Bibliografia
1. Global mortality associated with 33 bacterial pathogens in 2019: a systematic analysis for the Global Burden of Disease Study 2019. Lancet, 2022. 400(10369): p. 2221-2248.
2. Aarestrup, F.M., et al., A study of phage- and ribotype patterns of Staphylococcus aureus isolated from bovine mastitis in the Nordic countries. Acta Veterinaria Scandinavica, 1997. 38(3): p. 243-252.
3. Cheung, G.Y.C., J.S. Bae, and M. Otto, Pathogenicity and virulence of Staphylococcus aureus. Virulence, 2021. 12(1): p. 547-569.
4. Coppens, J., et al., Genomic analysis of methicillin-resistant Staphylococcus aureus clonal complex 239 isolated from Danish patients with and without an international travel history. Frontiers in Microbiology, 2022. 13: p. 9.
5. De Backer, S., et al., Remarkable geographical variations between India and Europe in carriage of the staphylococcal surface protein-encoding sasX/sesI and in the population structure of methicillin-resistant Staphylococcus aureus belonging to clonal complex 8. Clinical Microbiology and Infection, 2019. 25(5): p. 7.
6. Fetsch, A., D. Etter, and S. Johler, Livestock-Associated Meticillin-Resistant Staphylococcus aureus—Current Situation and Impact From a One Health Perspective. Current Clinical Microbiology Reports, 2021. 8(3): p. 103-113.
7. Fitzgerald, J.R., Livestock-associated Staphylococcus aureus: origin, evolution and public health threat. Trends in Microbiology, 2012. 20(4): p. 192-198.
8. Foster, T.J., Colonization and infection of the human host by staphylococci: adhesion, survival and immune evasion. Veterinary Dermatology, 2009. 20(5-6): p. 456-470.
9. Haag, A.F., J.R. Fitzgerald, and J.R. Penadés, Staphylococcus aureus in Animals. Microbiol Spectr, 2019. 7(3).
10. Kadariya, J., T.C. Smith, and D. Thapaliya, Staphylococcus aureus and staphylococcal food-borne disease: an ongoing challenge in public health. Biomed Res Int, 2014. 2014: p. 827965.
11. Larsen, H.D., F.M. Aarestrup, and N.E. Jensen, Geographical variation in the presence of genes encoding superantigenic exotoxins and β-hemolysin among Staphylococcus aureus isolated from bovine mastitis in Europe and USA. Veterinary Microbiology, 2002. 85(1): p. 61-67.
12. Mascaro, V., et al., Prevalence of Livestock-Associated Methicillin-Resistant Staphylococcus Aureus (LA-MRSA) Among Farm and Slaughterhouse Workers in Italy. J Occup Environ Med, 2018. 60(8): p. e416-e425.
13. Meroni, G., et al., Genomic Evidence Supporting a One Health Perspective on Staphylococcus aureus Bovine Mastitis. Antibiotics, 2026. 15(1): p. 98.
14. Peng, Q., et al., A Review of Biofilm Formation of Staphylococcus aureus and Its Regulation Mechanism. Antibiotics, 2023. 12(1): p. 12.
15. Pennone, V., et al., Antimicrobial Resistance Genes Analysis of Publicly Available Staphylococcus aureus Genomes. Antibiotics-Basel, 2022. 11(11): p. 19.
16. Piccinini, R., V. Borromeo, and A. Zecconi, Relationship between S. aureus gene pattern and dairy herd mastitis prevalence. Veterinary Microbiology, 2010. 145(1-2): p. 100-105.
17. Shepheard, M.A., et al., Historical Zoonoses and Other Changes in Host Tropism of Staphylococcus aureus, Identified by Phylogenetic Analysis of a Population Dataset. PLOS ONE, 2013. 8(5): p. e62369.
18. Stefani, S., et al., Meticillin-resistant Staphylococcus aureus (MRSA): global epidemiology and harmonisation of typing methods. International Journal of Antimicrobial Agents, 2012. 39(4): p. 273-282.
19. Vanderhaeghen, W., et al., Methicillin-resistant Staphylococcus aureus (MRSA) in food production animals. Epidemiology and Infection, 2010. 138(5): p. 606-625.
20. Wu, M., et al., Prevalence of methicillin-resistant Staphylococcus aureus in healthy Chinese population: A system review and meta-analysis. PLOS ONE, 2019. 14(10): p. e0223599.
21. Zaghen, F., et al., Epidemiology of Antimicrobial Resistance Genes in Staphyloccocus aureus Isolates from a Public Database in a One Health Perspective—Sample Characteristics and Isolates’ Sources. Antibiotics, 2023. 12(7): p. 1225.
22. Zaghen, F., et al., Epidemiology of Antimicrobial Resistance Genes in Staphylococcus aureus Isolates from a Public Database from a One Health Perspective—Sample Origin and Geographical Distribution of Isolates. Antibiotics, 2023. 12(12): p. 1654.
23. Zecconi, A., L.F. Calvinho, and K.L. Fox, Staphylococcus aureus intramammary infections. IDF Bulletin, 2006. 408: p. 1-42.
24. Zecconi, A. and F. Scali, Staphylococcus aureus virulence factors in evasion from innate immune defenses in human and animal diseases. Immunology Letters, 2013. 150(1-2): p. 12-22.
TORNA INDIETROEradicazione di M. hyopneumoniae nel suino: gli strumenti ci sono
I metodi storicamente impiegati per ridurre l’incidenza delle infezioni da M. hyopneumoniae non sembrano attualmente funzionare adeguatamente. I programmi di controllo per questo microrganismo si dividono in due macrocategorie: i programmi che prevedono l’eradicazione dell’agente patogeno e quelli che non la prevedono; a quest’ultima categoria appartengono le strategie che si basano su tre concetti: gestione, prevenzione e trattamento.