Title: Antimicrobial Therapy
1Antimicrobial Therapy
- Chemotherapy any treatment of patient with
chemicals to treat a condition. - Now word associated with cancer treatment
- Our focus is on antimicrobial agents
- Antibiotics antibiotics, semi-synthetic, or
synthetic - Antibiotics natural products made by microbes,
effective against other microbes - Semi-synthetic antibiotics use natural
antibiotic as base, but modified chemically most
of our new antibiotics - Synthetic made chemically in their entirety
2Spectrum
- Some antibiotics are considered broad spectrum
- By definition, these are effective against many
types of bacteria, both Gram negative and Gram
positive - Broad spectrum antibiotics can sometimes cause
problems because of damage to normal microbiota
of host - Microbiota (not plants!)
- Superinfection may result from this situation
- Overgrowth of normal microbes that cause
disease - Increased susceptibility to newly acquired
microbes
3Selective Toxicity the key to antibiotic therapy
- 3 concentration ranges ineffective, effective,
and toxic. A drug needs to have a wide effective
(therapeutic) range.
Selective toxicity is the ability of the drug to
harm the target without harming the host.
Bacteria have many targets that are biologically
different from us that the drugs can hit. As the
target becomes more like us, there are fewer and
fewer drugs that are selectively toxic fungi,
protozoa, worms, viruses, cancer.
4Selective Toxicity and side effects
- Drugs may fail to be selectively toxic and
interfere with mammalian biochemistry. They may
cause allergies. They may destroy too many
normal bacteria.
5Actions of antimicrobials
- Drugs work against microbes by these basic
mechanisms - Inhibition of cell wall synthesis
- Causes bacterium to commit suicide, but only
during growth when cells are cutting their own
PG. - Disruption of membrane function
- Often toxic to humans because we have membranes
too, cause leakage of vital molecules. - Inhibition of protein synthesis many
antibiotics - Bind to ribosomal RNAs, proteins.
- Inhibition of nucleic acid synthesis
- Attack transcription, DNA unwinding enzymes
- Act as anti-metabolites competitive inhibitors,
inhibit function of enzymes, usually
bacteriostatic.
6Ideal Antibiotic
- Good drug properties (e.g. soluble in body
fluids) - Selectively toxic, obviously
- Easily administered
- Non-allergenic
- Stable in vivo, slowly broken down and excreted
- Difficult for microbe to become resistant to.
- Long shelf life (chemically stable)
- low
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7Measurement of Efficacy
- Disk diffusion assay
- Paper disks with antibiotic applied to lawn in
Petri dish - Zone of inhibition indicates susceptibility to
drug - Broth dilution test to measure MIC
- Minimum inhibitory concentration
- Drug is diluted in broth which is inoculated
- Clear broth indicates that bacteria did not grow
or were killed. - That concentration of drug that first inhibits
MIC
8 Why bacteria might be resistant
- They are that way naturally
- Gram negative cell wall prevents antibiotics from
entering the cell and reaching their targets. - Some bacteria have no cell wall, so no target.
- The way they infect
- Some bacteria enter cells where antibiotic conc
is low. - Some bacteria are mutated
- Mutation changes the target for the antibiotic.
- Bacteria acquire new genes
- The new genes provide ways to foil the drugs
9Mechanisms of drug resistance(How do they do it?)
- Alteration of target active site of enzyme
changes, change in ribosome means drug no longer
binds. - Antibiotic either cant get in or cant stay in
transport protein changes, drug no longer enters
drug that does enter is actively pumped out. - Enzymatic destruction of drug penicillinases
(beta lactamases) - End around inhibitor bacteria learns to use
new metabolic pathway, drug no longer effective.
10Attack by penicillinase
Bacterial enzymes (beta lactamases
penicillinases) destroy this ring. Penicillins no
longer work. Some penicillins were created to
resist these enzymes.
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11Human behavior and antibiotic resistance
- Bacteria once under control are making a comeback
due to antibiotic resistance - S. aureus, Enterococcus, M. tuberculosis, et al.
- Human behavior
- Most diseases caused by viruses, non-cellular,
not treatable with antibiotics (but Doctor, do
something) - Full time course needed last bacteria left are
the most resistant, if they arent killed, they
become normal dont stop regimen because you
feel better. - Social behavior
- resistance in homeless/poor
- growth stimulants in agriculture
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12Fighting antibiotic resistance
- Use all drug at sufficiently high concentration
- Dont allow the least sensitive bacteria to
survive - Drugs in combination
- Odds of mutating to resist 2 drugs 1 in 106 x
106 - Synergism e.g. amoxicillin and clavulanic acid
- Limit antibiotic use
- gt50 of infections are viral not affected by
antibiotics - Constant exposure breeds resistance
- New drugs
13Penicillins Penicillins
amoxicillin Amoxil
ampicillin Penbritin
co-amoxiclav Augmentin
flucloxacillin Floxapen
phenoxymethylpenicillin Penicillin V
Common antibiotics inhibiting cell wall synthesis
Cephalosporins Cephalosporins
cefaclor Distaclor
cefalexin Ceporex, Keflex
cefotaxime Claforan
Other
vancomycin Vancocin
bacitracin
14Common antibiotics inhibiting protein synthesis
Macrolides Macrolides
clarithromycin Klaricid
erythromycin Erymax, Erythrocin, Erythroped
azithromycin Zithromax
Tetracyclines Tetracyclines
doxycycline Vibramycin
oxytetracycline Oxymycin, Oxytetramix
tetracycline Â
Aminoglycosides Aminoglycosides
gentamicin Cidomycin
neomycin Nivemycin
Others Others
chloramphenicol Â
clindamycin Dalacin C
15Common antibiotics nucleic acid targets
Quinolones Quinolones
ciprofloxacin Ciproxin
levofloxacin Levaquin
Others Others
metronidazole Flagyl
rifampicin Â
Disruption of membrane function
Others Others
polymyxin B Anti-fungal drugs (several)
16Antimetabolites
trimethoprim Monotrim
sulfamethoxazole
Combinations Amoxacillin and clavulanic
acid Augmentin Trimethoprim and
sulfamethoxazole Bactrim Neomycin, bacitracin
polymyxin Neosporin