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Appl. Environ. Microbiol., 09 1996, 3446-3452, Vol 62, No. 9
D Millar, J Ford, J Sanderson, S Withey, M Tizard, T Doran and J Hermon-Taylor
IS900 PCR for Mycobacterium paratuberculosis was applied to cream, whey,
and pellet fractions of centrifuged whole cows' milk. The test and
simultaneous control reactions gave correct results for spiked milk and for
native milk samples obtained directly from M. paratuberculosis- free,
subclinically infected, and clinically infected cows. The test was then
applied to units of whole pasteurized cows' milk widely obtained from
retail outlets throughout central and southern England from September 1991
to March 1993. With peak periods in January to March and in September to
November, when up to 25% of units were affected, an overall 22 of 312
samples (7%) tested positive for M. paratuberculosis. In 18 of the 22
positive samples (81%), the PCR signal segregated to the cream or pellet
fractions or both, consistent with the presence of intact mycobacteria.
Nine of 18 PCR-positive milk samples (50%) and 6 of 36 PCR-negative milk
samples (16%) yielded long- term liquid cultures which tested positive for
M. paratuberculosis after 13 to 40 months of incubation, despite overgrowth
by other organisms. Taken together with data on the prevalence of M.
paratuberculosis infection in herds in the United Kingdom, the known
secretion of M. paratuberculosis in milk from subclinically infected
animals, and the inability of laboratory conditions simulating
pasteurization to ensure the killing of all these slowly growing or
unculturable organisms, there is a high risk, particularly at peak times,
that residual M. paratuberculosis will be present in retail pasteurized
cows' milk in England.
Copyright © 1996, American Society for Microbiology
IS900 PCR to detect Mycobacterium paratuberculosis in retail supplies of whole pasteurized cows' milk in England and Wales
Department of Surgery, St. George's Hospital Medical School, London, United Kingdom.
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