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What is the main difference between bacteriostatic and bactericidal compounds in antimicrobial therapy?
Bacteriostatic compounds are for surface treatment, and bactericidal compounds are used as antibiotics
Bacteriostatic compounds and bactericidal compound have the same mode of action, and the terms can be used interchangeably
Bactericidal compounds kill bacteria, while bacteriostatic compounds inhibit bacterial growth
Bacteriostatic compounds kill bacteria, while bactericidal compounds inhibit bacterial growth
Bactericidal compounds kill bacteria, while bacteriostatic compounds inhibit bacterial growth
Bacteriostatic substances are most suitable for patients with:
Compromised immune systems
Slow bacterial growth rates
Intact immune systems
Rapid bacterial growth rates
Intact immune systems
What does the MIC test determine?
The lowest concentration of an antibiotic required to prevent bacterial growth
The highest concentration of an antibiotic that can kill bacteria
The concentration of an antibiotic that inhibits growth of gram-negative bacteria
The most inhibitory concentration of an antibiotic
The lowest concentration of an antibiotic required to prevent bacterial growth
What does the large size of the clearance zone in the Kirby-Bauer Assay indicate?
The high effectiveness of the antibiotic in inhibiting bacterial growth
The high resistance of bacteria to the antibiotic
The minimum antibiotic concentration required for inhibiting bacterial growth
The large size of the bacterial colony
The high effectiveness of the antibiotic in inhibiting bacterial growth
What is the primary difference between disinfectants and antiseptics?
Disinfectants are stronger and antiseptics are more toxic
Disinfectants primarily target bacteria, while antiseptics target a wider range of microorganisms
Disinfectants are used on surfaces, while antiseptics are used on the skin
Disinfectants are used internally, while antiseptics are used externally
Disinfectants are used on surfaces, while antiseptics are used on the skin
Which phase of antibiotic discovery is considered the most challenging and time-consuming?
Phase II clinical trials
Phase I clinical trials
Phase II clinical trials
Lead optimization
Lead optimization
Why have pharmaceutical companies lost interest in antibiotic discovery?
Decreased demand for antibiotics in the market
Challenges and costs involved in the process
Lack of intellectual property protection for antibiotics
Limited need for new antibiotics
Challenges and costs involved in the process
Why do antibiotics primarily focus on a limited set of targets?
These targets have been successful in the past
Eukaryotic and Prokaryotic cells lack these targets
The development cost of new antibiotics is high
These targets have the lowest toxicity
These targets have been successful in the past
What is the final step in peptidoglycan biosynthesis?
Transportation of amino sugars across the membrane
Polymerization of peptidoglycan
Cross-linking of peptidoglycan
Utilization of UDP derivatives of amino sugars
Cross-linking of peptidoglycan
What is the target of the antibiotic fosfomycin?
Transpeptidation enzymes
Dephosphorylation and recycling of undecapranyl pyrophosphate
Phosphor-NAM-pentapeptide transfer
Conversion of UDP-NAG to UDP-NAM
Conversion of UDP-NAG to UDP-NAM
Which step of peptidoglycan biosynthesis is targeted by bacitracin?
Phosphorylation and recycling of undecaprenyl pyrophosphate
Conversion of UDP-NAG to UDP-NAM
Transpeptidation
Transglycosylation
Phosphorylation and recycling of undecaprenyl pyrophosphate
Which antibiotics act on the transpeptidation step of peptidoglycan biosynthesis?
β-lactams
Moenomycin family of lipopolysaccharides
Tunicamycin
Glycopeptides
β-lactams
What is the role of penicillin-binding proteins (PBPs) in peptidoglycan biosynthesis?
Inhibition of transpeptidation enzymes
Formation of cross-bridges in peptidoglycan
Degradation of peptidoglycan
Catalyzation of transpeptidation reactions
Catalyzation of transpeptidation reactions
How do β-lactam antibiotics inhibit transpeptidase enzymes?
By opening the β-lactam ring and forming a covalent bond
By interacting with autolysins and degrading peptidoglycan
By irreversibly binding to the reactive serine residue
By inhibiting the cross-bridge formation in peptidoglycan
By opening the β-lactam ring and forming a covalent bond
What is the additional activity possessed by fourth-generation cephalosporins compared to third-generation cephalosporins?
Effectiveness against Enterobacteriaceae
Ability to target Haemophilus influenzae
Resistance to beta-lactamase enzymes
Increased coverage against Gram-positive bacteria
Resistance to beta-lactamase enzymes
Which enzyme do glycopeptides like vancomycin and teicoplanin bind to?
Beta-lactamase enzymes
Autolysins
Transpeptidase enzymes
Pyrophosphatase (PPiase) enzyme
Transpeptidase enzymes
What is the main use of bacitracin?
Internal use for systemic infections
Treatment of various skin infections
Prevention of Gram-negative bacterial infections
Sexually transmitted disease treatement
Treatment of various skin infections
How do aminoglycosides hinder protein synthesis?
By inhibiting transpeptidation enzyme
By blocking the 30S subunit from binding mRNA
By impeding the 50S subunit from joining the 30S subunit
By preventing the positioning of fMet-tRNA in the P site
By impeding the 50S subunit from joining the 30S subunit
What is a potential side effect of prolonged administration of aminoglycosides?
Hearing loss and kidney dysfunction
Liver damage and skin rash
Tooth discoloration and nausea
Sensitivity to light and muscle-related adverse effects
Hearing loss and kidney dysfunction
What is the primary mechanism of action for macrolides like erythromycin?
Disruption of DNA replication
Inactivation of beta-lactamase enzymes
Interference with protein synthesis
Inhibition of cell wall synthesis
Interference with protein synthesis
The main mechanism of action of quinolones and fluoroquinolones is by inhibiting:
Protein synthesis in bacteria
DNA gyrase activity in bacteria
Peptidoglycan synthesis
Cell wall synthesis in bacteria
DNA gyrase activity in bacteria
Tetrahydrofolate biosynthesis inhibitors affect bacterial cells by:
Interfering with cell wall synthesis
Inhibiting DNA replication
Targeting enzymes involved in folic acid synthesis
Blocking protein synthesis
Targeting enzymes involved in folic acid synthesis
Clavulanic acid is often combined with other β-lactam antibiotics to:
Block DNA replication in bacteria
Prevent degradation of β-lactam antibiotics
Enhance protein synthesis in bacteria
Inhibit bacterial cell wall synthesis
Prevent degradation of β-lactam antibiotics
What strategy have pharmaceutical companies adopted to combat resistance?
Reducing antibiotic research and development efforts
Enhancing existing antibiotics
Focusing on β-lactam and macrolide antibiotics
Developing new generations of antibiotics
Enhancing existing antibiotics
What are nosocomial infections also known as?
Healthcare-associated infections (HAIs)
Multidrug-resistant infections
Antibiotic-resistant infections
Community-acquired infections
Healthcare-associated infections (HAIs)
Which group of bacteria is referred to as ESKAPE pathogens?
Carbapenem-resistant Acinetobacter and Clostridioides difficle
Drug-resistant Campylobacter and ESBL-producing Enterobacteriaceae
Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannni, Pseudomonas aeruginosa, and Enterobacter species
Bacteria that escape the phagosome
Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannni, Pseudomonas aeruginosa, and Enterobacter species
How are bacteria classified as multidrug-resistant (MDR)?
If they are resistant to more than two categories of antibiotics
If they acquire mutations that prevent antibiotics from being activated
If they cause nosocomial infections
If they are resistant to one drug within a category
If they are resistant to more than two categories of antibiotics
Under what conditions do certain bacteria become more resistant to aminoglycosides?
Acidic conditions
Anaerobic conditions
Aerobic conditions
Alkaline conditions
Anaerobic conditions
What is the main function of efflux pumps in bacteria?
To prevent the expression of redundant transporters
To enhance the effectiveness of antibiotics withing the cell
To maintain cellular balance and remove toxins
To transport antibiotics into the bacterial cell
To maintain cellular balance and remove toxins
Which family of efflux pumps is particularly important in Gram-negative bacteria?
Small multidrug resistance (SMR) protein family
Major facilitator superfamily (MFS)
ATP-binding cassette (ABC) transporters
Resistance-nodulation-division (RND) family
Resistance-nodulation-division (RND) family
How do β-lactamases render β-lactam antibiotics inactive?
By preventing the production of β-lactamases during cell lysis
By attacking the β-lactam ring with an active-site serine residue
By inhibiting the release of water molecules
By preserving the β-lactam ring’s covalent bond
By attacking the β-lactam ring with an active-site serine residue
What are extended-spectrum β-lactamases (ESBLs) resistant to?
β-lactamase inhibitors only
Narrow-spectrum β-lactams, β-lactamase inhibitors, and later-generation extended-spectrum β-lactams
Later-generation extended-spectrum β-lactams only
Narrow-spectrum β-lactams only
Narrow-spectrum β-lactams, β-lactamase inhibitors, and later-generation extended-spectrum β-lactams
Which bacteria within the Enterobacteriaceae family can produce ESBLs?
Escherichia coli (E. coli), Klebsiella pneumoniae, Enterobacter spp, and Proteus mirabilis
Salmonella enterica
Enterobacter spp.
Salmonella and E. coli
Escherichia coli (E. coli), Klebsiella pneumoniae, Enterobacter spp, and Proteus mirabilis
Aminoglycoside resistance primarily occurs through:
β-lactamases
Enzyme inhibition
Efflux pumps
Ribosome modification
Ribosome modification
Chloramphenicol acetyltransferase (CAT) adds an acetyl group to chloramphenicol, preventing its:
Activation of gene expression
Binding to the ribosome
Uptake by the ribosome
Efflux from the cells
Binding to the ribosome
What is the role of the antitoxin in a TA system?
Inhibiting toxin activity
Blocking DNA replication
Halting bacterial growth
Upregulating stress-related genes
Inhibiting toxin activity