The most important mechanism by which tetracycline antibiotics exert antimicrobial action is

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Question 1 of 5

The most important mechanism by which tetracycline antibiotics exert antimicrobial action is

Correct Answer: B

Rationale: The correct answer is B) They bind to 30S ribosomes and inhibit bacterial protein synthesis. Tetracycline antibiotics act by binding to the 30S subunit of bacterial ribosomes, preventing the attachment of aminoacyl-tRNA molecules to the mRNA-ribosome complex. This inhibition halts the elongation of the polypeptide chain during protein synthesis, ultimately leading to bacterial cell death. Option A) They chelate Ca²⁺ ions and alter permeability of the bacterial cell membrane is incorrect because tetracyclines do not exert their antimicrobial action through this mechanism. Option C) They bind to 50S ribosomes and interfere with translocation of the growing peptide chain in the bacteria is incorrect as tetracyclines specifically target the 30S ribosomal subunit. Option D) They interfere with DNA-mediated RNA synthesis in bacteria is also incorrect as tetracyclines primarily target protein synthesis, not DNA replication or transcription. In an educational context, understanding the specific mechanism of action of tetracycline antibiotics is crucial for healthcare professionals to effectively prescribe these drugs and for students to grasp the fundamental principles of antimicrobial therapy. This knowledge helps in selecting the appropriate antibiotics for treating bacterial infections and avoiding resistance development.

Question 2 of 5

The most important mechanism by which gram-negative bacilli acquire chloramphenicol resistance is

Correct Answer: B

Rationale: In the context of drugs for the immune system, understanding mechanisms of antibiotic resistance is crucial for healthcare professionals. The correct answer to the question is B) Acquisition of a plasmid encoded for chloramphenicol acetyl transferase. This is because the production of chloramphenicol acetyl transferase enzyme inactivates chloramphenicol by acetylation, rendering it ineffective against the bacteria. This mechanism is a common way for bacteria to develop resistance to chloramphenicol. Option A) Decreased permeability into the bacterial cell is a mechanism seen in resistance to some antibiotics but not specifically chloramphenicol. Option C) Lowered affinity of the bacterial ribosome for chloramphenicol is not a common mechanism of resistance. Option D) Switching over from ribosomal to mitochondrial protein synthesis is unrelated to the acquisition of chloramphenicol resistance. In an educational context, understanding antibiotic resistance mechanisms is essential for effective patient care and for combatting the rise of multidrug-resistant bacteria. Healthcare professionals need to grasp these concepts to make informed decisions regarding antibiotic therapy and to prevent the spread of resistant strains.

Question 3 of 5

Which of the following drugs has demonstrated in vitro activity against Mycobacterium avium-intracellulare (MAI)?

Correct Answer: B

Rationale: The correct answer is B) Clarithromycin. Clarithromycin is a macrolide antibiotic that has demonstrated in vitro activity against Mycobacterium avium-intracellulare (MAI). This bacterium is known to cause opportunistic infections in immunocompromised individuals, particularly those with HIV/AIDS. Vancomycin (Option A) is a glycopeptide antibiotic commonly used to treat Gram-positive bacterial infections like MRSA and Enterococcus faecalis. It is not effective against MAI. Erythromycin base (Option C) is another macrolide antibiotic similar to clarithromycin, but it is less effective against MAI compared to clarithromycin. Troleandomycin (Option D) is a macrolide antibiotic that is not commonly used in clinical practice due to its potential for drug interactions and adverse effects. It is not a preferred agent for treating MAI infections. Understanding the specific antimicrobial activity of different drugs is crucial in the field of medicine, especially in infectious diseases and immunology. Knowing which drugs are effective against particular pathogens allows healthcare providers to make informed treatment decisions and provide optimal care to patients. In the context of immune system drugs, selecting the right antimicrobial agent can significantly impact patient outcomes, especially in cases of opportunistic infections like MAI in immunocompromised individuals.

Question 4 of 5

The aminoglycoside antibiotic which is distinguished by its resistance to bacterial aminoglycoside inactivating enzymes is

Correct Answer: C

Rationale: The correct answer is C) Amikacin. In the context of aminoglycoside antibiotics, amikacin is distinguished by its resistance to bacterial aminoglycoside inactivating enzymes. This property makes amikacin particularly effective against bacteria that produce these enzymes, allowing it to maintain its antibacterial activity where other aminoglycosides might be rendered ineffective. Looking at the other options: A) Kanamycin is susceptible to inactivation by bacterial enzymes. B) Sisomicin is also susceptible to inactivation by bacterial enzymes. D) Tobramycin, like kanamycin and sisomicin, can be inactivated by bacterial enzymes. Understanding the unique characteristics of each aminoglycoside antibiotic is crucial in clinical practice to ensure the selection of the most appropriate drug for a specific bacterial infection. By knowing that amikacin is resistant to bacterial inactivating enzymes, healthcare providers can make more informed decisions when prescribing antibiotics to treat infections caused by resistant strains of bacteria. This knowledge can contribute to better patient outcomes and help combat the issue of antibiotic resistance.

Question 5 of 5

Hepatitis with cholestatic jaundice occurs most frequently as an adverse reaction to the following preparation of erythromycin

Correct Answer: C

Rationale: The correct answer is C) Erythromycin estolate. Erythromycin estolate is known to be associated with an increased risk of cholestatic jaundice compared to other erythromycin preparations. This adverse reaction occurs due to the estolate salt form of erythromycin causing a higher incidence of hepatotoxicity, leading to cholestatic jaundice. Option A) Erythromycin base, B) Erythromycin stearate, and D) Erythromycin ethylsuccinate are less likely to cause cholestatic jaundice compared to erythromycin estolate. Erythromycin base is the basic form of the drug, stearate is a salt form with lower risk of liver toxicity, and ethylsuccinate is another salt form that is less likely to cause cholestatic jaundice. Educationally, understanding the differences in erythromycin preparations and their associated adverse effects is crucial for healthcare professionals to make informed decisions when prescribing medications. This knowledge helps in preventing potential harm to patients and in providing safer and more effective healthcare.

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