Wb. Mcnab et al., VARIABILITY IN BROILER CARCASS BACTERIAL LOAD AT 3 ABATTOIRS, AS MEASURED BY A HYDROPHOBIC GRID MEMBRANE-FILTER INTERPRETER, Journal of food protection, 56(8), 1993, pp. 700-705
In this observational study, the variability of broiler carcass bacter
ial load was investigated at three federally inspected abattoirs, usin
g an automated hydrophobic grid membrane filter interpreter system. Th
e measurement protocol involved: whole carcass rinses aided by a mecha
nical carcass shaker; filtration of rinse solutions through hydrophobi
c grid membrane filters (HGMF) (ISO-GRID(R), QA Laboratories, Ltd., To
ronto, Ont.); and use of an automated HGMF interpreter (MI-100 HGMF In
terpreter System, Richard Brancker Research, Ltd., Ottawa, Ont.). Carc
ass and lot mean bacterial loads were measured, respectively, in units
of log10 most probable number (MPN) of mesophylic aerobic colony form
ing units per gram of carcass (LgMPN/g), and slaughter lot mean LgMPN/
g (LMLgMPN/g). Whole carcass rinses were conducted on a total of 1,917
carcasses, among % slaughter lots from three abattoirs. Overall, the
LgMPN/g ranged from 1.054 to 4.180 with a mean of 2.585 and a variance
of 0.263. These corresponded to MPN/g counts from 11 to 15,135 and a
geometric mean of 385 MPN/g. Statistically significant differences wer
e observed between abattoirs and between lots within abattoirs. The in
tra-abattoir correlation coefficient of LgMPN/g was r = 0.180 (p < 0.0
01). The within abattoir intralot correlation coefficient was r = 0.25
9 (p < 0.001). In this data set, approximately 56, 26, and 18% of the
variability in LgMPN/g were attributed to factors operating at the ind
ividual bird, lot, and abattoir levels of organization, respectively.
Factors significantly associated with LMLgMPN/g included: abattoir (p
< 0.001), transportation time from farm to abattoir (p < 0.001), and w
aiting time from arrival at the abattoir yard to actual slaughter (p =
0.002). Analysis of a series of five repeat rinses, conducted on one
bird from each of the 96 study lots, demonstrated that bacterial count
s in the second to fifth sequential rinses were positively associated
with the bacterial count of the first rinse. Also, after adjusting for
the initial count, a pattern of decreasing counts was observed in sub
sequent rinses.