Bibliografia
1. Hagnestam, C.; Emanuelson, U.; Berglund, B. Yield Losses Associated with Clinical Mastitis Occurring in Different Weeks of Lactation. J. Dairy Sci. 2007, 90, 2260-2270.
2. Hussain, R.; Javed, M.T.; Khan, A. Changes in Some Biochemical Parameters and Somatic Cell Counts in the Milk of Buffalo and Cattle Suffering from Mastitis. Pak. Vet. J. 2012, 32, 418-421.
3. Lipkens, Z.; Piepers, S.; De Visscher, A.; De Vliegher, S. Evaluation of Test-Day Milk Somatic Cell Count Information to Predict Intramammary Infection with Major Pathogens in Dairy Cattle at Drying Off. J. Dairy Sci. 2019, 102, 4309-4321.
4. Bortolami, A.; Fiore, E.; Gianesella, M.; Corrò, M.; Catania, S.; Morgante, M. Evaluation of the Udder Health Status in Subclinical Mastitis Affected Dairy Cows through Bacteriological Culture, Somatic Cell Count and Thermographic Imaging. Pol. J. Vet. Sci. 2015, 18, 104.
5. Senft, B.; Neudecker, J. Defense Mechanisms of the Bovine Mammary Gland. Tierärztliche Prax. 1991, 19, 357-363. [
6. Nickerson, S.C. Immunological Aspects of Mammary Involution. J. Dairy Sci. 1989, 72, 1665-1678. [
7. Cobirka, M.; Tancin, V.; Slama, P. Epidemiology and Classification of Mastitis. Animals 2020, 10, 2212.
8. Bronzo, V.; Lopreiato, V.; Riva, F.; Amadori, M.; Curone, G.; Addis, M.F.; Cremonesi, P.; Moroni, P.; Trevisi, E.; Castiglioni, B. The Role of Innate Immune Response and Microbiome in Resilience of Dairy Cattle to Disease: The Mastitis Model. Animals 2020, 10, 1397.
9. Pighetti, G.M.; Sordillo, L.M. Specific Immune Responses of Dairy Cattle after Primary Inoculation with Recombinant Bovine Interferon-γ as an Adjuvant When Vaccinating against Mastitis. Am. J. Vet. Res. 1996, 57, 819-824.
10. Piotrowska-Tomala, K.K.; Siemieniuch, M.J.; Szóstek, A.Z.; Korzekwa, A.J.; Woclawek-Potocka, I.; Galváo, A.M.; Okuda, K.; Skarzynski, D.J. Lipopolysaccharides, Cytokines, and Nitric Oxide Affect Secretion of Prostaglandins and Leukotrienes by Bovine Mammary Gland Epithelial Cells. Domest. Anim. Endocrinol. 2012, 43, 278-288
11. Mishra, S. CD8+ Regulatory T Cell—A Mystery to Be Revealed. Front. Immunol. 2021, 12, 8874.
12. Rainard, P.; Foucras, G.; Martins, R.P. Adaptive Cell-Mediated Immunity in the Mammary Gland of Dairy Ruminants. Front. Vet. Sci. 2022, 9, 4890.
13. Pegolo, S.; Tessari, R.; Bisutti, V.; Vanzin, A.; Giannuzzi, D.; Gianesella, M.; Lisuzzo, A.; Fiore, E.; Barberio, A.; Schiavon, E.; et al. Quarter-Level Analyses of the Associations among Subclinical Intramammary Infection and Milk Quality, Udder Health, and Cheesemaking Traits in Holstein Cows. J. Dairy Sci. 2022, 105, 3490-3507.
14. De Vliegher, S.; Ohnstad, I.; Piepers, S. Management and Prevention of Mastitis: A Multifactorial Approach with a Focus on Milking, Bedding and Data-Management. J. Integr. Agric. 2018, 17, 1214-1233.
15. Ashraf, A.; Imran, M. Causes, Types, Etiological Agents, Prevalence, Diagnosis, Treatment, Prevention, Effects on Human Health and Future Aspects of Bovine Mastitis. Anim. Health Res. Rev. 2020, 21, 36-49.
16. Shaheen, M.; Tantary, H. A Treatise on Bovine Mastitis: Disease and Disease Economics, Etiological Basis, Risk Factors, Impact on Human Health, Therapeutic Management, Prevention and Control Strategy. Adv. Dairy Res. 2015, 4, 150.
17. Martins, S.A.M.; Martins, V.C.; Cardoso, F.A.; Germano, J.; Rodrigues, M.; Duarte, C.; Bexiga, R.; Cardoso, S.; Freitas, P.P. Biosensors for On-Farm Diagnosis of Mastitis. Front. Bioeng. Biotechnol. 2019, 7, 186.
18. Pyörälä, S. Indicators of Inflammation in the Diagnosis of Mastitis. Vet. Res. 2003, 34, 565-578.
19. Ouzzani, M.; Hammady, H.; Fedorowicz, Z.; Elmagarmid, A. Rayyan — a Web and Mobile App for Systematic Reviews. Available online: https://rayyan.ai/ (accessed on 1 August 2024).
20. Peters, M.D.P.; Silveira, I.D.B.; Fischer, V. Impact of Subclinical and Clinical Mastitis on Sensitivity to Pain of Dairy Cows. Animal 2015, 9, 2024-2028.
21. Ferreira, G.M.; Petzer, I.M. Injectable Organic and Inorganic Selenium in Dairy Cows—Effects on Milk, Blood and Somatic Cell Count Levels. Onderstepoort J. Vet. Res. 2019, 86, 1664.
22. Cheng, W.N.; Han, S.G. Bovine Mastitis: Risk Factors, Therapeutic Strategies, and Alternative Treatments-A Review. Asian-Australas J. Anim. Sci. 2020, 33, 1699-1713.
23. Hurley, W.L.; Theil, P.K. Perspectives on Immunoglobulins in Colostrum and Milk. Nutrients 2011, 3, 442-474.
24. Kibebew, K. Bovine Mastitis: A Review of Causes and Epidemiological Point of View. J. Biol. Agric. Healthc. 2017, 7, 1-14.
25. Bian, Y.; Lv, Y.; Li, Q. Identification of Diagnostic Protein Markers of Subclinical Mastitis in Bovine Whey Using Comparative Proteomics. Bull. Vet. Inst. Pulawy 2014, 58, 385-392.
26. Griffioen, K.; Velthuis, A.G.J.; Koop, G.; Lam, T.J.G.M. Effects of a Mastitis Treatment Strategy with or without On-Farm Testing. J. Dairy Sci. 2021, 104, 4665-4681.
27. Juronen, D.; Kuusk, A.; Kivirand, K.; Rinken, A.; Rinken, T. Immunosensing System for Rapid Multiplex Detection of Mastitis-Causing Pathogens in Milk. Talanta 2018, 178, 949-954.
287. Barreiro, J.R.; Gonçalves, J.L.; Grenfell, R.; Leite, R.F.; Juliano, L.; Santos, M.V. Direct Identification of Bovine Mastitis Pathogens by Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry in Pre-Incubated Milk. Braz. J. Microbiol. 2018, 49, 801-807.
29. El-Sayed, A.; Awad, W.; Abdou, N.E.; Castañeda Vázquez, H. Molecular Biological Tools Applied for Identification of Mastitis Causing Pathogens. Int. J. Vet. Sci. Med. 2017, 5, 89-97.
30. Awale, M.; Dudhatra, G.B.; Avinash, K.; Chauhan, B.N.; Kamani, D.R.; Modi, C.M.; Patel, H.B.; Mody, S.K. Bovine Mastitis: A Threat to Economy. Open Access Sci. Rep. 2012, 1, 1-10. Available online: https://www.omicsonline.org/scientific-reports/srep295.php (accessed on 28 May 2024).
31. National Mastitis Council Inc. Laboratory Handbook on Bovine Mastitis, 3rd ed.; National Mastitis Council Inc.: New Prague, MN, USA, 2017.
32. Kuang, Y.; Tani, K.; Synnott, A.J.; Ohshima, K.; Higuchi, H.; Nagahata, H.; Tanji, Y. Characterization of Bacterial Population of Raw Milk from Bovine Mastitis by Culture-Independent PCR-DGGE Method. Biochem. Eng. J. 2009, 45, 76-81.
33. Contreras, G.A.; Rodríguez, J.M. Mastitis: Comparative Etiology and Epidemiology. J. Mammary Gland Biol. Neoplasia 2011, 16, 339-356.
34. Klaas, I.C.; Zadoks, R.N. An Update on Environmental Mastitis: Challenging Perceptions. Transbound. Emerg. Dis. 2018, 65, 166-185.
35. Saidani, M.; Messadi, L.; Soudani, A.; Daaloul-Jedidi, M.; Châtre, P.; Ben Chehida, F.; Mamlouk, A.; Mahjoub, W.; Madec, J.Y.; Haenni, M. Epidemiology, Antimicrobial Resistance, and Extended-Spectrum Beta-Lactamase-Producing Enterobacteriaceae in Clinical Bovine Mastitis in Tunisia. Microb. Drug Resist. 2018, 24, 1242-1248.
36. Heikkilä, A.M.; Liski, E.; Pyörälä, S.; Taponen, S. Pathogen-Specific Production Losses in Bovine Mastitis. J. Dairy Sci. 2018, 101, 9493-9504.
37. Zi, C.; Zeng, D.; Ling, N.; Dai, J.; Xue, F.; Jiang, Y.; Li, B. An Improved Assay for Rapid Detection of Viable Staphylococcus Aureus Cells by Incorporating Surfactant and PMA Treatments in QPCR. BMC Microbiol. 2018, 18, 1-8.
38. Milanov, D.; Prunić, B.; Velhner, M.; Bojkovski, J. Diagnosis of Yeast Mastitis in Dairy Cows. Lucr. Stiint.-Univ. Stiint. Agric. A Banat. Timis. Med. Vet. 2014, 47, 56-64.
39. Abou-Elmagd, S.; Kotb, H.; Sabry, K.; Refai, M. Prevalence of Candida Albicans and Cryptococcus Neoformans in Animals and Chickens in Quena Governorate, with Special Reference to RAPD-PCR Patterns of the Isolates. J. Am. Sci. 2011, 7, 20-31.
40. Da Costa, G.M.; de Pereira, U.P.; Gomes Souza-Dias, M.A.; da Silva, N. Yeast Mastitis Outbreak in a Brazilian Dairy Herd. Braz. J. Vet. Res. Anim. Sci. 2012, 49, 239-243.
41. Tarazona-Manrique, L.E.; Villate-Hernández, J.R.; Andrade-Becerra, R.J. Bacterial and Fungal Infectious Etiology Causing Mastitis in Dairy Cows in the Highlands of Boyacá (Colombia). Rev. Fac. Med. Vet. Zootec. 2019, 66, 208-218.
42. Jagielski, T.; Krukowski, H.; Bochniarz, M.; Piech, T.; Roeske, K.; Bakuła, Z.; Wlazło, Ł.; Woch, P. Prevalence of Prototheca Spp. on Dairy Farms in Poland-A Cross-Country Study. Microb. Biotechnol. 2019, 12, 556-566. [
43. Shkromada, O.; Palii, A.; Palii, A.; Skliar, O.; Dudchenko, Y.; Necherya, T. Improvement of Milk Quality for Micro-Climate Formation on Cattle Farms. Bull. Sumy Natl. Agrar. Univ. Ser. Vet. Med. 2019, 4, 43-49.
44. Bezman, D.; Lemberskiy-Kuzin, L.; Katz, G.; Merin, U.; Leitner, G. Influence of Intramammary Infection of a Single Gland in Dairy Cows on the Cow’s Milk Quality. J. Dairy Res. 2015, 82, 304-311.
45. Wolfenson, D.; Leitner, G.; Lavon, Y. The Disruptive Effects of Mastitis on Reproduction and Fertility in Dairy Cows. Ital. J. Anim. Sci. 2015, 14, 650-654.
46. Van Soest, F.J.S.; Santman-Berends, I.M.G.A.; Lam, T.J.G.M.; Hogeveen, H. Failure and Preventive Costs of Mastitis on Dutch Dairy Farms. J. Dairy Sci. 2016, 99, 8365-8374.
47. Huijps, K.; Lam, T.J.G.M.; Hogeveen, H. Costs of Mastitis: Facts and Perception. J. Dairy Res. 2008, 75, 113-120.
48. Krishnamoorthy, P.; Goudar, A.L.; Suresh, K.P.; Roy, P. Global and Countrywide Prevalence of Subclinical and Clinical Mastitis in Dairy Cattle and Buffaloes by Systematic Review and Meta-Analysis. Res. Vet. Sci. 2021, 136, 561-586.
49. Aghamohammadi, M.; Haine, D.; Kelton, D.F.; Barkema, H.W.; Hogeveen, H.; Keefe, G.P.; Dufour, S. Herd-Level Mastitis-Associated Costs on Canadian Dairy Farms. Front. Vet. Sci. 2018, 5, 100.
50. Stevens, M.; Piepers, S.; De Vliegher, S. Mastitis Prevention and Control Practices and Mastitis Treatment Strategies Associated with the Consumption of (Critically Important) Antimicrobials on Dairy Herds in Flanders, Belgium. J. Dairy Sci. 2016, 99, 2896-2903.
TORNA INDIETRO
Eradicazione 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.