
To assess risk for cattle-to-human transmission of prions that cause uncommon forms of bovine spongiform encephalopathy (BSE), we inoculated mice expressing human PrP Met129 with field isolates. Unlike classical BSE agent, L-type prions appeared to propagate in these mice with no obvious transmission barrier. H-type prions failed to infect the mice. [ABSTRACT FROM AUTHOR]
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- 2008
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40. Effects of propranolol on the impulse activity of cardiovascular sympathetic afferent fibers.
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LOMBARDI, FEDERICO, CASALONE, CARLO, MALFATTO, GABRIELLA, RUSCONE, TOMASO GNECCHI, CASATI, RODOLFO, MALLIANI, ALBERTO, Lombardi, F, Casalone, C, Malfatto, G, Gnecchi Ruscone, T, Casati, R, and Malliani, A
- Published
- 1986
41. Dolphin Morbillivirus and Toxoplasma gondii coinfection in a Mediterranean fin whale (Balaenoptera physalus)
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Mazzariol Sandro, Marcer Federica, Mignone Walter, Serracca Laura, Goria Mariella, Marsili Letizia, Di Guardo Giovanni, and Casalone Cristina
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Dolphin Morbillivirus ,Toxoplasma gondii ,Fin whale ,DDT ,Mediterranean Sea ,Veterinary medicine ,SF600-1100 - Abstract
Abstract Background Although Morbillivirus and Toxoplasma gondii have emerged as important pathogens for several cetaceans populations over the last 20 years, they have never been identified together in a Mysticete. In particular, morbilliviral infection has been never described in the Mediterranean fin whale population. Case presentation On January 2011 an adult male of fin whale (Balaenoptera physalus) stranded along the Tyrrhenian coastline of Italy. During necropsy, tissue samples from heart, skeletal muscle, mesenteric lymph nodes, liver, spleen, lung, and kidney were collected and subsequently analyzed for Morbillivirus and Toxoplasma gondii by microscopic and molecular methods. Following the detailed necropsy carried out on this whale, molecular analysis revealed, for the first time, the simultaneous presence of a Dolphin Morbillivirus (DMV) and T. gondii infection coexisting with each other, along with high organochlorine pollutant concentrations, with special reference to DDT. Conclusion This report, besides confirming the possibility for Mysticetes to be infected with DMV, highlights the risk of toxoplasmosis in sea water for mammals, already immunodepressed by concurrent factors as infections and environmental contaminants.
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- 2012
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42. Resistance to classical scrapie in experimentally challenged goats carrying mutation K222 of the prion protein gene
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Acutis Pier Luigi, Martucci Francesca, D'Angelo Antonio, Peletto Simone, Colussi Silvia, Maurella Cristiana, Porcario Chiara, Iulini Barbara, Mazza Maria, Dell'Atti Luana, Zuccon Fabio, Corona Cristiano, Martinelli Nicola, Casalone Cristina, Caramelli Maria, and Lombardi Guerino
- Subjects
Veterinary medicine ,SF600-1100 - Abstract
Abstract Susceptibility of sheep to scrapie, a transmissible spongiform encephalopathy of small ruminants, is strongly influenced by polymorphisms of the prion protein gene (PRNP). Breeding programs have been implemented to increase scrapie resistance in sheep populations; though desirable, a similar approach has not yet been applied in goats. European studies have now suggested that several polymorphisms can modulate scrapie susceptibility in goats: in particular, PRNP variant K222 has been associated with resistance in case-control studies in Italy, France and Greece. In this study we investigated the resistance conferred by this variant using a natural Italian goat scrapie isolate to intracerebrally challenge five goats carrying genotype Q/Q 222 (wild type) and five goats carrying genotype Q/K 222. By the end of the study, all five Q/Q 222 goats had died of scrapie after a mean incubation period of 19 months; one of the five Q/K 222 goats died after 24 months, while the other four were alive and apparently healthy up to the end of the study at 4.5 years post-challenge. All five of these animals were found to be scrapie negative. Statistical analysis showed that the probability of survival of the Q/K 222 goats versus the Q/Q 222 goats was significantly higher (p = 0.002). Our study shows that PRNP gene mutation K222 is strongly associated with resistance to classical scrapie also in experimental conditions, making it a potentially positive target for selection in the frame of breeding programs for resistance to classical scrapie in goats.
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- 2012
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43. Evaluation of two sets of immunohistochemical and Western blot confirmatory methods in the detection of typical and atypical BSE cases
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Greenlee Justin J, Loiacono Christina M, Hamir Amir N, Acutis Pierluigi, Perazzini Alice Z, Iulini Barbara, Corona Cristiano, Martucci Francesca, Hall S Mark, Porcario Chiara, Richt Jürgen A, Caramelli Maria, and Casalone Cristina
- Subjects
Medicine ,Biology (General) ,QH301-705.5 ,Science (General) ,Q1-390 - Abstract
Abstract Background Three distinct forms of bovine spongiform encephalopathy (BSE), defined as classical (C-), low (L-) or high (H-) type, have been detected through ongoing active and passive surveillance systems for the disease. The aim of the present study was to compare the ability of two sets of immunohistochemical (IHC) and Western blot (WB) BSE confirmatory protocols to detect C- and atypical (L- and H-type) BSE forms. Obex samples from cases of United States and Italian C-type BSE, a U.S. H-type and an Italian L-type BSE case were tested in parallel using the two IHC sets and WB methods. Results The two IHC techniques proved equivalent in identifying and differentiating between C-type, L-type and H-type BSE. The IHC protocols appeared consistent in the identification of PrPSc distribution and deposition patterns in relation to the BSE type examined. Both IHC methods evidenced three distinct PrPSc phenotypes for each type of BSE: prevailing granular and linear tracts pattern in the C-type; intraglial and intraneuronal deposits in the H-type; plaques in the L-type. Also, the two techniques gave comparable results for PrPSc staining intensity on the C- and L-type BSE samples, whereas a higher amount of intraglial and intraneuronal PrPSc deposition on the H-type BSE case was revealed by the method based on a stronger demasking step. Both WB methods were consistent in identifying classical and atypical BSE forms and in differentiating the specific PrPSc molecular weight and glycoform ratios of each form. Conclusions The study showed that the IHC and WB BSE confirmatory methods were equally able to recognize C-, L- and H-type BSE forms and to discriminate between their different immunohistochemical and molecular phenotypes. Of note is that for the first time one of the two sets of BSE confirmatory protocols proved effective in identifying the L-type BSE form. This finding helps to validate the suitability of the BSE confirmatory tests for BSE surveillance currently in place.
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- 2011
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44. Multidisciplinary studies on a sick-leader syndrome-associated mass stranding of sperm whales (Physeter macrocephalus) along the Adriatic coast of Italy
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Daniela Berto, Daniele De Nurra, Vincenzo Olivieri, Michele Povinelli, S. Rubini, Giovanni Di Guardo, Cinzia Centelleghe, Bruno Cozzi, Alessandra Pautasso, Francesca Profeta, Sandro Mazzariol, Fulvio Garibaldi, Maria Cristina Fossi, Nicola Ferri, S. Guccione, Matteo Beverelli, Michela Podestà, Gabriella Di Francesco, Antonio Fernández, Paolo Cipriani, Federica Marcer, Maria Morell, Cristina Casalone, Paola Modesto, Letizia Marsili, Annalisa Zaccaroni, Simonetta Mattiucci, Federica Giorda, Yara Beraldo de Quiros, Giuliana Terracciano, Cristiano Cocumelli, Pasquale Troiano, Pietro Badagliacca, and Mazzariol S., Centelleghe C., Cozzi B., Povinelli M., Marcer F., Ferri N., Di Francesco G., Badagliacca P., Profeta F., Olivieri V., Guccione S., Cocumelli C., Terracciano G., Troiano P., Beverelli M., Garibaldi F., Podestà M., Marsili L., Fossi M.C., Mattiucci S., Cipriani P., De Nurra D., Zaccaroni A., Rubini S., Berto D., de Quiros Y.B., Fernandez A., Morell M., Giorda F., Pautasso A., Modesto P., Casalone C., Di Guardo G.
- Subjects
0301 basic medicine ,Adriatic Sea ,lcsh:Medicine ,Sperm whales, Adriatic Sea, Mass Stranding ,Multidisciplinary studies ,Biology ,Physeter macrocephalus ,Article ,03 medical and health sciences ,Mediterranean sea ,Sperm whale ,biology.animal ,Mass strandings ,Sperm whales ,Italy ,Mediterranean Sea ,Animals ,lcsh:Science ,Mass Stranding ,Multidisciplinary ,Adverse weather ,Sperm whales, mass stranding, multidisciplinary approach ,Behavior, Animal ,Sperm Whale ,Whale ,lcsh:R ,Health condition ,biology.organism_classification ,Sperm ,Fishery ,030104 developmental biology ,Morbillivirus ,lcsh:Q ,Morbillivirus Infections - Abstract
Mass strandings of sperm whales (Physeter macrocephalus) are rare in the Mediterranean Sea. Nevertheless, in 2014 a pod of 7 specimens stranded alive along the Italian coast of the Central Adriatic Sea: 3 individuals died on the beach after a few hours due to internal damages induced by prolonged recumbency; the remaining 4 whales were refloated after great efforts. All the dead animals were genetically related females; one was pregnant. All the animals were infected by dolphin morbillivirus (DMV) and the pregnant whale was also affected by a severe nephropathy due to a large kidney stone. Other analyses ruled out other possible relevant factors related to weather conditions or human activities. The results of multidisciplinary post-mortem analyses revealed that the 7 sperm whales entered the Adriatic Sea encountering adverse weather conditions and then kept heading northward following the pregnant but sick leader of the pod, thereby reaching the stranding site. DMV infection most likely played a crucial role in impairing the health condition and orientation abilities of the whales. They did not steer back towards deeper waters, but eventually stranded along the Central Adriatic Sea coastline, a real trap for sperm whales.
- Published
- 2018
45. Modeling Amyotrophic Lateral Sclerosis in hSOD1G93A Transgenic Swine
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Caterina Bendotti, Cesare Galli, Andrea Perota, Irina Lagutina, MN Chieppa, Cristiano Corona, Giovanna Lazzari, Cristina Casalone, Franco Lucchini, E. Vallino Costassa, Silvia Colleoni, Maria Caramelli, Roberto Duchi, A Grindatto, Chieppa MN, Perota A, Corona C, Grindatto A, Lagutina I, Vallino Costassa E, Lazzari G, Colleoni S, Duchi R, Lucchini F, Caramelli M, Bendotti C, Galli C, and Casalone C
- Subjects
Genetically modified mouse ,Genetics ,Somatic cell ,animal diseases ,Transgene ,hSOD1 ,SOD1 ,nutritional and metabolic diseases ,Biology ,Gene mutation ,medicine.disease ,Phenotype ,Neurology ,medicine ,Somatic cell nuclear transfer ,Neurology (clinical) ,Amyotrophic lateral sclerosis ,Transgenic Swine ,Amyotrophic Lateral Sclerosi - Abstract
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that occurs in two clinically indistinguishable forms: sporadic (SALS) and familial (FALS), the latter linked to several gene mutations, mostly inheritable in a dominant manner. Nearly 20% of FALS forms are linked to mutations in the Cu/Zn superoxide dismutase (SOD1) gene. Research on ALS relies on transgenic models and particularly on mice carrying a glycine-to-alanine conversion at the 93rd codon (G93A) of the hSOD1 gene. Although G93A transgenic mice have been widely employed in clinical trials and basic research, doubts have been recently raised from numerous reliable sources about their suitability to faithfully reproduce human disease. Besides, the scientific community has already foreseen swine as an attractive and alternative model to nonhuman primates for modeling human diseases due to closer anatomical, physiological and biochemical features of swine rather than rodents to humans. On this basis, we have produced the first swine ALS model by in vitro transfection of cultured somatic cells combined with somatic cell nuclear transfer (SCNT). To achieve this goal we developed a SOD1G93A (superoxide dismutase 1 mutated in Gly93-Ala) vector, capable of promoting a high and stable transgene expression in primary porcine adult male fibroblasts (PAF). After transfection, clonal selection and transgene expression level assessment, selected SOD1G93A PAF colonies were used as nuclei donors in SCNT procedures. SOD1G93A embryos were transferred in recipient sows, and pregnancies developed to term. A total of 5 piglets survived artificial hand raising and weaning and developed normally, reaching adulthood. Preliminary analysis revealed transgene integration and hSOD1G93A expression in swine tissues and 360° phenotypical characterization is ongoing. We believe that our SOD1G93A swine would provide an essential bridge between the fundamental work done in rodent models and the reality of treating ALS.
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- 2013
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46. Neurofilament light chain (Nf-L) in cerebrospinal fluid and serum as a potential biomarker in the differential diagnosis of neurological diseases in cattle.
- Author
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Di Muro G, Tessarolo C, Cagnotti G, Favole A, Ferrini S, Ala U, Bellino C, Borriello G, Gallo M, Iamone G, Iulini B, Pezzolato M, Casalone C, Caramelli M, Capucci L, Cavadini P, Corona C, and D'Angelo A
- Subjects
- Animals, Cattle, Diagnosis, Differential, Female, Male, Cattle Diseases diagnosis, Cattle Diseases blood, Cattle Diseases cerebrospinal fluid, Neurofilament Proteins blood, Neurofilament Proteins cerebrospinal fluid, Biomarkers blood, Biomarkers cerebrospinal fluid, Nervous System Diseases veterinary, Nervous System Diseases diagnosis, Nervous System Diseases blood, Nervous System Diseases cerebrospinal fluid
- Abstract
Neurofilament light chain (Nf-L) is a biomarker for axonal damage in human neurology but is understudied in cattle. With this study we wanted to determine Nf-L stability at two different storage temperatures and Nf-L levels in healthy cattle and the relationship with age, evaluate whether Nf-L holds diagnostic potential for neurological disorders, and whether an association exists between Nf-L in serum and in cerebrospinal fluid (CSF). To do this, we measured Nf-L levels in CSF and serum samples from 49 healthy and 75 sick cattle. Storage at -80 °C or -20 °C had no impact on Nf-L concentration. Physiological median Nf-L levels were 6.3 pg/mL (serum) and 414 pg/mL (CSF) in calves and 5.5 pg/mL (serum) and 828 pg/mL (CSF) in adult cattle. There was no association between Nf-L levels in CSF and calf age (r
2 0.07, p = 0.13), while a weak association was found for Nf-L in serum (r2 0.26, p = 0.01), and a significant association in adult cattle (CSF, r2 0.69, p = 0.0001; serum, r2 0.68, p = 0.0003). CSF Nf-L levels were higher in samples from animals with degenerative (median Nf-L 49971 pg/mL) and infectious central nervous system (CNS) disorders (median Nf-L, age < 2 months 8863 pg/mL; age 2-12 months 17474 pg/mL; age 1-6 years 3546 pg/mL), CNS anomalies and metabolic/toxic disorders. There was a significant association between CSF Nf-L and serum Nf-L in cattle with neurological disorders (r2 0.2, p = 0.009). Taken together, these findings suggest the potential of Nf-L as a diagnostic tool in cattle neurology., Competing Interests: Declarations. Ethics approval and consent to participate: This study adhered to current animal welfare regulations (Directive 98/58/EC and Italian Decree Law 146/2001). All procedures were conducted as described by the institutional guidelines in accordance with national (D.L.26/2014) and international laws and policies (EEC Council Directive 63/2010). Ethical approval for the study was obtained from the Bioethics Committee of the University of Turin (protocol no. 0251347) and from the Italian Ministry of Health (Auth. no. 242/2020–PR). Owners provided written informed consent for veterinary assessment and treatment of their animals. Competing interests: The authors declare that they have no competing interests., (© 2025. The Author(s).)- Published
- 2025
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47. Amyloid-β and phosphorylated tau screening in bottlenose dolphin (Tursiops truncatus) and striped dolphin (Stenella coeruleoalba) brains from Italy reveals distinct immunohistochemical patterns correlating with age and co-morbidity.
- Author
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Orekhova K, Testori C, Giorda F, Grattarola C, Mattioda V, Di Guardo G, Corona C, Castagnaro M, Sierra E, Casalone C, Favole A, Centelleghe C, and Mazzariol S
- Subjects
- Animals, Male, Female, Phosphorylation, Stenella metabolism, Italy, Aging metabolism, Comorbidity, Age Factors, Amyloid beta-Peptides metabolism, tau Proteins metabolism, Bottle-Nosed Dolphin metabolism, Brain metabolism, Brain pathology, Immunohistochemistry
- Abstract
Cetacean brains are uniquely adapted to diving, but can be affected by diseases and exposure to toxins, triggering neurodegenerative processes that may cause stranding. Some species exhibit a significant post-reproductive lifespan (PRLS), increasing the likelihood of observing cumulative and age-related pathology. Immunohistochemistry against amyloid-β and hyperphosphorylated tau proteins is increasingly implemented to assess Alzheimer's Disease-like neuropathology in cetaceans, but comparisons between geographically distinct populations, animals of different age groups, sex, and with concomitant pathologies are lacking. We tested 43 cetaceans' (30 Tursiops truncatus; 13 Stenella coeruleoalba) parietal cortex, our most consistently archived cerebral tissue, in immunohistochemical analyses with amyloid-β oligomer 42 (Aβ-42) and hyperphosphorylated tau (pTau AT180 and AT8) antibodies. Aβ-42 antibody cross-reacted with plaques in three aged bottlenose and two aged striped dolphins, but was more often detected within neurons, glia, and blood vessels of all the dolphins. Histoscore comparisons between dolphins of different ages, sexes, and pathologies revealed significant correlations between older age, viral infections, and plaque presence. Protozoan cysts cross-reacted with Aβ-42 antibody. pTau signal was observed as single foci in neurons and neuropil in two young and two aged bottlenose dolphins. To our knowledge, this study is the first of its kind for the Mediterranean region and will help establish baseline understanding of physiological and pathological expression of proteins associated with human neurodegenerative disease in cetacean brains., Competing Interests: The authors have declared that no competing interests exist., (Copyright: © 2024 Orekhova et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)
- Published
- 2024
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48. Anthropic Pressure on Cetaceans Stranded Along the Ligurian Coast Within the Pelagos Sanctuary: A Case Series.
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Mattioda V, Giorda F, Consales G, Testori C, Zoppi S, Goria M, Crescio MI, Serracca L, Varello K, Carta V, Marsili L, Baini M, Galli M, Fossi CC, Fontanesi E, Garibaldi F, Pietroluongo G, Mazzariol S, Brunelli F, Casalone C, and Grattarola C
- Abstract
Data collected by C. Re. Di. Ma over a 3-year period (2020-2022) were considered to assess anthropic pressure on cetaceans living in the Ligurian sea. Out of a total of 37 stranded cetaceans, a complete post mortem examination was performed on 23 cases. Of these, 14 were further selected considering at least one of these conditions: (i) confirmed, probable, or suspected interaction with fishing activities through the application of a standardized diagnostic framework (7/14; 50%), (ii) toxicological stress through the evaluation of OCs hazardous levels (14/14; 100%), and (iii) terrestrial pathogen-associated disease (systemic infection and/or associated lesions) (7/14; 50%). For 9 animals out of a total of 14 selected, the cause of death was classified as natural (6/14; 42,8%), anthropic (3/14; 21,4%), or not determined (5/14; 35,7%) based on gross and histological pathology and ancillary testing. These findings extend our knowledge of the anthropic pressure to which cetaceans stranded along the Ligurian coastline are subjected from a multidisciplinary point of view.
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- 2024
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49. Distribution and abundance of Aedes caspius (Pallas, 1771) and Aedes vexans (Meigen, 1830) in the Po Plain (northern Italy).
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Calzolari M, Mosca A, Montarsi F, Grisendi A, Scremin M, Roberto P, Tessarolo C, Defilippo F, Gobbo F, Casalone C, Lelli D, and Albieri A
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- Animals, Italy, West Nile Fever transmission, West Nile Fever epidemiology, Animal Distribution, West Nile virus isolation & purification, Population Density, Spatial Analysis, Aedes physiology, Aedes virology, Mosquito Vectors physiology, Mosquito Vectors virology
- Abstract
Background: Knowledge of the distribution and abundance of disease-causing mosquito vectors is fundamental for assessing the risk of disease circulation and introduction. Aedes caspius (Pallas, 1771) and Aedes vexans (Meigen, 1830) have been implicated, to different extents, in the circulation of several arthropod-borne viruses (arboviruses). These two mosquitoes are vectors of Tahyna virus in Europe and are considered potential vectors of Rift Valley fever virus, a virus not present but at risk of introduction on the continent., Methods: In this work, we analysed abundance data collected during West Nile virus (WNV) surveillance in northern Italy (Po Plain) via 292 CO
2 -baited traps to evaluate the distribution and density of these two non-target mosquitoes. We modelled the distribution and abundance of these two mosquito species in the surveyed area using two distinct spatial analysis approaches (geostatistical and machine learning), which yielded congruent results., Results: Both species are more abundant close to the Po River than elsewhere, but Ae. caspius is present in the eastern and western parts of the plain, linked with the occurrence of rice fields and wetlands, while Ae. vexans is observed in the middle area of the plain., Conclusions: Presence and abundance data at the municipality level were obtained and made available through this work. This work demonstrates the importance of maintaining and improving entomological surveillance programs with an adequate sampling effort., (© 2024. The Author(s).)- Published
- 2024
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50. Herpesvirus surveillance in stranded striped dolphins (Stenella coeruleoalba) and bottlenose dolphins (Tursiops truncatus) from Italy with emphasis on neuropathological characterization.
- Author
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Vargas-Castro I, Giorda F, Mattioda V, Goria M, Serracca L, Varello K, Carta V, Nodari S, Maniaci MG, Dell'Atti L, Testori C, Pussini N, Iulini B, Battistini R, Zoppi S, Nocera FD, Lucifora G, Fontanesi E, Acutis P, Casalone C, Grattarola C, and Peletto S
- Subjects
- Animals, Male, Italy epidemiology, Female, Herpesviridae genetics, Herpesviridae isolation & purification, Herpesviridae classification, Morbillivirus Infections veterinary, Morbillivirus Infections virology, Morbillivirus Infections pathology, Alphaherpesvirinae genetics, Alphaherpesvirinae isolation & purification, Alphaherpesvirinae pathogenicity, Mediterranean Sea, Gammaherpesvirinae genetics, Gammaherpesvirinae isolation & purification, Gammaherpesvirinae pathogenicity, Bottle-Nosed Dolphin virology, Stenella virology, Herpesviridae Infections veterinary, Herpesviridae Infections virology, Herpesviridae Infections pathology, Phylogeny, Morbillivirus genetics, Morbillivirus pathogenicity, Morbillivirus isolation & purification
- Abstract
Herpesvirus (HV) is widely distributed among cetacean populations, with the highest prevalence reported in the Mediterranean Sea. In this study, a comprehensive analysis was conducted, including epidemiological, phylogenetic, and pathological aspects, with particular emphasis on neuropathology, to better understand the impact of HV in these animals. Our results show a higher presence of HV in males compared to females, with males exhibiting a greater number of positive tissues. Additionally, adults were more frequently affected by HV infection than juveniles, with no infections detected in calves or neonates. The affected species were striped (Stenella coeruleoalba) and bottlenose dolphins (Tursiops truncatus). The highest positivity rates were observed in the genital system, cerebrum, and skin tissues. Phylogenetic analysis indicated a higher occurrence of Gammaherpesvirus (GHV) sequences but increased genetic diversity within Alphaherpesvirus (AHV). Key neuropathological features included astro-microgliosis (n = 4) and meningitis with minimal to mild perivascular cuffing (n = 2). The presence of concurrent infections with other pathogens, particularly cetacean morbillivirus (CeMV), underscores the complex nature of infectious diseases in cetaceans. However, the presence of lesions at the Central Nervous System (CNS) with molecular positivity for GHV, excluding the involvement of other potential neurotropic agents, would confirm the potential of this HV subfamily to induce neurological damage. Pathological examination identified lesions in other organs that could potentially be associated with HV, characterized by lymphoid depletion and tissue inflammation. These findings enhance our understanding of HV in odontocetes and highlight the need for ongoing research into the factors driving these infections and their broader implications., Competing Interests: The authors have declared that no competing interests exist., (Copyright: © 2024 Vargas-Castro et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)
- Published
- 2024
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