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Picorna viruses
Picorna viruses
OBJECTIVES
To learn about
• Classification
• Structure
• Pathogenesis
• Immunization
• Lab diagnosis of polioviruses.
INTRODUCTION
• Viruses comprises of pico=small rna =RNA
• SS RNA
• NON ENVELOPED
• DIAMETER = 27-30 NM
CLASSIFICATION
• Family- picornaviridae
• Divided - 6 genera
• Enterovirus
• Rhinovirus
• Cardiovirus
• Aphthovirus
• Hepatovirus
• Parechovirus
PROPERTIES
• SIZE 28- 30 NM
• VIRION ICOSAHEDRAL
• SS RNA LINEAR
• PROTEINS VP1 - VP3
antibody binding site
• INTERNAL PROTEIN
VP4
vpg associated with viral rna .
NONENVELOPE
REPLICATION - Cytoplasm .
CULTURE –
Many enterovirus - 37 deg
Monkey/human cells .
RHINO - Only human – 33 deg
COXASACKIE – Newborn mice
The cells from
which line was
initiated were
sampled from the
renal tissue of an
African green
monkey
(Cercopithecus
aethiops
ENTEROVIRUS
72 SEROTYPES
-poliovirus
-coxasackie virus
-echo virus
• they are all found in
intestine and excreted
in faeces.
• since 1969 classified as
type numbers .
POLIOVIRUS
CAUSES POLIOMYELITIS
MORPHOLOGY
• spherical - 27 nm
• capsid has - 60 subunits
• with proteins vp 1-4.
• ss rna of positive sense.
The Union Health Minister, Ghulam Nabi Azad received the
official certificate at a function here. 28 march 2014
RESISTANCE
• Among most stable virus
• Resistant to ether chloroform bile,intestinal
proteolytic enzymes
• In faeces survive for months at 37 deg
• Virus can survive for months at -20
• Room temp –several weeks
• Inactivated when heated at 55 deg for 30
min/drying /oxidising agents/chlorination
• Stable at ph -3
ANTIGENIC PROPERTIES
• TWO ANTIGENS
C ANTIGEN also called h or heated antigen
associated with empty noninfectious particle
D ANTIGEN
1. also called naive or n antigen asociated with
whole virion
2. anti – d is protective
3. potency of injectable poliovaccine – measured in
d antigen units
TYPES
• TYPE 1 – 3
• IDENTIFIED BY NEUTRALISATION TEST
– 1 common epidemic type
– 2 usually endemic type
– 3 involved in recent epidemics
HOST RANGE AND CULTIVATION
• PRIMARY MONKEY KIDNEY
– cells round off
– become refractile
– eosinophilic intranuclear inclusion bodies
PATHOGENESIS
• Transmitted by faeco oral route
• Inhalation or entry through conjunctiva of
droplets of respiratory secretions
• Ingested and multiplied in tonsil and small
intestine . It then spreads to regional lymph node
and enter blood stream .
• Spreads virus to target cells
• Where multiplication takes place
• Resulting in symptoms and Secondary viremia
• May ascend to brain tissues via infected nerves
Clinical features
• Incubation period 7-14 days
• 90 95 % presents with only serconversion
• 5% PRESENTS
• Asymptomatic illness- no symptoms
• Abortive Poliomyelitis The minor illness
fever/hdache/sorethroat malaise , 1-5 days
• Non paralytic - 3-4 d later, meningitis
• Paralytic - flaccid type
• Progressive postpoliomyelitis Muscle Atrophy
Precipitating Factors
• Proactive factors
– Fatigue
– Trauma
– Intramuscular injection
– DPT
– Operative procedures
Laboratory diagnosis
• SPECIMEN
– Blood
– CSF rare .
– Throat swabs first few days
– Faeces up to 30 days .
• CULTURE
– Primary monkey kidney cell
– Growth is indicated by cytopathic effect
– Isolated virus is identified and typed by antiserum
SEROLOGICAL TEST
Paired sera in CFT and neutralization .
IMMUNITY
• TYPE SPECIFIC
Humoral antibody protective
– IgM appears after one week and remain for 6 mths
– IgG persists for life
– IgA provides local – intestinal immunity
CMI not protective
PROPHYLAXIS
• IPV –SALK KILLED PV
• OPV – SABIN LIVE POLIO
• As national immunization programme
• 3 doses of opv ,month interval, 6,7,8 mth
• Booster dose is recommended 12 – 18 mths
• complete before 6 mths of age
• Between the age of 6mths – 3 years
KILLED/SALK SABIN/LIVE
• Developed by salk 1953
• Killed formalised
• Given s/c or i/m
• Induces antibody but no
local immunity
• Not useful in epidemics
• Lifelong
• Costlier
• Strict storage and
transport
• Developed by
Sabin1957
• Live attenuated
• Given orally
• Both humoral and
intestinal
• Useful herd immunity
• Booster is required
• Cheaper
• At zero degree
• trivalent • Monovalent/trivalent
• Mgcl2 or sucrose stabilise
against heat inactivation
Criteria of attenuated strains
• Should not be neurovirulent . Confirmed by
intraspinal inoculation.
• Following feeding—should be able to set up
intestinal infection and induce immunity.
• Should posess stable markers .
• Monoclonal antibodies.
• Nucleic acid sequencing .
Markers for differentiating wild from
the attenuated
wild strain attenuated
• D grow well in
low bicarbonate don’t grow
• Rct 40 at 40 deg don’t grow
• MS monkey kidney grow poorly
Global eradication
• By global immunisation with OPV
• Who made a campaign to eradicate by 2000
• America was declared –1994
• Western pacific region 2000
• Europe 2002
• India march 2014
Coxasackie viruses
• Two groups A (SEROTYPES 1- 24) and B (SEROTYPES 1- 6).
• Frequently found in faeces of healthy children.
Causes
• respiratory cold like illness
• illness resembling paralytic poliomyelitis.
• herpangina ,meningitis .
Can be cultured in cell culture and suckling
mouse . PCR.
Rhinoviruses
• Worldwide distribution.
• More than 100 antigenic types.
• Common cold.
• Transmission – droplets ,aerosol ,direct or indirect.
• Can be isolated and typed. WI- 38, MRC- 5 .
• Prevention – washing of hands , virucidal soaps.
• Treatment – supportive.
Refrences
• Essentials of medical microbiology. Apurba S Sastry.
• Textbook of Microbiology . Ananthannarayan and Paniker.
MCQs
1. Zero dose of OPV is given:
a. At one month
b. At birth
c. When child is having diarrhea
d. When child is having polio
2. Enterovirus 72 is:
a. Hepatitis A virus
b. Hepatitis E virus
c. Hepatitis B virus
d. Hepatitis C virus
3. Not true about salk vaccine:
a. Expensive than OPV
b. Not useful in epidemics
c. Contraindicated in low immunity
d. Booster doses are required
4. The most common viruses that can cause meningo encephalitis in children a
re:
a. Arboviruses
b. Herpesviruses
c. Japanese encephalitis virus
d. Enteroviruses.

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Picorna viruses

  • 2. Picorna viruses OBJECTIVES To learn about • Classification • Structure • Pathogenesis • Immunization • Lab diagnosis of polioviruses.
  • 3. INTRODUCTION • Viruses comprises of pico=small rna =RNA • SS RNA • NON ENVELOPED • DIAMETER = 27-30 NM
  • 4. CLASSIFICATION • Family- picornaviridae • Divided - 6 genera • Enterovirus • Rhinovirus • Cardiovirus • Aphthovirus • Hepatovirus • Parechovirus
  • 5. PROPERTIES • SIZE 28- 30 NM • VIRION ICOSAHEDRAL • SS RNA LINEAR • PROTEINS VP1 - VP3 antibody binding site • INTERNAL PROTEIN VP4 vpg associated with viral rna .
  • 6. NONENVELOPE REPLICATION - Cytoplasm . CULTURE – Many enterovirus - 37 deg Monkey/human cells . RHINO - Only human – 33 deg COXASACKIE – Newborn mice The cells from which line was initiated were sampled from the renal tissue of an African green monkey (Cercopithecus aethiops
  • 7. ENTEROVIRUS 72 SEROTYPES -poliovirus -coxasackie virus -echo virus • they are all found in intestine and excreted in faeces. • since 1969 classified as type numbers .
  • 8. POLIOVIRUS CAUSES POLIOMYELITIS MORPHOLOGY • spherical - 27 nm • capsid has - 60 subunits • with proteins vp 1-4. • ss rna of positive sense.
  • 9. The Union Health Minister, Ghulam Nabi Azad received the official certificate at a function here. 28 march 2014
  • 10. RESISTANCE • Among most stable virus • Resistant to ether chloroform bile,intestinal proteolytic enzymes • In faeces survive for months at 37 deg • Virus can survive for months at -20 • Room temp –several weeks • Inactivated when heated at 55 deg for 30 min/drying /oxidising agents/chlorination • Stable at ph -3
  • 11. ANTIGENIC PROPERTIES • TWO ANTIGENS C ANTIGEN also called h or heated antigen associated with empty noninfectious particle D ANTIGEN 1. also called naive or n antigen asociated with whole virion 2. anti – d is protective 3. potency of injectable poliovaccine – measured in d antigen units
  • 12. TYPES • TYPE 1 – 3 • IDENTIFIED BY NEUTRALISATION TEST – 1 common epidemic type – 2 usually endemic type – 3 involved in recent epidemics
  • 13. HOST RANGE AND CULTIVATION • PRIMARY MONKEY KIDNEY – cells round off – become refractile – eosinophilic intranuclear inclusion bodies
  • 14. PATHOGENESIS • Transmitted by faeco oral route • Inhalation or entry through conjunctiva of droplets of respiratory secretions • Ingested and multiplied in tonsil and small intestine . It then spreads to regional lymph node and enter blood stream . • Spreads virus to target cells • Where multiplication takes place • Resulting in symptoms and Secondary viremia • May ascend to brain tissues via infected nerves
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  • 16. Clinical features • Incubation period 7-14 days • 90 95 % presents with only serconversion • 5% PRESENTS • Asymptomatic illness- no symptoms • Abortive Poliomyelitis The minor illness fever/hdache/sorethroat malaise , 1-5 days • Non paralytic - 3-4 d later, meningitis • Paralytic - flaccid type • Progressive postpoliomyelitis Muscle Atrophy
  • 17. Precipitating Factors • Proactive factors – Fatigue – Trauma – Intramuscular injection – DPT – Operative procedures
  • 18. Laboratory diagnosis • SPECIMEN – Blood – CSF rare . – Throat swabs first few days – Faeces up to 30 days . • CULTURE – Primary monkey kidney cell – Growth is indicated by cytopathic effect – Isolated virus is identified and typed by antiserum SEROLOGICAL TEST Paired sera in CFT and neutralization .
  • 19. IMMUNITY • TYPE SPECIFIC Humoral antibody protective – IgM appears after one week and remain for 6 mths – IgG persists for life – IgA provides local – intestinal immunity CMI not protective
  • 20. PROPHYLAXIS • IPV –SALK KILLED PV • OPV – SABIN LIVE POLIO • As national immunization programme • 3 doses of opv ,month interval, 6,7,8 mth • Booster dose is recommended 12 – 18 mths • complete before 6 mths of age • Between the age of 6mths – 3 years
  • 21. KILLED/SALK SABIN/LIVE • Developed by salk 1953 • Killed formalised • Given s/c or i/m • Induces antibody but no local immunity • Not useful in epidemics • Lifelong • Costlier • Strict storage and transport • Developed by Sabin1957 • Live attenuated • Given orally • Both humoral and intestinal • Useful herd immunity • Booster is required • Cheaper • At zero degree
  • 22. • trivalent • Monovalent/trivalent • Mgcl2 or sucrose stabilise against heat inactivation
  • 23. Criteria of attenuated strains • Should not be neurovirulent . Confirmed by intraspinal inoculation. • Following feeding—should be able to set up intestinal infection and induce immunity. • Should posess stable markers . • Monoclonal antibodies. • Nucleic acid sequencing .
  • 24. Markers for differentiating wild from the attenuated wild strain attenuated • D grow well in low bicarbonate don’t grow • Rct 40 at 40 deg don’t grow • MS monkey kidney grow poorly
  • 25. Global eradication • By global immunisation with OPV • Who made a campaign to eradicate by 2000 • America was declared –1994 • Western pacific region 2000 • Europe 2002 • India march 2014
  • 26. Coxasackie viruses • Two groups A (SEROTYPES 1- 24) and B (SEROTYPES 1- 6). • Frequently found in faeces of healthy children. Causes • respiratory cold like illness • illness resembling paralytic poliomyelitis. • herpangina ,meningitis . Can be cultured in cell culture and suckling mouse . PCR.
  • 27. Rhinoviruses • Worldwide distribution. • More than 100 antigenic types. • Common cold. • Transmission – droplets ,aerosol ,direct or indirect. • Can be isolated and typed. WI- 38, MRC- 5 . • Prevention – washing of hands , virucidal soaps. • Treatment – supportive.
  • 28. Refrences • Essentials of medical microbiology. Apurba S Sastry. • Textbook of Microbiology . Ananthannarayan and Paniker.
  • 29. MCQs 1. Zero dose of OPV is given: a. At one month b. At birth c. When child is having diarrhea d. When child is having polio 2. Enterovirus 72 is: a. Hepatitis A virus b. Hepatitis E virus c. Hepatitis B virus d. Hepatitis C virus
  • 30. 3. Not true about salk vaccine: a. Expensive than OPV b. Not useful in epidemics c. Contraindicated in low immunity d. Booster doses are required 4. The most common viruses that can cause meningo encephalitis in children a re: a. Arboviruses b. Herpesviruses c. Japanese encephalitis virus d. Enteroviruses.