Microbiology Lecture Exam #3

Examples of Single Tissue Autoimmune Diseases

Blood Cells:
Autoimmune hemolytic anemia (RBC)
Endocrine Organs:
Thyroid - Graves' disease, Hashimoto's thyroiditis
Pancreas - type I diabetes
Nervous Tissue-
Multiple sclerosis
Connective Tissue-
Rheumatoid arthritis

Symbiosis

Relationship between organisms living together

Commensalism

One organism benefit, the other is not affected

Mutualism

Both organisms' benefit (us and normal flora)

Parasitism

One benefits (parasite) and the other organism is harmed (host)

Amensalism

One organism produces a substance that kills or inhibits another organism. (Penicillium mold produces penicillin that kills bacteria)

What is normal microbiota (flora)?

Bacteria we pick up through life based on numerous factors such as birth, diet, and environment

What is the difference between resident microbiota and transient microbiota?

Resident stays with you and transient is temporary

How do these organisms interact with the host and when is the normal microbiota developed?

The host is generally going to be benefited by microbiota

Probiotics

Promote bacterial growth

Prebiotics

Provide food to microbiota

What are opportunistic organisms?

A pathogen that usually does not cause us harm but can take advantage of an opportunity if we are immunocompromised

When do opportunistic organisms cause disease?

1. Introduction of an organism into a different area of the body
2. Immune suppression
3. Changes in the microbiome (Microbial competition and antagonism)
4. Stressful conditions

How does contamination differ from infection?

Contamination: The organism is present. Infection: Organism overcomes host defense and multiplies

What are reservoirs?

Continual source of the pathogen

Zoonosis

Animal (non-human) reservoirs

Human carriers

May not show symptoms but can pass on to others (Typhoid Mary)

Non living reservoirs

soil, water, food, etc. (typically fecal contamination and fecal-oral transmission

Portals of entry

the way that the microbe gets into the body

Parenteral entry

Bypasses normal barrier to enter

Numbers required

How many of a specific organism takes to cause infection (ID50 and LD50) 50% of those exposed

Adherence (adhesion)

microbes that are capable of establishing disease

What are pathogens?

microbes that are capable of establishing disease

When does microbe induced disease occur?

when the microbe is in sufficient numbers and has breached host defense

***What is pathology?

The scientific study of disease

How are infectious diseases classified?

Symptoms: Subjective: changes sensed or felt by individual
Signs: Objective: changes that can be observed or measured by someone else
Syndrome: a disease process that has a specific set of symptoms and signs associated with a particular disease
Asymptomat

Etiology

What the cause of the disease is

Germ Theory of Disease

idea that infectious diseases are caused by microbes

Virulence Factors

Anything that allows the microbe to be better able to establish disease

Pathogenicity

The ability to cause a disease

Virulence

Degree to which an organism can cause a disease
virulence factors

Extracellular enzymes

coagulase and kinase

Exotoxins

Released by the cell

Endotoxins

Gram - cells Lipid A portion of LPS (fever, inflammation, diarrhea, hemorrhaging, blood coagulation

Predisposing factors

make you susceptible

Development: (stages of disease)

1. Incubation: time from when organism first infects to body to when symptoms are shown
2. Prodromal period: start to feel that something is wrong
3. Illness: Most severe signs and symptoms are present
4. Decline: Either you are getting better or dying
5.

Portals of exit

Orifices on the body

Transmission

How a disease transfers from one host to another

Contact (diseases)

- Direct: touching
- Indirect: Fomite (inanimate object that has pathogen on it)
- Droplet: Passed in droplets from a sneeze or cough <1m

Vehicle

Through airborne, waterborne, and foodborne

Vector

- Biological: A specific pathogen
- Mechanical: Random

Acute disease

Symptoms develop rapidly and end quickly

Chronic disease

Milder symptoms which last longer

Subacute disease

Ranges between acute and chronic

Latent

Disease that appears a long time after infection

Communicable

Disease transmitted from one host to another

Contagious

A disease easily passed from one individual to another

Noncommunicable

Disease is not passed from person to person

Epidemiology

The study of when and where diseases occur and how they are transmitted (John Snow 1854)

Incidence

Number of new cases of the disease

Prevalence

Total number of cases in same population

Occurrence

Frequency of outbreaks

Endemic

Low levels in the population all the time

Sporadic

The disease happens occasionally

Epidemic

Sharp increase in number of cases in certain location

Pandemic

Epidemic in more than one continent at a time

Notifiable diseases

If health care facility diagnosis individual, facility is required by law to report to local health officials

Descriptive Epidemiology

Go to the source and ask questions, index case

Analytical Epidemiology

Analyzing the information that was obtained during the descriptive stage, try to determine etiology, transmission, etc.

Experimental Epidemiology

Application of Koch's postulates if possible

Exogenous HAIs

Pathogen comes from the environment in the healthcare facility

Endogenous HAIs

Pathogen comes from the patient's normal microbiota; superinfections (Clostridium difficile)

Iatrogenic infectious (HAIs)

Doctor-induced"
Factors: Presence of microorganisms in hospital environment, presence of immunocompromised patient, Transmission of pathogen between staff and patients and between patients

Control of HAI's

Aseptic practices, disinfection, antisepsis, cleaning the rooms properly, cleaning linens properly

How does epidemiology connect to Public Health?

How the data is conveyed to the public
-Educating the public
-CDC (more towards epidemiology) and the NIH (more towards research)
-World Health Organization (WHO)
-State public health agencies and local public health agencies

Host Defense (3 lines)

- 1st Line of defense (innate) Physical and chemical barriers
- 2nd Line of defense (Innate) Cells and other chemicals
- 3rd Line of defense (specific/immune response) Humoral immune response (antibody); cell mediated immunity (cellular response)

Species resistance

property that protects a type of organism from infection by pathogens of other, very different organisms

Skin and mucous membranes - first line of defense

These form a physical and chemical barrier to prevent the entry of pathogens

Dendritic cells

Multibranched phagocytes (found throughout the body but especially in skin and mucous membranes); antigen presenting cells (APC)

Oil and sweat gland secretions

Drop the pH on the skin from 3-5

Defensins

Chains of about 20-50 amino acids that have antimicrobial properties; produced by the sweat glands (dermicidins), Produced by neutrophils in mucous; broad spectrum

Mucous membranes and Other defense mechanisms

Traps microbes, contains antimicrobial peptides and can contain antibody (part of specific defense)

Ciliary escalator

Cilia pushes the mucous back out so that it does not reach the lungs

Lacrimal Apparatus

Flushing system for the eye, glands produce tears

Normal Microbiota and Microbial Antagonism

Organisms of the normal microbiota compete with potential pathogens and invaders to keep them out, release chemicals which kill invading bacteria

Antimicrobial Peptides

Found in mucous, production is triggered when the system has microbes on the surface

Plasma Components

About 90% water, electrolytes (conduct electricity), proteins (immunoglobulin, clotting factors), Waste products, dissolved O2 & Co2, hormones.

Transferrin

Binds and transports iron in the body

Ferritin

Protein that stores iron in the liver

Siderophores

Proteins produced by microbes that try to bind to our iron; take iron from transferrin

Lactoferrin

Protein that takes iron back away from siderophores

Serum

Does not contain clotting factors found in plasma

Eosinophils

2-4%: important in inflammatory infections, allergies, parasitic infections, limited phagocytic activity

Basophils

0.5-1%; inflammation and possibly blood clotting

Monocytes

3-8%; blood precursor to the macrophage

Lymphocytes

20-25%; Smallest of leukocytes, involved in specific defense: B cells, T cells and NK cells (nonspecific)

Wandering macrophages

Travel throughout the body

Fixed macrophages

Resident population in a specific organ: Kuppfer cells in liver, alveolar macrophages in alveoli, microglial cells in CNS

Natural Killer cells

Non-T, non-B lymphocyte; nonspecific defense; kill altered self-cells by punching a hole in the membrane

Diapedesis

movement of cells out of the blood into the tissue

Left Shift (Shift to the Left)

indicates an active infection process; cells are less mature

Phagocytosis

The cell eats

Stages of phagocytosis

1. Chemotaxis: Movement of a cell toward or away from a chemical stimulus
2. Adherence: Sticks to the pseudopod
3. Ingestion: Microbe is brought to the inside of the phagocyte, food vacuole forms around it
4. Phagosome Maturation and Microbial Killing: ly

How do microbes try to evade phagocytosis?

Using capsules, along with other virulence factors

Nonphagocytic Killing

Extracellular killing by leukocytes

What is meant by a disorder of the immune system?

Any situation where the immune system does not function normally is considered to be a disorder. These are divided into two different categories: hyperimmune responses (hypersensitivity and autoimmunity) where the immune system responds to non-dangerous a

Hypersensitivity

This is an "over the top" response to non-dangerous, environmental antigens.
The antigen in this case is called an allergen.

Type I (anaphylactic reactions) - Immediate type hypersensitivity

Type I reactions are called immediate type because the reaction happens very quickly after the person who is sensitive is exposed to the antigen.
It involves the action of IgE and MAST cells, basophils and eosinophils. This can have a genetic component (r

Sensitization

This is the process that happens the first time the person's system "sees" the allergen as dangerous. It causes the production of IgE instead of IgG during the immune response. IgE is homocytotrophic - meaning that it can bind to the surface of our cells

Degranulation of Sensitized cells

This occurs when the sensitized individual encounters the allergen again. The allergen must bind to two different IgE molecules on the surface of the granulated cells. This is called cross-linking. It sends a signal into the cell to release the content of

Roles of Degranulating Cells

The cells release their chemicals. The first cells involved are the mast cells and the basophils. Their granules contain potent chemicals that cause inflammation. These chemicals include histamine (vasodilator and effects smooth muscles), kinins (inflamma

Clinical Signs of Localized Reactions

Localized reactions include itching (skin and mucous membranes), runny nose, watery eyes, sneezing, rashes (urticaria - aka hives), swelling, and constriction of smooth muscle tissue causing the symptoms of asthma.

Clinical Signs of Systemic Reactions (Acute Anaphylaxis)

While localized reactions are uncomfortable, and sometimes dangerous (asthma symptoms), systemic reactions can be quickly deadly. These reactions happen in response to certain types of antigens. These would include insect venoms, certain vaccines, certain

Diagnosis of Type I

The two major categories of testing for type I reactions are skin tests and blood tests. The skin test is typically the most common form used, even though your book mentions it as secondary. In skin testing, a small amount of the purified antigen is injec

Prevention of Type I

AVOIDANCE! That is the primary prevention. Your book lists examples of methods used to help allergy sufferers avoid antigens (p. 529). Immunotherapy (allergy shots) are very beneficial to some. The concept is to give very small doses of the allergen, buil

Treatment of Type I

This is typically treated using antihistamines and/or antileukotrienes that help neutralize the effects of those chemicals, corticosteroids that suppress the immune response, bronchodilators that help open up airways, and epinephrine that neutralizes the

Type II (cytotoxic reactions)

These are called cytotoxic reactions because they result in the destruction of cells in the sensitive person. Antibody against the cell binds to the cell forming an antigen-antibody complex. These complexes activate complement through the classical pathwa

Type III (immune complex reactions)

Type III reactions happen when antibody binds to a soluble antigen, forming an immune complex (still an antigen-antibody complex) which can stick in our tissues. These activate complement (if they are not cleared out by the macrophages) resulting in destr

Hypersensitivity Pneumonitis

Typically caused when allergens are inhaled deeply into the lungs - the disease is often named for the occupation of the individual, since certain occupations expose people to certain types of inhalable antigens.

Glomerulonephritis

In the kidneys - causes damage to the glomeruli in the nephrons, and ultimately can cause kidney failure.

Rheumatoid Arthritis (autoimmune)

In the joints - complexes are deposited in the tissues of the joint, damaging it, causing pain and deformity of the joint

Systemic Lupus Erythematosus (autoimmune)

Antibody is produced against self molecules (including nucleic acid), the complexes form and lodge, and damage the tissues. Lupus is considered a systemic autoimmune disease since multiple areas of the body are affected. It can damage the heart, lungs, jo

Tuberculin Response

A small amount of purified protein from Mycobacterium tuberculosis is injected into the skin and then checked for a Type IV reaction. This is an indicator of someone being exposed to the disease or actually having had it.

Allergic Contact Dermatitis

Classic example is the reaction to poison oak and poison ivy, metals, etc.

Autoimmune Disease

This is a failure of self-recognition. Something triggers the immune system to inappropriately respond to its own tissues.

Single-Tissue Autoimmune Diseases

These are autoimmune diseases that affect a specific type of tissue or specific organ.

Systemic Autoimmune Diseases

These are disease that affect multiple systems and tissue types such as lupus.

Immunodeficiency Diseases

These are the opposite of the hyperimmune response diseases. They involve the inability of the immune system to respond against infectious agents the way that it should. These fall into two groups

Primary (Congenital) Immunodeficiency Diseases

These are typically genetic disorders that affect one or more areas of the immune system. They include SCIDs (severe combined immunodeficiency) that wipes out the entire response system that involves lymphocytes, DiGeorge syndrome where there is no T cell

Secondary (Acquired) Immunodeficiency Diseases

Secondary imunodeficiencies are acquired after the person is born. These can be due to infectious agents (such as HIV/AIDS) or exposure to chemicals or other components that cause suppression of the immune response.