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The use of pulsed-field gel electrophoresis to investigate the epidemiology of Mycoplasma bovis in French calf feedlots

► To investigate the epidemiological design of Mycoplasma bovis outbreaks in veal calf feedlots. ► We typed 39 strains from 5 feedlots, isolated during and 30 days after outbreak using PFGE. ► MluI, SmaI and KpnI provide a excellent discriminatory power, and allow fine typing of related strains. ► T...

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Published in:The veterinary journal (1997) 2012-04, Vol.192 (1), p.96-100
Main Authors: Arcangioli, Marie-Anne, Aslan, Hamidé, Tardy, Florence, Poumarat, François, Grand, Dominique Le
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Language:English
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Summary:► To investigate the epidemiological design of Mycoplasma bovis outbreaks in veal calf feedlots. ► We typed 39 strains from 5 feedlots, isolated during and 30 days after outbreak using PFGE. ► MluI, SmaI and KpnI provide a excellent discriminatory power, and allow fine typing of related strains. ► The same Mycoplasma bovis strain spreads clonally and persists in feedlots after an outbreak. Mycoplasma bovis is a major cause of respiratory outbreaks in cattle feedlots. In this study pulsed-field gel electrophoresis (PFGE) was used to trace field strains and provide information on M. bovis patterns of spread in calf feedlots. The suitability of KpnI, MluI and SmaI restriction enzymes was assessed on different sets of strains. The discriminative power of the first two enzymes was first assessed using 28 epidemiologically unrelated strains; stability was 100% on multiple isolates from in vivo experimental infection. Thirty-nine field isolates from six feedlots were then evaluated. In contrast to the unique fingerprints displayed by the unrelated strains, the isolates from the feedlots showed identical patterns at the time of the outbreak of respiratory disease and 4weeks later. The PFGE typing results suggest that M. bovis strains follow a clonal epidemic spread pattern at the herd level and that the same strain persists in calves of the herd after the clinical signs have disappeared.
ISSN:1090-0233
1532-2971
DOI:10.1016/j.tvjl.2011.05.004