Influence of Stress Connected with Moving to a New Farm on Potentially MAP-Infected Mouflons
Status PubMed-not-MEDLINE Jazyk angličtina Země Egypt Médium electronic-ecollection
Typ dokumentu časopisecké články
PubMed
24729908
PubMed Central
PMC3960726
DOI
10.1155/2014/450130
Knihovny.cz E-zdroje
- Publikační typ
- časopisecké články MeSH
There is no European legislation concerning paratuberculosis that requires that imported animals be kept in quarantine and commonly they are directly released into areas with other animals. In this study, detection of latent infection of paratuberculosis in healthy mouflons previously diagnosed as paratuberculosis-free, but originating from a real time quantitative PCR- (qPCR-) positive herd, occurred after their transport to a new farm. During a twelve-day quarantine period, all mouflons irregularly shed Mycobacterium avium subsp. paratuberculosis (MAP) in faeces, and in a small number of cases also in milk. After the animals were released from quarantine, MAP was detected for a further two days, after which, testing was negative, except in one case. Therefore, the stress connected with transport, novel environment, dietary change, or limited area with high density of animals might have contributed to the induction of paratuberculosis and the shedding of MAP from the animals, previously diagnosed as MAP-negative. According to these results, the keeping of imported animals in quarantine and their examination for MAP presence not only before the transport but also afterwards should be recommended. The designation of a particular area of a farm as a quarantine enclosure could help to mitigate the impact of stress caused by a confined space with a high density of animals.
Zobrazit více v PubMed
Deutz A, Spergser J, Wagner P, Rosengarten R, Köfer J. Mycobacterium avium subsp. paratuberculosis in wild animal species and cattle in Styria/Austria. Berliner und Munchener Tierarztliche Wochenschrift. 2005;118(7-8):314–320. PubMed
Robino P, Nebbia P, Tramuta C, Martinet M, Ferroglio E, de Meneghi D. Identification of Mycobacterium avium subsp. paratuberculosis in wild cervids (Cervus elaphus hippelaphus and Capreolus capreolus) from Northwestern Italy. European Journal of Wildlife Research. 2008;54(2):357–360.
Pribylova R, Slana I, Lamka J, Babak V, Hruska K, Pavlik I. Mycobacterium avium subsp. paratuberculosis in a moufon herd without clinical symptoms monitored using IS900 real-time PCR: a case report. Veterinarni Medicina. 2010;55(12):625–630.
Machackova M, Svastova P, Lamka J, et al. Paratuberculosis in farmed and free-living wild ruminants in the Czech Republic (1999–2001) Veterinary Microbiology. 2004;101(4):225–234. PubMed
Windsor PA, Whittington RJ. Evidence for age susceptibility of cattle to Johne’s disease. Veterinary Journal. 2010;184(1):37–44. PubMed
Council Directive 92/65/EEC of 13 July. Official Journal of the European Union. 1992
Nielsen SS. Programmes on paratuberculosis in Europe. Proceedings of the 10th International Colloquium on Paratuberculosis; 2009; Minneapolis, Minn, USA. International Association for Paratuberculosis; pp. 101–108.
Grandin T. Assessment of stress during handling and transport. Journal of Animal Science. 1997;75(1):249–257. PubMed
Carroll JA, Forsberg NE. Influence of stress and nutrition on cattle immunity. Veterinary Clinics of North America. 2007;23(1):105–149. PubMed
Dowd SE, Callaway TR, Morrow-Tesch J. Handling may cause increased shedding of Escherichia coli and total coliforms in pigs. Foodborne Pathogens and Disease. 2007;4(1):99–102. PubMed
Bailey MT, Dowd SE, Parry NMA, Galley JD, Schauer DB, Lyte M. Stressor exposure disrupts commensal microbial populations in the intestines and leads to increased colonization by Citrobacter rodentium . Infection and Immunity. 2010;78(4):1509–1519. PubMed PMC
Quist CF, Nettles VF, Manning EJB, et al. Paratuberculosis in key deer (Odocoileus virginianus clavium) Journal of Wildlife Diseases. 2002;38(4):729–737. PubMed
Soumya MP, Pillai RM, Antony PX, Mukhopadhyay HK, Rao VN. Comparison of faecal culture and IS900 PCR assay for the detection of Mycobacterium avium subsp. paratuberculosis in bovine faecal samples. Veterinary Research Communications. 2009;33(7):781–791. PubMed
Kopecna M, Trcka I, Lamka J, et al. The wildlife hosts of Mycobacterium avium subsp. paratuberculosis in the Czech Republic during the years 2002–2007. Veterinarni Medicina. 2008;53(8):420–426.
Kralik P, Slana I, Kralova A, Babak V, Whitlock RH, Pavlik I. Development of a predictive model for detection of Mycobacterium avium subsp. paratuberculosis in faeces by quantitative real time PCR. Veterinary Microbiology. 2011;149(1-2):133–138. PubMed
Slana I, Liapi M, Moravkova M, Kralova A, Pavlik I. Mycobacterium avium subsp. paratuberculosis in cow bulk tank milk in Cyprus detected by culture and quantitative IS900 and F57 real-time PCR. Preventive Veterinary Medicine. 2009;89(3-4):223–226. PubMed
Slana I, Kralik P, Kralova A, Pavlik I. On-farm spread of Mycobacterium avium subsp. paratuberculosis in raw milk studied by IS900 and F57 competitive real time quantitative PCR and culture examination. International Journal of Food Microbiology. 2008;128(2):250–257. PubMed
Rostagno MH. Can stress in farm animals increase food safety risk? Foodborne Pathogens and Disease. 2009;6(7):767–776. PubMed
Tham KM. Molecular and clinicopathological diagnosis of malignant catarrhal fever in cattle, deer and buffalo in New Zealand. Veterinary Record. 1997;141(12):303–306. PubMed
Radostits OM, Gay CC, Blod DC, Hinchcliff KW. Disease caused by viruses and chlamydia. In: Radostits OM, Gay CC, Blod DC, Hinchcliff KW, editors. Veterinary Medicine: A Textbook of the Diseases of Cattle, Sheep, Pigs, Goats and Horses. London, UK: WB Saunders; 1999. pp. 1019–1134.
Freeman ML, Sheridan BS, Bonneau RH, Hendricks RL. Psychological stress compromises CD8+ T cell control of latent herpes simplex virus type 1 infections. The Journal of Immunology. 2007;179(1):322–328. PubMed PMC
Radostits OM, Gay CC, Blod DC, Hinchcliff KW. General systemic diseases. In: Radostits OM, Gay CC, Blod DC, Hinchcliff KW, editors. Veterinary Medicine: A Textbook of the Diseases of Cattle, Sheep, Pigs, Goats and Horses. London, UK: WB Saunders; 1999. pp. 41–114.
Sweeney RW, Whitlock RH, Rosenberger AE. Mycobacterium paratuberculosis cultured from milk and supramammary lymph nodes of infected asymptomatic cows. Journal of Clinical Microbiology. 1992;30(1):166–171. PubMed PMC
Nebbia P, Robino P, Zoppi S, de Meneghi D. Detection and excretion pattern of Mycobacterium avium subspecies paratuberculosis in milk of asymptomatic sheep and goats by nested-PCR. Small Ruminant Research. 2006;66(1–3):116–120.
Dimareli-Malli Z. Detection of Mycobacterium avium subsp. paratuberculosis in milk from clinically affected sheep and goats. International Journal of Applied Research in Veterinary Medicine. 2010;8(1):44–50.
Khol JL, Kralik P, Slana I, et al. Consecutive excretion of Mycobacterium avium subspecies paratuberculosis in semen of a breeding bull compared to the distribution in feces, tissue and blood by IS900 and F57 quantitative real-time PCR and culture examinations. Journal of Veterinary Medical Science. 2010;72(10):1283–1288. PubMed
Buergelt CD, Williams JE. Nested PCR on blood and milk for the detection of Mycobacterium avium subsp paratuberculosis DNA in clinical and subclinical bovine paratuberculosis. Australian Veterinary Journal. 2004;82(8):497–503. PubMed