MECHANISM OF DRUG
RESISTANCE
SUBHANANTHINI JEYAMURUGAN,
18PY17, M.SC., MICROBIOLOGY.
AYYA NADAR JANAKI AMMAL COLLEGE SIVAKASI.
INTRODUCTION:
Antibiotics are secondary metabolites or biochemical
secreted by microorganisms.
 Inhibits the growth or kill other microbes.
 Soluble compounds derived from certain microorganisms.
 They are in the form of natural, synthetic and
semisynthetic.
ANTIBIOTIC RESISTANCE
It is the reduction in effectiveness of a drug in curing a
disease.
Loss of susceptibility of bacteria to the killing or growth
inhibiting properties of an antibiotic agent.
Resistance strain of bacteria : dominant…. It might be
untreatable and life threatening.
MECHANISM OF DRUG RESISTANCE
 Intrinsic (natural resistance)
inherent structural or functional characteristics, allows
tolerance
 Acquired resistance
changes in the usual genetic makeup
 Several common mechanisms for drug resistance and it
includes
1. Inactivation of the antibiotic
2. Efflux pumping of the antibiotic
3. Modification of the antibiotic target
4. Alternation of the pathway
Mechanism of drug resistance
MODIFICATION:
 Natural variants or acquired changes in the target sites of
antimicrobials that prevent drug binding is a common
mechanism of resistance.
 Bacteria can modify the antibiotics target to escape its
activity.
 It acts as a self resistance mechanism against several
classes of antibiotics.
 Bacteria can change the structure of the target, but the
modified target may also be able to function. This will be
achieved in two ways:
1. Mutation of the gene that codes for the target
protein.
2. Importing a gene that codes for a modified target.
Some methods of modifications:
 Alternation in the 30S subunit or 50S subunit
 Alternation in PBP
 Altered cell wall precursors
Mechanism of drug resistance
Alternation in Ribosomes
 Ribosomes leads to resistance to drugs that affect the
protein synthesis
 Example : Aminoglycosides, Macrolides, tetracyline,
chloramphenicol.
PBP:
 A specialized mechanism for the resistance of Gram
positive bacteria
 The presence of mutation in the PBP, leads to the reduced
affinity to beta lactam antibiotics.
 Examples: MRSA, Streptococcus pneumoniae.
Mechanism of drug resistance
CELL WALL PRECURSORS
 Inhibited by glycopeptides.
 Vancomycin or Teicoplanin, binding to the D-alanine- D-
alanine residues of peptidoglycan residues.
 It is changed to D-alanyl-lactate, as glycopeptide do not
cross link donot occur and resistance to them develops.
Mechanism of drug resistance
ALTERNATION OF THE TARGET SITE
 Alternation has been supposed to many antibiotics including : Beta lactams, Quinolones,
Glycopeptides, Chloramphenicol.
 Some drugs competitively inhibit metabolic pathways.
 Bacteria can overcome this method by using an alternative pathway.
Mechanism of drug resistance
Beta Lactam antibiotics
 Major mechanism involves the enzymatic action of Beta
lactam .
 Some other mechanisms also included:
PBP
MRSA
Alternations to PBPs.
Streptomycin
 It works on the mechanism of alternations in the
ribosomal subunit.
 Due to mutation changes in the protein structure occurs,
which prevents the binding of streptomycin .
 It induces the bacteria with resistance to very high
concentration of the drug.
Chloramphenicol & Erythromycin
 Alternations in the ribosomal subunit have been
implicated in resistance to both the antibiotics.
 Erythromycin resistance results more from methylation of
the 23S ribosomal RNA subunit.
 Dissociated resistance.
Fusidic acid
 Inhibiting the translocation of the growing polypeptide
chain.
 Mutational alternation
Quinolones
 Enzymatic target of antibiotic
 DNA gyrase and DNA topoisomerase II.
Mechanism of drug resistance
Rifampicin
 Alternation to the beta subunit of RNA polymerase.
Thank you

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Mechanism of drug resistance

  • 1. MECHANISM OF DRUG RESISTANCE SUBHANANTHINI JEYAMURUGAN, 18PY17, M.SC., MICROBIOLOGY. AYYA NADAR JANAKI AMMAL COLLEGE SIVAKASI.
  • 2. INTRODUCTION: Antibiotics are secondary metabolites or biochemical secreted by microorganisms.  Inhibits the growth or kill other microbes.  Soluble compounds derived from certain microorganisms.  They are in the form of natural, synthetic and semisynthetic.
  • 3. ANTIBIOTIC RESISTANCE It is the reduction in effectiveness of a drug in curing a disease. Loss of susceptibility of bacteria to the killing or growth inhibiting properties of an antibiotic agent. Resistance strain of bacteria : dominant…. It might be untreatable and life threatening.
  • 4. MECHANISM OF DRUG RESISTANCE  Intrinsic (natural resistance) inherent structural or functional characteristics, allows tolerance  Acquired resistance changes in the usual genetic makeup
  • 5.  Several common mechanisms for drug resistance and it includes 1. Inactivation of the antibiotic 2. Efflux pumping of the antibiotic 3. Modification of the antibiotic target 4. Alternation of the pathway
  • 7. MODIFICATION:  Natural variants or acquired changes in the target sites of antimicrobials that prevent drug binding is a common mechanism of resistance.  Bacteria can modify the antibiotics target to escape its activity.  It acts as a self resistance mechanism against several classes of antibiotics.
  • 8.  Bacteria can change the structure of the target, but the modified target may also be able to function. This will be achieved in two ways: 1. Mutation of the gene that codes for the target protein. 2. Importing a gene that codes for a modified target.
  • 9. Some methods of modifications:  Alternation in the 30S subunit or 50S subunit  Alternation in PBP  Altered cell wall precursors
  • 11. Alternation in Ribosomes  Ribosomes leads to resistance to drugs that affect the protein synthesis  Example : Aminoglycosides, Macrolides, tetracyline, chloramphenicol.
  • 12. PBP:  A specialized mechanism for the resistance of Gram positive bacteria  The presence of mutation in the PBP, leads to the reduced affinity to beta lactam antibiotics.  Examples: MRSA, Streptococcus pneumoniae.
  • 14. CELL WALL PRECURSORS  Inhibited by glycopeptides.  Vancomycin or Teicoplanin, binding to the D-alanine- D- alanine residues of peptidoglycan residues.  It is changed to D-alanyl-lactate, as glycopeptide do not cross link donot occur and resistance to them develops.
  • 16. ALTERNATION OF THE TARGET SITE  Alternation has been supposed to many antibiotics including : Beta lactams, Quinolones, Glycopeptides, Chloramphenicol.  Some drugs competitively inhibit metabolic pathways.  Bacteria can overcome this method by using an alternative pathway.
  • 18. Beta Lactam antibiotics  Major mechanism involves the enzymatic action of Beta lactam .  Some other mechanisms also included: PBP MRSA Alternations to PBPs.
  • 19. Streptomycin  It works on the mechanism of alternations in the ribosomal subunit.  Due to mutation changes in the protein structure occurs, which prevents the binding of streptomycin .  It induces the bacteria with resistance to very high concentration of the drug.
  • 20. Chloramphenicol & Erythromycin  Alternations in the ribosomal subunit have been implicated in resistance to both the antibiotics.  Erythromycin resistance results more from methylation of the 23S ribosomal RNA subunit.  Dissociated resistance.
  • 21. Fusidic acid  Inhibiting the translocation of the growing polypeptide chain.  Mutational alternation
  • 22. Quinolones  Enzymatic target of antibiotic  DNA gyrase and DNA topoisomerase II.
  • 24. Rifampicin  Alternation to the beta subunit of RNA polymerase.