Bacterial Growth & Nutrition Flashcards

1
Q

Describe general mechanisms of toxin action.

A
  1. damage cellular membrane (ex: staphylococcus aureus alpha-toxin)
  2. inhibit protein synthesis (ex: shiga toxin)
  3. activate host cell receptor => pathological signaling cascade (ex: C. diff)
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2
Q

Describe the role of type III secretory apparatus in gram negative bacterial pathogenesis.

A
  • composed of rings on the membranes and a hollow tube that acts as a needle
  • effector proteins are transferred from the bacteria into the injected host cell
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3
Q

Describe and outline the mechanisms of DNA, protein, and peptidoglycan synthesis. Identify specific steps that can be interrupted by antibiotic drugs.

A

DNA REPLICATION

  • carried out by DNA polymerase
  • both strands act as templates
  • novobiocin and synthetic quinolones inhibit DNA gyrase (disentangles finished replication products; unique from eukaryotic DNA gyrase)

PROTEIN SYNTHESIS

  • mRNA is translated by the ribosomes
  • mRNA transcription and translation are coupled (occur simultaneously)
  • antibiotics target the ribosome (erythromycin, tetracycline, streptomycin, spectinomycin)

PEPTIDOGLYCAN SYNTHESIS

  • subunits synthesized in cytoplasm
  • transferred across membrane by carrier proteins
  • cross-linked to existing peptidoglycan on outer membrane (facilitated by penicillin-binding proteins that make and break linkages during peptidoglycan maturation)
  • penicillin inhibits penicillin binding proteins (various drugs attack at each of these steps)
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4
Q

List the major steps in metabolism. How is this useful in understanding pathogenesis and treatment?

A
  1. nutrient molecules enter cell
  2. central metabolic pathways partially convert to energy by breakdown
  3. fermentation or respiration to remove more energy

USEFUL B/C

  • knowing requirements for energy production shows which environment best suits infection for that pathogens
  • identification of pathogen by preferred method of energy production
  • identifying toxic by-products of metabolism allows us to use reagents to combat bacterial defenses against them
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5
Q

Describe the siderophore system.

A
  • siderophores are secreted by host cells
  • sequester divalent cations in the ECF (ex: iron) to keep the free amount limited
  • bacteria have evolved to take in siderophore-cation complexes
  • dissociates in the cytoplasm
  • frees up nutrients for energy
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6
Q

Define and differentiate between fermentation and respiration. Describe the relevance of each in pathogenesis and diagnosis.

A

RESPIRATION
- def: electron transport and oxidative phosphorylation (via proton gradient)
=> drugs: disintegrate the cell envelope => destroy the gradient => kill cell
- causes buildup of ROS that must be removed by peroxidase (H2O2) and superoxide dismutase (superoxides)
=> drugs: H2O2 used as antimicrobial agent; overwhelms antioxidant enzymes

FERMENTATION

  • less efficient
  • anaerobic
  • can measure metabolic products
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7
Q
Describe the possible outcomes when bacteria encounter a specific environments. 
- general stress response
- pathogenic stress response
=> ex: location specific
=> ex: temporal
A
  • general stress response: starvation (sporulation) and heat (heat shock proteins)
  • pathogenic stress response: toxins and pili
    => salmonella enterica produces different type 3 systems and effectors depending on what location it inhabits
    => cholera must activates genes in a temporal sequence to induce pathogenesis (1. determine location. 2. adherence and colonization. 3. toxin)
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8
Q

List methods of entry for nutrients.

A
  1. facilitated diffusion
  2. active transport
  3. siderophore system
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9
Q

What factors determine rate of bacterial growth in cell culture?

A
  • nature of medium and presence of necessary nutrients
  • oxygen status
  • temperatures
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10
Q

exotoxin examples

A
  • botulinum does not grow well in the body so it doesn’t usually spread once inside; however, the exotoxin is very potent and can spread
  • enterotoxin isn’t fatal but assists in spread of organism by expelling spores in feces
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11
Q

List the major cellular targets of antibiotics.

A
  1. peptidoglycan synthesis (penicillin)
  2. RNA polymerase
  3. cell membrane
  4. ribosome inhibitors
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12
Q

List types of adaptive responses.

A
  1. sporulation in response to starvation
  2. heat shock proteins in response to heat to protect
  3. DNA repair in response to mutagenesis
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13
Q

Recall the phases of growth in culture.

A
  1. lag phase - no growth
  2. exponential growth - doubles over time
  3. stationary phase - growth = death; due to decreasing nutrients and buildup of toxins
  4. death phase
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