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Anaerobic ABC

A ctinomyces

B acteroides

C lostridium

Antimicrobial Agents - Inhibition of DNA and Protein Synthesis

Bacterial chromosome replication

DNA replication

Bacterial Topoisomerases 

maintain DNA in appropriate state of supercoiling 

cut and reseal DNA

DNA gyrase (topoisomerase II) introduces negative supercoils 

Topoisomerase IV decatenates circular chromosomes 

these are the targets of the quinolone antibacterial agents 

Quinolones

bind to bacterial DNA gyrase and topoisomerase IV after DNA strand breakage 

prevent resealing of DNA 

disrupt DNA replication and repair 

bactericidal (kill bacteria)

Fluoroquinolone is particularly useful against

Gram +ves: Staphylococcus aureus, streptococci 

Gram -ves: Enterobacteriacea; Pseudomonas aeruginosa 

Anaerobes: e.g. Bacteroides fragilis 

many applications e.g. UTIs, prostatitis, gastroenteritis, STIs 

Adverse effects

Relatively well tolerated

GI upset in ~ 5% of patients 

allergic reactions (rash, photosensitivity) in 1 - 2% of patients 

Inhibition of Bacterial Protein Synthesis 

Macrolides 

in 1952: Erythromycin was isolated as the first macrolide (Streptomyces erythreus) 

Newer macrolides: clarithromycin, azithromycin 

Structurally they consist of a lactone ring (14- to 16-membered) + two attached deoxy sugars 

Mode of action 

bind reversibly to bacterial 50S ribosomal subunit 

causes growing peptide chain to dissociate from ribosome → inhibiting protein synthesis 

bacteriostatic (stops reproduction)

Macrolides’ spectrum of activity

good antistaphylococcal and antistreptococcal activity 

treatment of respiratory & soft tissue infections and sensitive intracellular pathogens • e.g. Chlamydia, Legionella 

Adverse effects

Generally well tolerated

nausea 

vomiting 

diarrhoea 

rash 

Aminoglycosides

large family of antibiotics produced by various species of Streptomyces (“mycin”) and Micromonospora (“micin”) 

include: streptomycin, neomycin, kanamycin, gentamicins, tobramycin 

Structure = linked ring system composed of aminosugars and an aminosubstituted cyclic polyalcohol 

Mode of action of aminoglycosides

Bind irreversibly to 30S ribosomal subunit 

disrupt elongation of nascent peptide chain 

translational inaccuracy → defective proteins 

bactericidal 

Spectrum of activity 

broad spectrum; mainly aerobic G-ve bacilli (e.g. P. aeruginosa) 

used to treat serious nosocomial infections (hospital acquired infections)

First TB antibiotic

Used for cystic fibrosis 

Adverse effects

all aminoglycosides have low Therapeutic Index (only a small amount needed to become toxic)

renal damage, ototoxicity, loss of balance, nausea 

Medically Important Bacteria: Clasification

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Antibiotics: Protein Synthesis Inhibitors

Protein Synthesis

Formation of Initiation Complex (tRNA in P site)

aa incoorporation (tRNA in A site, aminoacyl-tRNA)

Formation of Peptide Bond (peptidyltransferase)

Translocation

MNEMONIC: “ALi  eSTá  Cuasi  MAL”

* Inhibit 1: “ALi”

A minoglycosides

Li nezolid

* Inhibit 2: “eSTá”

S treptogramins

T etracyclins

* Inhibit 3: “Cuasi”

C loramphenicol

* Inhibit 4:  "MAL"

M acrolides

A minoglycosides

L incosamides

Penicillin

Penicillin is a widely used antibiotic prescribed to treat staphylococci and streptococci bacterial infections. 

beta-lactam family 

Gram-positive bacteria = thick cell walls containing high levels of peptidoglycan

gram-negative bacteria = thinner cell walls with low levels of peptidoglycan and surrounded by a lipopolysaccharide (LPS) layer that prevents antibiotic entry 

penicillin is most effective against gram-positive bacteria where DD-transpeptidase activity is highest.

Examples of penicillins include:

amoxicillin

ampicillin

bacampicillin

oxacillin

penicillin

Mechanism(s)

Penicillin inhibits the bacterial enzyme transpeptidase, responsible for catalysing the final peptidoglycan crosslinking stage of bacterial cell wall synthesis.

Cells wall is weakened and cells swell as water enters and then burst (lysis)

Becomes permanently covalently bonded to the enzymes’s active site (irreversible)

Alternative theory: penicillin mimics D-Ala D-Ala

Or may act as an umbrella inhibitor

Resistance

production of beta-lactamase - destroys the beta-lactam ring of penicillin and makes it ineffective (eg Staphylococcus aureus - most are now resistant)

In response, synthetic penicillin that is resistant to beta-lactamase is in use including egdicloxacillin, oxacillin, nafcillin, and methicillin. 

Some is resistant to methicillin - methicillin-resistant Staphylococcus aureus (MRSA).  

Demonstrating blanket resistance to all beta-lactam antibiotics -extremely serious health risk.

Bacteria and fungi in petri dishes

Klari Reis uses plastics, paints and other mediums to create the idea of bacteria and biological matter within petri dishes

A fib =  no p wave 

Killed, inactivated Vaccines Available in the US

Killed vaccines induce only HUMORAL immunity

RIP   ACE 

R abies

I nfluenza (injected)

P olio (salk)

.

A Hepatitis

C holera 

E ncephalitis viruses (eg Japanese encephalitis)