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70 Cards in this Set

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Describe the defining characteristics of bacteria. Compare and contrast them to eukaryotic cells.
Outline the basic structure of bacteria including any special features.
Cell membrane
Peptidoglycan cell wall (no sterols)
Nucleoid; circular DNA chromosome
No introns
free floating ribosomes (70S)
Cell membrane
Peptidoglycan cell wall (no sterols)
Nucleoid; circular DNA chromosome
No introns
free floating ribosomes (70S)
Describe the 3 major morphological types of bacteria. Give examples of each and describe their characteristic clumping patterns.
Note: Vibrio are a type of bacilli (curved rod or comma shaped); 
Cocci: may arrange as grape-like clusters (Staph) or in chains (Strep), or in pairs (aka diplococci)--example: Neisseria form characteristic kidney bean shaped pairs.

Bacilli (a...
Note: Vibrio are a type of bacilli (curved rod or comma shaped);
Cocci: may arrange as grape-like clusters (Staph) or in chains (Strep), or in pairs (aka diplococci)--example: Neisseria form characteristic kidney bean shaped pairs.

Bacilli (aka rods)
Describe the steps of the gram staining procedure for bacteria. Define the test colors for a gram + vs. gram - bacterium.
1. Fixation of bacteria to slide with heat
2. Stain with crystal violet (all bacteria turn purple)
3. Iodine tx (gram + will stay purple)
4. Decolorize using EtOH (leaches out purple from gram-)
5. Counterstain with safrinin (makes gram- visib...
1. Fixation of bacteria to slide with heat
2. Stain with crystal violet (all bacteria turn purple)
3. Iodine tx (gram + will stay purple)
4. Decolorize using EtOH (leaches out purple from gram-)
5. Counterstain with safrinin (makes gram- visible again)

Gram stain a fast, cheap way to narrow down differential and candidate pathogens
Describe the differences in the external features of cell walls between Gram + and Gram - bacteria.

What is the role of peptidoglycan in bacteria? How is this exploited medically?
Peptidoglycan is unique to bacterial cells and it helps them retain their shape. It is exploited because it is a good drug target and well as target for innate immunity (i.e. lysozyme cleaves it). It is particularly vulnerable to the following drugs: cephalosporins, vancomycin, penicillins.
Describe the differences in the composition of the cell walls between Gram + and Gram - bacteria.
Gram +: no outer cell membrane, thick peptidoglycan layer, capsule, teichoic acid (can cause shock but rarer);

Gram -: Outer membrane, contains LPS/endotoxin (its LOS in Neisseria), thin peptidoglycan layer, has periplasmic space where beta lac...
Gram +: no outer cell membrane, thick peptidoglycan layer, capsule, teichoic acid (can cause shock but rarer);

Gram -: Outer membrane, contains LPS/endotoxin (its LOS in Neisseria), thin peptidoglycan layer, has periplasmic space where beta lactamases are found.
What is the third type of bacterial cell wall? Note: it does not stain gram + but is structurally different from other gram - bacteria.
Mycobacteria cell wall; stains with acid-fast stains. ex: mycobacterium tuberculosis
Describe the antigenic component of Gram + bacteria capable of causing shock.
Describe the antigenic component of Gram - bacteria capable of causing shock? Which portion is use for laboratory ID of the bacterium?
Lipid A--toxic/antigenic component
O-antigen used for lab ID
Lipid A--toxic/antigenic component
O-antigen used for lab ID
Describe the two types of bacterial glycocalyces; How do they function as virulence or pathogenic factors for the bacteria?
What are pili/fimbrae and what are they used for? Describe the pili of Gram + bacteria?
Describe the pili found in Gram - bacteria and their specialized functions.
Define adjuvant.
Adjuvant is a compound that increases the immunogenicity of an antigen. The most common adjuvant used in vaccines is Alum, an aluminum salt.
Define passive immunization.
It is the use of a immune serum to give an immediate resistance to an infection.
Define active immunization.
It is the act of immunizing with antigens to induce an immune response to a pathogen.
What is a live-attenuated vaccine?
It is a vaccine that contains a weakened virus that can replicate to limited extent.
Bacteriostatic
Refers to antimicrobial agents that <i>inhibit growth</i> and/or reproduction of bacteria <b>but</b> <i>does not kill them</i>.
Bacteriocidal
Refers to an antimicrobial agent that <i>kills </i>or irreversibly damages bacteria.;
Narrow spectrum antiobiotic
Refers to antimicrobial agents that are active against select groups of bacteria.;<br />Examples: older penicillins, macrolides, vancomycin (only effective against G+ bacteria)
Broad spectrum antibiotic
Antibiotic with activity against a wide array or bacteria including G+ and G- bacteria.;<br />These drugs often used to treat patients "empirically" before causative bacteria is a ID'd and when treatment delay could be detrimental.;<br />Examples: carbapenems, extended spectrum cephalosporins, newer fluoroquinones.
Critical items
Devices that enter the bloodstream or sterile parts of body (i.e. surgical instruments, implants, invasive monitors). These have potential to transmit infectious agents and MUST BE STERILIZED.
Semi-critical items
Devices in contact with mucous membranes or intact skin; Free of spores; Includes respiratory and anethesia equipment. These have moderate potential for transmitting infectious agents and must receive HIGH LEVEL DISINFECTION.
Non-critical items
Devices that are in contact with intact skin but NOT mucous membranes; Includes bedpans, BP cuffs etc..These have limited potential for transmitting infectious agents and require LOW LEVEL DISINFECTION.
Antiseptic (antisepsis)
The process of reducing microorganisms on living tissue (i.e. skin). It does NOT kill spores. ;An antiseptic is a chemical used to kill microorganisms on surface of skin and mucous membranes.
Disinfection
The process of killing many but not all, pathogenic microorganism (i.e. spores may survive).
Sterilization
The process of killing or eliminating all microorganisms, including bacterial spores. This process is carried out in health-care facilities by physical or chemical means.;
List the 6 methods of sterilization.
1. Steam/Autoclave2. Dry Heat3. Gas Plasma (i.e. STERRAD system)4. Liquid Sterilization (i.e. STERIS system)5. Gas (Ethylene Oxide)6. Filtration<br />
For steam/autoclave sterilization:1. Technique2. Use/Advantages3. Disadvantages
1. 121 degrees/15psi for 15 mins (standard)2. Good for surgical instruments; rapidly microbicidal; penetrates medical packing, most device lumens3. Damages microsurgical or heat sensitive instruments.
For ethylene oxide gas sterilization:1. Technique2. Uses/Advantages3. Disadvantages
1. Gas covers device instruments;2. Ok for most medical materials; gets into device lumens3. Requires additional aeration time to remove ETO residue (toxic)
For gas plasma sterilization:1. Technique2. Uses/Advantages3. Disadvantages
1. ;Portable Sterrad chamber filled with gas plasma (hydrogen peroxide) in vacuum under UV or microwaves (creates free radicals). Sterilizes instruments in ~1 hour.2. Good for endoscopes or temperature sensitive materials. Nontoxic.3. Some types endoscopes with small, narrow lumens can't be processed; Cellulose, linens and liquids can't be processed.
For Liquid sterilization describe:1. Technique2. Uses/Advantages3. Disadvantages
1. ;35% liquid paracetic acid (PAA) used; instruments immersed and sterilant flows through removing microbes, salt, protein.2. Rapid cycle (30-45 minutes); low temperature3. Can only be used for immersible instruments; Must use when needed--no sterile storage available.
List the 5 mechanisms by which viruses efficiently and effectively use their genomes?
1. No wasted space in genome (i.e. no junk DNA or RNA)2. Overlapping reading frames3. Ribosomal frame shifting4. Alternative splicing of RNA5. Polyprotein cleavage
Why do viruses have a high mutation rate?
1. Simple polymerase makes many mistakes2. No proofreading or error correction3. Some viruses do not have a second strand (so nothing to compare/correct against)
What is the significance of viruses high mutation rate?
1. Mutations can produce new antigens that avoid current immunity (i.e. influenza strains; aka antigenic shift).2. Mutations can lead to drug resistance (i.e. protease inhibitor resistant mutants of HIV)3. Integration of viral genomes can cause disease<br />(In addition, virus mutations can allow live vaccines to be made and also help epidemiologists trace disease in a population)
List the 4 types of virus interactions that facilitate changes in the viral genome.
1. Complementation2. Phenotypic mixing3. Recombination4. Reassortment<br /><br />
Define: Complementation
When a gene function of one virus replaces a mutated gene of another. Allows defective viruses to replicate and express their genes.;
Define: Phenotypic mixing
Exchange of capsid proteins. For example if 2 polio virus serotypes infect the same cell, the progeny might have capsids that are a mixture of each serotype.;
Define: Pseudotype
The genetic material of one virus in the capsid or envelope of another.
Define: Recombination
The exchange of genes by crossing over at regions of homology. Produces a hybrid virus which reproduces. Example: western equine encephalitis virus.
Define: Reassortment
The rearrangement of parts of a segmented genome to form a new set of segments. Example: influenza virus (antigenic shift), reovirus.
What is viral interference? How is this accomplished?
Refers to the fact that infection with one virus tends to prevent infection by another. Due to: blocking of receptors, competition for resources, production of interferon or other antiviral agents (stimulates immunity)
In terms of mutation which types of genomes are most susceptible?
RNA genomes are most susceptible to mutation (inherently unstable)--they average 1 mutation per generation.;<br />DNA genomes are pretty stable averaging 1 mutation per several hundred or thousand generations.
What is a conditional lethal mutation?
A mutation that allows a virus to grow only under certain conditions (i.e. temperature sensitive mutants or host range mutants).
Autograft
A transfer of one's own tissue to another site on the body. There is no transplant rejection with this type of graft.
Syngeneic graft
A tranfer of tissue between genetically identical individuals (e.g. identical twins). This type of transplant usually "takes" --minimal (if any) rejection. Note: this type of transplant is often referred to as an isograft.;
Xenograft
A transfer of tissue between different species. This type of graft is always rejected by an <u>immunocompetent host.</u> Immunosuppressive drugs would be needed for it to take.
Allograft
A transfer of tissue between genetically different members of the same species (e.g. human to human). This type of transplant is rejected unless the recipient receives immunosuppressive drugs.
Graft-versus-host disease (GVHD)
A special type of rejection that occurs with bone marrow transplantation. ;Mature T cells in the <i>grafted </i>bone marrow attack the recipient's tissues.;
List the 4 blood types in the ABO system and indicated the antibodies that each makes.
<u>Blood Type</u>A: makes anti-B antibodiesB: makes anti-A antibodiesAB: makes no antibodies against A or BO: makes anti-A and anti-B antibodies
Hyperacute rejection
The most severe and immediate form of transplant rejection. Results from recipient's pre-existing antibodies reacting to the graft. Most commonly caused by ABO blood type mismatch. Alternatively, may result from mismatched HLA.;<br />Note: this type of rejection is sometime called "white graft" rejection due to the appearance of the rejected graft (i.e. becomes white due to loss of blood).
Acute rejection
A type of transplant rejection in which the <i>recipient's T cells</i> become<i> reactive against</i> the<i> graft. </i>This process may takes several days to weeks.<b> Strongest immune reaction results from graft tissue that expresses MHC class II. </b>May also result from antigen presentation by APC's via MHC class I.;<b><br /></b>Note: Acute rejection is the most common type of rejection. It is the focus of most immunosuppressive therapies.;
Chronic rejection
A type of transplant rejection that takes months or years to develop. It results from the recipient's indirect immune recognition of the graft via MHC molecules or minor transplantation antigens. ;It is usually associated with the presence of antibodies to HLA-class I antigens in the graft. This type of rejection acts on the vasculature of the graft.;
Describe the Panel Reactive Antibody (PRA) test. What is it used for?
The PRA is a quick test for HLA-antibodies. ;Serum from the transplant recipient is tested against a panel of donor leukocytes to see if they have antibodies to HLA. ;The test is presented as a percentage 0-100%. A low % is good, whereas a high % suggests potential difficulty in finding a suitable transplant donor (i.e. recipient has too many anti-HLA antibodies).
Describe cross-matching in the context of transplantation.
It is a test to compare compatibility between donor and recipient based on ABO blood type antigens. It is the most basic type of pre-transplantation matching that must be done.;
Describe the immunologic mechanism of hyperacute rejection.
<img src="paste-20315195310083.jpg" />
Describe the immunologic mechanism of acute rejection (direct pathway).
<img src="paste-20581483282435.jpg" />
Describe the immunologic mechanism of acute rejection (indirect pathway).
<img src="paste-20860656156675.jpg" />Indirect pathway: recipient APC process antigen from donor cells and initiate immune response/rejection.
Describe the immunologic mechanism for chronic rejection.
<img src="paste-21238613278723.jpg" />Note: chronic rejection acts mostly on vasculature of graft.
What is the most common type of transplantation?
Blood transfusions
List the 3 major classes of drugs used to immunosuppress transplant patients.
1. Corticosteroids2. Cytotoxic drugs3. Monoclonal antibodies
List the 2 most commonly used immunosuppressive corticosteroids and their mechanism of action.
Prednisone and Prednisolone; they work by interfering with transcription factor for T cell activation. This results in a "knocked down" T cell response.
Describe the major effects of corticosteroid therapy on the immune system.
<img src="paste-23519240912899.jpg" />
List the monoclonal antibodies used for immunosuppressive therapy.
1. Muromonab (Visilizumab): binds to CD3 molecule on T cells.2. Daclizumab or Basiliximab: target IL-2 receptor; inhibits activated T cells.
List the newest treatments for transplant immunosuppressive therapy. How do they work?
Belatacept (CTLA4-IG): recombinant DNA produced protein; combines CTLA4 extracellular portion with Fc region of human IgG1 antibody. MOA: blocks co-stimulation of T cells by covering up B7.;
Describe the mechanism of GVHD.
<img src="paste-24318104829955.jpg" />
Describe the tissues reactions in the 4 grades of GVHD.
<img src="paste-24567212933123.jpg" />
Identify and describe the 3 main classes of helminths?
Define the following types of parasitic hosts:
Intermediate
Definitive
Zoonotic
Intermediate: A host in which the asexual cycle occurs or larva is present.
Definitive: a host in which the sexual cycle occurs or an adult is present.
Zoonotic: a host that exists in the environment.
List the 5 neglected parasitic diseases in the United States.
Identify the 5 classes of protozoa and their characteristic features.