• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/204

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

204 Cards in this Set

  • Front
  • Back
sterilization
destruction or removal of all forms of microbial life with an exception of PRIONS
sterilant
a sterilizing agent -heat is the most common
commercial sterilization
sufficient heat treatment to kill CLOSTRUDIUM BOTULINUM in canned foods
disinfection(disinfectant)
destruction of vegetatiove pathogens (harmful microbes)
antisepsis(antispeptic)
destrustion of vegetative pathogens on living tissue
degerming
REMOVAL of microbes from a limited area
sanitization
treatment intented to lower microbial counts on eat8ing and drinking utensils to safe public levels
"cide"
suffix on treatment names that KILL microbes
"stat" or "stasis"
suffix on treatments that inhinit the growth of mutiplication of microbes
aseptic
the absence of significant contamination
for each min of antimicrobial tretment what percent of the popluation is killed?
90%
factors that effect anitmicrobial tretment
1. number of microbes
2. enviornmental influences
3. time of exposure
4. microbial characteristics
how antimicrobial agents inhibit microbs thro membrane
damages the lipids and protiens causing leakage of cellular content which interfers growth
heat radiation and chemicals do what to microbes
1. break hygrogen bonds
2. attack covalent bonds
3. breaak disulfide bridges
4. damage nucleic acid (rna dna) which makes cell no longer to replicate/carry out metabolic functions
what does heat do to microbes?
denatures their enzymes chaning their 3d shape making them inacctive and killling them
thermal death point
lowest temp all microbes in a liquid will be killed within 10 min
thermal death time
the minimal length of time for all bacteria in a liquid to be killed at a given temp.
decimal reduction time
the time in min. that kills 90% of bacteria at a given temp.
type of moist heat sterilization
boiling - kills MOST not all
autoclave
above boiling point steam underpressure
steam at what pressure will kill alll organisims in 15min
15psi
pasteurization
mild heating to kill a sufficent amount of microbsto keep from spoil but preserve flavor
phosphatase test
test that determines if dairy has been pasteurized
high temperature short time pasteurization
72 degrees for 15min
ultra high temperatures
sterilizing milk treatment -allows storage without refrigeration for several months
equivalent treatments
as temp increases less time is needed to kill the same number of microbes
how does dry heat kill?
but oxidation effects
flaming
a type of dry heating
incineration
dry heating way to dispose of contaminated paper cups, bags . and dressings
hot air sterilization
dry heating in an oven
-
what heats faster...moist heat or dry heat?
moist
filtration
a passage of lighid or gas thro a screen like material with pore that retain microbes
what is fitration used for
heat sensitive materials
high efficiency particulate air filters
remove all microbes larger than .3 mircometers in diameter
fiterable viruses
pathogens that could pass thro filtrates
membrane filters
.1micrometers thick more retainable filter system
low temperaures
slow the metabolic rate of microbes and kill some
-slow freezing more effective
high pressures
atler molecular structures and kill buy inactivating vegetative microbs
desiccation
the absence of water which enables the growth of microbes.
osmotic pressure
high concentrations of salts ans sugar cause hypertonic enviornments that cause desiccation
what is more laikley to for in low moist, high osmotic pressure areas, bateria mold, or yeast ?
moldds and yeasts
ionization radiation
gamma rays, x-rays, high energy elecron beam, create mutations in microbe cells
nonionizing radiation
uv light damages dna by causing bonds btw adjcent thymines inhibit replication
mocrowaves
not very good at killin microbes
use dilution test
test the effectivness of disinfectants
disk diffusion method
used in teaching labs to evaluate the efficentcy of a chemical agent
2 types of disinfectants
1. phenol-throat lozenges
2. phenolics-disinfect pus saliva and feces
cresols
type of phnolic that is a good surface disinfectant
bisphenols
derivative of pheol with two phonolic groups

-hexachlorophene
-triclosan
biguanides
most effective against gram postive
-chlorhexidrine
-alexidine
halogens
iodine, chlorine effective antimicrobial agents
tincture
solution in aqueous alcohol
idophor
iodine and orgainic molecule mixture
alcohols
kill fungi and bacteria by protien denaturation
oligodynamic action
the ability for metals to exter antimicrobial activity
-silver, copper, zinc
sufactants
decease surface tension among molecules
emlusification
when oily filimants are fomed throu scrub of soap
acic anionic sanitizers
surface active
-quats
chemical food preservatives
sulfur dioxide
nitroaminies
nitrite reacting with amino acids
antibiotics
nasin and natamycin used in foot preservation to
aldyhydes
most effective antimicrobial
chemical sterilization
not a pratical sterilent
plasma
state of matter when the gas is excited
supercritical fluids
chemical and physical methods
peroxygens
oxidizing agents that include hydrogen peroxcide and peracetic acid
pathology
the study of disease
concerns of pathologists
1. etiology(cause)
2. pathogenisis(growth)
3. structural and functional changes
infection
invation and colonization
disease
change in normal state of health
normal microbiota/ normal flora
microbes that made perminate residence in the body
transient microbiota
microbes that only stay in the body for a short period of time
microbial antagonism/ competetive exclusion
competition among microbes for nutrients, portect against invasion of harmful pathogens
SYMBIOSIS
one ogranism is dependent on the other
commensalism
one benifits the other is unaffected
mutualism
both benifit
probiotics
live microbial cultures applied or ingestes for benificial effects
prebiotics
promoted bacterial growth
parasitism
one beifits the other is harmed
opportunistic pathogens
normally harmless in normal conditions but in change in environmewnt can be harful
does cooperation and competition between microbes cause disease?
yes
koch postulate requirements
1. pathogen present in every case of the disease
2. pathogen isolated from disease host and gown in pure culture
3. pathogen from pure culture inoculated into healthy lab animal cause disease
4. pathogen isolated from inoculated animal and grown on pure culture must be the orignal pathogen from 1st
what is the nitch in koch postulate
not all pathogens can be grown on pure cultures
syptoms
change in body function
1. subjective -cants see
2. objective -physician obverved
signs
lesions, swelling, fever, paralysis
syndrome
syntoms or signs always associated to a specific disease
communicatable disease
transfered directly or indirectly from host to host
contagious disease
EASILY spread from one person to the next
noncommunicable disease
not spread from on person to the next
syptoms
change in body function
1. subjective -cants see
2. objective -physician obverved
incidence
number of people in a population with a disease
signs
lesions, swelling, fever, paralysis
prevalence
number of people who develope a disease at a specific time (old and new cases)
soporatic disease
occuring occationally
syndrome
syntoms or signs always associated to a specific disease
endemic disease
constantly present
communicatable disease
transfered directly or indirectly from host to host
contagious disease
EASILY spread from one person to the next
noncommunicable disease
not spread from on person to the next
incidence
number of people in a population with a disease
prevalence
number of people who develope a disease at a specific time (old and new cases)
soporatic disease
occuring occationally
endemic disease
constantly present
predesposing factor
makes the body more suseptible to a disease

ex: gender, age, fatigue, nutrition
development process of disease
incubation period(inital-1st symptom)
prodromal period(ealy mild symptoms)
period of illness(most severe)
period of decline (symptoms subside)
period of convalescence(recovery)
something that provides a parthogen with adequate conditions for survival
resiovir of infection
human
animal
nonliving
carriers
people who have and spread disease but dont show symptoms
zoonoses
disease in aminals transmitted to humans
nonliving resevrvior
soil, water, badly prepared foods
transmission occurs through
contact -person to person
vehical -by medium, water air food
vectors-aminal transmition
nonliving resevrvior
soil, water, badly prepared foods
formite
the nonliving host intermidiate btw contact transmition
transmission occurs through
contact -person to person
vehical -by medium, water air food
vectors-aminal transmition
types of vectors
mechanical-passive
biological -active
formite
the nonliving host intermidiate btw contact transmition
types of vectors
mechanical-passive
biological -active
nonsocomial infection
recieved from a hospital
compromised host
resistance to infection is compromised by a disease
emerging infectious disease
new or changing, increase in incidences
epidemiology
the study of when where occur and how disease is transmitted
descriptive epidemiology
all data that describes the occurance of the disease
analytical epidemiology
anaylze to determine the probable cause
experimental epidemiology
hypothesis then experiments to test it
case study
evidence of a chain of transmission
incidence
number of peopl ein a population who develope a disease
prevalence
number of poeple who develope a diseae in a certain time period
soporatic disease
occurs occasionally
endemic disease
constantly present
epidemic disease
many people infected in a short period of time
most pathogens enter though
mucus membranes of the gastrointestinal tract and respritory tracts
skin
where microbes can enter but it is very difficult
parental route
deposited directly under skin/into muscus membranes
preferred portal entry
routes microbes prefer and in some case wont cause disease unless eneter this way
adherance
microbes attcking themselve to host
biofilms
microbes that can attach to living and nonliving surfaces
adhesin/ligands
binder that bind to surface receptors
m protein
found in fimbrae and surface of cell
increase the virulence of microorganisms
how does bacteria attack to the host
fmbrae and op
waxy lipid
increases virulence but resisting digestion by phgocytes
coagulases
bacteria that clot fimbrinogen in the blood
fimbrinogen
is plama protien produced by the liver
kinases
enzyme that breaks down fibrin digests clots
collagenase
breaks down collagen protein
Iga proteases
destroies Iga antibodies
antigenic variation
when pathogens alter surface antigens making the pathogen immune to antibodies
actin
cytoskeleton protein that is used by microbes to penetrate a hosts cell
invasions
surface proteins produces by microbes that rearrange actin
4 ways microbes damage host cell
1. using its nutrients
2. damage in the vicinity of invasion
3. producing toxins
4. inducing hypersensitivity reactions
siderdphores
protiens secreted by microbes that go out a take iorn away frm iron transporters
direct damage is done through
rupture, toxins, passing thorugh, penatration
toxin
posionous substances released by miicrobes
toxigenicity
capacity of microbes to produce toxins
toxemia
toxins in the blood
2 types of toxins
1. exotoxins -inside
2. endotoxins -outide
antioxidants
antibodies that provide immunity to exotoxins
exotoxins
inhibit certain metabolic functions

release into body thro lysis

very deadly
toxoids
exotoxins inactivated that only now produce antitoxins
endoxins
relseased into the body when cell wall breaks

part of the outter membrane
lysogenic conversion
bacterial cell becomes immune to infection by the same type of phage
cytopathic effects
visible effects of viral infection of an animal virus
Selective toxicity
A drug that kills harmful microbes without damaging the host.
Chemotherapy
the use of drugs to treat a disease
antibiotic
a substance produced by a microbe that, in small amounts, inhibits another microbe
Superinfection
when a broad spectrum antibiotic kills the normal flora and allows other normal microbiota to over grow
Bactericida
kills microbes directly
Bacteriostatic
prevents microbes from growing, the hosts immune usually destroys the microbe
Macrolides
Inhibits cell wall synthesis: targets peptidoglycan formation, therefore selectively toxic
gram positive
Natural penicillins
Primarily useful against gram positives therefore narrow spectrum of activity
Semisynthetic penicillins
Broader range of activity; many are effective against gram positives and gram negatives
Methicillin
1st semisynthetic penicillin cause mrsa
vancomycin
last line of defense against mrsa
inhibits cell wall synthesis
inhibitors of cell wall synthesis
bacitracin
vancomycin
Isoniazid (INH)
Ethambutol
inhibitor of nucleic acid synthesis
Rifamycin
Quinolones
fluoroquinolones
injuries the plasma membrane
Polymyxin B
antibiotic resistance
Enzymatic destruction of drug.
Prevention of penetration of drug.
Alteration of drug's target site.
Rapid ejection of the drug
cause of antibiotic resistance
Failure to complete the prescribed regimen
Using outdated or weakened antibiotics.
Using antibiotics for the common cold and other inappropriate conditions.
Use of antibiotics in animal feed.
using someone elses perscription
Pathogenicity
the ability to cause disease
Pathogen
microbes that cause disease
Virulence
the extent to pathogenicity
portals of entry for pathogens
Mucous membranes
Skin
Parenteral route
Oral
Respiratory tract
Gastrointestinal tract
Urinary tract
Preferred portal of entry
the perfered route a pathogen likes to take and sometime the only router it can take to create disease
id 50
infection dose for 50% of the population
LD50
lethal dose for 50% of the population
pathogens bind to host receptors by
adhesion and ligands
the bound pathogens form
biofilms
pathogens penetrate hosts defense in capsule by
preventing phagocytosis in capsule
pathogens penetrate hosts defense in enzymes by
Coagulase: Coagulates fibrinogen
Kinases: Digest fibrin clots
Hyaluronidase: Hydrolyzes hyaluronic acid
Collagenase: Hydrolyzes collagen
IgA proteases: Destroy IgA antibodies
pathogens penetrate hosts defense in the cell wall by
M protein resists phagocytosis
Opa protein inhibits T helper cells
Mycolic acid (waxy lipid) resists digestion
invasion
Penetration into the Host Cell Cytoskeleton
what does a pathogen use to move from cell to cell
actin
pathogens cause disease by
Disrupt host cell function
Produce waste products
Toxins
toxin
Substance that contributes to pathogenicity
Toxigenicity
the ability to prodice a toxin
Toxemia
presence of toxins in the host blood
Toxoid
inactivated toxins used in vaccines
Antitoxin
antibodies against a specific toxin
exotoxin
inside the cell
endotoxin
around the outside of cell the cell wall ish
pathogens lyse host cell by
creating channels in the plasma membrane and Disrupting phospholipid bilayer
Leukocidins
kill white blodd cells
Hemolysins
lyse red blood cells
Streptolysin
toxins made byy streptococcus
superantigens
Cause an intense immune response due to release of cytokines from host cells
Symptoms: fever, nausea, vomiting, diarrhea, shock, and death
portals of exit
Respiratory tract
Coughing and sneezing
Gastrointestinal tract
Feces and saliva
Genitourinary tract
Urine and vaginal secretions
Skin
Blood
Biting arthropods and needles or syringes