• 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

1/50

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;

50 Cards in this Set

  • Front
  • Back
Infection
invasion or colonization of the body by pathogens, presence of pathogens in the body (ex. HIV+, HCV)
Disease
when the growth of the pathogens damages all or part of body so that it is incapable of performing normal functions (ex. HIV infection AIDS, HBV infection hepatitis)
Normal flora
• Organisms that normally colonize a host without causing disease
• Includes: bacteria, viruses, fungi, protozoa
• Body cells = 1013
• Bacterial cells = 1014 ten times more than body cells
• Microbes outnumber human cells 10 to 1
Sites that harbor normal flora
skin
upper respiratory tract
most of GI tract, large intestine highest #
outer opening of urethra
vagina
Microbe-free anatomical sites
All internal tissues & organs

Fluids within an organ or tissue
blood
urine in kidneys, ureters, bladder
cerebrospinal fluid
semen prior to entering urethra
amniotic fluid surrounding embryo & fetus
Predisposing factors – make a person more likely to allow the microbes to overgrow & get sick
old age & extreme youth
genetic defects in immunity
AIDS
surgery & organ transplants
diseases: cancer, diabetes
physical & mental stress
other infections
Portals of entry
Site where microbes enter the body
Skin
Mucous membrane
Parenteral- deposited under the skin or mucous membrane
Infectious dose
Number of microbes required to initiate an infection
Varies with infectious agent
It usually takes more than 1 to start an infection.
1 rhinovirus cold; RARE SITUATION
10,000 HIV  HIV positive
10,000 bacterial cells gonorrhea
8,000-50,000 anthrax spores  anthrax
Virulence factors
Factors a microbe uses to invade and colonize a host. Pathogenic bacteria have more of these than bacteria of the normal flora.
Adherence factors
Exoenzymes – dissolve host defense barriers, promote spread into deeper tissues
Toxins – poisons
antiphagocytic factors – help in avoiding WBCs
Adherence factors
Fimbrae
Capsules
spikes
hooks
flagella
Examples of a few Exoenzymes
Mucinase – digests protective coating of mucous membranes
hyaluaronidase – digests hyaluaronic acid, which cements cells together
coagulaeses – cause blood clots
Kinases- break clots
Antiphagocytic factors
leukocidins – kill WBCs
slime layers & capsules – make it difficult for phagoctyes to engulf bacteria

Mycobacterium and Legionella may replicate within WBC
4 periods of disease
Incubation- time from initial contact with microbe; microbe multiplies
Prodromal – microbe multiplies, appearance of first symptoms
Invasion – microbe multiplies to high levels, exhibits greatest toxicity, becomes well established in target tissue
Convalescent - mo are cleared, recovery
Portals of exit
respiratory & saliva
skin scales
feces
urine
urogenital tract
blood
Reservoir of infection
Primary habitat where a pathogen originates
either living organism or inanimate object
provides pathogen with adequate conditions for
Survival

Replication

Opportunity for transmission
3 types of reservoirs
Human reservoirs - People with or without signs & symptoms
Animal reservoirs- contact with infected animals, wastes, or hides, or insects; animal may or may not have symptoms
Zoonoses - diseases that occur primarily in animals & can be transmitted to humans
Nonliving reservoirs- soil, water, food
Measures to prevent nosocomial infections
Hand-washing
gloves
gowns
masks
surgical asepsis – practices to maintain a microbe-free surgery
medical asepsis – practices that lower loads of mo in patients, personnel & hospital
Most common sites of nosocomial infections
Urinary tract infection
surgical wound infection
lower respiratory tract infection
bacteremia
cutaneous infection
Koch’s Postulates
Purpose: determine the causative agent of a disease
Find evidence of a particular microbe in every case of a disease.
Isolate mo from an infected subject & grow it in the lab.
Inoculate a susceptible healthy subject & observe resultant disease.
Reisolate the agent from this subject.
Exceptions to Koch’s Postulates
Bacteria and viruses that cannot be grown on artificial media - syphilis
Some diseases are caused by a variety of mo: diarrhea, pneumonia
Some pathogens cause several different diseases: Streptococcus pyogenes
Exclusively human diseases: no animal model, immoral to infect human with incurable disease.
Physical barriers at body’s surface
skin pH 4 – acidic; layers of tightly packed cells
perspiration - flushes skin, high salt, contains lysozyme- degrades bacterial cell wall
Saliva
mucus traps mo
ciliary escalator of lower respiratory tract moves continuously propelling dust & mo toward throat
Stomach acid
2nd level -Innate Defense System
Innate immunity serves as a rapid response system for detecting & clearing infections by microbes.
When an invader is detected, many signaling proteins are produced that induce inflammation & direct the body to mount a full-fledged immune response.
Phagocytes – dendritic cells, macrophages, monocytes & neutrophils
Engulf & destroy invaders.
Take antigen to lymph node & present to the T cells.
Some microbes may reproduce inside the phagocytes
5 types of leukocytes (WBCs)
Neutrophils (55-90%) phagocytes
Monocytes (3-7%) differentiate into phagocytic macrophages after leaving the blood & going into tissues
Eosinophils (1-3%) somewhat phagocytic, produces toxins against parasites
Basophils (0.5-1%) involved in allergic response

Lymphocytes (20-35%) B & T types, involved in specific immune response, Not phagocytic
Functions of the lymphatic system
Route for return fluid to circulatory system
Drain off system inflammatory response
renders surveillance, recognition, & protection against foreign materials
Lymph
Formed when blood components move out of blood vessels into extracellular spaces & diffuse into lymph capillaries
plasmalike liquid carried by lymphatic system
contains: water, dissolved salts & 2-5% protein
transports WBCs
Lymph node
small, bean-shaped organs stationed in clusters along lymphatic channels, large blood vessels
aggregations occur in armpit, groin, & neck
Contains large numbers of B&T cells
Filter lymph, allowing pathogens to encounter B & T lymphocytes
Inflammatory response
The elements of the innate system work together
Inflammatory cytokines such as tumor necrosis factor (TNF) & IL-1 are released into the tissues, summoning beneficial cells & fluids into the injured area
Causes: swelling, pain, fever, fatigue and malaise.
stages of inflammation
tissue damage – complement & phagocytes act
Triggers blood vessels to dilate (vasodilation) & increase their permeability
WBCs leave blood vessels, enter tissue and phagocytosis & more inflammation mediators released.
If needed more inflammatory cytokines such as tumor necrosis factor (TNF) & IL-1 are released into the tissues, causing fever, fatigue and malaise.
tissue repair
Functions of Inflammation
Attract immune components to site of injury
Repair tissue damage, localize & clear away harmful substances
Destroy microbe & block further invasion

Inflammation may cause collateral damage
where normal healthy host cells are killed
Fever
Does NOT directly kill mo
Inhibits growth of temp sensitive mo
Decreases amount of iron available, impeding bacterial nutrition
Increase metabolism & stimulates immune reactions
Phases of phagocytosis
Chemotaxis
contact & ingestion
Lysosome fuses with vesicle
killing, digestion of microbe
release of debris
Interferon
Protein secreted by a virus infected cell
Binds to neighboring cells and causes them to produce antiviral proteins that block virus replication
Signals cell to apoptosis (suicide) if infected.
Not virus specific
Host species specific, (human interferon for humans, etc.)
Complement
A group of 20 proteins present in the bloodstream in inactive forms
Cleavage of complement proteins activate them
Functions: (OIL)
Opsonization – coating with C proteins facilitates phagocytosis
Inflammation – summons other immune cells into the area
Lysis -may initiate membrane attack complexes that destroy cells & inactivate viruses
When microbes breach the barrier defenses
Complement binds – opposonization, inflammation & lysis
Dendritic cells phagocytize & release cytokines.
Activated NK cells, neutrophils, macrophages & interferon attack
If large amounts of cytokines & dead cells are produced, dendritic cells exit the tissues & migrate to lymph nodes
In lymph nodes, they present antigen to TH and B cells & signal the type of response needed.
(Dendritic cells are like the “coach” & TH cells the “quarterback”)
The immune system has 2 divisions.
The innate part acts near entry points into the body & is always at the ready.
If it fails to contain a pathogen,
The adaptive division kicks in later by mounting a highly targeted attack against the specific invader.
The adaptive immune system
Helper T cells –activate other T & B cells
Cytotoxic T cells – kill infected cells by secreting perforin
B cells produce antibodies to
Opsonize microbes

Agglutinate microbes

Neutralize microbes
2 branches of the adaptive immune system
Humoral immune system- takes place in body fluids; B cells secrete antibodies that “attack” antigens
Cellular immune system – takes place between the T cells and antigens (infected, cancerous or other types of cells.
Antigen
(foreign invader) a substance that is recognized as foreign or “nonself” by the immune system. May be a whole microorganism or a portion of it.
Antibody
(defensive weapon) a Y-shaped protein which is produced & secreted by B cells in response to a specific antigen. Antibodies bind to & contribute to the destruction
Structural & chemical characteristics of antibodies
Also called immunoglobulins
highly specific proteins that interact with only one antigenic determinant (epitope) on an antigen
serve as antigen receptors for B cells
each Ab has 2 identical binding sites for antigen
a typical Ab monomer has 4 protein chains
a. 2 identical Light (L) chains
b. 2 identical Heavy (H) chains
each H & L chains has a variable region & a constant region
variable region
located at the end of the Y arms
account for ability to bind specific Ag
thousands of possibilities
constant region
located at the stem & lower parts of the Y arms
5 major types of constant H regions ( G,M,A,D,E)
2 major types of constant L regions ( kappa, lambda)
stem of the Y called Fc region
Fc can bind to host cells
Fc of G & M classes of Ab can activate complement
Characteristics of each of the 5 classes of antibodies
IgG
cross placenta & confer passive immunity to fetus
trigger complement system

IgM
pentamer – 5 monomers & a J chain
trigger complement system
first antibody to appear after initial exposure to Ag

3. IgA
high amounts are in mucous, saliva, & breast milk
secretory IgA – dimmer- 2 monomers & a J chain & a secretory component
main function is to prevent attachment of pathogens to mucous membranes
4. IgD
acts as antigen receptor on B cells
No known function in serum
5.IgE
bound to mast cells & basophils by Fc end, serve as Ag receptors & binding causes release of histamine & chemicals  allergies
useful against parasitic worms
What happens after antibodies bind to antigen?
Neutralization - block virus attachment to cell, block toxin's active site
Activation of complements(opsonization, inflammation, lysis)
Agglutination - clumps Ag together -helps phagocytosis
Opsonization -helps phagocytosis
Primary immune response
Slower
Weak response
Few specific B & T cells
Few antibodies made
Secondary immune response
Faster
Strong response
More specific B & T cells
Lots of IgG made quickly
Basis for vaccines & booster shots
How does the Cellular Immune System distinguish between “self” and “nonself”?
All body cells have Major Histocompatability Complex (MHC) class I proteins on their surfaces that mark the cells as “self”
Immune system tries to destroy anything that does not have class I proteins because they are “nonself”, or antigens
T cells
Derived from bone marrow and mature in the thymus
Make up 70-80% of circulating lymphocytes
Each has a T cell antigen receptor which recognizes a peptide bound to a self MHC molecule
Do not recognize soluble, Extracellular antigen
Antigen must be displayed on surface of an antigen presenting cell like a B cell or macrophage
4 Types of T cells
Helper T4 Conductor of immune system
Cytotoxic T8 Destroy target cells on contact
DH Allergic responses, kill cancer cells
Suppressor Turn off immune responses
Cytokines
Chemical messengers of the immune cells
Signal cells to move into area, become active, replicate, etc.
used to communicate among WBCs
Interleukin 1 (IL-1)
Interferon (IFN)
Tumor Necrosis Factor (TNF)