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Dengue Virus
 Characterized by fever of sudden onset,
headache, retro bulbar pain, conjunctival
infection, pain in the back and joints
 Break bone fever
 Lymphadenopathy, and maculopapaular
lesion
 Four sero types
 DEN 1
 DEN 2
 DEN 3
 DEN 4
 Transmitted by aedes aegypti
Clinical features
 Two forms
 Classical dengue fever
 Dengue in more serious forms with
hemorrhagic manifestations
Classical dengue fever
 Affects older children and adults
 Fever, headache, pain in muscles and bones
 Fever- biphasic
 Incubation period 5-8 days
 Maculopapular rash appears on 3rd or 4th day
 Febrile illness lasts for 10 days
 Rarely fatal

Dengue in more serious forms with
hemorrhagic manifestations
 Dengue hemorrhagic fever( DHF) and
dengue shock syndrome (DSS)
 Mostly in 5-10 years age group
 In area where multiple dengue viruses
cause disease
 It appears to be hyper immune response
 It is seen in patients previously infected
dengue virus
 On reinfection with a different type of
dengue virus antibody formed against the
first virus reacts with the second serotype
virus forming immune complexes
 Symptoms- fever associated with
hemorrhagic rash, thrombocytopenia,
and shock
 Mortality 5-10%
Laboratory diagnosis
 SPECIMENS:
 For antibody and antigen detection –
serum
 For isolation of virus and PCR- serum,
plasma, whole blood, autopsy
specimens, mosquitoes collected
innature
 Hematological diagnosis:
 Thrombocytopenia
 haemoconcentrtion
 Microbiological diagnosis:
 Detection of antibody
 IgM ab in serum
 Appear after 5 days
 ELISA is used
 IgG ab appears later than IgM
 Detection of NS1 antigen
 Immunochroamtographic test
 Rapid test
 Detects on the first day of fever
 Takes 15 mins
 Isolation of virus:
 Done by inoculating clinical specimens in
to mosquitoes, mosquitoes cell lines or
suckling mice
 Further identification is done by
fluorescent antibody technique
 PCR:
 Viral RNA can be detected in clinical
specimens by RTPCR
Prophylaxis
 Elimination of mosquitoes
 No effective vaccine
 Vaccine Under clinical trails
DENGUE.ppt/ dengue virus/ dna viruses/virology

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DENGUE.ppt/ dengue virus/ dna viruses/virology

  • 2.  Characterized by fever of sudden onset, headache, retro bulbar pain, conjunctival infection, pain in the back and joints  Break bone fever  Lymphadenopathy, and maculopapaular lesion
  • 3.  Four sero types  DEN 1  DEN 2  DEN 3  DEN 4  Transmitted by aedes aegypti
  • 4. Clinical features  Two forms  Classical dengue fever  Dengue in more serious forms with hemorrhagic manifestations
  • 5. Classical dengue fever  Affects older children and adults  Fever, headache, pain in muscles and bones  Fever- biphasic  Incubation period 5-8 days  Maculopapular rash appears on 3rd or 4th day  Febrile illness lasts for 10 days  Rarely fatal 
  • 6. Dengue in more serious forms with hemorrhagic manifestations  Dengue hemorrhagic fever( DHF) and dengue shock syndrome (DSS)  Mostly in 5-10 years age group  In area where multiple dengue viruses cause disease  It appears to be hyper immune response  It is seen in patients previously infected dengue virus
  • 7.  On reinfection with a different type of dengue virus antibody formed against the first virus reacts with the second serotype virus forming immune complexes
  • 8.  Symptoms- fever associated with hemorrhagic rash, thrombocytopenia, and shock  Mortality 5-10%
  • 9. Laboratory diagnosis  SPECIMENS:  For antibody and antigen detection – serum  For isolation of virus and PCR- serum, plasma, whole blood, autopsy specimens, mosquitoes collected innature
  • 10.  Hematological diagnosis:  Thrombocytopenia  haemoconcentrtion
  • 11.  Microbiological diagnosis:  Detection of antibody  IgM ab in serum  Appear after 5 days  ELISA is used  IgG ab appears later than IgM
  • 12.  Detection of NS1 antigen  Immunochroamtographic test  Rapid test  Detects on the first day of fever  Takes 15 mins
  • 13.  Isolation of virus:  Done by inoculating clinical specimens in to mosquitoes, mosquitoes cell lines or suckling mice  Further identification is done by fluorescent antibody technique
  • 14.  PCR:  Viral RNA can be detected in clinical specimens by RTPCR
  • 15. Prophylaxis  Elimination of mosquitoes  No effective vaccine  Vaccine Under clinical trails