B. Svensson et al., Involvement of a pasteurizer in the contamination of milk by Bacillus cereus in a commercial dairy plant, J DAIRY RES, 67(3), 2000, pp. 455-460
Bacillus cereus is a common contaminant in raw milk. The spores survive pas
teurization and psychrotrophic strains of B. cereus often limit the keeping
quality of pasteurized milli stored at > 6 degrees C (Griffiths, 1992). Hi
gh numbers of B. cereus in pasteurized milk are most frequent when the cows
are grazing (Slaghuis et al. 1997), mainly owing to increased levels of sp
ores in ram milk resulting from teat contamination by soil (Christiansson e
f al. 1999). However, high numbers can also be found in pasteurized milk wh
ile the cows are housed indoors, and this is probably caused by additional
contamination at the dairy plant (te Giffel et al. 1996; Larsen & Jorgensen
: 1997: Lin et nl. 1998). There is little information available about the s
ites of recontamination in the dairy. The use of typing techniques capable
of discrimination below the species level, such as fatty acid profiles and
random amplification of polymorphic DNA-polymerase chain reaction (RAPD-PCR
), could be helpful in demonstrating contamination routes (Lin et al. 1998.
Nilsson et al. 1998).
Spores of B. cereus are very hydrophobic and readily adhere to surfaces of
steel, glass and rubber (Ronner et al. 1990), and short cleaning-in-place p
rogrammes do not always eliminate all the spores (Ronner St Husmark, 1992).
Spores adhering to surfaces are more difficult to eliminate by disinfectan
ts than spores in solution (te Giffel et al. 1995). Many B. cereus spores g
erminate rapidly in milli upon heat activation and, if allowed to propagate
undisturbed on surfaces: may form biofilms that are extremely difficult to
eliminate (Mosteller & Bishop, 1993. Wirtanen et al. 1996; Kumar & Anand,
1998).
This paper describes how we demonstrated the involvement of a pasteurizer i
n the contamination of pasteurized milli by B. cereus in a commercial dairy
plant using a combination of classic microbiological analyses and typing o
f strains by RAPD-PCR.