Antimicrobial Chemotherapy 1 Flashcards

1-5

1
Q

Describe what is meant by MIC.

A

Minimal inhibitory concentration.
= the concentration of antimicrobial needed to inhibit growth of bacteria.

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2
Q

Describe what is meant by MBC.

A

Minimal bactericidal concentration.
= The minimum concentration of microbial required to kill a given organism.

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3
Q

Describe what is meant by sensitive bacteria.

A

Sensitive bacteria are inhibited or killed by antimicrobial available at site of infection.

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4
Q

Describe what is meant by resistant bacteria.

A

Resistant bacteria are not killed or inhibited by antimicrobial at site of infection.

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5
Q

Describe what is meant by bactericidal antimicrobials.

A

Bactericidal antimicrobials kill bacteria.

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6
Q

Describe what is meant by bacteriostatic antimicrobial.

A

Bacteriostatic antimicrobials inhibit bacteria.

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7
Q

Describe what is meant by synergy.

A

Antimicrobial synergy is where two agents exert greater activity when added together.

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8
Q

Describe what is meant by antagonism (in antimicrobials)

A

This is when the exertion from the combination of two agents is lesser than expected from the addition.

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9
Q

State the 3 different mechanisms of action of antibiotics.

A

Inhibition of cell wall synthesis.
Inhibition of protein synthesis.
Inhibition of nucleic acid synthesis.

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10
Q

Describe the process of inhibition of cell wall synthesis in Beta-Lactams (Penicillin).

A

Beta-Lactams are effective mostly against Gram-positive bacteria.
For the cell wall to be synthesised (in tact), the proteins of the cell walls need to be cross-linked.
So, Penicillin inhibits peptidoglycan synthesis by inhibiting enzymes (penicillin binding protein) responsible for cross linking the carbohydrate chains.

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11
Q

Describe Beta-Lactams.

A

Beta-Lactams are antimicrobials that inhibit cell wall synthesis.
They posses a Beta-Lactam ring within their structure.

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12
Q

Describe the process of inhibition of cell wall synthesis by glycopeptides.

A

Act on cell wall a stage prior to Beta-Lactams.
They inhibit the assembly of peptidoglycan precursor.
The PBP is taken up by glycopeptides.

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13
Q

Describe glycopeptides.

A

Glycopeptides are bactericidal antibiotics and their inability to penetrate the gram-negative cell wall means they only act on gram-negative organisms.
e.g. Vancomycin, Teicoplanin

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14
Q

Describe the process of inhibition of protein synthesis by aminoglycosides.

A

The binding of aminoglycosides to the 30s subunit of the ribosome, impairs translational proof reading leading to misreading of RNA message premature termination and inaccuracy of the translated protein.

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15
Q

Describe aminoglycosides.

A

Concentration dependent bactericidal antibiotics.
Useful in treatment of serious gram negative infection (e.g. gentamycin)

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16
Q

Describe the process of inhibition of protein synthesis by macrolides and tetracyclines.

A

Macrolides inhibit the bacterial protein biosynthesis, by preventing peptidyltransferase from adding the growing peptide attached to tRNA to the next amino acid as well as inhibiting ribosomal translation.

17
Q

Describe a macrolide.

A

Macrolides depend on concentration and bacterial species.
These are bactericidal and bacteriostatic.
(e.g. erythromycin, clarithromycin)

18
Q

Describe the process of inhibition of protein synthesis by oxazolidinones.

A

They prevent two subunits (of the ribosome) from meeting, stopping protein synthesis.

19
Q

Describe tetracyclines.

A

Tetracyclines are bacteriostatic antibiotics.
Used for treatment of Gram positive infections.
Bacteria have become increasingly resistant.

20
Q

Describe oxazolidinones.

A

Bacteriostatic and bactericidal treatment of gram positives.
(e.g. linezolid, used for serious MRSA infection, given orally)

21
Q

Describe cyclic lipopeptides.

A

These are strong bactericidal antibiotics used for treatment of gram positive bacteria.
e.g. daptomycin

22
Q

Describe the process of inhibition of protein synthesis by daptomycin.

A

Aggregation of daptomycin alters the curvature of the membrane, creating holes.
This leaks ions out of the cell, causing rapid depolarisation = loss of membrane potential.
= inhibition of protein, DNA, RNA synthesis.
= CELL DEATH>

23
Q

Describe, generally the inhibitors of nucleic acid synthesis (purine synthesis)

A

Inhibition of DNA synthesis either directly or indirectly by interrupting the supply of precursors for DNA synthesis.
Bacteriostatic, when combined Bactericidal.

24
Q

Name some examples of inhibitors of nucleic acid synthesis (purine synthesis stage).

A

Trimethoprim (UTIs or chest infections)
Sulphamethoxazole (when combined cotrimoxazole).

25
Q

Describe fluoroquinolones.

A

These are bactericidal.
They are effective against gram-negative organisms.
They inhibit DNA synthesis by working on DNA gyrase.
(e.g. ciprofloxacin, levofloxacin).

26
Q

Name some examples of fluoroquinolones.

A

Ciprofloxacin
Levofloxacin