the use of antimicrobial (antibiotics) in the treatment of infections [ch9] Flashcards
what are the characteristics of antibiotics.
Selective toxicity Highly soluble - contact Effective concentration Immune system –not affected Target isolated species Prevent resistant strains No side effects Not bind to host proteins/ inactivated
what is the general mode of action of antibiotics
Inhibiting the synthesis of cell walls;
• Inhibiting the synthesis of proteins;
• Inhibiting the synthesis of nucleic acids;
• Damaging cell membranes;
• Or by inhibiting of specific enzyme systems by antimetabolites.
Classify antibiotics according to the class that they belong.
Note that penicillin ,cephalosporins, carbapenems and monobactams are b-lactam agents.
1) Penicillin’s :ends with cillin
2) cephalosporins: Starts with cef or cep
3) monobactams: Ends with am
4) carbapenems :ends with penem
5) Glycopeptides: ends with in
6) aminoglycosides:end with cin
7) Tetracycline:cycline
8) chloramphenicol-phenicol
9) macrolides:ends with romycin
10) lincomycins:mycin
11) quinolones/fluoroquinolones: ends with oxacin
12) ansamycin:starts with rifa
13) nitroimidazole:ends with idazole
14) sulphonamides:
15) polyenes
16) polypeptides
describe the mode of action of B-lactam agents
are bactericidal, and act by inhibiting the synthesis of the peptidoglycan layer of bacterial cell walls.
describe the mode of action of aminoglycosides
Inhibition of protein synthesis. Once inside the bacterial cell, aminoglycosides bind to the 30s ribosomal sub-unit and cause a misreading of the genetic code. This subsequently leads to the interruption of normal bacterial protein synthesis.
describe the mode of action of tetracycline
Inhibition of protein synthesis. Once tetracyclines have been transported into the cell, this class of antibiotic reversibly binds to receptors on the 30S ribosomal subunit of the bacteria, preventing attachment of aminoacyl-tRNA to the RNA-ribosome complex.
describe the mode of action of macrolides
inhibition of bacterial protein biosynthesis, and they are thought to do this by preventing peptidyltransferase from adding the growing peptide attached to tRNA to the next amino acid (similarly to chloramphenicol) as well as inhibiting bacterial ribosomal translation.
describe the mode of action of Chloramphenicol
Chloramphenicol is a bacteriostatic by inhibiting protein synthesis. It prevents protein chain elongation by inhibiting the peptidyl transferase activity of the bacterial ribosome
describe the mode of action of Quinolones
mode of action is by inhibition of DNA replication. Quinolones bind to the topoisomerase IV/DNA gyrase–DNA complexes and this results in the inhibition of DNA replication.
describe the mode of action of Lincosamides
Lincomycin inhibits bacterial protein synthesis by binding to the 23S RNA of the 50S subunit of the bacterial ribosome. Lincomycin is predominantly bacteriostatic in vitro.
describe the mode of action of Sulphonamides
antimetabolite -Inhibition of other metabolic processes. Sulfonamides interfere with folic acid synthesis by preventing addition of para-aminobenzoic acid (PABA) into the folic acid molecule through competing for the enzyme dihydropteroate synthetase.
What types of infections do the different class of antibiotics treat ?
1)Penicillins are used in the treatment of infections affecting skin, teeth, ears, urinary tract and
respiratory tract infections, as well as gonorrhoea.
2)Cephalosporins :Pneumonia, Streptococcal throat, Staphylococcal infections, tonsillitis, bronchitis, otitis media, various types
of skin infections and gonorrhoea may be treated with Cephalosporins which are bactericidal. (note they differ with the types of generations )
3)Glycopeptides:It is used in the treatment of infections
caused by oxacillin-resistant staphylococci and other gram-positive bacteria.
4)Polypeptides : topically-applied drug for treating skin-infections caused by Gram-positive bacteria
5) Aminoglycosides: are used in the treatment of systemic infections caused by
Gram-negative bacteria as well as Mycobacteria.
6)Tetracycline:bacteriostatic drugs include tetracycline, doxycycline and minocycline which are used in the treatment
of infections caused by Chlamydia, Mycoplasma, Rickettsia and some Gram-positive and Gram-negative
bacteria
7). Macrolides: can also be used to treat infections caused
by gram-positive and Campylobacter bacteria in patients with allergies to penicillin.
8) Chloramphenicol is an antibiotic. It’s mainly used to treat eye infections (such as conjunctivitis) and sometimes ear infections
9) Oxazolidones :It is the drug of choice to treat infections caused by Enterococci
10)Lincosamides :It is used to treat
Staphylococcal infections as well as anaerobic gram-negative infections.
11)Quinolones:
Naladixic acid, a narrow spectrum antibiotic, was initially used for the treatment of urinary tract infections
caused by Gram-negative rods until resistance to this drug developed in these bacteria
12)Nitroimidazoles:Metronidazole belongs to this class and it is used to treat anaerobic infections as well as amoebiasis and giardiasis.
13) Rifampin: is an antibiotic used to treat several types of bacterial infections, including tuberculosis, Mycobacterium avium complex, leprosy, and Legionnaires’ disease.
14) Sulphonamides :They may be prescribed to treat urinary tract infections (UTIs), bronchitis, eye infections, bacterial meningitis, pneumonia, ear infections, severe burns, traveler’s diarrhea, and other conditions
15) Trimethoprim: It’s used to treat urinary tract infections (UTIs), such as cystitis. Occasionally, trimethoprim is used to treat other types of infections, such as chest infections and acne.
Discuss the type, mode of action and function of the different types of antiviral drugs
Action : Inhibit nucleic acid synthesis ,synthetic antibiotics ,nucleoside analogues
Selectivity has been a problem because viruses use the metabolic machinery of the
host
B. Antiviral drugs target specific steps of life cycle, especially enzymes that function in
the life cycle (e.g., amantadine, vidarabine, acyclovir, and azidothymidine)
C. Human interferon is used to treat some viral infections
Differentiate between intrinsic and
acquired resistance.
Inherent resistance occurs as a result of lack of affinity of the drug for the bacterial
target, inaccessibility of the drug into the bacterial cell, extrusion of the drug by chromosomally encoded
active exporters and innate production of enzymes that inactivate the drug. More than one of these
mechanisms may be responsible for inherent resistance.
Acquired resistance occurs when an organism that is initially susceptible to an antibiotic, becomes resistant
to it
Describe the strategies used by bacteria to
resist the action of antibiotics
refer to written book notes