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JAPANESE ENCEPHALITIS

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Title: JAPANESE ENCEPHALITIS


1
JAPANESE ENCEPHALITIS
Lin Chaoshuang The Third Affiliated Hospital
Sun-Yet sen University
2
Overview
  • Etiology
  • Epidemiology and history
  • Pathogenesis and Pathology
  • Clinical Manifestation
  • Diagnosis
  • Treatment
  • Prevention and Control

3
Etiology The Organism
  • Arbovirus
  • Flavivirus
  • Enveloped
  • Single positive-stranded RNA virus 11kb
  • Morphology sphere 4050nm
  • The name is Latin for flavus
  • Flavus means yellow
  • Refers to yellow fever virus

Flaviviridae
4
  • It has three proteins
  • Envelope protein
  • Core protein
  • Membrane protein

Etiology The Organism
5
Replication
Flaviviruses replication process includes the
entry by receptor-mediated endocytosis,
uncoating, protein synthesis, viral genome
synthesis, assembly, and virus release by budding
from plasma membrane or internal membrane.
6
History
  • 1870's Japan
  • Summer encephalitis epidemics
  • 1924 Great epidemic in Japan
  • 6,125 human cases 3,797 deaths
  • (62 case-fatality rate)
  • 1935 First isolated in Japan
  • From a fatal human encephalitis case
  • 1938 Isolated from Culex tritaeniorhynchus

7
History
  • 1940-1978
  • Disease spread with epidemics in China. Korea
    5,548 human cases in 1949
  • India recognized in 1954, over 6,000 cases in
    1978
  • 1983 Immunization in South Korea
  • Started as early as age 3
  • Endemic areas started earlier
  • 1983-1987 Vaccine available in U.S. on
    investigational basis

8
Epidemiology
  • Geographic Distribution
  • Endemic in temperate and tropical regions of Asia
  • Reduced prevalence in Japan
  • 30,000-50,000 cases annually
  • Less than 1 case/year in U.S.

www.cdc.gov/ncidod/dvbid/jencephalitis
9
JE Outbreaks in India
  • Outbreaks of JE occur in India for 27 years
  • Larger outbreak 1988 1228 deaths
  • Total deaths in 27 years 4000 deaths
  • Outbreak 2004 50 deaths

10
Outbreak 2005 in India
  • Index case Nepal, mid-June
  • First case India July 20th
  • First outbreak alert August 12th
  • Confirmation JE August 21th
  • Total death 1302
  • Total cases gt 5000

11
JE in CHINA
  • Pandemic from 1960s to early 1970s.
  • Incident rate decreased since late 1970s
  • Case reports were 500010000 cases /y these few
    years.
  • Outbreak in some areas.
  • Prevalence in Shanxi Province Yuncheng From
    13 July to 14 Augest, 2006.
  • 65 cases,19 deaths.

12
Transmission Sources of Infection
  • Arthropod-borne viruses (Arboviruses, ????)
  • Enzootic or zoonoses disease
  • Amplifying hosts
  • Pigs (the main reservoir)
  • Wading birds (egrets, herons), Bats
  • Incidental hosts
  • Horses, humans (dead-end hosts)
  • Others

herons
13
Transmission Routes of Transmission
  • Vectors Mosquitoes
  • Culex species tritaeniorhynchus
  • The mosquitoes that transmit the virus breed in
    rice fields, and standing water.
  • In winter, virus persist in arthropod (????) eggs
    or migrate with birds.
  • Death of infected no-human vertebrates occurs
    before human outbreak.

14
Transmission Susceptible Population
  • Age 2-10 years
  • Living in rural areas
  • People who live near
  • stagnant water
  • (mosquito breeding)

15
Epidemiologic Feature
  • The major outbreaks coincided with the heavy
    rainfall or floods.
  • Seasonal more common in summer, July to October
  • Infection provides life long immunity.

16
DYNAMICS OF JE TRANSMISSION
Vector Mosquito
Environment
Victim-Accidental
Recovery with residual complications
Full Recovery
Death
Host - Amplifying
Host - Carrier
17
Pathogenesis
  • The nature of flavivirus disease is determined
    primarily by
  • The specific tropisms of the individual virus
    type
  • The concentration of infecting virus
  • Individual host response to the infection

18
Pathogenesis
  • JE Virus
  • mononuclear phagocyte
  • blood circulation
  • viremia
  • Adequate immunological
    Weak immunological
  • response

    response
  • subclinical or mild invades
    the CNS
  • systemic disease induce
    mortality

19
Pathogenesis
  • Initial viral replication may occur in local
    regional lymph nodes
  • Initially brain damage is due to viral infection
    and multiplication in neurons per se
  • Later immunopathological mechanisms may play a
    role.

20
Pathology
  • Degeneration and necrosis of neurocyte
  • Formation of malacoma focus (???)
  • Blood vessel change and inflammatory reaction
  • Hyperplasy of colloid (??) cell

21
Manifestation
  • Most asymptomatic or mild signs
  • Ratio of subclinical to clinical ratio
    (2503001)
  • 50 develop permanent neurological damage
  • Incubation Period - 5 to 15 days

22
Clinical Manifestations
  • Clinical manifestations depend upon
  • Severity of infection
  • Susceptibility of the host
  • Location of the agent

23
Four stages
  • A Prodromal Stage
  • An Acute encephalitic Stage
  • The Convalescence Stage
  • A Sequela Stage

24
Prodromal Stage
  • The Prodromal stage usually lasts for 1 to 6
    days. It can be as short as less than 24 hours or
    as long as 14 days
  • Acute
  • Fever with severe rigors, headache and malaise
  • Nausea, Vomiting, Abdominal pain
  • Drowsy
  • Neck rigidity
  • Convulsions, Seizures

25
The Acute Encephalitic Stage
  • Begins by the third to fifth day.
  • The symptoms include
  • High fever for about 710 days
  • Changes in consciousness dullness, tremor,
    stupor, ataxia, focal or diffuse paralysis, coma
  • Convulsions localized or generalized, Tremors in
    fingers, tongue, eyelids and eyes
  • Respiratory failure maybe due to high
    intracranial pressure, edema of the brain, hernia
    of the brain.
  • Meningeal irritation sign Stiff neck, positive
    Kernigs sign and pathological reflexes.

26
The Convalescence Stage
  • Defervescence of fever
  • Defervescence of neurologic improvement
  • Usually lasts for at least two weeks.

27
A Sequela Stage
  • Neuropsychiatric sequelae
  • 30-50 of survivors
  • Characterised by
  • Persistance of signs of CNS injury
  • Mental impairment     
  • Increased deep Tendon reflexes     
  • Paresis either of the upper or lower motor neuron

  • (???????)     
  • Speech impairment     
  • Epilepsy, Abnormal movements, Behaviour
    abnormalities

28
Clinical spectrum of JE infection
Die
Severe
Moderate
Mild
Asymptomatic
  • For every symptomatic JE case, there are likely
    to be about 300 1000 people infected with JE
    virus but without any clinical manifestation
  • People of any age can be infected. Adult
    infection most often occurs in areas where the
    disease is newly introduced.

29
Laboratory Investigation
  • Peripheral blood analysis
  • leucocytosis (1020)X109/L with
    neutrophilicgt80
  • Cerebrospinal fluid (CSF) analysis
  • Routine clear, tension elevated,
  • leucocytosis (50500)X106/L
  • Neutrophils may
    predominate in early CSF samples but a
    lymphocytic pleocytosis is typical
  • Biochemistry
  • protein is moderately elevated
  • glucose and chloride normal
    level

30
Laboratory Investigation
  • Serological tests
  • Specific IgM antibody
  • A significant rise in IgG antibody titer
    should be seen with paired samples from the
    acute and convalescent stages.
  • The virus isolation
  • Isolated from CSF by inoculating into 2-4
    day old mice and the virus is identified by
    haemagglutination inhibition.
  • JE virus may also be identified by infection
    of cell cultures (chicken embryo or hamster
    kidney cells, or the mosquito cell line C3/36).

31
Diagnosis
  • Materials of epidemiology
  • Clinical
  • Laboratory Tests
  • Tentative diagnosis
  • Antibody titer HI, IF, CF, ELISA
  • JE-specific IgM in serum or CSF
  • Definitive diagnosis
  • Virus isolation Blood, CSF sample, brain

32
Differential Diagnosis
  • Toxic shigellosis and other Toxic Encephalopathy
  • Cerebral Malaria
  • Meningitis (other viral meningitis or
    encephalitis, partially treated bacterial
    meningitis, meningococcal meningitis, tuberculous
    or fungal meningitis)
  • Febrile Convulsions
  • Reys Syndrome
  • Rabies

33
Prognosis
  • Approximately 5-35 of cases are fatal, some with
    a fulminate course lasting a few days and others
    run a more protracted course in coma.
  • About 30-50 of those who survive may have
    serious neurologic sequelae.

34
Treatment
  • No specific therapy
  • Supportive care intensive life support is
    indicated
  • Surveillance for cases of encephalitis

35
Treatment
  • Treatment of high fever
  • Physical method ice, alcohol, cool saline.
  • Artificial hibernation
  • Seizure and convulsions management
  • Sedation, Corticosteroids may be used
  • For respiratory failure
  • Oxygen supply, artificial respiration
  • For raised intracranial pressure
  • Mannitol iv.drip 1mg/Kg every 68 hrs.

36
Prevention
  • Vector (Mosquito) control
  • Eliminate mosquito breeding areas Chemical
    larvicides, Biolarvicides, Environmental
    management
  • Adult and larval control Anti-larval treatment
  • Vaccination
  • Personal protective measures
  • Avoid prime mosquito hours from dusk to dawn
  • Indoor spray and fogging Use of Insecticide

37
Vaccination
  • Live attenuated vaccine
  • Successful for reducing incidence
  • SA 14-14-2 (Chinese live attenuated vaccine at
    affordable cost, safe, effective).
  • This vaccine was developed in China and has been
    used since 1988.
  • It has been licensed and used in South Korea.

38
Vaccination
  • Inactivated mouse brain vaccine(JE-VAX)
  • Comprising 3 doses 0.5ml each time and
  • the interval is 12 weeks in infancy,
  • boosting 1.0ml in children.
  • Used for endemic or epidemic areas.
  • Recommended for travelers visiting
  • endemic areas for gt 30 days.

39
THANKS
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