Antibiotics Flashcards

1
Q

Difference between bacteriostatic and bactericidal antibiotics?

A
Bacteriostatic = prevent growth and allow immune system to kill
Bactericidal = kill bacteria directly
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2
Q

When should you start a broad range antibiotic? What are the side effects?

A

If the microbe is unknown and treatment needs to be started immediately. Causes disruption of natural flora and Gi distress.

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3
Q

What does an antibiogram consist of?

A

Susceptibility profile including Minimum inhibitory concentrations (MIC). Identifying effective therapies to exceed MIC and MBC levels.

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4
Q

What are common side effects of antibiotics?

A

Tetracycline = discoloration of teeth
Streptomycin = auditory damage
Chloramphenicol = anemia
- alters flora, diarrhea, prophylaxis, Abx Resistance

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5
Q

What is the problem with treating C. Difficle?

A

The antibiotics used to treat C.Diff can also prevent the natural flora from recolonizing allowing C.Diff to continue to populate without competition.

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6
Q

How can bacteria develop resistance?

A

Horizontal gene transfer and spontaneous mutations.

  • modify abx or target
  • reduction in abx concentration by pumps/permeability
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7
Q

What are the key differences in Gram Positive vs Negative?

A

Gram Positive = Significant amount of peptidoglycan layer and no outer membrane
Gram Negative = small amount of peptidoglycan with an outer membrane and porins

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8
Q

What are the three main steps in synthesis of peptidoglycan?

A
  1. Synthesis of the precursors that have the terminal D-Ala + D-Ala
  2. Transport across the membrane to the extracellular space
  3. Polymerization and cross-linking of L-Ala+L-Ala to Lys and D-Ala
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9
Q

Where do beta-lactams work and how?

A

Beta-Lactams bind Penicillin Binding Proteins (PBPs) inhibiting them from cross-linking the peptides to make peptidoglycan. Beta-Lactams mimic the natural substrate in the active site.

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10
Q

What are the two types of resistance from penicillin?

A

Encoding Beta-Lactamases and extended spectrum that degrade more than one B-lactams
Mutations of PBP

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11
Q

What organism has B-lactamase encoded in their genome?

A

Pseudomonas. (E. Coli is frequently resistant as well)

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12
Q

What type of organisms usually have Beta-Lactamase compared to mutations in PBP?

A

Beta-Lactamase = Gram Negative

PBP Mutations = Gram Positive

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13
Q

How can you overcome an organism with B-lactamase?

A

Clavulanic Acid inhibits the B-lactamase and use a B-lactam at the same time.

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14
Q

What are the most common organisms that are gram positive to become resistant to B-lactams?

A

Streptococcus and Staph (MRSA)

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15
Q

How can you overcome gram positive cocci that is resistant to B-lactams?

A

There is not a remedy other than using a different type of antibiotic such as Vancomycin.

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16
Q

What is a common Glycopeptide and how does it work?

A

Vancomycin. Binds the D-Ala-D-Ala end of the precursor peptide to prevent synthesis of peptidoglycan.

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17
Q

When is Vancomycin primarily used?

A

Gram Positive organisms when resistant to B-lactams.

Can’t fit well through outer membrane of gram negative

18
Q

What organism is typically associated with vancomycin resistance?

A

enterococci in hospital settings. Vancomycin-Resistant Enterocci. (VRE) Be aware it can transfer the resistance to Staph if in the same wound or area.

19
Q

Where does cycloserine act in peptidoglycan synthesis?

A

Structurally similar to D-Ala, prevents the D-Ala-D-Ala synthesis due to having higher affinity than endogenous substrate and preventing cross-linking.
-inhibits Alanine Racemase and Synthase

20
Q

When is cycloserine usually used?

A

Used as a second-line therapy for TB treatment.

21
Q

How does Bacitracin work and where is it used?

A

Binds to Bactoprenol-PP preventing the recycling of lipid carriers moving peptidoglycan.
– TOPICAL ONLY – Used for both Gram +/-

22
Q

What are the two lipopeptides in the class and how do they work?

A

Daptomycin - Gram Positive Only - binds cytoplasmic membrane, narrow spectrum.
Polymyxins - Gram Negative - binds LPS on outer membrane. Toxic, limited use.

23
Q

What are the difference between bacterial ribosomes and human?

A

Bacterial - 30S and 50S = 70S

Human - 40S and 60S

24
Q

What do the tetracyclines target and what are in the class?

A

Tetracyclins target - 30S subunit to inhibit protein synthesis. Broad spectrum/bacteriostatic
Include: Doxycyline, Tetracycline, and Minocycline

25
Q

How can an organism become resistant to Tetracyclines?

A

Efflux Pumps and Ribosome mutations.

- Much more common/wide spread due to overuse

26
Q

What can be used on hard to kill Gram Negatives such as Pseudomonas Aeruginosa?

A

Aminoglycosides. Irreversibly bind 30S causing misreading and inhibition of protein synthesis.

27
Q

How are aminoglycosides typically resisted by bacteria?

A

Modifying the antibiotic with transferases inactivating it.

28
Q

How do Macrolids work and who do they work on?

A

Gram Positive. Bacteriostatic. Binds 50S and blocks elongation. Useful when allergic to B-lactams.
Included: Erythromycin and Azithromycin

29
Q

How can bacteria become resistant to Macrolids?

A

Methylating the binding site on the 50S blocking the abx

30
Q

What kind of infections is Chloramphenicol typically used for?

A

Severe infections like Typhoid or Rocky Mountain Fever, due to causing anemia because of nonselectivity.
- inhibits pepidyl transferase

31
Q

What kind of bacteria does Clindamycin usually treat?

A

Gram Positive - Community MRSA and S. Aureus (skin)

–binds 50S preventing elongation– Bacteriostatic

32
Q

What kind of cross reactivity does Clindamycin have?

A

If the bacterium is resistant to Macrolids, then they are also resistant to Clindamycin.

33
Q

How does Linezolid work?

A

Binds a unique site of the 50S Ribosome preventing formation of the 70S complex.
Gram Positive Only

34
Q

When would someone use Linezolid?

A

Used with complicated skin and structure infections, can become resistant by a single point mutation of the ribosome. Usually Staph strains.

35
Q

What are the inhibitors of DNA synthesis?

A

1st Generation - Nalidixic Acid - narrow
2nd Generation - Fluoroquinolones - Broad
- Cipro, Levo, Moxi

36
Q

What is the mechanism of action of DNA synthesis antibiotics?

A

Binds DNA Gyrase/Topoisomerase disrupting DNA replication and repair.
Resistance: Point mutations and Drug modification

37
Q

What is Metronidazole commonly used to treat?

A

Typically Anaerobic infections due to targeting DNA with free radicals.
– C. Difficle Treatment

38
Q

What are two RNA Polymerase inhibitors?

A

Rifampin and Fidaxomicin

-binds RNA Polymerase inhibiting it’s action

39
Q

What are two inhibitors of the Tetrahydrofolate pathway?

A

Sulfonamides - similar to p-aminobenzoic acid

Trimethoprim - inhibits dihydrofolate reductase

40
Q

When two antibiotics complement one another’s action they are thought to be?

A

Synergistic

41
Q

Why do bacteriostatic and bactericidal drugs not work well together?

A

Due to the bactericidal drugs killing the bacterium when they are dividing, but bacteriostatic prevent them from dividing.

42
Q

Where are biofilms typically located and how do they effective treatment?

A

Biofilms are usually found on implanted devices or tubes and the bacteria can reside there unaffected by antibiotics. Only cure is to remove the device.