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what aspects of the skin make it an effective defensive barrier?
tightly packed, dead epithelial cells
dry → microbes need moisture to grow
constantly sloughing off our outer later of dead skins cells (mechanical removal) → microbes can’t attach to our skin
large amounts of keratin: tough, durable protein → most microbes can’t digest keratin
where are mucous membranes found?
epithelium lining the gastrointestinal, respiratory, and genitourinary tracts
what do mucous membranes secrete?
mucus
what is mucus beneficial for?
glycoprotein that keeps the membrane moist
keeps live cells from drying out
allows for nutrients to be brought in and waste to be sent out
where do most infections occur?
most infections occur through mucous membranes
thin layer of dead cells
more vulnerable to attack
what are other defenses of mucous membranes?
epiglottis
nose hair
what does the epiglottis do?
prevents food from entering the respiratory tract
what do nose hairs do?
filters incoming air, removes microbes
get stuck in the mucus in your nose hairs so they don’t get in your lungs
what do tears do to physically prevent infection?
constantly wash the surface of the eye
water
mucus
lipids
where do tears go?
drain into the nose/throat
what does irritation in your eye cause?
increases tear production (mostly water)
what does saliva do to physically prevent infection?
keeps the mouth moist and washes bacteria off surfaces
what does peristalsis do to physically prevent infection?
keeps substances moving along
what does defecation do to physically prevent infection?
removes materials from the intestines
infecting bacteria must find a spot to attach or they will simply pass through us
what does skin sloughing do to physically prevent infection?
microbes can’t attach to our skin
what does urination do to physically prevent infection?
washes unattached bacteria away
what do vaginal secretions do to physically prevent infection?
move unwanted microbes out
how does the respiratory tract prevent infection?
mucus produced in the lungs trap most bacteria
what removes the bacteria in your lungs?
removed by ciliated epithelium
where does the trapped bacteria go?
ciliary escalator moves trapped bacteria up and out
mucus gets moved up and grabbed by the next set of cilia until you clear your throat
goes down to your stomach
sneezing/coughing will also remove mucus
what is a lysozyme?
antibacterial enzyme found in sweat, saliva, and tears
how does lysozymes attack bacteria?
digests peptidoglycan cell walls
are skin oils protective?
short fatty acids that are toxic to most microbes
insert themselves into bacterial membranes and reduce their capacity for growth
how is the stomach effective to killing bacteria?
gastric acid in the stomach: very acidic
kills most bacteria
why are acid blockers a potentials problem for infections?
stops acid production
get food-borne infections more
what are defensins?
small antibacterial proteins
found in sebum, saliva, tears, and mucus in the lungs
how do resident intestinal bacteria protect against infection?
block attachment
inhospitable environment
how do resident intestinal bacteria block attachment?
take up available attachment sites
how do resident intestinal bacteria make it an inhospitable environment?
use up available nutrients/resources
produce antibacterial chemicals
change the environment
give an example of resident intestinal bacteria producing antibacterial chemicals
E. coli produces anti-Salmonella compounds
give an example of resident intestinal bacteria changing the environment
lactic acid bacteria in the vagina produce acid byproduct from their metabolism
make it a slightly acidic environment → yeast does not like this
do anatomical barriers require any prior exposure to a pathogen to protect against it?
no!
jules bordet discovered 2 factors (in plasma) that killed bacteria, what were they?
heat-stable (heat-resistant) factor
heat-labile (heat-sensitive) factor
what was the heat-stable (heat-resistant) factor?
killed specific bacteria
turned out to be antibodies
what was the heat-labile (heat-sensitive) factor?
killed non-specific bacteria
complement
what is the complement?
defensive proteins found in the blood, act in a cascade to respond to pathogens
system of over 30 proteins
can complement recognize some pathogens without have been exposed previously?
yes!
what are the key facts about complement?
present at birth, genetically determined
recognizes certain molecules as “non-self”
capable of attacking cells marked by these molecules
what signals set off complement?
antibodies
foreign substances
how do antibodies set off complement?
complement reacts to presence of multiple antibodies bound to a surface (adaptive immunity)
how do foreign substance set off complement?
has proteins that recognize certain characteristic bacterial proteins/carbohydrates
the targeting of complement to foreign surfaces is in place at birth and never changes
define PAMP
pathogen-associated molecular patterns
non-host molecules that are commonly associated with pathogens
examples of PAMPs
lipopolysaccharides, peptidoglycan, etc.
when do PAMP receptors develop?
receptors for recognition of PAMPs are present at birth as a key part of the innate immune system
what are the 3 responses when the complement system recognizes an intruder?
opsonization
cytolysis
inflammation
what opsonization?
coating of an object with immune system proteins
what does opsonization promote?
phagocytosis → makes it easier for phagocytic defenses to see the marked cells
if they spot something coated in complement → they’re going to kill it
what is cytolysis?
punches holes in the plasma membrane
lyses cells
how does complement cause inflammation?
signals for inflammatory response
also attract phagocytic cells
what happens when a complement recognizes that it’s bound to a target that shouldn’t be there?
complement system has protein members that are cytokines (cell signals) that send out an inflammatory signal
region becomes inflamed
immune system focuses its attention on that region
does complement act only on its own, or can it also act to enhance adaptive immunity?
enhances adaptive immunity by recognizing antibody-bound objects