WBR0088: Difference between revisions
No edit summary |
No edit summary |
||
Line 1: | Line 1: | ||
{{WBRQuestion | {{WBRQuestion | ||
|QuestionAuthor={{Ochuko}} | |QuestionAuthor={{Ochuko}} (Reviewed by Will Gibson) | ||
|ExamType=USMLE Step 1 | |ExamType=USMLE Step 1 | ||
|MainCategory=Microbiology | |MainCategory=Microbiology |
Revision as of 00:44, 21 March 2014
Author | [[PageAuthor::Ogheneochuko Ajari, MB.BS, MS [1] (Reviewed by Will Gibson)]] |
---|---|
Exam Type | ExamType::USMLE Step 1 |
Main Category | MainCategory::Microbiology |
Sub Category | SubCategory::Neurology, SubCategory::Infectious Disease |
Prompt | [[Prompt::A 38-year old male is brought to the emergency department by his mother with complaints of hydrophobia and disorientation. She reports that he has had three episodes of seizures in the past 2 weeks. Three days later, the patient experiences vivid visual hallucinations, lapses into a coma and dies. The most likely causal organism binds to which of the following cell surface molecules?]] |
Answer A | AnswerA::SNARE proteins |
Answer A Explanation | [[AnswerAExp::SNARE proteins are responsible for neurotransmitter release at synaptic junctions. Clostridium tetani and clostridium botulinum produce toxins that cleave SNARE proteins and thereby cause paralysis.]] |
Answer B | AnswerB::CD4 receptors |
Answer B Explanation | AnswerBExp::HIV-1 binds to CD4 through its viral envelope protein gp120 to gain entry into host T-cells. The number of CD4-positive T cells in the blood is a marker of disease progression in HIV infected patients. |
Answer C | AnswerC::LDL receptors |
Answer C Explanation | [[AnswerCExp::LDL receptor mutations cause familial hypercholesterolemia, an autosomal dominant lipid disorder. Familial hypercholesterolemia is associated with accelerated atherosclerosis, tendon (Achilles) xanthomas and corneal arcus.]] |
Answer D | AnswerD::CCR5 receptors |
Answer D Explanation | [[AnswerDExp::CCR5 receptor is a co-receptor for HIV found on macrophages and Th cells. Individuals with CCR5 mutations are protected from HIV infection.]] |
Answer E | AnswerE::Acetylcholine receptors |
Answer E Explanation | [[AnswerEExp::The rabies virus binds to nicotinic acetylcholine receptors to travel from peripheral nerves to the brain.]] |
Right Answer | RightAnswer::E |
Explanation | [[Explanation::The patient in this vignette has rabies encephalitis, a viral infection that is transmitted from dog, bat, raccoon and skunk bites. The disease progresses from fever, malaise to agitation, photophobia, hydrophobia, seizures, hallucination and then to paralysis, coma and death. After the bite from an infected animal, the virus infiltrates peripheral nerves by binding to nicotinic acetylcholine receptors at the site of inoculation. The virus moves by retrograde axoplasmic transport to dorsal root ganglia and the spinal cord. The brain becomes rapidly infected when the virus gets to the spinal cord. The incubation period during which patients do not display symptoms is typically months. However, death usually occurs within days of symptom onset.
On autopsy, the brains of patients will display negri bodies (pictured below), hallmark cytoplasmic inclusions found in neurons infected with the virus. Treatment for suspected rabies infection consists of wound debridement, prophylactic vaccination (active immunity) and anti-rabies IgG (passive immunity). Rabies virus is a rhabdovirus, consisting of single-stranded negative sense RNA with helical capsid symmetry. It is famous for its bullet-shaped appearance. Negri Bodies |
Approved | Approved::Yes |
Keyword | WBRKeyword::Rabies, WBRKeyword::Virus, WBRKeyword::Viruses, WBRKeyword::Microbiology, WBRKeyword::Neurodegenerative, WBRKeyword::Hallucination, WBRKeyword::Seizure |
Linked Question | Linked:: |
Order in Linked Questions | LinkedOrder:: |