RO TA RUS V CCI E
     VI    A N
T E T SAVE YOUR K
 IM O            IDS




  DR.SMRUTIRANJAN PATANAIK
RO TA RUS
                  VI
 A VIRUS OF THE FAMILY
  REOVIRIDAE
 WHEEL SHAPED APPEARANCE –
  ROTA
 MAJOR CAUSE OF DIARRHEA AND
  GASTROENTERITIS UNDER THE
  AGE OF FIVE
 MORTALITY 6 LAKHS ACROSS THE
  GLOBE (29 TO 45 % OF ALL
  DIARRHEAL DEATHS)
 OVER 2 MILLION HOSPITALIZED
  EACH YEAR
STRUCTURE




CLASSIFICATION
BASIS :- IMMUNOLOGICAL REACTIVITIES OF VARIOUS
         COMPONENTS OF PARTICLES & FROM
 GENOMIC COMPOSITION INTO GROUPS A-G:-
GROUP A HAVING SEROTYPES & GENOTYPES
REPLI TI N
               CA O
SITE- CYTOPLASM OF ENTEROCYTES
        REMOVAL OF OUTER CAPSID

            mRNA SYNTHESIS

          mRNA (CYTOPLASM)
                    TRANSLATION

            VIRAL PROTEINS

              VIROPLASM
                    REPLICATION

                ds RNA

    DOUBLE SHELLED PARTICLES FORMED

            VIRUS RELEASED
ROUTE OF TRANSMISSION-FAECO ORAL
 ROUTE (1012 VIRIONS PER GM. OF EXCRETA
 IN ACUTE INFECTION)
INFECTIVE DOSE-LOW (100-1000 VIRAL
 PARTICLES)
INCUBATION PERIOD-2 TO 3 DAYS
IMMUNITY:-
        IgA ANTIBODIES
        CTL
NEED FO R AV CCI E
                       A N

 NATURALLY ACQUIRED IMMUNITY AFTER THE DISEASE.
 TRANSMISSION RATES UNAFFECTED BY IMPROVING
  SANITATION.
 UNAVAILABILITY OF LIFE SAVING I.V. TREATMENT TO
  ALL PATIENTS.
 COST EFFECTIVE METHODS.


 HISTORYOF VACCINE DEVELOPMENT
• 1993-94—LIVE ATTENUATED ROTAVIRUS VACCINE
           FROM RHESUS MONKEY.
• 1996-COCKTAIL VACCINE (RRV-TV).
• 1998-ROTASHIELD
PRESEN V CCI ES A ALA LE
      T A N      VI B
CHALLEN GES FO R V CCI E
                         A N
  I TRO DUCTI N& FUTURE PRO SPECTS
   N         O


UNCERTAIN DEMAND, INSUFFICIENT SUPPLY
 AND HIGH PRICES OF THE VACCINE.
LACK OF INFORMATION ON BURDEN OF
 DISEASE IN SOME COUNTRIES.
NEW EMERGING MUTANT & RECOMBINANT
 STRAINS OF VIRUS.
I AN
          N UTSHELL
THE 2 VACCINES ROTATEQ AND ROTARIX
LAUNCHED IN THE YEAR 2006 HELP IN
PREVENTION OF ROTAVIRUS INFECTION AT THE
ENTEROCYTE LEVEL HAVING A PROMISING
EFFICACY OF AROUND 95 TO 100%.
Rotavirus

Rotavirus

  • 1.
    RO TA RUSV CCI E VI A N T E T SAVE YOUR K IM O IDS DR.SMRUTIRANJAN PATANAIK
  • 2.
    RO TA RUS VI  A VIRUS OF THE FAMILY REOVIRIDAE  WHEEL SHAPED APPEARANCE – ROTA  MAJOR CAUSE OF DIARRHEA AND GASTROENTERITIS UNDER THE AGE OF FIVE  MORTALITY 6 LAKHS ACROSS THE GLOBE (29 TO 45 % OF ALL DIARRHEAL DEATHS)  OVER 2 MILLION HOSPITALIZED EACH YEAR
  • 3.
    STRUCTURE CLASSIFICATION BASIS :- IMMUNOLOGICALREACTIVITIES OF VARIOUS COMPONENTS OF PARTICLES & FROM GENOMIC COMPOSITION INTO GROUPS A-G:- GROUP A HAVING SEROTYPES & GENOTYPES
  • 4.
    REPLI TI N CA O SITE- CYTOPLASM OF ENTEROCYTES REMOVAL OF OUTER CAPSID mRNA SYNTHESIS mRNA (CYTOPLASM) TRANSLATION VIRAL PROTEINS VIROPLASM REPLICATION ds RNA DOUBLE SHELLED PARTICLES FORMED VIRUS RELEASED
  • 5.
    ROUTE OF TRANSMISSION-FAECOORAL ROUTE (1012 VIRIONS PER GM. OF EXCRETA IN ACUTE INFECTION) INFECTIVE DOSE-LOW (100-1000 VIRAL PARTICLES) INCUBATION PERIOD-2 TO 3 DAYS IMMUNITY:- IgA ANTIBODIES CTL
  • 6.
    NEED FO RAV CCI E A N  NATURALLY ACQUIRED IMMUNITY AFTER THE DISEASE.  TRANSMISSION RATES UNAFFECTED BY IMPROVING SANITATION.  UNAVAILABILITY OF LIFE SAVING I.V. TREATMENT TO ALL PATIENTS.  COST EFFECTIVE METHODS. HISTORYOF VACCINE DEVELOPMENT • 1993-94—LIVE ATTENUATED ROTAVIRUS VACCINE FROM RHESUS MONKEY. • 1996-COCKTAIL VACCINE (RRV-TV). • 1998-ROTASHIELD
  • 7.
    PRESEN V CCIES A ALA LE T A N VI B
  • 8.
    CHALLEN GES FOR V CCI E A N I TRO DUCTI N& FUTURE PRO SPECTS N O UNCERTAIN DEMAND, INSUFFICIENT SUPPLY AND HIGH PRICES OF THE VACCINE. LACK OF INFORMATION ON BURDEN OF DISEASE IN SOME COUNTRIES. NEW EMERGING MUTANT & RECOMBINANT STRAINS OF VIRUS.
  • 9.
    I AN N UTSHELL THE 2 VACCINES ROTATEQ AND ROTARIX LAUNCHED IN THE YEAR 2006 HELP IN PREVENTION OF ROTAVIRUS INFECTION AT THE ENTEROCYTE LEVEL HAVING A PROMISING EFFICACY OF AROUND 95 TO 100%.