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STRUCTURE: Smallest of RNA viruses, ss (+) RNA, non-enveloped, linear, infectious. No cap but there is a viral protein linked to the 5' end.
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Rigid capsule makes fecal-oral transmission possible
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A large number of infectious viral particles is produced. Humoral immunity is crucial to fighting these.
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Non-enveloped structure makes it a good GI pathogen, able to survive in GI tract.
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REPLICATION: Cytoplasmic, RNA-Dependent RNA Polymerase.
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Entire genome is immediately translated into a polyprotein.
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Polyprotein is cleaved into several small constituents:
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Viral RNA-Dependent RNA Polymerase
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Structural proteins
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RNA Dependent RNA Polymerase then makes a minus-strand RNA out of the plus-strand RNA.
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The minus-strand RNA is then used as a template for making additional (plus-strand) viral particles.
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ENTEROVIRUSES:
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CONDITIONS:
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Stable at pH 3, thus it can replicate in stomach.
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Optimal temp is 37C, favoring GI tract.
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EPIDEMIOLOGY: Highly communicable. Fecal-oral transmission, respiratory, person-to-person.
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Peak occurrence in summer and fall.
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Incubation period of 3-5 days for localized infections, or longer for generalized illnesses.
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Virus is tropic for lymphoid tissue in small intestine and pharynx.
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General Manifestations: Usually asymptomatic or associated with mild illness. Even though GI tract is a major site of replication, GI symptoms are rarely seen (except as a consequence of generalized illness).
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IMMUNITY: Acquired immunity is lifelong and serotype specific. Humoral and mucosal immunity is important, to counteract free viral particles.
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Enteroviruses that infect the gut produce a good IgA response, whereas viruses that infect only the upper respiratory tract do not produce as good a response.
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POLIOVIRUS:
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STRUCTURE: 3 serotypes.
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Ig-Superfamily cell-surface receptor protein has been identified.
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DIAGNOSIS:
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MANIFESTATIONS: Only 1 in 200 infections come down with Paralytic Poliomyelitis.
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Infection of anterior horn cells of spinal cord (spinal poliomyelitis) or pontine nuclei (bulbar poliomyelitis).
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Symptoms: Myalgia, generalized weakness, followed by flaccid paralysis.
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Post-Polio Syndrome (PPS): Strange symptoms, thought to be due to nerve cell attrition, very late in the course of disease. Fatigue, muscle weakness, and respiratory difficulty.
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VACCINE: Sabin (live, oral) and Salk (dead). Most remaining cases of Polio today are residuals of the live attenuated vaccine.
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The Sabin Oral Polio vaccine should not be given to people with HIV. Other live vaccines (measles, mumps, HBV, influenza) can be given.
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Enhanced Polio Inactivated Vaccine has been developed recently. Will be given as the first shot -- inactivated vaccine, in order to prevent patient from getting polio from vaccine. Subsequent booster shots will then be the oral polio vaccine.
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COXSACKIEVIRUSES:
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COXSACKIEVIRUS A: 26 serotypes.
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MANIFESTATIONS: Usually just mild respiratory disease.
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ASEPTIC MENINGITIS:
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Viral Meningitis occurs in Summer and Fall -- not Winter and Spring as in Mumps virus.
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Coxsackie A&B, and Echovirus account for 80-90% of all cases of viral aseptic meningitis.
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Important to distinguish it with partially treated bacterial meningitis: lumbar puncture will show lymphocytes (not PMN's), and a normal glucose (not low glucose).
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HERPANGINA: Severe febrile, vesicular pharyngitis -- vesicles or nodules on soft palate.
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Acute Hemorrhagic Conjunctivitis. Very contagious pain and swelling of eyelids. Occurs in Coxsackie A24.
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HAND-FOOT-AND-MOUTH DISEASE: Vesicular rashes. Coxsackie A9 and A16.
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Hemolytic Uremic Syndrome (HUS): Can be seen in strains of Coxsackie A and B, and Echovirus. Also due to E. Coli strains.
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COXSACKIEVIRUS B: 6 serotypes.
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MANIFESTATIONS: The leading viral cause of myocarditis and pericarditis.
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Myocarditis and Pericarditis.
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Aseptic meningitis.
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Pleurodynia: Sharp muscle pain. Peak age of incidence in adolescent -- older than most enteroviral infections.
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Newborn Disease: Myocarditis, encephalitis, hemorrhagic hepatitis. Also found in Echovirus. Non-immune neonate (no maternal antibodies) is susceptible, and can be fatal.
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ECHOVIRUS: Enteric Cytopathic Human Orphan Virus
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STRUCTURE: 30 serotypes. Called "orphan" because it wasn't associated with any disease state. Generally non-pathogenic.
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MANIFESTATIONS: Asymptomatic or mild respiratory disease, and can cause aseptic meningitis and HUS, severe diseases of newborn.
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ENTEROVIRUSES 68-72: Newer numbered enteroviruses.
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ENTEROVIRUS-70:
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MANIFESTATIONS: Acute Hemorrhagic Conjunctivitis. Very contagious pain and swelling of eyelids. Also seen with Coxsackie A24.
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ENTEROVIRUS-71:
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MANIFESTATIONS:
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Hand-foot-and-mouth Disease: Herpetiform lesions in hand, foot, and mouth.
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ENTEROVIRUS-72: HEPATITIS-A
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STRUCTURE: Single stranded RNA, non-enveloped, stable to ether, temperature.
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TRANSMISSION: Fecal-oral, sexual. Found in shellfish, where viral particles can become concentrated.
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MANIFESTATIONS: Unlike the other picornaviruses, it is not cytocidal.
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Damage to liver is due to hypersensitivity, cytotoxic T-Cells -- not due to viral cytopathic effect.
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As opposed to HBV and HCV, HAV is only acute -- there is no persistent infection.
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DIAGNOSIS: Look for Anti-HAV IgM to diagnose acute infection.
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AST will be high early on.
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Anti-HAV IgM, increases slowly, and drops off after a few weeks.
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Anti-HAV IgG starts afer 5-6 weeks and persists for life.
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VACCINE: Available, and given to people traveling to endemic areas. Three doses.
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RHINOVIRUS:
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STRUCTURE: more than 100 serotypes. "Rhino" = nose.
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ICAM cell-surface receptor protein has been identified.
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CONDITIONS:
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Labile at pH 3, thus it is inactivated in the stomach.
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Optimal temp = 33C, thus it likes to grow in the nose.
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IMMUNITY: Acquired immunity is poor.
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DIAGNOSIS: It isn't cultured, but must distinguish it from bacterial otitis media or pharyngitis. Culture for Strep-A.
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MANIFESTATIONS:
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Common Cold: 30-50% of cases, occurring throughout year and peaking in summer.
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Category: Microbiology Notes
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