Match each patient's clinical presentation with the primary molecular mechanism by which the causative pathogen survives within host cells.
- A 65-year-old man develops severe pneumonia and confusion after attending a convention. Sputum Gram stain shows numerous neutrophils but no organisms.Inhibits phagosome-lysosome fusion via a Type IV secretion system, establishing a replicative vacuole surrounded by host ribosomes.
- A 24-year-old traveler presents with a step-wise fever and rose spots on his abdomen. Blood cultures grow H2S-producing, motile bacteria.Employs a Type III secretion system to remodel the containing vacuole, protecting the organism from reactive oxygen species.
- A 40-year-old sheep farmer presents with high fever, headache, and atypical pneumonia; transaminases are elevated.Actively relies on the fusion of the phagosome with lysosomes, requiring a highly acidic environment for metabolic activation.
- A 70-year-old woman develops meningitis after eating unpasteurized cheese. Cerebrospinal fluid grows Gram-positive rods with tumbling motility.Produces a pore-forming toxin that lyses the phagosomal membrane, enabling the organism to escape into the cytosol.
Answer
Legionella pneumophila (convention pneumonia) inhibits phagosome-lysosome fusion. Salmonella typhi (typhoid fever) remodels its vacuole using a Type III secretion system. Coxiella burnetii (Q fever) requires the highly acidic environment of the fused phagolysosome. Listeria monocytogenes (cheese-associated meningitis) escapes the phagosome by producing a pore-forming toxin.
Each correct pair accurately links a classic clinical presentation to the specific, distinct molecular strategy used by that causative pathogen to survive and replicate within host cells.
Step-by-Step Solution
Key Concept
Intracellular pathogens utilize distinct molecular mechanisms to survive within host phagocytes, including preventing phagosome-lysosome fusion, escaping into the cytosol, remodeling the enclosing vacuole, or adapting to the highly acidic environment of the mature phagolysosome.