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Body locations with normal Microbiota
Skin - Commensal, human unaffected microbes get nutrients
Small Intestine - Mutual, microbiota help digestion while they get stable enviroment
Throat - Commensal, humans unaffected microbes dont harm or hurt
Body location which are sterile
Brain
Heart
Blood
Why are some body parts sterile
They contain barriers that prevent microbes, Microbes would impair function, strong immune surveillance and no benefit for microbes to be there
Why do some body parts contain microbiota
Relationships exist where either the host or microbe are benefiting, some areas are constantly exposed to the outside world, helps train the immune system, the eviroment supports growth
What is an opportunistic infection?
caused by microbes that normally don’t cause disease in a healthy person but take advantage of certain conditions to become harmful. often part of your normal microbiota (commensal) or are common in the environment. They only cause problems when given the right “opportunity.”
What are some “opportunities” that allow opportunistic infections to cause disease?
Can occur from weakened immune system, breach of a physical barrier, antibiotics flushing good bacteria, entering the wrong body system
The difference between ENDO- and EXO-toxins?
Endotoxins originate as a part of the bacterial cell wall, whereas exotoxins are produced and secreted by the bacteria
Collagenase
Breaks down collagen, allowing pathogen to spread through tissues.
Hyaluronidase
Breaks down hyaluronic acid, allowing pathogen to spread through tissues.
Coagulase
Catalyzes the production of fibrin clots.
Kinase
Allows bacteria to escape from fibrin clots.
Order of Infection process
Portal of entry, Adhesion, Invasion, Multiplication, Infection of target, disease, and portal of exit.
Can you identify a virulence factor for each step of the infection process?
Portal of entry - Enzymes or penetration mechanisms hyaluronidase or collagenase
Adhesion - Fimbriae, Pili, Surface proteins
Invasion - Invasive enzymes, streptokinase - dissolves clots so bact. can spread
Multiplication - Biofilm formation protects microbes while they multiply
Infection of target - Evasion of immune system through capsules, immune inhibitors
Disease - Endotoxins (direct cell damage), Exotoxins (trigger inflammation)
Portal of exit - Toxins inducing excretion help pathogen spread
Infection ≠ Disease: why not?
Infection infections multiplication, disease indicates damage or symptoms
Contact transmission - Direct, indirect, droplets
Requires you to be in close proximity to someone (or to objects they have been in contact with); involves short distances. (touching, fomites, sneezing, coughing) <1M
Vehicle transmission - Airborne, Waterborne, Foodborne
Carried by a nonliving intermediary
Aerosols, Contaminated water or food
Vector - Mechanical, Biological
Carried by a living intermediary
Biological - Mosquito, Tick, Mite, Flea, Biting fly
Mechanical - Housefly, Roach
Zoonotic transmission
From animal to human, can be direct, indirect, waterborne, foodborne, or biological or mechanical vector
What route of transmission would be a rabies bite on a human
Zoonotic, Direct
Cow excretes in water, person drinks water, gets E. Coli. What kind of transmission
Zoonotic, Fecal oral, Waterborne
Mosquito bites bird, gets west nile, then bites human
Biological Vector, Zoonotic, and not communicable
Mosquito bites girl infected w/ malaria then bites another person
Biological Vector, not zoonotic, not communicable, not contagious
Isolation vs Quarantine
Isolation separates sick people with contagious disease from people who are not sick
Quarantine seperates those exposed to see if they will become sick
Lists cases of notifiable conditions by region and state
Smallpox, Botulism, Measles, Tuberculosis
Anthrax, Covid-19, West nile, HIV/AIDS
Types of HAI’s
Exogenous - external source, MRSA
Endogenous - patients normal microbiota are the source, E. Coli
Iatrogenic - infection directly caused by a medical procedure, Catheter AUTI
List at least 4 of the universal precautions for EVERY hospital interaction
Wear gloves, Wash hands, Wear masks, Avoid injury from needles, Vaccinate
Distinguish between signs and symptoms of disease (give examples)
Signs are Objective, measurable, and observable evidence of disease that a healthcare provider (or others) can detect. Fever, Rash, Hypertension, Elevated WBC count
Symptoms are subjective experiences felt and reported by the patient.
Pain, Nausea, Fatigue, Dizziness, Headache
What is a hospital acquired infection
a nosocomial infection—is an infection that a patient develops while receiving care in a healthcare facility that was not present or incubating at the time of admission
What are the 3 contributing factors to HAIs (why are they common in the hospital
setting
Immunocompromised patients, increase presence of infectious agents, many opportunities for spread
Where do innate immune responses take place
Outside and Inside the body
Barrier surface like skin and mucus membranes
In the blood WBC’s circulate
The lymphatic system helps detect and transport pathogens to immune cells
Where do adaptive immune responses take place
Inside the body
Lymph nodes and spleen
As well as blood
1st line of defense physical and chemical (innate)
Skin - preventing entry
Mucus - lines respiratory, digestive, and urogenital tracts
Sebum - acidic inhibiting bacteria
Lysozyme - break down bacterial cell walls
2nd line of defense 4 components (innate)
Compliment - 30 proteins that cascade to help phago + destroy pathogens
Phagocytosis - WBC engulfing its invaders
Inflammation - Red, Swelling, Pain, Heat
Interferon - Cells produced when infected to warn nearby cells
Neutrophil
Engulf and destroy through phagocytosis
Macrophages
Bridge adaptive and innate through activating the adaptive
Phagocytose pathogens and clean up dead cells
Dendritic cells
Capture pathogens and present antigens to T cells
Basophils + Mast cells
Release histamine to trigger inflammation
B cells
Produce antibodies specific to a pathogen
Form memory B cells for a faster future response
Helper T cells (CD4+)
Coordinate immune response, activate B cells and other immune cells
Cytotoxic T cells (CD8+)
Kill infected cells directly
Memory T cells
Provide long-term immunity after infection
Eosinophils
Attack large parasite by releasing toxic granules, since too small to eat
Stages of phagocytosis
Chemotaxis - pathogens or damaged cells release chemical signals, phago attracted
Adhesion - phagocyte sticks to the pathogen, recognition occurs via immune cell
Ingestion - Engulfment, membrane wraps around it forming phagosome
Fusion - phagosome fuses with a lysosome
Killing - enzymes and toxic substances destroy the pathogen, micro fractionated
Elimination - waste expelled by exocytosis
What is interferon and what produces it
Like Paul Revere these are signaling proteins released when a cell is infected by a virus, they help nearby cells and limit the spread. They don’t kill they just interfere with viral replication
What are the 3 complement pathways and what do they do
Classic - Antibody–antigen complex forms, Links adaptive immunity → complement activation, Antibodies (IgG or IgM) bound to a pathogen, lead to patho destruction
Alternative - Starts spontaneously when complement proteins bind to microbes, Rapid, innate response, Direct contact with pathogen surfaces (no antibodies needed), Continuous “surveillance” defense against invaders
Lectin - Recognizes carbohydrate patterns on pathogens, Lectins (like mannose-binding lectin) binding to sugars on microbes, Activates complement cascade like the other pathways, require no antibodies
What is the result of complement activation
the destruction and removal of pathogens through a coordinated set of immune actions in Innate immunity. Opsonization, Inflammation, Cell lysis (MAC), Enhanced immune clearance.
4 properties of inflammation and why they occur
Heat - Vasodilation bring warm blood from the core
Redness - more blood flow since BV’s dilate
Swelling - BV’s become more permiable allowing fluid, proteins, and immune cells to leak into the tissus
Pain - prostaglandins and histamine stimulate pain receptors, pressue from swelling
3 ways the first and/or second line of defense work together to prevent infection in the
body (interactions of multiple factors)
Mucus traps bacteria, Lysozyme and stomach acid kill micrbobes
Skin and Mucus are physical barriers, if broken, inflammation is triggered bringing phagocytes to the area
Cilia moves microbes through mucus out of airways, macrophages destroy microbes that manage to make it through
Complement deficiency results in
Recurrent bacterial infections
Lysozyme deficiency results in
Eye infections
Goblet cell deficiency results in
Respitory infections
Gastroferritin deficiency results in
Intestinal infections
Interferon deficiency results in
Viral infection
What cell types can do phagocytosis
Neutrophils, Macrophages, and dendritic cells
Opsonization
What is complement? Where is it found?
The complement system is a group of blood plasma proteins that work together to enhance (“complement”) immune defenses. It is part of Innate immunity, but it can also be activated by antibodies. Mainly in the blood plasma (circulating in an inactive form), Also present in tissue fluids, Produced mostly by the liver
5 aspects of the adaptive response
Specificity - immune system targets one specific antigen (pathogen marker) Each B or T cell recognizes only one unique shape/structure
Inducible - response is not always active, turned on when pathogen is encountered
Clonal - deletion via apoptosis and proliferation. Effector cells fight infection, Memory cells are for future protection
Tolerance to self - the immune system does not attack itself
Memory - some lymphocytes remain as memory cells, response = stronger + faster
Apoptosis
programmed cell death to remove damaged or infected cells
Differentiation
process by which a less specialized cell becomes a more specialized cell with a specific structure and function.
Proliferation
Proliferation means the rapid increase in the number of cells by cell division.
It is an important process in both normal growth and in Adaptive immunity.
true or false Lymphocytes secrete cytokines
Lymphocytes—especially T helper cells—do secrete cytokines. Cytokines are chemical signaling proteins that help regulate and coordinate immune responses in Adaptive immunity.
Cell mediated response
Kills host cell instead of antibodies - T cells attack infected cells directly
Antibody mediated (humoral) response
Production of antibodies, uses B cells to produce antibodies that act in body fluids (“humors” like blood and lymph).
IL-2
a cytokine (signaling protein) released by helper 1 T cells that activates and clones cytotoxic T cells, enhancing NK cell activity
IL-4
produced by T helper 2, mast and basophils in order to stimulate B cell activation, antibody production, and IgE-mediated immune response
IL-12
a signaling protein produced by dendritic cells and macrophages that produces Th1 differentiation, activates NK, cells and strengthens cell-mediated immunity
What do IL-2 IL-4 IL-12 signaling proteins do
IL-2 = T cell expansion
IL-4 = B cell / antibody response (IgE, allergy)
IL-12 = Th1 / NK activation (cell-mediated immunity)
Antigen
Exogenous
Endogenous