In-house testing for microorganisms such as Escherichia coli is routine for most food manufacturers. An increasing number of companies, however, are also performing in-house testing for Staphylococcus aureus. In fact, 62% of the 1,400 manufacturers surveyed in 2000 were already doing their own evaluations.
One of those manufacturers is The Schwan Food Company (Marshall, Minn.), a producer of frozen foods that serves approximately 50 countries through home delivery, grocery stores, online shopping, and sales to food service. The company has multiple brands and offers pizza, entrees, convenience foods, fruit, vegetables, bakery items, and desserts.
Some manufacturers may have concerns about in-house testing for S. aureus since it is classified as a pathogen. “However, there is a difference between Staph and Listeria or Salmonella,” says Anne Sherod, director of Food Safety, Microbiology, at Schwan’s Research and Development, Inc.
“Illness is not caused directly by the Staph organism. Any illness would be due to enterotoxin, which is produced by Staph aureus, and a large number of Staph aureus organisms would be required to produce sufficient enterotoxin to cause illness,” Sherod adds. She insists that if well-trained personnel employ appropriate methodologies and good laboratory practices, there should not be any more or any less risk involved in testing for S. aureus in house than in testing for any other organism. Sherod identifies four key steps to follow in setting up an in-house testing program for S. aureus: establishing, monitoring, evaluating, and correcting.
Before testing begins, determine acceptable microbiological criteria for sampling of S. aureus, along with limits on where enterotoxin testing should be performed. “Base those levels on literature, past experience in your plant, ingredients, finished products and processes, and the potential for toxin production in your setting,” says Sherod. “Staph aureus is generally found on animals, but humans can also carry Staph aureus.” She adds that an effective testing program can provide verification of a hazard analysis and critical control point (HACCP) system.
Monitoring Manufacturing
“Manufacturers must understand their processes as well as the potential for Staph aureus growth and cross-contamination,” Sherod says. “Consider where Staph aureus could be found or grow to levels that would produce enterotoxin.”
She recommends scheduled monitoring of ingredients; components such as batters, mixes, or fillings; work in progress; and finished products and manufacturing equipment, including dipping bays, waterfalls, or recirculating systems. “Look for equipment that is aging or no longer fully cleanable, and determine if the equipment needs repair. For instance, do small parts like O-rings need to be replaced to avoid hosting microorganisms?”
Monitoring employee behavior is also necessary to guarantee that good practices are being followed. For instance, make sure that employees are wearing gloves appropriately and changing them often enough.
Evaluating Samples
The Schwan Food Company uses a two-part approach to test for S. aureus. Primary testing identifies levels of S. aureus present. Depending on those results, secondary testing may be done to determine if enterotoxin has been produced.
Schwan uses Petrifilm Staph Express Count Plates from 3M (St. Paul, Minn.) for their primary testing; the plates are approved as an official method of analysis by AOAC International, an organization that provides and facilitates validated analytical methods and laboratory quality assurance programs. The sample-ready plates are coated with rehydratable nutrients, a cold-water-soluble gelling agent, and chromogenic, modified Baird-Parker medium, which is selective and differential for S. aureus. Only one incubation temperature is required.
While equivalent to the bacteriological analytical manual, three plate, Baird-Parker agar and tube coagulase method, Petrifilm Staph Express Count Plates produce results more quickly. Distinctive, red-violet colonies are counted as S. aureus and appear within 22 to 29 hours instead of 69 to 78 hours.
ACCESS THE FULL VERSION OF THIS ARTICLE
To view this article and gain unlimited access to premium content on the FQ&S website, register for your FREE account. Build your profile and create a personalized experience today! Sign up is easy!
GET STARTED
Already have an account? LOGIN