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MEASLES VIRUS
Saroj Kumar Thakur
B.Sc.MLT, M.Sc. Medical Microbiology
(Medical Microbiologist)
Madesh Institute of Health Sciences
(Provincial Hospital)
MORPHOLOGY
 Spherical , pleomorphic
 120-250nm size
 Possesses a lipoprotein
envelop having
haemagglutinin(H) spikes but
no neuraminidase activity
 It has fusion protein(F) that
mediated cell fusion &
haemolytic activities.
PATHOGENESIS
 Measeles is also known as rubeola
 Highly infectious childhood disease transmitted by
inhalation of virus present in respiratory secretion of
patients
Infects RT----Multiply in RT----Invades blood stream------
spread to RES----Multiply further in RES-----Transported
via blood to epithelial surfaces-skin,mouth,RT &
conjunctva
CLINICAL FEATURES
 IP-10-14 days
 Prodromal stage characterised by fever, conjunctivitis,
malaise, running nose & cough
 Koplik’s spot-bright red lesions with a white, central dot on
buccal mucosa are diagnostic
 A few later- a red maculopapular rash appears 1st on the
face & spread downwards. Rash disappears in 3-6 days
LABORATORY DIAGNOSIS
 Specimens: Nasopharyngeal swab & blood
 Microscopy: Demonstration of multiple gaint cells in Giemsa-stained
smears of nasal secretions for early diagnosis, even before the rash
appears
 Culture:
 Human or monkey kidney cell culture
 Continuous cell culture (HeLa,VERO)
 Observed for cytopathic effects (CPE
 Serological diagnosis
 CFT
 ELISA-IgM
 Neutralization test
 HAI
EPIDEMIOLOGY AND PROPHYLAXIS
 Man is the only natural host of measles & monkey
acquires infection from man
 Maximum incidence in children 1-5 years
 Measles is endemic throughout the world & eidemics
usually occurs in later winter & early spring.
TREATMENT
 MMR
Measles.pptx

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Measles.pptx

  • 1. MEASLES VIRUS Saroj Kumar Thakur B.Sc.MLT, M.Sc. Medical Microbiology (Medical Microbiologist) Madesh Institute of Health Sciences (Provincial Hospital)
  • 2. MORPHOLOGY  Spherical , pleomorphic  120-250nm size  Possesses a lipoprotein envelop having haemagglutinin(H) spikes but no neuraminidase activity  It has fusion protein(F) that mediated cell fusion & haemolytic activities.
  • 3. PATHOGENESIS  Measeles is also known as rubeola  Highly infectious childhood disease transmitted by inhalation of virus present in respiratory secretion of patients Infects RT----Multiply in RT----Invades blood stream------ spread to RES----Multiply further in RES-----Transported via blood to epithelial surfaces-skin,mouth,RT & conjunctva
  • 4. CLINICAL FEATURES  IP-10-14 days  Prodromal stage characterised by fever, conjunctivitis, malaise, running nose & cough  Koplik’s spot-bright red lesions with a white, central dot on buccal mucosa are diagnostic  A few later- a red maculopapular rash appears 1st on the face & spread downwards. Rash disappears in 3-6 days
  • 5. LABORATORY DIAGNOSIS  Specimens: Nasopharyngeal swab & blood  Microscopy: Demonstration of multiple gaint cells in Giemsa-stained smears of nasal secretions for early diagnosis, even before the rash appears  Culture:  Human or monkey kidney cell culture  Continuous cell culture (HeLa,VERO)  Observed for cytopathic effects (CPE
  • 6.  Serological diagnosis  CFT  ELISA-IgM  Neutralization test  HAI
  • 7. EPIDEMIOLOGY AND PROPHYLAXIS  Man is the only natural host of measles & monkey acquires infection from man  Maximum incidence in children 1-5 years  Measles is endemic throughout the world & eidemics usually occurs in later winter & early spring.