Antibiotics TBL Quiz Flashcards
MOA of penicillins
disruption of cell wall synthesis by binding PBPs and enzymes responsible for peptidoglycan synthesis
cephalosporin and cephamycins MOA
disruption of cell wall synthesis by binding PBPs and enzymes responsible for peptidoglycan synthesis
MOA of carbapenems
disruption of cell wall synthesis by binding PBPs and enzymes responsible for peptidoglycan synthesis
MOA of monobactams
bind PBPs and enzymes responsible for peptidoglycan synthesis
MOA of beta lactams
disruption of cell wall by beta lactamases and prevents the enzymatic inactivation of beta lactam
MOA of vancomycin
disruption of cell wall via inhibiting cross linkage of peptidoglycan layers
daptomycin MOA
causes depolarization of cytoplasmid membrane resulting in disruption of ion concentration gradients
bacitracin MOA
inhibits bacterial cytoplasmic membrane and movement of peptidolycan precursos
polymixins MOA
inhibits bacterial membrane synthesis
isoniazid MOA
inhibits mycolic aicd synthesis
ethionamide MOA
inhibits mycolic acid synthesis
ethambutol MOA
inhibits arabinogalactan synthesis
cycloserine MOA
inhibits cross linkage of peptidoglycan layers
what are the beta lactam antibiotics
penicillins, cephalosporins, cephamycins, carbapenems monobactams and beta lactamase inhibitors
Resistance mechanisms of beta lactam antibiotics
prevention of interaction between antibiotic and the target PBP
modification of the binding of the antibiotic to the PBP
hydrolysis of the antibiotic by bacterial enzymes (beta lactamases)
MOA of aminoglycosides
produces premature release of peptide chain from 30S ribosome
MOA of tetracyclines
prevents polypeptide elongation at the 30S ribosome
glycyclines MOA
binds the 30S ribosome and prevents initiation of protein synthesis
oxazolidonone MOA
prevents initiation of protein synthesis at the 50S riboosome
Macrolides MOA
prevent polypeptide elongation at the 50S ribosome
ketolides MOA
prevents polypeptide elongation at the 50S ribosome
clindamycin MOA
prevents polypeptide elongation at the 50S ribosome
streptogramins MOA
prevents polypeptide elongation at the 50S ribosome
quinolones MOA
binds with the alpha subunit of DNA gyrase
MAO of rifampin and rifabutin
prevents transcription by byinding DNA dependent RNA polymerase
_______disrupts bacterial DNA
metronidazole
______-inhibits dihydropteroate synthase and disurpts folic acid synthesis
sulfonamides, dapsone and trimethoprim
the carbapenems include
imipenem, meropenem, ertapenem, and doripenem
monobactans include
aztreonam
monobactams are active against
aerobic, gram negative bacteria
______and _____are resistant to monobactans
anaerobes and gram positive bacteria
_____interacts with teh D alanine D alanine termini of the pentapeptide side chains
vancymycin
vancomycin is inactive against
gram neg.
_______has potent activity against gram positive bacteria but gram neg are resistant and disrupts the ionic gradients of the bacteria
daptomycin
_________is used for treatment of skin infections caused by gram positive bacteria
bacitracin
____________inhibits with dephosphorylation and the recycling of the lipid carrier responsible for moving the peptidoglycan precuorses through the cytoplasmic membrane
bacitrcin
_______insert into the bacterial membranes like detergents
polymyxins
___________, __________, _______- and _______are cell wall active antibiotics used for the treatment of mycobacterial infections
isoniazid, ethionamide, ethambutol and cycloserine
__________interferes with the synthesis of arabinogalactan in the cell wall
ethambutol
_______-inhibits D ala D ala synthetase and alanine racemase
cycloserine
resistance to isoniaxid, ethionamide, ethambutol and cycloserine results mainly from
reduced drug uptake into the bacterial cell or alteration of the target sites `
what are the two effects of binding to the 30 S ribosomal protein
production of aberrant proteins and interruption of protein synthesis causing the premature release of the ribosome from mRNA
_________is also known as spectinomycin and is active against what
aminocyclitol, Neisseria gonorrhoae
_________are used to treat infections with gram-negative rods
aminoglycosides
__________is the most active aminoglycoside
amikacin
_______and _________are used to treat enterococcal infections
streptomycin and gentamicin combined with cell wall active antibiotic
what type of aminoglycoside is active versus mycobacteria and selected gram neg rods
streptomycin
_____are broad spectrum antibiotics against gram pos bacteria and some gram negative , mycoplasmas, chlamydia, and richettsiae
tetracyclines (tetracycline, doxycycline, and minocycline)
aminoglycosides include
streptomycin, kanamycin, gentamycin, tobramycin and amikacin)
__________are more active against gram negative bacteria and rapidly growing mycobacteria
glycylcyclines (tigecycline)
_____________are active against staphylococcus, enterococcus, streptococcus, gram positive rods, and clostridium and anaerobic cocci; not active against gram neg bacteria
oxazolidinone
linezolid is an example of
oxazolidone
_______are broad spectrum antibiotics active against gram positive and some gram negative bacteria
macrolides (erthrymycin, azithromycin, clarithrymycin and roxithrymycin)
_________are broad spectrum antibiotic similar to macrolides that are active against macrolide resistant staphylcocci and enterococci
ketolides (telithromycin)
________are broad spectrum against aerobic gram positive cocci and anaerobes
lincoasmide (clindamycin)
__________-are active against gram positive bacteria, good activity against methicillin-susceptible and resistant staphylococci, streptoccci, vancomycin susceptible and resistant E. faecium, haemophilus, moraxella and anaerobes not active against enterobacteriacae or gram neg rods
streptogramins (quinopristin-dalfopristin)
aminoglycosides are considered
bactericidal
___are considered to be resistant to
aminolycosides
_________is considered to best for treatment of systemic infections caused by susceptible gram neg. bacteria that are resistant gentamicin and tobramycin
amikacin
what are the four ways resistance can develop for aminoglycosides
mutation of ribosomal binding site
decreased uptake of antibiotic
increased expulsion of antibiotic
enzymatic modification of the antibiotic
most common cause of tetracycline resistance is
active efflux of tetracyclines from the cell
what species are generally resistant to tigecycline
proteus
morganella
providencia
p aeruginosa
______blocks initiation of protein synthesis by interfering with formation of the initiation complex consisting of tRNA, mRNA and ribosome by binding to 50S ribosomal subunit
linezolid (oxazolidones)
_____has activity against ALL staph, strep, and enterococci
linezolid
___________has a broad antibacterial spectrum similar to that of tetracycline but is not commonly used in the US because it disrupts protein synthesis in human bone marrow and can produce blood dyscrasias such as aplastic anema
chloraamphenicol
____________bind to the 23 and 50S ribosomal subunit which blocks polypeptide elongation
macrolides
resistance to macrolides is from
methylation of the 23s rRNA, inactivation of the macrolides by enzymes or mutations in 23s rRNA ribosomal proteins
what type of bacteria are commonly resistant to macrolides
gram neg bacteria
examples of macrolides
erythromycin
azithromycin
clarithrymycin
roxithrymycin
what is the name of the ketolide that is currently available in the US
telithromycin
_________binds to 50s ribosomal subunit and blocks protein synthesis
telithromycin
_________is a ketolide that has good resistance against staphylococci, s pneumoniae and other respiratory pathogens, gram pos rods and some anaerobes
telithrymycin
________-inhibits peptidyl transferse by interfering with the binding of amino acid acyl tRNA complex
clindamycin
_______binds to DNA dependent RNA polymerase and inhibits the initiation of RNA synthesis
rifampin
rifampin resistance results from
mutation in chromosomal gene that codes for the beta subunit of RNA polymerase
Rifabutin binds
DNA dependent RNA polymerase
produces cytotoxic compounds that disrupts the host DNA
metronidazole
_________compete with p aminobenzoic acid and prevent synthesis of folic acid
sulfonamides
_____-inhibits dihydrofolate reductase
trimethoprim
________ and ____________are antifolates that have proved to be useful for treating mycobacterial infections
dapsone and p-aminosalicylic acid
bacteria that use exogenous thymidine are
intrisically resistant to antimetabolites
__________is a lipophilic antibiotic that binds mycobacterial DNA
clofaziimine
___________is active against M tuberculosis at a low pH and mechanism is unkown
PZA