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90 Cards in this Set

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Eukaryotes
Light microscope allowed differentiation. have high degree of internal complexity, have a true nucleus enclosed by a membrane, membrane bound organelles, mitosis, and complex lipids
Prokaryotes
Archea and bacteria, no nucleus, no membrane bound organelles, have D-amino acids, have muramic acid
Why are things that prokaryotes have important?
We can take advantage of these uniquely prokaryotic structure to serve as targets for the action of antibiotics
Shapes of bacteria
1) Cocci- Sphere
2) Bacilli- Rod
3) Vibrios- Comma Shaped
4) Spirochetes- helical, flexible
5) Spirilla- helical, rigid
6) Staphylococci- grapelike group of cooci
7)Streptobacilli- long line of connected rod shaped cells
Why are gram-stain and shape so important?
They are stable characteristics that help identify bacteria
Structure of Capsule or Slime Layer
Slime is a mucilaginous exterior covering with no distinct boundaries. Capsule is a mucilaginous exterior covering with optically distinct boundary
Chemical Composition of Slime layer
Variable.
Generally made of either protein or complex carbs.
Function of Capsule or Slime Layer
No metabolic function. Probably prevents dessication. Often absent in laboratory cultured cells. WIthin the host the capsule can increase virulance by avoiding phagocytosis due to slipperiness. The capsule can also serve as a disguise by mimicing molecules on the host tissue. Finally, the capsule can promote adherence. Some capsular material is antigenic- results in Quellung Rxn.
Gram Positive Cells
Stain Purple. Cell surface is delineated by cell wall that is relatively thick and composed of a thick layer of covalently bonded peptidoglycan
Gram- Negative Cells
Stains pink. Outer layer is delineated by outer membrane followed by a thin cell wall with little peptidoglycan and little cross-linking and no peptide bridges.
Medical Significance of the cell surface.
1)It determine interaction with host defese mechanisms

2) Allows serological ID bc of antigens on surface

3)Provides many of the structures unique to bacteria that are targeted by abx's
Gram Stain History and Significance
Devised by Christian Gram in late 1980's. Central to ID'ing most bacteria in most situations. Can determine prognosis and treatment. More difference between gram neg and pos cells than between us and yeast.
Gram Stain Procedure
-Sample dried and fixed on side
-flooded with crystal violet, both pos and neg take it up
-Add gram's iodine that complexes with crystal violet to make large conjugate (mordant)
-Washed with alcohol removes complexed stain from neg because of thinner cell wall but pos retains the complex and stays purple
-Flooded with pink safranin stain which now only shows up in the neg cells
Cell Wall Biosynthesis and Antibiotics
All antibiotics that will work on gram neg will also work on gram pos cells. The steps of the process the abx targets are common to both cell types. Often takes longer and larger doses to work on gram negative because of the permeability barrier of the gram negative outer membrane
Cell Wall Synthesis
Occurs in 3 sites
1) Synth of water soluble peptidoglycan subunits in the cytoplasm (no ribosomes or rna)

2)Transfer to and modification of cell wall components at the cell membrane. Gram pos cells get peptidoglycan crosslinks here

3)Polymer growth at the cell wall
Antibiotics acting on Cell wall Biosynthesis
1) D-cyclosporine- inhibits racemase that converts l-alanin to d-alanine

2) Vancomycin- blocks subunit transfer from carrier lipid to growing peptide

3)Bacitracin- topical, blocks dephosphorylation to lipid carrier is not regenerted

4)Penicillin- inhibits transpeptidase reaction by preventing cross-peptide bridge formation
Lysozyme
-Not an Antibiotic
-an enzyme
-doesn't require cell to be actively growing
-won't affect gram neg until outer wall is removed
Function of Cell Wall
-Give shape and provide rigitidy under different osmotic conditions
-In the right osmotic condition some gram neg bacteria without cell wall (spheroplasts) can survive
Gram Negative Outer Membrane
-External to peptidoglycan cell wall
- made of phospholipid, protein, and lipopolysaccharide (LPS)
-Has porin proteins that make it sieve-like
Periplasmic Space
-Only in gram negative cells
-between outer membrane and cytoplasmic membrane
-variety of degradative enzymes, carrier enzymes
LPS
- only in gram negative
-Located on the outer leaflet of the outer membrane
-its carbohydrate groups face outward
Cytoplasmic Membrane Makeup
-Structure is same for gram pos and gram neg
-Phospholipid bilayer with proteins involved in cell envelope biosyntehsis, transport, and the cytochrome
Function of Cytoplasmic Membrane
-Selective permeability barrier
-Site of active transport
-site of oxidative phosphorylation through electron transport sytem
Bacterial Cytoplasm
-contains 50% of protein and most enzymes
-no membrane bound organelles
Visible Structures in Cytoplams
*only visible with electron microscope
-Chromosomes- single closed circular, double stranded
- Plasmids- autonomously replicating covalently closed circular DNA elements that cary greatly in size and don't encode info vital for growth but things like abx resistance
-Ribosomes- large RNA-protein complexes functioning in protein synthesis
Flagella
-imparts motility
-polymarized subunits of flagellin added at the tip
-very thin
-antigenic so of diagnostic value
-cells are peritrichous, monotrichous, or lophotrichous
Axial Filaments
-Spirochetes
-like flagella in structure and fx in motility
-originate at the poles and extend toward center of cell
-enclosed in the outer membrane of the cell so not external to the cell
Pili
-filamentous and made of protein
-pili are thinner and shorter than flagella
- Assembled from the base
-Don't confer motility
-work in attachment
-Function in Conjugation
Spores
-Bacillus and Clostridium
-sporulation is not a reproductive stage but instead is a mechanism for survival in poor conditions
-Resist killing by heat, drying, freezing, abx, and UV radiation
-Autoclave can kill
-Metabolically quiescent and dehydrated
Why do we like antibiotics directed against cell wall of bacteria?
Unique to bacteria so side effects are reduced
What kind of carbon compounds to bacteria of medical importance require?
Reduced carbon sources- they breakdown and oxidize them for energy.
All medically important bacteria are chemotrophs or phototrophs? Organotrophs or lithotrophs?
heterotrophs or autotrophs?
-Chemotrophs- obtain energy from a chemical sources, not the sun

-They get their energy from organic sources to they are organotrophs.

-Generate energy in tth form of ATP from electron transport chain and from substrate-level phosphorylation

-They are heterotrophs- need growth factors like vitamins, amino acids etc.
Temperature Requirements
-All are mesophilic (prefer 20-40 degrees C)
-temperature at which an organism grows best does not preclude it from growing at other temperatures (ex) listeria can grow at low temps)
Aerobes
Some bact like e-coli, neisseria, and mycobacterium are aerobic
- can be obligate and have to have oxy
- facultative and oxy is utilized but not required
- microaerophillic and need a little oxy but too much is bad (lots like this bc in bloodstream ex) gonorrheae)
Anerobes
Strepto and clostridium
-obligate anerobes- oxy is toxic (C. botulism)
-Aerotolerant- oxy is tolerated but not used
Toxicity of Oxygen
-All bacteria have enzymes capable of reacting with oxy can result in toxic hydrogen peroxide or superoxide

-aerobes and aerotolerant orgs have peroxidases and superoxide dismutase and catalase

-All obligate anaerobes lack superoxide dismutase +/- catalase

-Org lacking catalase may not be sesitive to oxy
Salt
-ok with 1-2% salt and most dont do well with more

-Exception is staphylococcus aureus that does well in up to 8%
PH
between 6-8 for most but as low as 1 and as high as 10
CO2
Some capnophilic bacteria do better with higher proportion of CO2 like that found in blood
Anabolic
Catabolic
Amphibolic
Anabolic- Building ex) synth of tryptophan

Catabolic- Breaking down ex) embden meyerhof (glycolic)

Amphibolic- link catabolism and anabolism ex)TCA cycle
Fermentation
Nonoxidative breakdown of carbs to yield energy good for differentiating bacteria based on products and types of carbs that can be fermented
Quiescent State
Very few bacteria cause trouble while in the quiescent state so if DNA replication is blocked then growth stops event hough bacteria may not be dead
Nalidixic Acid
inhibits bacterial DNA synthesis by inhibiting DNA gyrase which gets rid of supercoiling of DNA generated during replication
Transcription
DNA into RNA
-involves RNA polymerase sensitive to abx
Rifampcin
antibiotic that binds beta subunit of RNA polymerase and presents reading of DNA and transcription generally
Protein Synthesis
bacteria have 70s ribosomes (we have 80s) different enough to have antibiotics that target the bacterial ribosome but will cause side effects because we still have mitochondria with 70s ribosomes
Chloramphenicol
inhibits protein synthesis and peptidyl transferase- side effects
Bacteria Cellular Division
Divide by binary fission can be complete or incomplete and form two equally sized daughter.
Incomplete remain connected as in staphylococcus or streptobacilli
Population Growth
Generation time (20m-20h) is time it takes for population to double which depends on nutrients and physical and chemical environment
Measure Cell Growth
- by turbidity
- by bacterial mass
- plate count
Cell Death
a cell that cannot grow is said to be dead- what about vaccines
Mutation
-affect the production of the gene product or the products ability to act
-change in nucleotide sequence
Substitution Mutation
- change of one nucleotide for another
Insertion or Deletion
-One or more nucleotides are inserted or deleted
- can be a frameshift mutation if what is inserted or deleted is not a multiple of three
Mutagens
Agents that increase mutation frequency
- disrupts or interferes with normal ydrogen bodning
-UV light= Thymine Dimers
- Base analogs
- Relatively high mutation rate
Gene Transfer
-Plasmids
-lysogenic bacteriphages
- transformation
- conjugation
-transduction
Transformation
transfer of naked DNA released by donor cell though lysis or artificially through chemical extraction
- then recombination can occur=> transformation
Conjugation
Mating of two cell types
-e-coli
-males have F factor (autonomously replicating plasmid) F+
- F factor can integrate into chromosome
- F+ and F - mating- F+ donates copy of F factor
- F and F'- F prime is f+ that integrated into chrom and excised improperly taking a small frag of dna with it

-HFR and F- has whole chromosome and can integrate
R Factors
plasmids that transmit resistance to one or more antibiotics ex) shigella
Bacteriocinogenic
plasmids that encode products that kill other bacteria ex) Colv
Transduction
transfer of genetic info by a phage can be either
- generalized- during packaging of virus picks up strand of bacterial DNA accidentally
-specialized- involves particular phage that carries restricted region of DNA that is often adjacent to phage insertion site
Selective Media
inhibit the growth of certain bacteria while allowing the growth of other bacteria
Differential Media
Distinguish one type of bacteria from another based on physiological differences which are indicated by color changes in the media or bacterial colony ex) MacConkey Agar
Importance of immunology
-can benefit host with immunity or harm with autoimmune disease
-can id infectious organisms through serology
-skin testing for atopic dematitis
Innate Immunity
-non specific
- first line of defense
-rapid
-no memory
- skin, mucous, tears, saliva, cilia involved
- humoral factors like complement, cell secreted factors like cytokines, and host leukocytes
Inflammation in Innate Immunity
- bacteria enter
- swelling, redness, pain, and heat
- infiltration of plasma and leukocytes
Phagocytes
Neutrophils, dendritic cells, macrophages
- can phagocytose and kill bacteria
- can produce chemical messages that attract more host antibacterial cells (cytokines)
- Process and internalize bacteria and present to lyphocytes
Bactericidal Mechanism
-antimicrobial peptides that damage mebranes
- opsonization- host molecules bind to and cause enhanced uptake of bacteria by phagocytes
-phagocytosis
Adaptive Immunity
-Second line of defense
-Specific to antigens
-generated over time
-characterized by immunological memory
Initiation of Adaptive Immunity
Dendritic cells, macrophages, and B Lymphocytes are antigen present, present to T Cells that become activated, proliferate and generate clones that are specific to the antigen
Types of Lymphocytes
All originate in bone marrow
1)B lymphocytes differentiate in bone marrow and become antibody secreting plasma cells when activated by antigen
2) T Cells differentiate in the thymus to become either Helper T cells or cytotoxic T cells
Humoral Immunity
mediated by antibodies
-recognize and bind to antigens on bacteria to help clear the bacteria by preventing it from binding to or entering host or opsonizing it or fixing complement
Cellular Immunity
Deal with bacteria within host cells
mediated by T cell that provide help (cytokines) or kill host cells harboring intracellular bacteria
Antibody Structure
Two identical heavy and two identical light chains with variable regions of amino acid sequence and has two binding sites (Bivalent) which allows cross-linking and agglutination
IGM
On B cell surfaces
complement fixation and agglutination
primary immune response
IGG
In tissue spaces
complement fixation and neutralization
Secondary Immune Response
IGA
In secretions
neutralization on mucosal surfaces
IGE
Mast Cell sensitization
IGD
receptor for antigen on B cells
Serology
Diagnostic science that allows ID of specific antimicrobial antibodies in serum or microbes/microbial antigens through the se of antimicrobial antibodies
Types of Lymphocytes
All originate in bone marrow
1)B lymphocytes differentiate in bone marrow and become antibody secreting plasma cells when activated by antigen
2) T Cells differentiate in the thymus to become either Helper T cells or cytotoxic T cells
Humoral Immunity
mediated by antibodies
-recognize and bind to antigens on bacteria to help clear the bacteria by preventing it from binding to or entering host or opsonizing it or fixing complement
Cellular Immunity
Deal with bacteria within host cells
mediated by T cell that provide help (cytokines) or kill host cells harboring intracellular bacteria
Antibody Structure
Two identical heavy and two identical light chains with variable regions of amino acid sequence and has two binding sites (Bivalent) which allows cross-linking and agglutination
IGM
On B cell surfaces
complement fixation and agglutination
primary immune response
IGG
In tissue spaces
complement fixation and neutralization
Secondary Immune Response
IGA
In secretions
neutralization on mucosal surfaces
IGE
Mast Cell sensitization
IGD
receptor for antigen on B cells
Serology
Diagnostic science that allows ID of specific antimicrobial antibodies in serum or microbes/microbial antigens through the se of antimicrobial antibodies