PICORNAVIRIDAE

on 2.2.09 with 0 comments



  • STRUCTURE: Smallest of RNA viruses, ss (+) RNA, non-enveloped, linear, infectious. No cap but there is a viral protein linked to the 5' end.

    • Rigid capsule makes fecal-oral transmission possible

    • A large number of infectious viral particles is produced. Humoral immunity is crucial to fighting these.

    • Non-enveloped structure makes it a good GI pathogen, able to survive in GI tract.

  • REPLICATION: Cytoplasmic, RNA-Dependent RNA Polymerase.

    • Entire genome is immediately translated into a polyprotein.

    • Polyprotein is cleaved into several small constituents:

      • Viral RNA-Dependent RNA Polymerase

      • Structural proteins

    • RNA Dependent RNA Polymerase then makes a minus-strand RNA out of the plus-strand RNA.

    • The minus-strand RNA is then used as a template for making additional (plus-strand) viral particles.

  • ENTEROVIRUSES:

    • CONDITIONS:

      • Stable at pH 3, thus it can replicate in stomach.

      • Optimal temp is 37C, favoring GI tract.

    • EPIDEMIOLOGY: Highly communicable. Fecal-oral transmission, respiratory, person-to-person.

      • Peak occurrence in summer and fall.

      • Incubation period of 3-5 days for localized infections, or longer for generalized illnesses.

      • Virus is tropic for lymphoid tissue in small intestine and pharynx.

    • 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).

    • IMMUNITY: Acquired immunity is lifelong and serotype specific. Humoral and mucosal immunity is important, to counteract free viral particles.

      • 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.

    • POLIOVIRUS:

      • STRUCTURE: 3 serotypes.

        • Ig-Superfamily cell-surface receptor protein has been identified.

      • DIAGNOSIS:

      • MANIFESTATIONS: Only 1 in 200 infections come down with Paralytic Poliomyelitis.

        • Infection of anterior horn cells of spinal cord (spinal poliomyelitis) or pontine nuclei (bulbar poliomyelitis).

        • Symptoms: Myalgia, generalized weakness, followed by flaccid paralysis.

        • 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.

      • VACCINE: Sabin (live, oral) and Salk (dead). Most remaining cases of Polio today are residuals of the live attenuated vaccine.

        • The Sabin Oral Polio vaccine should not be given to people with HIV. Other live vaccines (measles, mumps, HBV, influenza) can be given.

        • 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.

    • COXSACKIEVIRUSES:

      • COXSACKIEVIRUS A: 26 serotypes.

        • MANIFESTATIONS: Usually just mild respiratory disease.

          • ASEPTIC MENINGITIS:

            • Viral Meningitis occurs in Summer and Fall -- not Winter and Spring as in Mumps virus.

            • Coxsackie A&B, and Echovirus account for 80-90% of all cases of viral aseptic meningitis.

            • Important to distinguish it with partially treated bacterial meningitis: lumbar puncture will show lymphocytes (not PMN's), and a normal glucose (not low glucose).

          • HERPANGINA: Severe febrile, vesicular pharyngitis -- vesicles or nodules on soft palate.

          • Acute Hemorrhagic Conjunctivitis. Very contagious pain and swelling of eyelids. Occurs in Coxsackie A24.

          • HAND-FOOT-AND-MOUTH DISEASE: Vesicular rashes. Coxsackie A9 and A16.

          • Hemolytic Uremic Syndrome (HUS): Can be seen in strains of Coxsackie A and B, and Echovirus. Also due to E. Coli strains.

      • COXSACKIEVIRUS B: 6 serotypes.

        • MANIFESTATIONS: The leading viral cause of myocarditis and pericarditis.

          • Myocarditis and Pericarditis.

          • Aseptic meningitis.

          • Pleurodynia: Sharp muscle pain. Peak age of incidence in adolescent -- older than most enteroviral infections.

          • Newborn Disease: Myocarditis, encephalitis, hemorrhagic hepatitis. Also found in Echovirus. Non-immune neonate (no maternal antibodies) is susceptible, and can be fatal.

    • ECHOVIRUS: Enteric Cytopathic Human Orphan Virus

      • STRUCTURE: 30 serotypes. Called "orphan" because it wasn't associated with any disease state. Generally non-pathogenic.

      • MANIFESTATIONS: Asymptomatic or mild respiratory disease, and can cause aseptic meningitis and HUS, severe diseases of newborn.

    • ENTEROVIRUSES 68-72: Newer numbered enteroviruses.

      • ENTEROVIRUS-70:

        • MANIFESTATIONS: Acute Hemorrhagic Conjunctivitis. Very contagious pain and swelling of eyelids. Also seen with Coxsackie A24.

      • ENTEROVIRUS-71:

        • MANIFESTATIONS:

          • Hand-foot-and-mouth Disease: Herpetiform lesions in hand, foot, and mouth.

    • ENTEROVIRUS-72: HEPATITIS-A

      • STRUCTURE: Single stranded RNA, non-enveloped, stable to ether, temperature.

      • TRANSMISSION: Fecal-oral, sexual. Found in shellfish, where viral particles can become concentrated.

      • MANIFESTATIONS: Unlike the other picornaviruses, it is not cytocidal.

        • Damage to liver is due to hypersensitivity, cytotoxic T-Cells -- not due to viral cytopathic effect.

        • As opposed to HBV and HCV, HAV is only acute -- there is no persistent infection.

      • DIAGNOSIS: Look for Anti-HAV IgM to diagnose acute infection.

        • AST will be high early on.

        • Anti-HAV IgM, increases slowly, and drops off after a few weeks.

        • Anti-HAV IgG starts afer 5-6 weeks and persists for life.

      • VACCINE: Available, and given to people traveling to endemic areas. Three doses.

  • RHINOVIRUS:

    • STRUCTURE: more than 100 serotypes. "Rhino" = nose.

      • ICAM cell-surface receptor protein has been identified.

    • CONDITIONS:

      • Labile at pH 3, thus it is inactivated in the stomach.

      • Optimal temp = 33C, thus it likes to grow in the nose.

    • IMMUNITY: Acquired immunity is poor.

    • DIAGNOSIS: It isn't cultured, but must distinguish it from bacterial otitis media or pharyngitis. Culture for Strep-A.

    • MANIFESTATIONS:

      • Common Cold: 30-50% of cases, occurring throughout year and peaking in summer.

Category: Microbiology Notes

POST COMMENT

0 comments:

Post a Comment