MD.KABIUL AKHTER ALI
       Vector Borne Disease Consultant
                      NVBDCP, NRHM
District Heath & Family Welfare Samiti
                        Uttar Dinajpur
Overview
Economic impact
History
Epidemiology
Transmission
Clinical Signs
Diagnosis and Treatment
Disease in Humans
Prevention and Control
Actions to Take/Program mode
Japanese Encephalitis
Flaviviridae
  Flavivirus
The name is derived from
 the Latin ‘flavus’
  Flavus means “yellow”
       Refers to yellow fever virus
Enveloped
Single stranded RNA virus
Morphology not well defined
History
 1870s: Japan
    “Summer encephalitis” epidemics
1924: Great epidemic in Japan
   6,125 human cases; 3,797 deaths
1935: Virus first isolated
   From a fatal human encephalitis case
1938: Isolated from Culex tritaeniorhynchus
1952: First evidence of J E
1955:First case in India
1958:First viral isolation in India
1973:First outbreak inBankura/Burdwan
1978:widespread occurance/monitoring NMEP
Initiation of immunisation –killed mouse brain vaccine
Economic Impact
Animals
  Porcine
      High mortality in piglets
  Equine
      Up to 5% mortality rate
  Humans
      Cost for immunization and medical treatment
Geographic Distribution
Endemic in temperate and
 tropical regions of Asia
Reduced prevalence in                      Korea   Japan


 Japan                              China

Has not occurred in U.S.   India             Philippine
                                              s


                                              Indonesia
Morbidity/Mortality
Swine
  High mortality in piglets
  Death rare in adult pigs
Equine
  Morbidity: 2%, during an outbreak
  Mortality: 5%
Humans
  Mortality: 5-40%
  Serious neurologic sequelae: 45-70%
Transmission
Vector-borne disease
Enzootic cycle
  Mosquitoes: Culex species
    Culex vishnuii/pseudovishnui/tritinorinchus
    Paddy fields

  Reservoir/Amplifying hosts
    Pigs, bats
    Ardeid (wading) birds
    Possibly reptiles and amphibians

  Incidental hosts
      Horses, humans,(dead end)
Global Problem
Leading cause of viral encephalitis
3 billion live in endemic areas
50000 cases reported annually
10-15 thousand deaths annually
INDIA-33o million live in endemic areas in 15
 states/ut
135 districts are affected
Clinical Signs: Swine
Incubation period not known
Exposure early in pregnancy more harmful
Birth of stillborn or mummified fetuses
Piglets: Neurological signs, death
Boars: Infertility, swollen testicles
Post Mortem Lesions
Horses
  Non-specific
  Nonsuppurative
   meningoencephalitis
Swine
  Fetuses
    Mummified and dark in appearance
    Hydrocephalus

    Cerebellar hypoplasia

    Spinal hypomyelinogenesis
Differential Diagnosis
Equine
   Other viral encephalitides, Hendra, rabies,
   neurotoxins, toxic encephalitis
Swine
  Myxovirus-parainfluenza 1, coronavirus, Menangle
   virus, porcine parvovirus
Sampling
Before collecting or sending any samples, the proper
 authorities should be contacted

Samples should only be sent under secure conditions
 and to authorized laboratories to prevent the spread
 of the disease
Diagnosis
Clinical
  Horses: Fever and CNS disease
  Swine: High number of stillborn piglets
Laboratory Tests
  Definitive: Viral isolation
       Blood, spinal cord, brain, CSF
  Rise in titer
     Neutralization, HI, IF, CF, ELISA
     Cross reactivity of Flaviviruses
Treatment
No effective treatment
Supportive care
Clinical Signs-Humans
Incubation period: 5 to 15 days
Most asymptomatic or mild signs
Children < 15 years and Elderly
  At highest risk for severe disease
     Elderly: High case fatality rate (30%)
     For every case 200-1000 undetected/asymptomatic cases

     Disease clinical perspective divided into
      mild/moderate/severe/asymptomatic cases
Clinical Signs: Severe
Acute encephalitis
  Headache, high fever, stiff neck, stupor
Severe encephalitis
  Paralysis, seizures, convulsions, coma, and death
Neuropsychiatric sequelae
  45-70% of survivors
In utero infection possible
  Abortion of fetus
Post Mortem Lesions
Pan-encephalitis
Infected neurons scattered
 throughout CNS
Occasional microscopic
 necrotic foci
Thalamus generally severely
 affected
Diagnosis and Treatment
Clinical
Laboratory Tests
  Tentative diagnosis
     Antibody titer: HI, IFA, CF, ELISA
     JE-specific IgM in serum or CSF

  Definitive diagnosis
       Virus isolation: CSF sample, brain
No specific treatment
  Supportive care
Public Health Significance
Strengthening of surveillance
Capacity building for diagnosis/case management to
 reduce fatality
Clinical laboratory support/adequacy of medicines in
 hospitals
Vector surveillance strengthening
Focused IEC for early reporting
Increasing indigenous capacity of vaccine production
Disinfection
Biosafety Level 3 precautions
Chemical
  Ethanol, glutaraldehyde, formaldehyde
  Sodium hypochlorite (bleach)
  Iodine, phenols, iodophors
Physical
  Deactivation at 133oF (for 30 minutes)
  Sensitive to ultraviolet light and gamma radiation
Prevention
Vector control
   Eliminate mosquito breeding areas
   Adult and larvae control( chemical larvicides, Biolarvicides,
    larvivorous fish)
   Environmental management
Vaccination
   Equine and swine
   Humans
Personal protective measures
   Avoid prime mosquito hours/IVM
   Space spray-Fogging with pyrethrum/malathion
   Use of repellants /ITN/curtains
Prevention(Program mode)
Strengthening JE surveillance- identifying /setting of
 50 sentinel sites
12 Apex Referral laboratories(Diagnosis)
Guidelines for AES/JE surveillance
VBD Control Surveillance Unit at BRD Medical
 College Gorakhpur
Sub office ROHFW Lucknow at Gorakhpur
NIV Pune unit at BRD Medical College
 Gorakhpur(funded by GOI/ICMR)
Vaccination
Live attenuated vaccine
  Used in equine and swine
  Successful for reducing incidence
Inactivated vaccine (JE-VAX)/SA 14-14-2 Chinese-
 Single dose IM(Children 1-15 years)
     Used for human beings
     2006-11 districts in 4 states(Assam,Karnataka,WB &UP)

     2007 – Expanded to 27 districts in 9 states

     2008- 23 districts in 9 states covered

     Left out and new cohorts covered in routine immunisation
THANK YOU

JE ppt

  • 1.
    MD.KABIUL AKHTER ALI Vector Borne Disease Consultant NVBDCP, NRHM District Heath & Family Welfare Samiti Uttar Dinajpur
  • 2.
    Overview Economic impact History Epidemiology Transmission Clinical Signs Diagnosisand Treatment Disease in Humans Prevention and Control Actions to Take/Program mode
  • 3.
    Japanese Encephalitis Flaviviridae Flavivirus The name is derived from the Latin ‘flavus’ Flavus means “yellow”  Refers to yellow fever virus Enveloped Single stranded RNA virus Morphology not well defined
  • 4.
    History  1870s: Japan  “Summer encephalitis” epidemics 1924: Great epidemic in Japan  6,125 human cases; 3,797 deaths 1935: Virus first isolated  From a fatal human encephalitis case 1938: Isolated from Culex tritaeniorhynchus 1952: First evidence of J E 1955:First case in India 1958:First viral isolation in India 1973:First outbreak inBankura/Burdwan 1978:widespread occurance/monitoring NMEP Initiation of immunisation –killed mouse brain vaccine
  • 5.
    Economic Impact Animals Porcine  High mortality in piglets Equine  Up to 5% mortality rate Humans  Cost for immunization and medical treatment
  • 6.
    Geographic Distribution Endemic intemperate and tropical regions of Asia Reduced prevalence in Korea Japan Japan China Has not occurred in U.S. India Philippine s Indonesia
  • 7.
    Morbidity/Mortality Swine Highmortality in piglets Death rare in adult pigs Equine Morbidity: 2%, during an outbreak Mortality: 5% Humans Mortality: 5-40% Serious neurologic sequelae: 45-70%
  • 8.
    Transmission Vector-borne disease Enzootic cycle Mosquitoes: Culex species  Culex vishnuii/pseudovishnui/tritinorinchus  Paddy fields Reservoir/Amplifying hosts  Pigs, bats  Ardeid (wading) birds  Possibly reptiles and amphibians Incidental hosts  Horses, humans,(dead end)
  • 10.
    Global Problem Leading causeof viral encephalitis 3 billion live in endemic areas 50000 cases reported annually 10-15 thousand deaths annually INDIA-33o million live in endemic areas in 15 states/ut 135 districts are affected
  • 11.
    Clinical Signs: Swine Incubationperiod not known Exposure early in pregnancy more harmful Birth of stillborn or mummified fetuses Piglets: Neurological signs, death Boars: Infertility, swollen testicles
  • 12.
    Post Mortem Lesions Horses Non-specific Nonsuppurative meningoencephalitis Swine Fetuses  Mummified and dark in appearance  Hydrocephalus  Cerebellar hypoplasia  Spinal hypomyelinogenesis
  • 13.
    Differential Diagnosis Equine  Other viral encephalitides, Hendra, rabies, neurotoxins, toxic encephalitis Swine Myxovirus-parainfluenza 1, coronavirus, Menangle virus, porcine parvovirus
  • 14.
    Sampling Before collecting orsending any samples, the proper authorities should be contacted Samples should only be sent under secure conditions and to authorized laboratories to prevent the spread of the disease
  • 15.
    Diagnosis Clinical Horses:Fever and CNS disease Swine: High number of stillborn piglets Laboratory Tests Definitive: Viral isolation  Blood, spinal cord, brain, CSF Rise in titer  Neutralization, HI, IF, CF, ELISA  Cross reactivity of Flaviviruses
  • 16.
  • 17.
    Clinical Signs-Humans Incubation period:5 to 15 days Most asymptomatic or mild signs Children < 15 years and Elderly At highest risk for severe disease  Elderly: High case fatality rate (30%)  For every case 200-1000 undetected/asymptomatic cases  Disease clinical perspective divided into mild/moderate/severe/asymptomatic cases
  • 18.
    Clinical Signs: Severe Acuteencephalitis Headache, high fever, stiff neck, stupor Severe encephalitis Paralysis, seizures, convulsions, coma, and death Neuropsychiatric sequelae 45-70% of survivors In utero infection possible Abortion of fetus
  • 19.
    Post Mortem Lesions Pan-encephalitis Infectedneurons scattered throughout CNS Occasional microscopic necrotic foci Thalamus generally severely affected
  • 20.
    Diagnosis and Treatment Clinical LaboratoryTests Tentative diagnosis  Antibody titer: HI, IFA, CF, ELISA  JE-specific IgM in serum or CSF Definitive diagnosis  Virus isolation: CSF sample, brain No specific treatment Supportive care
  • 21.
    Public Health Significance Strengtheningof surveillance Capacity building for diagnosis/case management to reduce fatality Clinical laboratory support/adequacy of medicines in hospitals Vector surveillance strengthening Focused IEC for early reporting Increasing indigenous capacity of vaccine production
  • 22.
    Disinfection Biosafety Level 3precautions Chemical Ethanol, glutaraldehyde, formaldehyde Sodium hypochlorite (bleach) Iodine, phenols, iodophors Physical Deactivation at 133oF (for 30 minutes) Sensitive to ultraviolet light and gamma radiation
  • 23.
    Prevention Vector control  Eliminate mosquito breeding areas  Adult and larvae control( chemical larvicides, Biolarvicides, larvivorous fish)  Environmental management Vaccination  Equine and swine  Humans Personal protective measures  Avoid prime mosquito hours/IVM  Space spray-Fogging with pyrethrum/malathion  Use of repellants /ITN/curtains
  • 24.
    Prevention(Program mode) Strengthening JEsurveillance- identifying /setting of 50 sentinel sites 12 Apex Referral laboratories(Diagnosis) Guidelines for AES/JE surveillance VBD Control Surveillance Unit at BRD Medical College Gorakhpur Sub office ROHFW Lucknow at Gorakhpur NIV Pune unit at BRD Medical College Gorakhpur(funded by GOI/ICMR)
  • 25.
    Vaccination Live attenuated vaccine Used in equine and swine Successful for reducing incidence Inactivated vaccine (JE-VAX)/SA 14-14-2 Chinese- Single dose IM(Children 1-15 years)  Used for human beings  2006-11 districts in 4 states(Assam,Karnataka,WB &UP)  2007 – Expanded to 27 districts in 9 states  2008- 23 districts in 9 states covered  Left out and new cohorts covered in routine immunisation
  • 26.

Editor's Notes