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prokaryotic cell vs eukaryotic cell
prokaryotic has no nucleus or organelles making it smaller, eukaryotic cells have a nucleus and organelles making them much larger and complex.
different types of bacteria
obligate aerobes
obligate anaerobes
facultative anaerobes (can live in anaerobic and aerobic)
live in extreme conditions
may form endospores (can survive anything)
bacteria morphology
unicellular but often live in “groups”
good vs bad bacteria
small fraction cause infection or illness, most are harmless. Some are opportunistic pathogens (normally not but can become pathogenic).
normal flora
the bacteria, fungi, and viruses that live in/on our bodies all the time
bacterial cells of normal flora
body contains same amount of human cells as it does bacterial cells but are not found in urine, blood, lymph, or CSF.
locations of bacteria in our body
skin, digestive tract, and respiratory tract act as mini ecosystems to bacteria, providing us with specific benefits.
controlling bacterial infections
antiseptics and disinfectant can kill bacteria or inhibit their growth.
Antibiotics and antimicrobial drugs prevent growth but are not toxic to host with minimal side effects (can lead to antibiotic resistance)
antibiotic resistance
one “generation” for bacteria is a short period of time, many generations = more opportunities for random mutations that could make the bacteria resistant to the antibiotics.
viruses structure
acellular (no cell membrane)
cant reproduce on their own
cant make/use their own energy (invades host cells cellular machinery to copy genetic info and make more particles)
genetic info contained in a “protein coat”
lytic cycle
virus invades host cell, makes new copies of the virus, then causes lysis of the host cell to release the virus.
lysogenic cycle
virus invades host cell, viral DNA gets incorporated into host genome and stays there until a condition changes (can be long time). Can later re-enter the lytic cycle.
control of viral infection
hand washing
avoiding germs
masks
vaccination
antiviral medications disrupt but can be harmful to host
fungi structure
eukaryotic cells but have unique cell wall
not always microscopic (mushrooms vs yeast)
part of our normal flora but can be opportunistic pathogens
common ones: thrush, athletes foot, ring worm
control of fungal infections
anti fungal medication (sometimes toxic to human cells)
fungal pathogens develop resistance
protozoa structure
eukaryotic
unicellular
most aren’t pathogenic but some are important pathogens with serious effects on human health
complex lifestyles involving more than one host
associated with contaminated drinking water
typically have locomotion
control of protozoan infection
avoid contact
ensure access to clean drinking water
vaccines
metazoan parasites structure
eukaryotic
multicellular (bigger, complex)
adult form can be large and visible but are often identified by eggs or larval from (microscopic)
can include pinworm, tapeworm, filariasis
control of metazoan infections
avoid contact (uncooked meat, skin, fecal-oral route)
some medications are available
antibiotics to kill bacteria in the gut of the parasite
ways microorganisms can cause disease
consuming nutrients/resources in your body
triggering vomiting/diarrhea
causing structural damage
provoking an immune response
disrupting your normal flora
nosocomial infections
acquired in a clinical setting due to poor hand hygiene, antibiotic resistant strains of bacteria, resistant endospores, patients are more susceptible.
barrier defences
skin forms a tight barrier, mucous traps pathogens, clotting response prevents pathogens from entering.
adaptive responses
lymphocytes are capable of response and cells of the immune system use secreted signals and cell-to-cell interactions to communicate
cells associated with innate defenses
phagocytic cells destroy/engulf pathogens, granular cells harm/kill pathogens, cells of immune system communicate via cytokines
innate immunity (non-specific)
born with it
defense against anything foreign/abnormal
first line of defense
includes physical barriers, NK cells, inflammation, etc.
adaptive immunity (specific)
develops after birth, after exposure to antigen
4 properties (specificity, versatility, memory, tolerance)
includes actions of cytotoxic T cells and B cells.
specificity
ability to target specific cells
versatility
ability to respond/build defences against things we don’t know exist and adapt to environment
memory
ready to act quick if exposed again because our body remembers
tolerance
need to destroy other cells but not our normal ones
communication across cell membranes
antigens are “specific chemical targets” that stimulate immune response and be displayed on surface of cells (MHC)
body can detect “self” from “non-self” antigens
antigen presenting cells
pick up and display antigens on their surface without being infected themselves
have class II MHC proteins on their membranes
activate helper T cells
includes dendritic cells, macrophages, microglia.
NK cells
non-specific
recognize foreign antigens/abnormal antigens on cells
release perforins to create holes in target cells and destroy
destroy body cells infected by viruses (including cancer cells)
T cells/lymphocytes
cell-mediated immunity (attack by phagocytosis)
formed in bone marrow but developed in thymus
T cell receptors and CD markers on membranes
includes helper T cells, cytotoxic T cells, memory T cells, regulatory T cells
B cells/lymphocytes
antibody-mediated immunity
formed in bone marrow
B cell receptors and class II MHC proteins on membrane
includes inactive B cells, sensitized B cells, plasma cells, memory B cells
what happens if there is a “breach” in immune response?
innate defenses keep thing under control until specific defenses are ready where they will destroy the specific antigen.
class I MHC
on all nucleated cells
communicates with CD8 T cells (cytotoxic T cells)
results in destruction of infected cell
class II MHC
on specialized cells (APCs, B cells)
communicates with CD4 T cells (helper T cells)
results in stimulation of immune response
IgG antibodies
largest, account for 80% of antibodies, responsible for resistance against viruses, bacteria, and bacterial toxins.
IgE antibodies
attaches as an individual molecule to the exposed surfaces of basophils and mast cells. Causes stimulation of a cell to release histamine.
IgD antibodies
is an individual molecule on the surfaces of B cells where it binds antigens in the extracellular fluid.
IgM antibodies
first class of antibody secreted after an antigen is encountered, circulates as a five-antibody starburst.
IgA antibodies
found in glandular secretions such as mucous, tears, saliva, and semen. Attack pathogens. before they gain access to internal tissues.
primary response
first exposure to specific antigen, takes time to develop; some IgM first then IgG
secondary response
second exposure to same antigen, much more rapid as you are now “immune” to the pathogen. Some IgM but much more IgG
artificially acquired active immunity (vaccines)
antigen is administered triggering immune response, individual will produce antibodies against the antigen so youre ready if ever exposed to the “real” antigen
inflammation
non-specific defense
innate
a response to invasion/infection, tissue damage, or both
symptoms include redness, heat, swelling, and pain
purpose of inflammation
deliver leukocytes and plasma proteins to site of injury to destroy any invaders, clean up the mess, and facilitate healing/repair
how do cells get to inflammation sites?
mast cells release histamine triggering vasodilation and increased capillary permeability. Neutrophils and monocytes also undergo margination and diapedesis.
immunological surveillance and cancer
any cell may undergo a mutation that affects its cell division, becoming cancerous. cancer cells are “self” but are abnormal so can be recognized by your body defenses.
balance between immunity and autoimmunity
immune response is essential to preventing infection but an overactive immune response could lead to autoimmunity.