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Published byWilfred Marshall Modified over 9 years ago
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MECHANISMS OF ACTION OF ANTIBIOTICS
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BACTERIOSTATIC AGENTS Sulfonamides Drugs inhibiting protein synthesis except aminoglycosides (macrolides, chloramphenicol, tetracyclines etc).
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BACTERICIDAL AGENTS Beta lactams (penicillins, cephalosporins, imipenem) Trimethoprim/sulfamethoxazole Vancomycin Fluoroquinolones Aminoglycosides
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MECHANISMS OF ACTION Inhibitors of cell wall synthesis Drugs altering cell membranes Inhibitors of protein synthesis Antimetabolites Inhibitors of nucleic acid synthesis.
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DRUGS INHIBITING CELL WALL SYNTHESIS Penicillins Cephalosporins Imipenem Vancomycin Fosfomycin β-lactams
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www.uccs.edu/
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Plus penicillin Spheroplast Emerging Spheroplast Dividing Bacteria Division Growth site Growth
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www.chem.qmul.ac.uk/
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www.uccs.edu/
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Mur NAc X Glycopeptide Polymer X Mur NAc Glycopeptide Polymer X Glycopeptide Polymer D-Alanine Transpeptidase
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Penicillin Binding Proteins Transpeptidases Carboxypeptidases Endopeptidases Penicillin
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AUTOLYSINS
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All Beta lactam antibiotics act by the same mechanism
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PENICILLINS ACTIVE VS GRAM - BACTERIA
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S C C C C C NCOOH O CH 3 NC O R Penicillinase S C C C CNCOOH CH 3 N C O R OH O Penicilloic Acid (β-Lactamase)
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COMBINATIONS WITH BETA LACTAMASE INHIBITORS Penicillin plus a beta lactamase inhibitor.
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CEPHALOSPORINS AND IMIPENEM Same mechanism of action as penicillins but bind to different binding proteins.
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FOSFOMYCIN Inhibits peptidoglycan synthesis at an earlier stage than where the beta lactams act.
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Fosfomycin UDP-GNAc-pyruvate enol ether UDP-NAc-muramyl- L -Ala- D -Glu- L -Lys- D -Ala- D -Ala UTP + N-acetylglucosamine-1-P UDP-GNAc PP Phosphoenolpyruvate (Biel pp 24-26)
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VANCOMYCIN
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E nz y m e NAG-NAM D-ALA L-GLU LYS D-ALA Transpeptidase PENICILLINS X
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NAG-NAM D-ALA L-GLU LYS D-ALA E nz y m e VAN Transglycosylase
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RESISTANCE TO BETA LACTAMS Penicillinase Beta lactamases
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RESISTANCE Increased production of beta- lactamase (penicillinase) enzymes.
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S C C C C C NCOOH O CH 3 NC O R Penicillinase S C C C CNCOOH CH 3 N C O R OH O Penicilloic Acid
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METHICILLIN RESISTANCE Altered PBP’s.
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RESISTANCE TO OTHER BETA LACTAM ANTIBIOTICS Most prevalent mechanism is hydrolysis by beta lactamases. Cephalosporins have variable susceptibility to βlactamases. Some even induce formation of the enzymes.
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RESISTANCE TO VANCOMYCIN
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ANTIBIOTICS AFFECTING CELL MEMBRANES Polymyxins Daptomycin
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POLYMYXINS Surface active amphipathic agents. Interact strongly with phospholipids and disrupt the structure of cell membranes.
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DAPTOMYCIN Depolarizes the cell membrane
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ANTIBIOTICS INHIBITING PROTEIN SYNTHESIS Macrolides Clindamycin Linezolid Streptogramins Chloramphenicol Tetracyclines Aminoglycosides
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50S 30S Procaryotic Ribosome 70S-- M.W.2,500,000 60S 40S Eucaryotic Ribosome 80S--M.W. 4,200,000
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Antibiotics binding to the 50S ribosomal subunit and inhibiting protein synthesis Erythromycin and other macrolides Chloramphenicol Linezolid Streptogramins
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Antibiotics binding to the 30S ribosomal subunit and inhibiting protein synthesis Aminoglycosides Tetracyclines
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CLE an S AT
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Macrolides (Erythromycin, Azithromycin and Clarithromycin)
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aa A 50S 30S mRNA template Transferase site P Nascent polypeptide chain MACROLIDES TRANSLOCATION
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CHLORAMPHENICOL
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aa A 50S 30S mRNA template Transferase site P Nascent polypeptide chain Chloramphenicol Mechanism of action of Chloramphenicol
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INITIATION
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STREPTOGRAMINS Quinupristin/Dalfopristin (30:70)
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aa A 50S 30S mRNA template Transferase site P Nascent polypeptide chain QUINUPRISTIN (MACROLIDE) DALFOPRISTIN
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MECHANISM OF ACTION Act synergistically to inhibit bacterial protein synthesis. They bind to separate sites on the 50 S ribosomal subunit and form a ternary complex with the ribosome.
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MECHANISM OF ACTION Quinupristin binds at the same site as the macrolides and has a similar effect. Dalfopristin directly blocks peptide bond formation by inhibiting peptidyl transferase. Dalfopristin results in a conformational change in the 50S ribosome subunit.
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INITIATION
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AMINOGLYCOSIDES Bind irreversibly to the 30S subunit. Exact mechanism of cell death is unknown. Postantibiotic effect.
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A 50S 30S mRNA template Transferase site P Nascent polypeptide chain Tetracycline aa
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INHIBITION OF MITOCHONDRIAL PROTEIN SYNTHESIS Mitochondrial ribosome resembles bacterial ribosome. May account for some toxic effects (e.g. chloramphenicol, linezolid).
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RESISTANCE Alterations in ribosomal proteins (e.g. macrolides). Decreased permeability to the antibiotic.
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Tetracycline ATP TETRACYCLINE RESISTANCE
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ANTIBIOTICS ACTING AS ANTIMETABOLITES Sulfonamides Trimethoprim plus sulfamethoxazole
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2 HNCOOH DIHYDROPTERIDINE PYROPHOSPHATE DERIVATIVE DIHYDROPTEROIC ACID DIHYDROFOLIC ACID FOLIC ACID BIOSYNTHESIS Glutamic Acid 2 ATP 2 HN SO 2 NH 2 Dihydropteroate Synthetase
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TRIMETHOPRIM- SULFAMETHOXAZOLE 2 HNCH 2 OCH 3 80 mg TRIMETHOPRIM O 2 HN SO 2 NH NCH 3 400 mg SULFAMETHOXAZOLE
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PABA DIHYDROPTEROIC ACID DIHYROFOLIC ACID TETRAHYDROFOLIC ACID + Pteridine SULFONAMIDE TRIMETHOPRIM Dihydrofolate Reductase Dihydrofolate Synthetase Dihydropteroate Synthetase
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Advantages of sulfonamide- trimethoprim combination
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Results from multiple mechanisms. Altered dihydropteroate synthetase. Cross-resistance among all sulfonamides. SULFONAMIDE- RESISTANCE
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ANTIBIOTICS AFFECTING NUCLEIC ACID SYNTHESIS. Fluoroquinolones Metronidazole Rifampin
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FLUOROQUINOLONES
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Gyrase (Topoisomerase I)-older quinolones Topoisomerase IV-3 rd and 4 th gen quinolones.
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FQ RESISTANCE Changes in gyrase and topoisomerase Increased efflux
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Inactive End Products Metronidazole Metronidazole Short lived intermediates Inactive end products products DNA RNA Protein Other targets Mechanism of action of metronidazole on an anaerobic organism Ferredoxin reduced
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RIFAMPIN
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