1 / 20

Antibiotic Resistance

Antibiotic Resistance. By: E. Salehifar Faculty of Pharmacy Department of Clinical Pharmacist. Antibiotic Usage. Transplants. Dialysis. Suppressed Immune Systems. Joint Replacements. Antibiotic Overuse. Overprescribing Continuous use in livestock feed. Humans = 30% antibiotic use.

rangsey
Download Presentation

Antibiotic Resistance

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Antibiotic Resistance By: E. Salehifar Faculty of Pharmacy Department of Clinical Pharmacist

  2. Antibiotic Usage Transplants Dialysis Suppressed Immune Systems Joint Replacements

  3. Antibiotic Overuse • Overprescribing • Continuous use in livestock feed Humans = 30% antibiotic use Animals = 70% https://amr-review.org/file/327

  4. Three possible outcomes after antibiotic use: • Death (Bacteriocidal) • Growth Inhibition (Bacteriostatic) • Resistance

  5. The most challenging MDROs in HealthcareHighly Intelligent! • Methicillin-resistant Staphylococcus aureus(MRSA) • Vancomycin-resistant enterococcus (VRE) • Extended-spectrum beta-lactamase-producing bacteria (ESBLs) • Carbapenem-resistant enterobacteriaceae (CRE) • Multi-drug resistant Acinetobacterbaumanii (MDR-A)

  6. Carbapenem-resistant enterobacteriaceae (CRE) • Significantly limited treatment options for life-threatening infections • No new drugs are under development for gram-negative infections • Resistance mechanisms (carbapenemases) spread readily via plasmids • Co-resistance to other agents is common

  7. Mechanisms of Resistance • Drug inactivation or modification • β-lactamases • Klebsiella pneumoniae carbapenemases (KPCs) • New Delhi metallo-β-lactamase (NDM) carbapenemases • originally identified in Sweden in 2008 and have spread worldwide rapidly • Adding of acetyl or phosphate group to a specific site on the antibiotic→ ↓ its ability to bind to the cites of action

  8. Mechanisms • Beta-lactam antibiotics permanently inactivate PBP (transpeptidase) leads to inhibition of peptidoglycan synthesis • MRSA: • expresses a PBP that does not allow the antibiotic into its active site

  9. Mechanisms of Resistance • Alteration of target- or binding site • Alteration of PBP • MRSA and other penicillin-resistant bacteria. • Ribosomal protection proteins • binding of the ribosomal protection proteins to the ribosomes of the bacterial cell → conformational changes • Alteration of metabolic pathway • Some Sulfonamide-resistant bacteria do not require PABA • Resistant MO uses preformed folic acid • Efflux pump antibiotics • FQs  resistance, AGs, Tetra, Pen, Macrolides

  10. Resistant Genes • Horizontal Gene Transfer • Plasmid-mediated resistance genes produce proteins that can bind to DNA gyrase • Point mutations (1 in 108 per chromosomal replication) • mutations at key sites in DNA gyrase or topoisomerase IV

  11. Horizontal Gene Transfer

  12. To limit the spread of Resistance • Prudent antimicrobial prescribing • Surveillance • C&S tests (sampling, transport, kits, method, interpretation) • DUE studies • RUD committee, D&C committee • Infection control

More Related