Pathogen Contamination
from Human Sources
In addition to the contamination
of raw food supplies that occurs during growing, shipping, and processing,
there is the problem of food contamination caused by people who are carriers
of pathogens. (See Table 4-1.) While most food codes require
that when an employee is sick, he or she should stay home, people actually
shed pathogenic bacteria a few hours to many days before they have major
symptoms of illness. Food workers can become permanent carriers of
pathogens and yet exhibit no signs of illness (e.g., Salmonella
carriers). Therefore, the only safe assumption is that all employees
who work with food every day carry pathogens (on their skin and in their
urine and feces) that must be kept out of the food. The following
table is a list of some pathogens that commonly originate from human sources.
Table 4-1. Pathogen Contamination Common from Human Sources*
|
|
|
| Shigella spp., hepatitis A, Norwalk virus, E. coli, Salmonella spp., Giardia lamblia | Feces |
| Norwalk virus | Vomit |
| Staphylococcus aureus | Skin, nose, boils, skin infections |
| Streptococcus Group A | Throat and skin |
* 1 in 50 (2%) of the employees who come to work each
day are highly infective.
(This calculation is based on 16,000,000 people who are
ill each year for 2.5 days, of which 5,000,000 work in food operations
each day.)
Foodborne Illness
Hazards: Threshold and Quality Levels
The next step in the systematic
approach to hazard control is to recognize that certain pathogens can be
selected as the basis for process control criteria. Table 4-2 shows
the levels of microorganisms that caused illness, based on volunteer feeding
tests of healthy people. Hazardous levels of chemicals and hard foreign
objects in food are also listed.
Spores of the pathogenic
bacteria B. cereus, C. botulinum, and
C. perfringens must
germinate after the food is cooked, and the vegetative cells must multiply
to a level of at least 104 to 106 in order to make
the food a hazard to consumers. Low levels of these spore-forming
organisms (102 to 103) in food are not a hazard,
with the exception of C. botulinum found in honey. Honey must
not be fed to infants at an age of less than one year (103). Infants
have few competitive gut microflora, and the C. botulinum in the
honey is able to germinate and then multiply in the infant's intestinal
tract and produce toxin at a level sufficient to cause illness and even
death. This hazard can be controlled by educating family members
not to feed honey to babies.
Campylobacter jejuni
is a principal cross-contamination problem. This pathogenic microorganism
may be present in poultry at a "natural" level after slaughter that will
cause illness without having to multiply. Raw chicken and other poultry
can be contaminated at high levels (i.e., 106 to 107
organisms / chicken) (84). The threshold for illness in healthy people
is approximately 500 organisms in 180 ml of milk, which means approximately
2 organisms per ml. Comparing this infective level with those for
Salmonella,
E.
coli,
Vibrio,
etc., it is obvious that C.
jejuni, in poultry that is grossly
contaminated, will be a major cause of foodborne illness.
(If Table
4-2 does not print properly, click
here for separate image.)

Assumed Contamination
Levels for Raw Food
A series of beginning contamination
levels for raw food coming into typical foodservice systems is shown in
Table 4-3. It is based on threshold levels that make healthy people
ill and normal contamination as listed in the literature.
These figures pertain to
food in the U.S. Contamination levels in other countries may be higher
or lower. When designing a safe food process, these are the levels
of contamination that must be controlled and eliminated by methods of processing,
preservation, and storage.

Often there is the question for retail food operators, "What is a microbiological standard for good food quality?" Neither the USDA nor the FDA provides an answer to this question. Table 4-4 lists suggested microbial specifications that can be used when communicating with suppliers as to the microbial quality of raw food (171).
Table 4-4. Microbial Criteria for Food Quality
| Number of Spoilage Microorganisms Aerobic Plate Count at 70°F (21.1°C) | Rating |
| < 10,000 CFU / gram | Good |
| 10,000 to 5,000,000 CFU / gram | Average |
| 5,000,000 to 50,000,000 CFU / gram | Poor |
| > 50,000,000 CFU / gram | Spoiled |
The purpose of foodservice is to provide food that is safe and pleasurable to consume. Therefore, in addition to providing safe food by controlling and eliminating pathogens in food, the growth of spoilage microorganisms must be limited and controlled as much as possible in order to provide food products of a specified quality.
Assumed Microbiological
Criteria for Food Handlers and Food Contact Surfaces
In addition to microbial
contamination expected in food, it is also necessary to define contamination
levels for food handlers, facilities, and equipment. Based on the
estimate that as many as 16 million people may get foodborne illness each
year (15), for a period of 2 to 5 days. It can be estimated through
calculations that 1 in 50 people working in the 500,000 food establishments
in the U.S. is shedding billions of pathogens in his or her feces.
If 0.001 gram of fecal material leaks through or gets around toilet
paper, fingertips and underneath fingernails will become contaminated with
fecal pathogens. Hands and fingertips can also become contaminated
when changing diapers, cleaning up vomit, or cleaning up after animals
at home. The double hand wash method using a fingernail brush must
be used to reduce fecal microorganisms to less than 10 on the fingertips
and under the fingernails.
The facilities and equipment
will also be contaminated. If the food contact surfaces are washed
and rinsed every 4 hours, and if the facilities are cleaned and sanitized
adequately at the end of production, the pathogenic build-up on the equipment
and facilities can be kept to a safe level. Note that L. monocytogenes
is an environmental pathogen that arrives on food or on the people who
enter the facility. It is essential that the facility be as well
maintained as possible in critical locations, so that cracks in the floors,
walls, or ceilings (where L. monocytogenes can accumulate)
are minimal. When cleaning is done regularly, L. monocytogenes
can be reduced to an undetectable level immediately after cleaning.
It is also essential that food processing areas be kept at a humidity of
less than 65% to minimize mold multiplication in dry food and in the environment
of the facility. In a food production area where pasteurized, cooked,
cooled food is being assembled and packaged for refrigerated meals, there
must be no pathogens on food contact surfaces. This is defined as
no vegetative pathogens (e.g., Salmonella spp., Shigella
spp., and C. jejuni) in a 50-sq.-cm. swabbed area of a surface.
The Standards for Number
of Spoilage Microorganisms on Food Contact Surfaces are shown in Table
4-5. If these standards are maintained, industry experience has shown
that foods with long shelf lives can be produced.
Table 4-5. Standards for Number of Spoilage Microorganisms on Food Contact Surfaces
|
|
|
| <1 CFU / 50 sq. cm. or <1/ml. of rinse solution | Excellent |
| 2 to 10 CFU / 50 sq. cm. | Good |
| 11 to 100 CFU / 50 sq. cm. | Clean-up time |
| 101 to >1,000 CFU / 50 sq. cm. | Out of control, shut down and find the problem |
Food Pathogen Control
Data Summary
The next step is to develop
the microbiological basis for the time and temperature and pH process standards.
Table 4-6 provides the database for process standards development.
Since Y. enterocolitica
and
L.
monocytogenes both begin to multiply at 29.3ºF (-1.5ºC) (76),
food must be kept below a temperature of 30ºF (-1.1ºC) if the
multiplication of these pathogens is to be totally stopped. This
means only having frozen food, which is impractical. Another solution
is to use time with temperature from 29.3 to 127.5ºF (-1.5 to 52.2ºC)
so that the pathogens do not multiply to an unsafe level. Salmonella
spp. will multiply at a pH as low as 4.1. Therefore, it is essential
that if food such as mayonnaise is made with raw eggs (notorious for being
contaminated with Salmonella spp.), the pH of the product must be
below 4.1. Smittle (167) determined that there is no Salmonella
spp. growth at pH 4.1 (when acidified with acetic acid), and in fact, Salmonella
spp. in mayonnaise is destroyed when held at 70ºF (21.1ºC) for
72 hours.
The data for C. jejuni
point
out that it grows very poorly over a limited range and is quite easily
destroyed. Therefore, the major problem with C. jejuni is
cross-contamination, as mentioned earlier. It can be assumed that
10,000 Campylobacter spp. per 50 square cm (177) will be deposited
on the food contact surface by raw food such as chicken, and it must be
reduced to less than 100 per 50 square cm to be tolerable.
Spores of C. botulinum
type E are inactivated at 180ºF (82.2ºC). However, many
foods do not reach this temperature when cooked or pasteurized. It
must be assumed, then, that C. botulinum type E and other non-proteolytic
C.
botulinum spores will survive the cooking process. (If Table
4-6 does not print properly, click
here for separate image.)

Many foods, 0.25 inch below
the surface, have an oxidation reduction potential at which C. botulinum
will grow. For control, if the food is a probable carrier of non-proteolytic
C.
botulinum, the food must be stored below 38ºF (3.3ºC) in
order to prevent outgrowth of the spores. Staphylococcus aureus
begins
to multiply at 43ºF (6.1ºC) but does not begin to produce a toxin
until it reaches a temperature of 50ºF (10.0ºC). Since
there may be recontamination of food with S. aureus when people
make salads with their hands, if salad ingredients are pre-chilled to less
than 50ºF (10.0ºC) and are kept below this temperature when mixed,
there will be no chance of S. aureus toxin production. Food
containing 1,000 S. aureus organisms per gram is not hazardous.
A population of 106S. aureus per gram of food is necessary
to produce a sufficient amount of toxin to cause illness. However,
if the toxin is produced, it is virtually impossible to destroy the toxin
when the food is cooked or reheated. Therefore, reheating food to
165ºF (73.9ºC) should never be used as a critical control procedure.
After food is cooked, the best method of control is to prevent the production
of toxin by controlling cross-contamination and by keeping the temperature
of food below 50ºF (10.0ºC).
Some types of B. cereus
begin to multiply below 40ºF (4.4ºC) (192). It is a very
common contaminant of many cereal products, spices, and even fresh sprouts.
This spore-forming pathogen will survive cooking. To be safe for
long-term storage (greater than 10 days), cooked food must be cooled and
maintained at less than 38ºF (3.3ºC) in order to prevent the
growth of both type E C. botulinum and B. cereus.
Proteolytic strains of C.
botulinum (types A and B) do not begin to multiply and produce a toxin
until they reach a temperature of 50ºF (10.0ºC). Therefore,
if produce such as fruits and vegetables, which today are frequently vacuum
packaged and contaminated with low levels of C. botulinum, are kept
at a temperature of less than 50ºF (10.0ºC), types A and B C.
botulinum will not cause illness.
Finally, C. perfringens
is considered to be another control organism. Actually, the highest
known growth temperature for a foodborne pathogenic bacterium is that of
C.
perfringens at 126.1°F (52.3°C) and is referred to as the Phoenix
phenomenon (164). Therefore, the upper temperature limit for pathogenic
microorganism control is 126.1°F (52.3°C) [rounded to 130ºF
(54.4ºC)]. Because of its rapid growth, as rapidly as once every
7.2 minutes at 105.8ºF (41.0ºC) (196), this pathogen dictates
the heating and cooling rates for food. Food must be heated from
40 to 130ºF (4.4 to 54.4ºC) in less than 6 hours in order to
assure no multiplication. Food must be cooled from 130 to 45ºF
(54.4 to 7.2ºC) within 15 hours in order to prevent the outgrowth
of C. perfringens spores during cooling (98).
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A)
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Contents
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