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Contents
Battling Food-Poisoning Bacteria

Microbiologist Irene Wesley examines the growth of microbes obtained from a hog
carcass swab. Her work is part of the National Food Safety Initiative, which
has as a major goal reducing foodborne pathogens on the farm and in foods.
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In 1931, USDA's Bureau of Home Economics published the fourth edition of
Aunt Sammy's Radio Recipes, a compilation of the most popular recipes
and menus from "Housekeepers' Chats," a 1926 radio program for women.
Today, USDA is still concerned with the preparation of food. But the
spotlight now is on food safety rather than cookbookson doing everything
possible to make sure our food is safe and wholesome.
Every year, 6.5 to 33 million people in the United States get foodborne
illnesses. The estimated medical costs and productivity losses range from $6 to
$34 billion a year. And the food industry loses moneyand product
reputationsthrough embargoes, recalls, and voluntary destruction of
products.
For these reasons, the National Food Safety Initiative was begun in 1997.
It's a comprehensive national program to improve the safety of food all the way
from where food startson the farmto where it winds upon your
table. USDA carries out the initiative along with the Food and Drug
Administration, Centers for Disease Control and Prevention, and U.S.
Environmental Protection Agency.
Across the country, Agricultural Research
Service laboratories at 10 locations are leading the scientific battle
against food pathogens in fresh and processed meats, milk, grains, fruits,
vegetables, and other foods. The work of just one of these labs is profiled
herethe National Animal Disease
Center (NADC) in Ames, Iowa.
Researchers at Ames are battling four major bacterial pathogens in food:
Campylobacter jejuni, Salmonella, Escherichia coli
O157:H7, and Listeria monocytogenes. One major battle is already won:
finding faster ways to identify the enemy.
"Each strain of bacteria has a specific genetic fingerprint,"
says ARS microbiologist Irene V. Wesley. When an outbreak of foodborne illness
occurs, Wesley obtains samples of both the food and bacterial isolates taken
from individuals who became ill. Her basic studies show that DNA fingerprints
of the patients' harmful bacteria match those in foods that made them ill.
In the last 3 years, Wesley and her NADC colleagues have developed several
quick and accurate tests to identify foodborne pathogens. The tests use a
gene-multiplying technique called polymerase chain reaction (PCR) to recognize
pathogens in animal, human, and food samples in less than 8 hours. Culturing
techniques, by comparison, can take up to 2 weeks.

Campylobacter requires complex media for growth. Biological technician
Sharon Fanklin searches a blood agar plate for typical Campylobacter
colonies.
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Now the PCR tests are being put to the ultimate test. Wesley and researchers
at Iowa and North Carolina State Universities are participating in a project
funded by USDA's Food Safety and Inspection Service. They are tracking the
spread of Campylobacter, Salmonella, and Yersinia
enterocolitica in pigsfrom the nursery stage to slaughter. Usually
kept in a separate facility, nursery pigs have been weaned but are not yet
developed into what is called the grower stage.
The study, which includes eight farms and two slaughterhouses, compares two
different ways of raising hogs in Iowa and North Carolina. The results of this
study will be used to determine which farm management practices reduce
foodborne pathogens.
With a PCR test, Wesley has shown that 90 percent of nursery stage pigs
harbor Campylobacter. At slaughter, the organism was found on 17 percent
of hog carcasses.
C. coli is a less severe pathogen than its ugly relativeC.
jejuni. The latter organism is the leading cause of foodborne bacterial
infection in people. Four million C. jejuni infections occur in humans
each year in the United States, according to the Centers for Disease Control
and Prevention.
Like twins that can trade places without anyone knowing the difference,
these two microorganisms are difficult to tell apart. But the PCR test is one
of the best ways to do it.
"Because they're so genetically similar, these two bacteria can
exchange DNA on the farm. Where C. coli exists, there is also the
probability that C. jejuni exists," says Wesley.
In another study, Wesley used the PCR tests to identify C. coli in
about 70 percent of 1,300 market-weight hogs. Less than 1 percent of the test
hogs harbored C. jejuni. Neither strain of Campylobacter was
detected in 29 percent of the hogs sampled.
Keeping an Eye on Cleanliness
Public concern over E. coli O157:H7 has skyrocketed since 1993, when
the microbein undercooked hamburger pattieskilled four children in
the Pacific Northwest. In that single outbreak, 477 people were infected from
the undercooked, contaminated hamburger.
Foodborne disease-causing bacteria such as E. coli O157:H7 are found
in feces and spread to food through fecal contamination. One of the prime ways
to reduce bacterial contamination is to reduce fecal contamination in livestock
and poultry slaughter facilities. Current federal regulations mandate zero
tolerance for visible fecal contamination and for E. coli O157:H7.

Microbiologists Tom Casey (left) and Mark Rasmussen evaluate a new laser for
use in their fecal contamination detection system for meat carcasses. They are
working in the laser lab of an Iowa State University collaborator, photochemist
Jacob Petrich.
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At the slaughterhouse, visual inspections and carcass cleaning have been
two of the standard tools for reducing the likelihood of E. coli and
other bacterial contaminants in meat.
But "the human eye is not very sensitive and often can't tell the
difference between feces and blood clots that can be on a carcass," says
ARS microbiologist Mark A. Rasmussen at Ames.
Now Rasmussen, ARS microbiologist Thomas A. Casey, and Iowa State University
photochemist Jacob W. Petrich have invented a new prototype instrument based on
fluorescent spectroscopy.
"We think this instrument has the potential to greatly improve the
ability of inspectors to identify small amounts of fecal contamination not
detected visually on carcasses," says Casey.
The technology uses specific wavelengths or colors of light to illuminate
the carcass. Collected light returned from the carcass is electronically
analyzed to determine if the carcass is contaminated. The results are displayed
as a numerical value relative to the amount of feces. A contaminated carcass
would then be trimmed or sanitized to remove the fecal contamination.
Instruments can be designed to meet the needs of any slaughter facility.
They could range in size from a portable, hand-held device similar to metal
detector wands used at airports to a larger device capable of detecting fecal
contamination on an entire carcass.
The researchers have applied for a patent on the instrument and are
constructing and testing other prototype designs. About 60 companies and
industry organizations have contacted the researchers. ARS plans to choose an
industry partner for a cooperative research and development agreement to
develop the prototype into a commercial instrument. By
Linda Cooke McGraw,
Agricultural Research Service Information Staff.
This research is part of an ARS National Program on Food Safety described on
http://www.nps.ars.usda.gov/programs/108s2.htm.
Irene V. Wesley,
Mark A. Rasmussen,and
Thomas A. Casey are scientists at
the USDA-ARS National Animal Disease
Center, P.O. Box 70, Ames, IA 50010; phone (515) 663-7200, fax (515)
663-7458.
"Battling Food-Poisoning Bacteria" was published in the
February 1999 issue of
Agricultural Research magazine.
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