9 Flashcards

1
Q

sterilization

A

In its strictest sense, sterilization refers to the removal or
destruction of all microbes, including viruses and bacterial endospores,
in or on an object. (The term does not apply to prions,
which are infectious proteins, because standard sterilizing techniques
do not destroy them.)
- In practical terms, sterilization indicates only the eradication
of harmful microorganisms and viruses; some innocuous
microbes may still be present and viable in an environment
that is considered sterile.

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2
Q

aseptic

A

describes an environment or procedure

that is free of contamination by pathogens

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3
Q

disinfection

A

refers to the use of physical or chemical
agents known as disinfectants, including ultraviolet light, heat, alcohol, and bleach, to inhibit or destroy microorganisms,
especially pathogens. Unlike sterilization, disinfection does
not guarantee that all pathogens are eliminated; indeed, disinfectants
alone cannot inhibit endospores or some viruses. Further,
the term disinfection is used only in reference to treatment
of inanimate objects.

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4
Q

antisepsis

A

When a chemical is used on skin or other
tissue, the process is called antisepsis3 (an@te@sep´sis), and the
chemical is called an antiseptic. Antiseptics and disinfectants
often have the same components, but disinfectants are more
concentrated or can be left on a surface for longer periods of
time

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5
Q

degerming

A

the removal of microbes from a surface by
scrubbing, such as when you wash your hands or a nurse prepares
an area of skin for an injection. Though chemicals such
as soap or alcohol are commonly used during degerming, the
action of thoroughly scrubbing the surface may be more important
than the chemical in removing microbes.

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6
Q

sanitization

A

the process of disinfecting places and utensils
used by the public to reduce the number of pathogenic microbes
to meet accepted public health standards. Thus, the difference between disinfecting dishes at
home and sanitizing dishes in a restaurant is the arena—private
versus public—in which the activity takes place.

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7
Q

pasteurization

A

the use of heat to kill pathogens and
reduce the number of spoilage microorganisms in food and
beverages.

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8
Q

two major types of microbial

control

A

sterilization, which is the elimination of all
microbes, and antisepsis or disinfection, which each denote the
destruction of vegetative (nonspore) cells and many viruses.
Modifications of disinfection include degerming, sanitization,
and pasteurization

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9
Q

-stasis/-static

A

indicate that a chemical or physical
agent inhibits microbial metabolism and growth but does not
necessarily kill microbes.

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10
Q

-cide/-cidal

A

refer to agents that destroy

or permanently inactivate a particular type of microbe

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11
Q

microbial death

A

the permanent loss of

reproductive ability under ideal environmental conditions.

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12
Q

microbial death rate

A

One technique for evaluating the efficacy of an antimicrobial
agent is to calculate the microbial death rate, which is usually
found to be constant over time for any particular microorganism
under a particular set of conditions

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13
Q

There are many types of chemical and physical microbial controls,
but their modes of action fall into two basic categories:

A

those that disrupt the integrity of cells by adversely altering
their cell walls or cytoplasmic membranes and those that interrupt
cellular metabolism and reproduction by interfering with
the structures of proteins and nucleic acids.

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14
Q

hypotonic

A

surroundings < cell. water go in

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15
Q

virus covering

A

In enveloped viruses, the envelope is a membrane composed
of proteins and phospholipids that is responsible for the
attachment of the virus to its target cell. Damage to the envelope
by physical or chemical agents fatally interrupts viral replication.
The lack of an envelope in nonenveloped viruses accounts
for their greater tolerance of harsh environmental conditions,
including antimicrobial agents.

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16
Q

As we have seen, a protein’s function
depends on an exact three-dimensional shape, which is
maintained by

A

hydrogen and disulfide bonds between amino

acids.

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17
Q

ribozyme

A

that portion of a
ribosome that actually catalyzes the synthesis of proteins is a
ribozyme—that is, an enzymatic RNA molecule. For this reason,
physical or chemical agents that interfere with nucleic
acids also stop protein synthesis.

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18
Q

Ideally, agents used for the control of microbes should be

A

inexpensive,

fast acting, and stable during storage.

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19
Q

most resistant microbes

A
  • bacterial endoposres (bacillus, clostiridum) – most resilient forms of life
  • mycobacterium (tb)
  • protoozoa cysts
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20
Q

y mycobacterium resilient

A

contain a large
amount of a waxy lipid. The wax allows these bacteria to
survive drying and protects them from most water-based
chemicals

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21
Q

y cysts resilient

A

A protozoan cyst’s wall prevents entry
of most disinfectants, protects against drying, and shields
against radiation and heat.

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22
Q

high level germicides

A

kill all pathogens, including
bacterial endospores. Health care professionals use them
to sterilize invasive instruments such as catheters, implants, and
parts of heart-lung machines.

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23
Q

intermediat elevel germicides

A

kill fungal
spores, protozoan cysts, viruses, and pathogenic bacteria but
not bacterial endospores. They are used to disinfect instruments
that come in contact with mucous membranes but are noninvasive,
such as respiratory equipment and endoscopes.

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24
Q

low level germicides

A

Low-level
germicides eliminate vegetative bacteria, fungi, protozoa, and some
viruses; they are used to disinfect items that contact only the skin
of patients, such as furniture and electrodes

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25
Q

Temperature and pH affect microbial death rates and the efficacy
of antimicrobial methods.

A

Warm disinfectants, for example,
generally work better than cool ones because chemicals
react faster at higher temperatures (Figure 9.3). Acidic conditions
enhance the antimicrobial effect of heat.

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26
Q

bsl 1

A

suitable for handling microbes,
such as E. coli, not known to cause disease in healthy humans.
Precautions in BSL-1 are minimal and include hand washing
with antibacterial soap and washing surfaces with disinfectants

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27
Q

bsl 2

A
  • for handling moderately hazardous agents, such as hepatitis
    and influenza viruses and methicillin-resistant Staphylococcus
    aureus
  • Access to BSL-2 labs
    is limited when work is being conducted, extreme precautions
    are taken with contaminated sharp objects, and procedures that
    might produce aerosols are conducted within safety cabinets
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28
Q

bsl 3

A
  • requiring that all manipulations be done
    within safety cabinets containing high-efficiency particulate
    air (HEPA) filter
  • special design features: entry through double sets of
    doors and ventilation such that air moves into the room only
    through an open door. Air leaving the room is HEPA-filtered
    before being discharged outside the room.
  • designed for
    experimentation on microbes such as tuberculosis and anthrax
    bacteria and viruses of yellow fever and Rocky Mountain spotted
    fever.
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29
Q

bsl 4

A

designated
for working with dangerous or exotic microbes that cause severe
or fatal diseases in humans, such as Ebola, smallpox, and
Lassa fever viruses. BSL-4 labs are either separate buildings or
completely isolated from all other areas of their buildings. Entry
and exit are strictly controlled through electronically sealed
airlocks with multiple showers, a vacuum room, an ultraviolet
light room, and other safety precautions designed to destroy all
traces of the biohazard. All air and water entering and leaving
the facility are filtered to prevent accidental release. Personnel
wear “space suits” supplied with air hoses (Figure 9.4). Suits
and the laboratory itself are pressurized such that microbes are
swept away from workers.

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30
Q

thermal death pt

A

the

lowest temperature that kills all cells in a broth in 10 minutes

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31
Q

thermal death time

A

the time it takes to completely sterilize

a particular volume of liquid at a set temperature

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32
Q

deciaml reduction time (D)

A

When measuring the effectiveness of heat sterilization, researchers
calculate the decimal reduction time (D), which is the time
required to destroy 90% of the microbes in a sample (Figure 9.5).
This concept is especially useful to food processors because
they must heat foods to eliminate all the endospores of anaerobic
Clostridium botulinum, which could germinate inside sealed cans

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33
Q

boiling time

A

It
is impossible to boil something more quickly simply by applying
more heat; the added heat is carried away by the escaping
steam. Boiling time is the critical factor. Further, it is important
to realize that at higher elevations water boils at lower temperatures
because atmospheric pressure is lower; thus, a longer boiling
time is required in Denver than in Los Angeles to get the
same antimicrobial effect.

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34
Q

pressure fo rsterilization

A

Practically speaking, true sterilization using heat
requires higher temperatures than that of boiling water. To
achieve the required temperature, pressure is applied to boiling
water to prevent the escape of heat in steam. The reason
that applying pressure succeeds in achieving sterilization is that
the temperature at which water boils (and steam is formed) increases
as pressure increases

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35
Q

autoclave

A

consists of a pressure chamber, pipes to introduce
and evacuate steam, valves to remove air and control
pressure, and pressure and temperature gauges to monitor the procedure

36
Q

autoclave conditions

A

121C, 15 psi f pressure above that of normla air pressure, 15min

37
Q

autoclave bio indicator of sterility

A

endospores of bacillus stearothermophilus impregnated into tape. After autoclaving, the tape is aseptically
inoculated into sterile broth. If no bacterial growth appears,
the original material is considered sterile.

38
Q

batch method

A

Historically, milk was pasteurized

by the batch method for 30 minutes at 63°C

39
Q

flash pasteurization

A

most milk processors
today use a high-temperature, short-time method known
as flash pasteurization, in which milk flows through heated tubes
that raise its temperature to 72°C for only 15 seconds. This treatment
effectively destroys all pathogens.

40
Q

ultra high temp pasteurization

A

heats the milk to at least 135°C for only 1 second,

but some consumers claim that it adversely affects the taste.

41
Q

ultra high temp sterilization

A

flash heating milk or other liquids
to rid them of all living microbes. The process involves passing
the liquid through superheated steam at about 140°C for
1 to 3 seconds and then cooling it rapidly. Treated liquids can
be stored indefinitely at room temperature without microbial
spoilage, though chemical degradation after months of storage
results in flavor changes.

42
Q

ultra high temp sterilization

A

flash heating milk or other liquids
to rid them of all living microbes. The process involves passing
the liquid through superheated steam at about 140°C for
1 to 3 seconds and then cooling it rapidly. Treated liquids can
be stored indefinitely at room temperature without microbial
spoilage, though chemical degradation after months of storage
results in flavor changes.

43
Q

moist vs dry heat

A
  • dry heat requires
    higher temperatures for longer times than moist heat because
    dry heat penetrates more slowly
  • water beyter conductor than air
44
Q

hot air

A

denatures
proteins and fosters the oxidation of metabolic and structural
chemicals

45
Q

psychrophilic

A

cold loving

46
Q

fridge n freezing

A

These processes decrease microbial
metabolism, growth, and reproduction because chemical reactions
occur more slowly at low temperatures and because liquid
water is not available at subzero temperatures.

47
Q

slow freezing

A

Slow freezing, during which ice crystals have time to form
and puncture cell membranes, is more effective than quick freezing
in inhibiting microbial metabolism

48
Q

dessication

A

inhibits microbial growth because

metabolism requires liquid water.

49
Q

lyophilzation

A

a technique
combining freezing and drying, to preserve microbes and other
cells for many years. In this process, scientists instantly freeze
a culture in liquid nitrogen or frozen carbon dioxide (dry ice);
then they subject it to a vacuum that removes frozen water
through a process called sublimation, in which the water is transformed
directly from a solid to a gas. Lyophilization prevents
the formation of large, damaging ice crystals. Although not all
cells survive, enough are viable to enable the culture to be reconstituted
many years later.

50
Q

membrane filters

A

Scientists today typically use thin
(only 0.1 mm thick), circular membrane filters manufactured of
nitrocellulose or plastic and containing specific pore sizes ranging
from 25 μm to less than 0.01 μm in diameter (Figure 9.10b).
The pores of the latter filters are small enough to trap small viruses

51
Q

osmotic pressure

A

Another ancient method of microbial control is the use of high
concentrations of salt or sugar in foods to inhibit microbial
growth by osmotic pressure. The removal of water inhibits cellular metabolism
because enzymes are fully functional only in aqueous
environments.

52
Q

osmotic pressure limitations

A

Fungi have a greater ability than bacteria to tolerate hypertonic
environments with little moisture

53
Q

electromagnetic radiation

A

energy without mass traveling in waves at the speed of

light

54
Q

particulate radiation

A

Particulate radiation consists of
high-speed subatomic particles, such as protons, that have been
freed from their atoms.

55
Q

ionizing radiation

A

Electron beams, gamma rays, and some X rays, all of which
have wavelengths shorter than 1 nm, are ionizing radiation because
when they strike molecules, they have sufficient energy
to eject electrons from atoms, creating ions. Such ions disrupt
hydrogen bonding, oxidize double covalent bonds, and create
highly reactive hydroxyl radicals (see Chapter 6). These ions in
turn denature other molecules, particularly DNA, causing fatal
mutations and cell death.

56
Q

nonionizing radiation

A

UV (only this has enough energy), visible, infrared, radio waves.
- Electromagnetic radiation with a wavelength greater than 1 nm
does not have enough energy to force electrons out of orbit, so it
is nonionizing radiation. However, such radiation does contain
enough energy to excite electrons and cause them to make new
covalent bonds, which can affect the three-dimensional structure
of proteins and nucleic acids.

57
Q

UV light

A

UV light with a wavelength of 260 nm is specifically absorbed
by adjacent pyrimidine nucleotide bases in DNA, causing
them to form covalent bonds with each other rather than
forming hydrogen bonds with bases in the complementary
DNA strand (see Figure 7.25). Such pyrimidine dimers distort the
shape of DNA, making it impossible for the cell to accurately
transcribe or replicate its genetic material. If dimers remain uncorrected,
an affected cell may die.
- but doesnt penetrate well

58
Q

phenolics

A

Phenolics are compounds derived from phenol (carbolic acid) molecules
that have been chemically modified by the addition of halogens
or organic functional groups

59
Q

bisphenolics

A

Bisphenolics are composed of two covalently linked phenolics

60
Q

phenolics effectiveness

A

Phenol and phenolics denature proteins and disrupt cell
membranes in a wide variety of pathogens. They are effective
even in the presence of contaminating organic material, such as
vomit, pus, saliva, and feces, and they remain active on surfaces
for a prolonged time.

61
Q

alcohols

A

Alcohols are bactericidal, fungicidal, and virucidal against enveloped
viruses; however, they are not effective against fungal spores
or bacterial endospores

62
Q

alcohols effectiveness

A

Alcohols are considered intermediatelevel
disinfectants. Isopropanol is slightly superior to ethanol as a disinfectant and
antiseptic.

63
Q

Surprisingly, pure alcohol is not an effective antimicrobial

agent because

A

the denaturation of proteins requires water

64
Q

halogens

A

Halogens are the four very reactive, nonmetallic chemical elements:
iodine, chlorine, bromine, and fluorine.

65
Q

halogens effectiveness

A

Halogens are
intermediate-level antimicrobial chemicals that are effective
against vegetative bacterial and fungal cells, fungal spores, some
bacterial endospores and protozoan cysts, and many viruses.

66
Q

oxidizing agents

A

Peroxides, ozone, and peracetic acid kill microbes by oxidizing their
enzymes, thereby preventing metabolism. work by releasing oxygen radiclas.

67
Q

oxidizing agents effecgiveness

A

Oxidizing agents are
high-level disinfectants and antiseptics that work by releasing
oxygen radicals, which are particularly effective against anaerobic
microorganisms. Health care workers use oxidizing agents
to kill anaerobes in deep puncture wounds

68
Q

Hydrogen peroxide does not make a good antiseptic for

open wounds because

A

catalase—an enzyme released from damaged
human cells—quickly neutralizes hydrogen peroxide by
breaking it down into water and oxygen gas, which can be seen
as escaping bubbles.

69
Q

paracetic acid

A

Peracetic acid is an extremely effective sporicide that can be
used to sterilize surfaces.

70
Q

surfactants

A

Surfactants are “surface active” chemicals. One of the ways surfactants
act is to reduce the surface tension of solvents such as
water by decreasing the attraction among molecules. One result
of this reduction in surface tension is that the solvent becomes
more effective at dissolving solute molecules.
- soaps, detergents

71
Q

detergents

A

Synthetic detergents are positively charged organic surfactants
that are more soluble in water than soaps.

72
Q

quats

A

The most popular
detergents for microbial control are quaternary ammonium
compounds, or quats, which are composed of an ammonium
cation (NH4
+ ) in which the hydrogen atoms are replaced by
other functional groups or hydrocarbon chains

73
Q

quats effectiveness

A

Quats function by disrupting cellular membranes so that affected
cells lose essential internal ions, such as K+. cidal to everything except nonenveloped viruses, mycobacteria,
or endospores

74
Q

heavy metal ions

A

Heavy-metal ions, such as ions of arsenic, zinc, mercury, silver,
and copper, are antimicrobial because they combine with sulfur
atoms in molecules of cysteine, an amino acid. Such bonding denatures
proteins, inhibiting or eliminating their function.

75
Q

heavy metal ions effectiveness

A

Heavymetal
ions are low-level bacteriostatic and fungistatic agents, and
with few exceptions their use has been superseded by more effective
antimicrobial agents.

76
Q

aldehydes

A

compounds containing terminal —CHO groups; glutaraldehyde, formaldehyde

77
Q

gaseous agents

A

bulky items can be sterilized within a closed chamber
containing highly reactive microbicidal and sporicidal gases
such as ethylene oxide, propylene oxide, and beta-propiolactone

78
Q

antimicrobial enzymes

A

Many organisms produce chemicals that inhibit or destroy a variety
of fungi, bacteria, or viruses. Among these are antimicrobial
enzymes, which are enzymes that act against microorganisms.

79
Q

lysozyme

A

antimicrobial enzyme in human tears that digests the peptidoglycan cell walls of bacteria,
causing the bacteria to rupture because of osmotic pressure

80
Q

antimicrobials

A

Antimicrobials include antibiotics, semisynthetics, and synthetics.
- The main
difference between these antimicrobials and the chemical agents
we have discussed in this chapter is that antimicrobials are typically
used for treatment of disease and not for environmental
control of microbes.

81
Q

antibiotics

A

antibiotics are antimicrobial chemicals produced
naturally by microorganisms. When scientists chemically modify
an antibiotic, the agent is called a semisynthetic. Scientists have
also developed wholly synthetic antimicrobial drugs.

82
Q

who popularized phenol

A

joseph lister; antiseptic during surgery

83
Q

use dilution test

A

In
this test, a researcher dips several metal cylinders into broth
cultures of bacteria and briefly dries them at 37°C. The
researcher then immerses each contaminated cylinder into a
different dilution of the disinfectants being evaluated. After
10 minutes, each cylinder is removed, rinsed with water to remove
excess chemical, and placed into a fresh tube of sterile
medium for 48 hours of incubation. The most effective agent is
the one that entirely prevents microbial growth at the highest
dilution

84
Q

use dilution test trivia

A
  • curent standard in US
  • Some government agencies
    have expressed concern that the test is neither accurate, reliable,
    nor relevant so a new one being developed
85
Q

kelsey sykes capacity test

A
  • standard in EU
  • researchers
    add a suspension of a bacterium to a suitable concentration of the chemical being tested.
    Then at predetermined times, they move samples of the mixture
    into growth medium containing a disinfectant deactivator. After
    incubation for 48 hours, turbidity in the medium indicates that
    bacteria survived treatment. Lack of turbidity, indicating lack of
    bacterial reproduction, reveals the minimum time required for
    the disinfectant to be effective.
86
Q

Though phenol coefficient, use-dilution, and Kelsey-Sykes capacity
tests can be beneficial for initial screening of disinfectants,

A

they can also be misleading. These types of evaluation are
measures of effectiveness under controlled conditions against
one or, at most, a few species of microbes, but disinfectants are
generally used in various environments against a diverse population
of organisms that are often associated with one another in
complex biofilms affording mutual protection

87
Q

in-use test

A
  • more realistic, more time consuming
  • swabs are taken from actual objects,
    such as operating room equipment, both before and after the application of a disinfectant or an antiseptic. The swabs are then
    inoculated into appropriate growth media that, after incubation,
    are examined for microbial growth.