Jm. Woody et al., Role of bacterial association and penetration on destruction of Escherichia coli O157 : H7 in beef tissue by high pH, J FOOD PROT, 63(1), 2000, pp. 3-11
This study was undertaken to determine if association with collagen enables
Escherichia coli O157:H7 to resist high-pa treatments and to determine the
effects of high pH on the survival of E. coli O157:H7 within different lay
ers of beef tissue. E. coli O157:H7 was inoculated onto purified bovine typ
e I collagen on 12-mm(2) circular grass coverslips, plain 12-mm(2) circular
grass coverslips (control), and 12-mm2 irradiated (cobalt-60) lean beef ti
ssue. The rates of destruction of E. coli O157: H7 inoculated on coverslips
in pH 10.5 NaHCO3-NaOH buffer at 35 degrees C were determined at various s
ampling times. E. coli O157:H7 cells associated with collagen and treated i
n the same manner were also examined using scanning electron microscopy to
determine if association with collagen enabled the organism to resist high-
pa treatments. The inoculated tissue was treated in pH 13.0 NaHCO3-NaOH buf
fer at 25 degrees C, and penetrating cells of E. coli O157:H7 were recovere
d using a cryostat technique. There was no significant difference (P < 0.05
) between the rates of destruction of collagen-associated E. coli O157:H7 a
nd non-collagen-associated E. coli O157:H7 following exposure to high-pH tr
eatments. Scanning electron micrographs showed that collagen-associated E.
coli O157:H7 cells appeared physically damaged by exposure to high-pH treat
ments, and association of E. call O157:H7 to collagen did not increase the
resistance of the organism to destruction by high-pH rinses. No significant
differences were seen between 20 ml of NaHCO3-NaOH buffer at pH 13.0 (trea
tment) and 20 mi of distilled water at pH 7.0 (control) when E. coli O157:H
7 cells were recovered in beef tissue at depths of up to 2,000 mu m (P < 0.
05). The ability of E. coli O157:H7 to penetrate beef tissue may be an impo
rtant factor in reducing the effectiveness of high-pH treatments in killing
this organism on beef tissue. This funding should be considered in the fut
ure when designing treatments to decontaminate beef carcasses.