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Why do you get sick?How do you get better?What’s the best way for you to avoid
getting sick in the first place?
For years, people thought diseases were caused by curses, spirits, etc.
In the nineteenth century, Louis Pasteur and Robert Koch concluded that infectious diseases were caused by microorganisms (germs) = the Germ Theory of Disease
In the summer of 1975, many children in Lyme, CT developed a rare form of childhood arthritis
Allen Steere realized the children developed their problems after having a skin rash from a deer tick bite
Steere’s colleague, Dr. Burgdorfer, found an unusual spiral-shaped bacterium in the ticks and the child patients
Steere injected lab mice with the bacterium and they developed similar symptoms = Lyme Disease
So, Lyme disease is caused by a bacterium
Koch developed a series of guidelines to identify the microorganism that causes a specific disease 1. The pathogen should always be found in the body of a
sick organism and should not be found in a healthy one. 2. The pathogen must be isolated and grown in the
laboratory in pure culture. 3. When the purified pathogens are placed in a new host,
they should cause the same disease that infected the original host.
4. The injected pathogen should be re-isolated from the second host and be identical to the original pathogen.
Disease no longer seems unavoidable consequences, but now pathogens could be identified and diseases could be prevented or cured.
The pathogen should always be found in the body of a sick organism and should not be found in a healthy one.
The pathogen must be isolated and grown in the laboratory in a pure culture.
When purified pathogens are placed in a new host, they should cause the same disease that infected the host.
The very same pathogen should be reisolated from the second host. And it should be the same as the original pathogen.
No pathogen Suspected pathogen Suspected pathogen
Injection of organisms from
pure culture
Pathogen
Dead mouse Dead mouse
Dead mouse
Healthy mouse
Healthy mouse
Suspected pathogen grown in pure culture.
Section 40-1
Disease = any change, other than injury, that disrupts the normal functions of the body Diseases can be inherited (ex. Hemophilia) Diseases can be caused by materials in the
environment (ex. Cigarette smoke) Diseases can be produced by agents (ex. Bacteria,
viruses, fungi) = pathogens Pathogens = “sickness-makers” Diseases caused by pathogens = infectious
diseases, because they enter, or infect, the body
The human body provides great conditions for pathogenic growth
You have many different microorganisms living in your body that are actually harmless or beneficial
However, some microorganisms are dangerous Some bacteria break down body tissues and others
release toxins (poisons) Some protists, fungi, and worms are parasites that live
inside you and use up your nutrients or destroy blood/nerve cells
Viruses are nonliving pathogens that use a host cell to make copies of the virus and destroy other cells
Infectious diseases are spread From person to person: coughing, sneezing,
or physical contact▪ Common cold, mumps, measles, influenza, STDs
(AIDS), meningitis, athlete’s foot Contaminated water and/or food
▪ Cholera, dysentery, E.coli infection, salmonellosis Vectors: infected animals (ticks/mosquitoes)
▪ Lyme disease, malaria, West Nile virus, rabies
Viruses
Protists
Worms
Fungi
Disease Agent That Causes Disease
Method of Transmission
Common coldInfluenza
Chicken pox
Measles
Tuberculosis
Meningitis
CholeraTetanusAfrican sleeping sicknessMalariaAmoebic dysenterySchistosomiasisBeef tapeworm
Athlete’s foot
Ringworm
RhinovirusTwo types (A, B), plus subtypesVaricella
Paramyxovirus
Mycobacterium tuberculosisNeisseria meningitidisVibrio choleraeClostridium tetaniTrypanosoma
PlasmodiumEntamoeba histolyticaSchistosomaTaenia saginata
Imperfect fungi
Imperfect fungi
Airborne; direct contact with infected personAirborne; droplet infection; direct contact with infected personAirborne; direct contact with infected personDroplets in air; direct contact with secretions of infected personDroplets in air; contaminated milk and dairy products
Direct contact with a carrier
Contaminated drinking waterContaminated wound; usually puncture wound
Spread by tsetse fly
Spread by Anopheles mosquitoes
Contaminated drinking waterFreshwater streams and rice paddies Contaminated meat
Contact with infected personExchange of hats, combs, or athletic head gear with infected person
Section 40-1
Pathogen Types
Bacteria
Drugs have been developed to use against pathogens
Antibiotics = chemicals that kill bacteria without harming the cells of humans or animals Penicillin = interferes with the synthesis of cells
walls by Eubacteria (breaks down peptidoglycan in their cell walls))
Streptomycin = interferes with bacterial growth by blocking protein synthesis in ribosomes
Antivirals = inhibit the ability of viruses to invade cells or multiply inside cells
A series of defenses that guard against diseases = body’s protection
Nonspecific defenses = “walls” of the immune system keeping everything out
Specific defenses = “security guards” identifying and inhibiting pathogens
Skin = most important nonspecific defense Physical barrier Acidic environment on surface kills bacteria
Mucus, sweat, tears and saliva Traps pathogens and removes them from the body by cilia or
destroys them using the enzyme lysozyme, which breaks down cell walls
Inflammatory response = reaction to tissue damage caused by injury or infection Blood vessels around wound expand, white blood cells enter
infected tissue and phagocytes (special WBCs) engulf and destroy bacteria, tissue becomes swollen and painful, body temperature increases (fever) to slow pathogen growth and increase circulation and activity of WBCs
Interferon = proteins that “interfere” with the virus Proteins released by virus-infected cells to help other cells
resist viral infection by inhibiting viral protein synthesis, blocking viral replication
SkinWound
Bacteria enter the wound
Phagocytes move into the area and engulf the bacteria and cell debris
Capillary
Section 40-2
A series of specific defenses that attack the pathogens = immune response Humoral immunity Cell-mediated immunity Permanent immunity
Antigen = a substance that triggers the immune response (organic molecules on the surface of pathogens)
Antibody = protein that helps destroy pathogens by binding to antigen and attracting phagocytes to engulf and destroy them
Pathogen:Pathogen: any any disease causing agentdisease causing agent Ex. Fungus, Bacteria, Ex. Fungus, Bacteria,
Virus etc.Virus etc. Antigen:Antigen: any any
substance that substance that triggers an immune triggers an immune response. response. Antigens are chemicals Antigens are chemicals
present on the surface present on the surface of viruses, bacteria, of viruses, bacteria, pollen grains etc.pollen grains etc.
Antibody:Antibody: a protein a protein that helps to destroy that helps to destroy pathogens.pathogens.
Antigen-binding
sites
Antigen Antibody
Prentice Hall Biology Presentation Pro, 2002
Immunity against pathogens in the body fluids (blood/lymph)
Immunity produced by lymphocytes (type of WBC) B lymphocytes (B cells) produce antibodies to
mark pathogens and prevent future infections B Cell (a.k.a. B-lymphocyte) is activated by antigens on
the pathogen (will eventually produce antibodies.) Macrophage (a type of phagocyte): engulfs pathogen and
then displays the antigens on its surface. T Cell: binds to activated macrophage (one with the
antigens on surface) and then becomes a helper T cell (or a killer T cell).
Helper T Cell: helps the activated B cell to begin producing antibodies.
Antibodies bind to the pathogen marking them for destruction by other immune cells like phagocytes.
Bacteria With Antigens on Surface
Macrophage
T cell
B cell
A large phagocyte called a macrophage engulfs a bacterium
Circulating antibodies bind to bacterial antigens, helping other immune cells to identify and destroy bacteria
Active B cells proliferate to produce clones of memory cells
Helper T cell assists the activated B cell to develop into an antibody-producing plasma cell
T cell, activated by macrophage, becomes a helper T cell
Antigens are displayed on surface of macrofage after digestion of bacterium
T cell binds to activated macrophage
Section 40-2
Bacterial antigens also stimulate B cells
Plasma cell produces large amounts of antibody proteins, released intothe bloodstream
Immunity that relies on lymphocytes (cells) Killer T cells (cytotoxic T cells) can attack
infected cells and destroy their cell membranes T cells bind to activated macrophages and become
Helper T cells Helper T cells activate Killer T cells. Killer T Cells (a.k.a. cytotoxic T cells) bind to infected
cells, disrupt their cell membranes which causes the contents of the infected cell to leak out and it dies.
Killer T cells are what make organ transplants difficult, because they see the new organ as foreign and begin to attack it = rejection. Rejection can be limited by finding donors that are well
matched to the recipients and by administering drugs to the recipient that will suppress the cell-mediated immune response.
Macrophage
T Cell
Helper T Cell
Killer T Cell
Infected CellAntigens are displayed on surface of macrophage
T cell binds to activated macrophage
T cell, activated by macrophage, becomes a helper T cell
Helper T cell activates killer T cells and B cells
Killer T cells bind to infected cells, disrupting their cell membranes and destroying them
Section 40-2
Here, the smaller cytotoxic T cell or Tc (arrow) is attacking and killing a much larger virus-infected cell. The T cell will survive while the infected cell is destroyed.
People that survived infectious diseases, never developed the same disease again
Memory B and T cells remain capable of producing specific antibodies to that pathogen, ensuring the disease never gets a chance to develop again
Interval between exposures
First exposure
Second exposure
Time
Ant
ibod
y C
once
ntra
tion
Section 40-2
An immediate active immune response against the pathogen in a vaccine
Vaccination = injection of a weakened or mild form of a pathogen to produce immunity Prevents serious human diseases by
stimulating the immune system to create plasma cells capable of producing the specific antibodies for another possible infection
Active Immunity lasts long term (permanent)
Antibodies produced by other animals for a pathogen are injected into the bloodstream The antibodies will produce passive
immunity against a pathogen as long as they remain in circulation (several weeks)
Antibodies from the mother are passed to the fetus through the placenta or to the infant in the mother’s milk = maternal immunity The antibodies will produce passive
immunity against most infectious diseases for the first few months of life or longer if breast-fed
Although the immune system defends the body from potential pathogens, sometimes disorders occur The immune system may overreact to
an antigen, producing discomfort or disease
The cellular nature of the immune response is a potential weak point
Overreaction of the immune system Allergies occur when antigens from allergens
(pollen, dust, dust mites) bind to mast cells (type of immune cell common in nasal passages)
Activated mast cells release chemicals = histamines, which increase the flow of blood and fluids to the surrounding area (sneezing, runny eyes/nose, etc)
Antihistamines = drugs used to reduce allergy symptoms by counteracting the effects of histamines
Asthma = allergic reaction where smooth muscle contractions reduce the size of air passageways in the lungs making breathing difficult
The immune system has the ability to distinguish “self” from “nonself”
The immune system makes a mistake and attacks the body’s own cells (“it attacks itself”) Juvenile-onset diabetes (immune system attacks
insulin-producing cells in pancreas) Myasthenia gravis (attacks neuromuscular
junctions) Multiple Sclerosis (destruction of myelin sheath –
attacks nervous system) Lupus (attacks cells and tissues resulting in
inflammation and tissue damage: heart, joints, skin, lungs, blood vessels, liver, kidneys and nervous system)
Acquired Immune Deficiency Syndrome (AIDS) = when cells of the immune system are weakened by infection
Caused by HIV (human immunodeficiency virus) and spread by contact with body fluids (drug needles, unprotected sexual intercourse, breast milk, blood during birth, blood transfusions)
HIV attaches and destroys most helper T cells, so body is more susceptible to infections
People DO NOT die from HIV/AIDS, they die from the infections they get because the HIV virus has left their immune system unable to respond to the infections
Infection;Immune system eliminates most of HIV
Symptoms, such as swollen lymph nodes, are few
Loss of immunefunction moreapparent; appearanceof characteristic diseases such asyeast infections
Almost total loss of cellular immunity; AIDS
Relative HIV concentration
T cell concentration
Section 40-3
Years
There are many different types of drugs being used. Each drug has a different approach: Stop the virus from attaching to cells. Stop the virus from creating its protein coat. Stop the virus from replicating its genetic
information. Doctors are now treating people with HIV
with drug cocktails (several different drugs at the same time) These cocktails have dramatically increased the
amount of time people are living with HIV and their quality of life – VERY expensive!
ACQUIRED IMMUNODEFICIENCY SYNDROME ACQUIRED IMMUNODEFICIENCY SYNDROME (AIDS)(AIDS)
Worldwide HIV infection, 1999
HIV virus particle
Total population 2007: 6,625,000,000Total population 2007: 6,625,000,000Adults age 15-49 with HIV/AIDS,Adults age 15-49 with HIV/AIDS, 20052005 – 38 mill – 38 millNew HIV infections,New HIV infections, 20052005 – 4.9 mill, – 4.9 mill, 20072007 – 2.5 mill– 2.5 millAdult HIV prevalence (%),Adult HIV prevalence (%), 20052005 - 1.1, - 1.1, 20072007 – 0.8– 0.8Women age 15-49 with HIV/AIDS, Women age 15-49 with HIV/AIDS, 20052005 – 17.5 mill – 17.5 millChildren with HIV/AIDS, Children with HIV/AIDS, 20052005 – 2.3 – 2.3 millmill,, 20072007 – 2.5 – 2.5
millmill
AIDS orphans (ages 0-17), AIDS orphans (ages 0-17), 20032003 – 15 mill – 15 millAIDS deaths,AIDS deaths, 20052005 – 3.1 mill, – 3.1 mill, 20072007 – 2.1 mill– 2.1 mill
The number of people with HIV/AIDS has been The number of people with HIV/AIDS has been decreasingdecreasing..Source: http://hivinsite.ucsf.edu/global?page=cr-00-01Source: http://hivinsite.ucsf.edu/global?page=cr-00-01
Viral RNA genome is converted to double-stranded DNA by a virally encoded reverse transcriptase that is present in the virus particle.
The viral DNA is then integrated into the cellular DNA by a virally encoded integrase, along with host cellular co-factors, so that the genome can be transcribed.
Once the virus has infected the cell, two pathways are possible: the virus becomes latent and the infected cell
continues to function the virus becomes active and replicates, and a large
number of virus particles are liberated that can then infect other cells
HIV-1 is the virus that was initially discovered and termed LAV. It is more virulent, relatively easily transmitted, and is the cause of the majority of HIV infections globally.
HIV-2 is less transmittable than HIV-1 and is largely confined to West Africa.
HIV differs from many viruses in that it has very high genetic variability.
This diversity is a result of its fast replication cycle, with the generation of 109 to 1010 viruses every day, coupled with a high mutation rate and recombinogenic properties of reverse transcriptase.
This leads to many variants of HIV in a single infected patient in the course of one day.
This variability is compounded when a single cell is simultaneously infected by two or more different strains of HIV.
Cells multiply uncontrollably and destroy healthy tissue
Cancer begins when cells lose the ability to regulate cell growth and division Tumor: mass of growing tissue
▪ Benign: tumors that will not spread to surrounding tissue (non cancerous)
▪ Malignant: tumors that can spread to other tissues and organs invading and destroying tissue (cancerous)
Metastasis: the spread of cancerous tumors beyond their original site to new places in the body
As cancer cells spread, they absorb nutrients, block nerve connections, and prevent proper functioning, disrupting the body’s balance
Cancer is caused by defects in the genes that regulate cell growth and division Inherited genes Viruses: interfere with cell cycle (mitosis)
▪ Ex. Human papilloma virus (HPV: an STD) can lead to cervical cancer or genital warts (non cancerous)
Radiation: causes mutations in DNA▪ Ex. X-rays, nuclear radiation, sunlight (UV Rays)
Chemicals: cause mutations in DNA▪ Carcinogens = chemicals that cause cancer▪ Ex. Chloroform and benzene (industrial solvents used
in production of drugs, plastics and synthetic rubber, small component in gasoline), cigarette smoke
Prevention by protecting your DNA from agents that cause cancer (not smoking, balanced diet with regular exercise)
Treatments Surgery: remove tumors to prevent spread of cancer
▪ Problem: cancerous tumors spread, so some cancerous cell may remain in the body forming new tumors
Radiation therapy: destroy cancer cells▪ Problem: also damages healthy cells in the vicinity and there
is a limit to how much a person can have Drug therapy (chemotherapy): using chemicals to
destroy cancer cells or just stop the growth of cancer cells▪ Problem: also damages healthy cells, uncomfortable side-
effects
Section 40-4
includes a knowledge of
which may include a
including including
which may consist of
which are classified as
The Study of Cancer
Symptoms Causes Treatments
Benign Malignant X-rays Sunlight Nuclear radiation
Surgery
Tumor Viruses Radiation Chemicals
Drug therapy
Radiation therapy
Blood Type of Donor
A
B
AB
O
Blood Type of Recipient
A B AB O
Unsuccessful transfusion Successful transfusion
Prentice Hall Biology Presentation Pro, 2002
Blood Types (review)Blood Types (review)
Humans: Humans: 4 Main types classified by their antigens4 Main types classified by their antigens Type A: Type A: A antigensA antigens B antibodiesB antibodies Type B: Type B: B antigensB antigens A antibodiesA antibodies Type AB: Type AB: A & B antigensA & B antigens no antibodiesno antibodies Type O: Type O: no antigensno antigens A&B antibodiesA&B antibodies