Streptococcus pneumoniae: Polysaccharide capsule crucial for virulence
Question 4: Actin Polymerization
Question: Which of these bacteria polymerize actin behind them to propel themselves through eukaryotic cells?
Answer: c. Listeria monocytogenes
Explanation:
Listeria monocytogenes hijacks the host cell's actin to form "actin tails," pushing itself through the cytoplasm and neighboring cells.
Incorrect options:
Plasmodium vivax: A protozoan parasite causing malaria and does not use actin polymerization like Listeria.
Bacillus anthracis: Causes anthrax, doesn't use actin to move.
Escherichia coli: Some strains invade cells but do not polymerize actin like Listeria.
Question 5: Opa Proteins and Immune Evasion
Question: Which of these bacteria makes Opa proteins that can be variable and allow for immune evasion?
Answer: c. Neisseria gonorrhea
Explanation:
Neisseria gonorrhea uses opaque proteins (Opa) that can vary their expression to avoid the immune system, helping them persist in host tissues and cause gonorrhea.
Incorrect options:
Staphylococcus aureus: Immune evasion occurs through factors like protein A, not Opa proteins.
Listeria monocytogenes: Doesn't make Opa proteins; uses other virulence mechanisms.
Shigella flexneri: Causes dysentery but does not have Opa proteins.
Escherichia coli: Doesn't have Opa proteins.
Question 6: Superantigens
Question: Which of the following are superantigens?
Answer: c. TSST, SEA, Streptococcal pyrogenic exotoxin
Explanation:
TSST-1 is toxic shock syndrome toxin.
SEA is staphylococcal enterotoxin A.
Streptococcal pyrogenic exotoxin. All are classified as superantigens
Question 7: Endocytosis
Question: Which of these bacteria primarily invades by inducing endocytosis?
Answer: c. Shigella
Explanation:
Shigella tricks host epithelial cells into endocytosing it, allowing it to invade and replicate intracellularly.
Question 8: A-B Toxins
Question: Which of the following contains an A-B structure?
Answer: e. Cholera toxin
Explanation:
The "A" component is the active part (enzymatic activity).
The "B" component is the binding part (binding to host cells).
Cholera toxin is the textbook example. Shiga toxins are phage encoded.
Question 9: Limulus amebocyte lysate (LAL) assay
Question: Which of the following are not correct names for this assay?
Answer: a. LPS from Gram-negative bacteria is the LAL assay- none of the options listed are correct names.
Question 10: Lysogeny
Question: Which disease is lysogeny related?
Answer: e. Cholera toxin is lysogeny related.
Question 11: Protein Synthesis Inhibition
Question: Which of the following inhibits protein synthesis?
Answer: c. Diphtheria toxin
Explanation:
Diphtheria toxin inhibits protein synthesis by ADP ribosylating EF-2.
The toxin gene is carried on a bacteriophage.
Question 12: Response to Endotoxin
Question: Which cytokine is released early in response to endotoxin?
Answer: d. IL-1
Explanation:
IL-1 is a major pro-inflammatory cytokine released early in response to endotoxin, especially LPS from Gram-negative bacteria.
Question 13: Treatment of Tuberculosis
Question: Which is harder to treat?
Answer: d. Tuberculosis
Explanation:
Tuberculosis has a thick waxy cell wall, is intracellular, and requires long-term, multi-drug therapy.
Question 14: Mechanism of Antibiotic Resistance
Question: What is target site modification?
Answer: c. MRSA
Explanation:
MRSA acquires the mecA gene, which encodes a modified penicillin-binding protein that does not bind beta-lactam antibiotics effectively. This is a classic example of resistance due to alteration of the drug's target site.
Question 15: Common Antibiotic Target
Question: The most common antibiotic target?
Answer: d. Ribosome
Explanation:
The ribosome is the most common antibiotic target because many major antibiotic classes act by disrupting bacterial protein synthesis.
Question 16: Microbe Produced Antimicrobial Compounds
Question: Which antimicrobial compounds are produced by microbes?
Answer: e. All of these (Polymyxin B, Chloramphenicol, Tetracycline, Streptamycin)