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Aminoglycosides
bacteriocidal. Freeze the 30s subunit of tRNA,
causing frameshift in protein synthesis by
misreading of DNA. Effective on Gram -ves. Can
be used as a synergist with penicillin - enters
cell after cell wall destruction. e.g.
streptomycin.
Tetracyclines
bacteriostatic. Broad spectrum antibiotic.
Bind to acceptor site of ribosome, 30s subunit.
e.g. tetracycline, deoxycycline.
Macrolides
bacteriostatic. Prevent translocation of the
50S subunit of tRNA from A to P site. Active
against Gram +ves and mycoplasma e.g
erythromycin, azithromycin.
Lincosamides
bacteriostatic. Broad-spectrum. Inhibits
protein synthesis.
Chloramphenicol
bacteriostatic. Broad-spectrum. Inhibits
protein synthesis. Only used for bacterial
meningitis as it can be toxic.
Oseltamivir (Tamiflu): Interupts action of neuroaminidase
Non-Antibiotic mode of action (NA)(cleaves bond between syalic acid and
haemagluttinin (HA))
Amphotericin B and Nyostatin Bind to ergosterol and form pores in the fungal
membrane.
5-flurocytosine
inhibits cytosine deaminase, inhibits fungal
protein, DNA, RNA synthesis.
Echinocandin
inhibits beta-glucan chains in the fungal cell
wall.
Optochin
for alpha haemolytic Streptococci. If resistant,
"viridans" streptococci. If sensitive, S.
pneumoniae.
Campylobacter jejuni
(only if severe): Macrolides (see above)
Giardia lamblia:
Though this is not a bacteria, it can be treated
with metronidazole.
HIV:
treatments targeting: reverse transcriptase,
DNA integration, protease, HIV binding.
Vaccines difficult to develop due to mutation
(reverse transcriptase often makes mistakes).