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113 Cards in this Set

  • Front
  • Back
Prophylaxis
use of a drug to prevent imminent infection of a person at risk
Semisynthetic Drugs
drugs that are chemically modified in the lab after being isolated from natural sources
Synthetic Drugs
drugs produced entirely by chemical reactions
Spectrum
Narrow & Broad- antimicrobials effective against an array of microbial types
Primary sites of action of antimicrobial drugs on bacterial cells
cell wall
cell membrane
DNA/RNA
Ribosomes
Folic Acid
Inhibitors of protein synthesis
work at level of ribosome, 70S ribosomes not 80S
Cell wall inhibitors
block synthesis and repair
ex: penicillin, bacitracin
Folic acid synthesis
inhibits metabolism
Anitmicrobial resistance
requires a change in the DNA
-mutation, horizontal transfer between species, transformation, transduction, conjugation
Acquired Drug Resistance Mechanisms
drug inactivation
decrease permeability
drug pump
change in binding site
use of alternative metabolic pathway
drug inactivation
microbe makes an enzyme that cleaves a portion of molecule and changes it (becomes inactive)
decrease permeability
receptor that transports the drug is altered, so the drug cannot enter the cell
drug pump
specialized membrane proteins are activated and continually pump the drug out of the cell
change in binding site
binding sie on target (ribosome) is altered so drug has no effect
use of alternative metabolic pathway
drug blocked pathway, so microbe uses unblocked pathway
Nosocomial infections
infections you get in a hospital/ other healthcare facilities
drugs in animal feed
decrease infection and increase growth rate
Strategies to limit drug resistance
-physicians must make correct diagnosis and prescribe the right drug
-patients must follow recommendations for taking the drug
-take 2 or more drugs
Drug Research
-develop shorter term, higher dose microbial's that are less expensive, more effective, and fewer side effects
-develop new antimicrobials
Antibiotics
do not get rid of infection, but buys time
5 Long Term Strategies
1. Proposal to help educate workers to encourage patients to take all antibiotics
-proposal that all doctors must justify each antibiotic prescription
2. valuable antimicrobials may be limited in use to only 1 or 2 types of infections
3. banning the use of antibiotics in animal feed
4. make effective therapy to low income populations
5. recommending vaccines as an alternative
Probiotics
contain living cultures and will supplement normal flora and help protect from digestive upsets and sometimes work
Prebiotics
nutrients to encourage growth of microbes
ex: Cranberry Juice
3 Interactions between drug & host
Selective Toxicity
Allergic Reaction
Alternation of Microbiota
Selective toxicity
want a microbe that will kill disease with no side effect, may be toxic to kidneys, organ, liver, etc
Allergic Reaction
Unpredictable, have to be exposed twice
ex: skin rash
Alternation of Microbiota
microbes that normally live on/in you to protect them from infection, if wiped out other things can grow
ex: Yeast infection
Selecting antimicrobial drug
-what is the microbe causing infection
-degree of microorganisms sensitivity to various drugs
-overall medical condition of patient
Kirby-Bauer Disc diffusion test
senses sensativity
Kirby-Bauer Disc Steps
-take pure culture and spread on dish
-take disc covered in antibiotic
-antibiotic diffuses out of disc and onto pure culture
-clear path by disc of antibiotic worked
-bigger the zone, better it worked (measure with ruler and view chart)
Minimum Inhibitory Concentration
-same amount of bacteria in each test tube, add drug
-when turns purple, that is the min amount of dosage needed
Actions of antiviral drugs
-inhibit attachment/entry
-inhibition of nucleic acid synthesis
-inhibition of viral assembly or release
2 Pathogenic microbes
opportunistic
frank/true
opportunistic
will not make you sick, but if you give opportunity they will cause and infection
frank/true
not part of normal flora, comes from outside and sets up infection
ex: flu, herpes
normal flora
large and mixed collection of microbes adapted to the body
include array of bacteria, fungi, protozoa, and certain extent of virus's and arthropods
how do babies pick up normal flora?
right out of birth, from food, and other people touching them
host defenses
healthy, nourished, vaccinated
microbial virulence factors
ability to establish in host and cause damage
Virulence
determined by its ability to establish itself in the host and cause damage
Human host and microorganism outcomes
-microbe passes through unnoticed
-microbe becomes established without disease
-microbe causes disease
Factors that weaken host defenses
old age, genetic defects, surgery/operations, underlying disease, chemotherapy, physical, and mental stress
terminology
itis: inflammation
emia:in the blood
osis: disease cause
oma: swelling
infected host
exit, mode of transmission, entry to susceptible host
susceptible host
able to catch disease
-overcome host defenses
-cause damage to host
-become infected host
fomites
anything that is not alive
ex: fork, pen
reservoir
detour for the microbe
biological reservoir
alternate host, ex: deer for lymes
carriers: have infection but no signs/symptoms
zoonotic: diseases of animals
nonbiological reservoir
soil, water
Symptoms
non quantifiable
ex: nauseous,
Signs
Quantifiable
ex: blood pressure, temperature
Classic stages of clinical infections
incubation period, prodromal stage, period of invasion, convalescent period
Incubation period
initial exposure to microbe, infected but no signs or symptoms
prodromal stage
mild symptoms
active/period of invasion
microbe has invaded, is growing, body trying to fight it off
(heigh of infection)
convalescent phase
antibiotics, now white cells protect
antiphagocitic factors
phagocytes=wbc
capsules make it hard for white cell to kill bacteria
leukocidins
kills white blood cells
exoenzymes
made by cell and released
ex: chimases- dissolve clots, allows microbes to spread, no clots
endotoxins
LPS at gram- bacteria symptoms are non-specefic
exotoxins
made and released from bacterial cells, mostly proteins. diseases/symptoms are specefic
localized infection
microbe enters body and remains confined to a specific tissue
systematic
when an infection spreads to several sites and tissue fluids, usually in the blood stream
focal infection
localized infection that spreads
mixed infection
multiple infections at the same time
nosocomial infections
acquired in a health care setting
Aseptic techniques
medicare/medicaid won't pay for catheter uti, surgical sight infection...the hospital pays for it
5-10 billion a year
Infection control committee
tracks infections
training in aseptic techniques
implement practices/products
Standard precautions for nosocomial infections
-hand hygiene
-use of personal protective equipment
-respiratory hygiene and cough etiquette
-safe infection practices
-safe handling of potentially contaminated equipment or surfaces
Koch's Postulates
-find evidence of a particular microbe in every case of disease
-isolate the microbe in pure culture
-cause the disease in a susceptible host
-re-isolate the same organism
Lab Safety Levels
1- regular techniques
2- lab coats, gloves, signs
3- dangerous microbes, specialized clothing, no unsterilized materials can leave lab
4- most dangerous organisms, clothing change and showers required for people entering/leaving
Epidemiology
study of disease in populations
endemic
with in the population
ex: valley fever
epidemic
out breaks of disease in populations
sporadic
isolated, few cases
pandemic
pan=total/all, could affect the entire world
CDC
center for disease control and prevention
WHO
world health organization
prevalence
total number of cases in a population divided by total number of people in population x 100.
incidence
measures number of new cases divided by the number of susceptible persons
-per 100,000
point source epidemic
single source of infection
ex: food poisoning
common source
single source, but over time
ex: contaminated well
propagated epidemic
not one source, but disease passes from person to person
First line defenses
always there whether there is a threat or not
ex: tears, urine
second line defense
cellular defenses
ex: phagocytes eat bacteria
Acquired defenses
get it naturally or artificially after exposure to microbe
naturally acquired
active- get disease, don't die, won't get it again
passive- protection you get from another individual ex:antibodies made by mom
Artificially acquired
active- vaccination
passive- bitte by snake
RBC, WBC, Platelets
RBC- no nucleus (erythrocytes)
WBC- leucocytes
Platelets- fragments
development of blood cells and platelets- 1
start with hematopoietic cell, splits into lymphs or anything but lymphs
development- 2
lymphoid stem cell splits into lymphoblasts, lymphocytes are T or B cells, which are agranuloctyes
development -3
stem cell for all blood cells except lymphocytes
-red blood cells
megakaryocytes -->platelets
Granuloctyes: neutrophils, basophils, eosinophils
wrights stain
differential that allows us to determine which cell is which
WBC's and Dyes
neutrophils- don't favor one dye, 55%
eosinophils- red dye, 2-3%
basophils- all granulocytes, named by how they stain, purple <.5%
Agranulocytes
Monocytes 5%
lymphocytes (t-cells and b-cells)- 20%
macophage
phagocytes, better than monoctyes. found free in blood, fixed in tissues
mast cell
specialized tissue cells similar to basophils that trigger local inflammatory reactions and are responsible for many allergic symptoms
natural killer cells
related to T cells, except are non specific, wonder body and kill cancer and infected cells
2nd line defenses
inflammation, phagocytosis, fever, antimicrobial peptides
inflammation
complex series of steps, goes as far as needed.
cardinal signs
reactions you an see and feel
rubor- redness
calor- heat
tumor- swelling
dolor- pain
Stages of injury
vascular changes
cellular responses
late steps
vascular changes
vasodilation, increase blood flow to are edima, fluid leaks out blood vessels, contains protein
cellular responses
involves accumulation of WBC
neutrophils- 24hrs, attracted to the area by bacteria and damaged cells
monocytes- 48hrs attracted by chemicals of dead neutrophils
Late steps
a. resolution- healing
b. scarring- connective tissue repair, usually b/c so much injury, no healing.
c. phagocytes- activates immune system responses
chemotaxis
movement of white blood cells toward an area of injury/infection
Phases of phagocytosis
chemotaxis
attachment/adhesion
engulfment
phagosome
lysosome
killing and destruction of bacterial cells
release of residual debris
attachment/ adhesion
bacteira adhering to phagocyte PRR's by their PAMPs.
PAMP
pathogen associated molecular patterns
PRR
pattern recognition receptors
Fever
systemic, increase in temp throughout the body
-can kill you b/c it denatures proteins
-inhibits bacterial reproduction
chemical defenses
antimicrobial peptides, complement found in blood as a series of inactive proteins --> cascade, forms pores in cell membranes
interferon
made by cells infected with viruses
controls spread of a viral infection
activates natural killer cells