5. Control of Microbial Growth Flashcards

1
Q

disinfection

A

destruction or removal of vegetative pathogens but NOT bacterial endospores. usually used only on inanimate objects

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2
Q

sterilization

A

complete removal or destruction of all viable microorganisms. used on inanimate objects

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3
Q

antisepsis

A

chemicals applied to body surface to destroy or inhibit vegetative pathogens

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4
Q

chemotherapy

A

chemicals used internally to kill or inhibit growth of microorganisms within host tissues
-antibacterials
-antibiotics
-antivirals
-antifungals

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5
Q

impact of biocide exposure

A

most to least:
antisepsis
sanitization
disinfection
sterilization (moist heat, best/quickest way)

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6
Q

“cidal” agents

A

kill

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7
Q

static agents

A

inhibit growth

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8
Q

pattern of microbial death

A

microorganisms are not killed instantly
population death usually occurs exponentially
measure of agent’s killing efficiency
-decimal reduction time: time to kill 90%
must be sure viable but nonculturable cells are dead
-once they recover, they may regain the ability to reproduce and cause infection

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9
Q

D and Z values

A

D values are the time or dose required for a 90% reduction in microbial concentration via a sterilization process.
Z values measure the resistance of the microorganism to death by the sterilization source.

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10
Q

Filtration

A

reduces microbial population or sterilizes solution of heat-sensitive materials by removing microorganisms
-also used to reduce microbial populations in air

ex: sterile glucose or sterile penicillin

membrane filters, filtering air

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11
Q

moist heat

A

destroys viruses, fungi, and bacteria
boiling will not destroy endospores and does not sterilize
degrades nucleic acids, denatures proteins, and disrupts membranes

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12
Q

dry heat is

A

less effective than moist heat sterilization, requiring higher temperatures and longer exposure times

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13
Q

pasteurization

A

controlled heating at temperatures well below boiling
used for milk, beer, and other beverages
process does not sterilize but does kill pathogens present and slow spoilage by reducing the total load of organisms present
*increase shelf life

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14
Q

ultraviolet radiation

A

wavelength of 260 is most bactericidal (DNA absorbs)
-causes thymine dimers preventing replication and transcription

UV limited to surface sterilization because it does not penetrate glass, dirt films, water, and other substances
-has been used for water treatment

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15
Q

ionizing radiation

A

gamma radiation penetrates deep into objects (sterilizing foods)
destroys bacterial endospores; not always effective against viruses
used for sterilization and pasteurization of antibiotics, hormones, sutures, plastic disposable supplies, and food

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16
Q

chemotherapeutic agents

A

chemical agents used to treat disease
destroy pathogenic microbes or inhibit their growth within host

17
Q

penicillin

A

gram positive activity; beta lactamase and acid sensitive
inhibits cell wall synthesis (“beta-lactam” antibiotics)

penicillin is a beta lactam
beta lactamase breaks down ring and stops action of beta lactam

18
Q

protein synthesis as a drug target

A

most of the antibiotics targeting protein synthesis will target translation by binding to the bacterial ribosome
-aminoglycosides
-tetracyclines
-marcolide antibiotics

19
Q

nucleic acid synthesis as a drug target

A

quinolones are antibacterial compounds that interfere with DNA gyrase
e.g. cirpofloxacin

20
Q

growth factor analogs

A

other antibacterial drug targets
structurally similar to growth factors but do not function in the cell
-analogs similar to vitamins, amino acids, and other compounds

21
Q

isoniazid

A

a growth analog effective only against mycobacterium
-interferes with synthesis of mycolic acid (only found in mycobacteria- acid fast)

22
Q

platensimycin

A

new structural class of antibiotic
broad-spectrum; effective against MRSA and vancomycin-resistant enterococci

23
Q

antibiotic targets that target the cell membrane and wall

A

polymyxins disrupt the membrane and cause leakage and death

24
Q

antibiotic targets that target peptidoglycan synthesis

A

beta-lactams
vancomycin
bacitracin

25
Q

b-lactams

A

penicillin, cephalosporin, derivatives
interfere with transpeptidation
(formation of cross-links)

26
Q

vancomycin

A

binds to pentapeptide precursor and prevents interbridge formation

27
Q

bacitracin

A

binds to bactoprenol and prevents new peptidoglycan precursors from reaching site of synthesis

28
Q

types of drug resistance

A

intrinsic
acquired
Persisters

29
Q

intrinsic

A

born with it in them
mycoplasma resistance to beta-lactam antibiotics and other cell wall inhibitors simply because these bacteria lack a cell wall
(no cell wall- walking pneumonia- should never be prescribed penicillin- useless since no cell wall)

30
Q

acquired

A

occurs when there is a change in the genome of a bacterium that converts it from one that is sensitive to an antibiotic to one that is resistance

31
Q

Persisters

A

drug-tolerant bacteria lack the mechanisms for antibiotic resistance and “ignore” the presence of antibiotics, usually because they are embedded in biofilms that antibiotics cannot effectively penetrate or are growing too slowly to be inhibited

32
Q

mechanisms of drug resistance

A

-modify the target of the antibiotic
-drug inactivation
-minimize the concentration of antibiotic in the cell
-bypass the biochemical reaction inhibited by the agent or increase the production of the target metabolite

33
Q

antiviral drugs

A

-drug development has been slow because it is difficult to specifically target viral replication
-antiviral drugs have had mixed success and the vast majority of viral infections cannot be cured
-some antiviral drugs simply limit the duration of the illness or its severity (flu and HIV)
-drugs currently used inhibit virus-specific enzymes and life cycle processes

34
Q

antiviral drugs for influenza

A

tamiful
-anti-influenza agent
-a neuraminidase inhibitor
-though not a cure for influenza, has been shown to shorten course of illness

35
Q

antifungal drugs

A

fewer effective agents because of similarity of eukaryotic fungal cells and human cells
-superficial and more common
-many have low therapeutic index and are toxic

easier to treat superficial mycoses than systemic infections
-combinations of drugs may be used