P2-60 Attachment of Shiga Toxigenic Escherichia coli (STEC) on Stainless Steel Hex Nuts in Minimal and Full Nutrient Broth

Tuesday, July 30, 2013
Exhibit Hall (Charlotte Convention Center)
Amy Parks, Texas Tech University, Lubbock, TX
Kendra Nightingale, Texas Tech University, Lubbock, TX
J. Chance Brooks, Texas Tech University, Lubbock, TX
Michael San Francisco, Texas Tech University, Lubbock, TX
Leslie Thompson, Texas Tech University, Lubbock, TX
Guy H. Loneragan, Texas Tech University, Lubbock, TX
Mindy M. Brashears, Texas Tech University, Lubbock, TX
Introduction: Formation of biofilms on processing equipment within food production facilities can have a detrimental effect on both quality and safety of the products by harboring pathogens and spoilage bacteria.  Recent regulations identifying six additional serogroups (O26, O45, O103, O111, O121, and O145) of Shiga toxigenic Escherichia coli (STEC) plus the original designation of E. coli O157 as adulterants in non-intact beef product underscores the importance of understanding how these strains grow and interact within the food processing environment. 

Purpose: The objective of this research is to determine if strains of each STEC serogroup can attach to stainless steel and potentially form biofilms.

Methods: Four strains for each serogroup with variation in presence of stx1 and stx2 and origin of strain were examined.  Stainless steel hex nuts, with a rough or smooth surface, were incubated in either minimal or full nutrient broth inoculated with a single strain of STEC at 25°C up to 48 h.  At the time interval (4, 8, 12, 24, or 48 h), the nut was removed, rinsed, stained with crystal violet, and the crystal violet was removed from the nut to determine solution absorbance at 590 nm to measure resultant biomass.

Results: Significant differences (P < 0.05) between strains within serogroup were found within the rough surface/minimal media combination for O45, O103 and O111 with some evidence of differences (P < 0.08) for O157 with no differences found over time.  Significant differences between strains within serogroup were also found within the smooth surface/minimal media combination for O26, O45, O103, and O121 and no differences over time except for STEC O45 serogroup. 

Significance: These data indicate differences in attachment ability between strains within serogroup.  Further research utilizing strains with greater attachment abilities is needed to examine the effectiveness of commonly used detergents and sanitizing agents on STEC biofilm renewals as well as improvements of current methodologies to determine formation of STEC biofilms.