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1843-1910




• Discriminating between organisms and associating
 organisms with particular diseases
• formulated a set of conditions that needed to be met in
 order to ‘prove’ a causal relationship
Koch's postulates
1. The microorganism must be found in abundance in all
   organisms suffering from the disease, but not in healthy
   organisms.

2. The microorganism must be isolated from a diseased organism
   and grown in pure culture

3. The cultured microorganism should cause disease when
   introduced into a healthy organism.

4. The microorganism must be re-isolated from the inoculated,
   diseased experimental host and identified as being identical to
   the original specific causative agent.
Which germ?
Which disease?




Signature of organism
Why may it be difficult to prove causation using Koch’s
                     postulates ?



             1.   chronic or minor conditions
             2.   multiple causes
             3.   pathogen can't be grown
             4.   no suitable animal model
             5.   Long incubation period
"Molecular Koch's Postulates":
                     Stanley Falklow (1988)

1. Identify gene (or gene product) responsible for virulence determinant
2. Show gene present in strains of bacteria that cause the disease
3. Not present in avirulent strains
4. Disrupting the gene reduces virulence
5. Introduction of cloned gene into avirulent strain confers virulence.
6. The gene is expressed in vivo
7. Specific immune response to gene protects
•   Guillain Barre Syndrome
•   Hepatitis A
•   Boil
•   Leprosy (Hanson’s disease)
•   Tetanus
•   Typhoid fever
•   Yellow fever
•   Rheumatic Fever
Guillain Barre Syndrome & Campylobacter jejuni




 Scanning electron microscope image of            Blood-free, charcoal-based selective
 Campylobacter jejuni, illustrating its corkscrew medium agar (CSM) for isolation of
 appearance and bipolar flagella.                 Campylobacter jejuni at 42 C

 Evidence of link between campylobacter jejuni and GBS

•For more than 100 years, a variety of preceding infectious diseases have been described
in association with GBS.
•But the relation with Campylobacter jejuni was discovered recently.
•However gastrointestinal illnesses occurring in up to 20% of GBS patients were
recognized many decades ago.
•Campylobacter infection was first reported as a potential cause of GBS in 1982 in a 45-
year-old man who developed severe GBS with irreversible neurologic damage 2 weeks
after a gastrointestinal illness caused by Campylobacter infection .
Guillain Barre Syndrome & Koch’s postulates
Koch’s postulates can not be applied to prove the etiological relationship
                between GBS and Campylobacter jejuni
Koch's postulates 01
   In GBS only 40 % of the cases Campylobacter jejuni can be isolated as an antecedent event
   But in the other cases no such association is found.
   Campylobacter can be found in patients with no evidence of GBS and in patients with
   gastroenteritis.

Koch's postulates 02
   Only 40% of cases this can be done. It requires special culture media for culture and special
   conditions. (E.g. Blood-free, charcoal-based selective medium agar (CSM) at 420C)
   Organism will also be absent in stool by the time the patient gets the disease.

Koch's postulates 03
   It does not cause GBS in all cases only few cases progress in to Guillan Barre syndrome.
   Only 1:1000 cases will get GBS from C.jejuni infection.

Koch's postulates 04
   Development of GBS can be related to the inoculation of C. jejuni in to a healthy
   individual or it can be a purely an incidental cause.
   So organism isolation is not always definite.
Robert Koch



Blood-free, charcoal-based
selective medium agar (CSM) for
isolation of Campylobacter jejuni
at 42 C




Scanning electron microscope image of          A patient with Guillain Barre
Campylobacter jejuni, illustrating its       syndrome showing acute flaccid
corkscrew appearance and bipolar             paralysis of lower limbs with areflexia
Koch’s postulates can not be applied to prove the etiological relationship
  between GBS and Campylobacter jejuni
1.   Koch's postulates 01
      The microorganism must be found in abundance in all organisms suffering from the disease, but should
      not be found in healthy animals.
             In GBS only 40 % of the cases Campylobacter jejuni can be isolated as an antecedent event
      but in the other cases no such association is found. Campylobacter can be found in patients
      with no evidence of GBS and in patients with gastroenteritis
2. Koch's postulates 02
    The microorganism must be isolated from a diseased organism and grown in pure culture.
           Only 40% of cases this can be done. It requires special culture media for culture and special
    conditions. E.g. Blood-free, charcoal-based selective medium agar (CSM) at 42 C

3. Koch's postulates 03
    The cultured microorganism should cause disease when introduced into a healthy organism.
           It does not cause GBS in all cases only few cases progress in to Guillan Barre syndrome.
4. Koch's postulates 04
    The microorganism must be reisolated from the inoculated, diseased experimental host and identified as
    being identical to the original specific causative agent
             Development of GBS can be related to the inoculation of C. jejuni in to a healthy
      individual or it can be a purely an incidental cause. So organism isolation is not always
      definite.
  HAV is a Heat stable, Picornavirus (ssRNA)
  Mode of transmission by Fecal-oral route
  Water & food borne disease
  HAV causes inflammation of the liver
  Signs & symptoms
                  Jaundice, Fever, Abdominal pain, Nausea ,Diarrhoea,
                  Sharp pain in right upper quadrant of the abdomen.
 During Hippocrates's era - Infectious icterus
 1956, Dr. Saul Krugmann - Labelled the of two forms of hepatitis
                               By their aetiological agents
(In 1956 Dr. Krugman conduct a study among mentally retarded, disabled children in
Willow brook State School (New York), and he fed & injected infected serum to the
children. And ethics of his experiment aroused controversy & it was censured by NY
senate.)
 1973, Feinstone & Purcell - identified Hepatitis A virus –
                                1st visualized by Immune electron microscopy
HAV & Koch’s postulates
• First postulate –
        90% of infected children <= 5 yrs are Asymptomatic
        Not all the subjects who have infected get the symptoms, infants
• Second postulate –
        Pure cultures for the viruses were not available during that time.
        Nowadays HAV grows in primate cell cultures.
                                            (chimpanzees/marmosets)
• Third postulate –
        No evidence of disease by Pure cultured virus.
  BUT ;
        1944, McCollam, Transmission of the infected serum to volunteers
        1956, Dr.Saul Krugman, feed & inject infected serum to the mentally
        retarded, disabled children in Willow brook State School (New York)
        and they developed the hepatitis
• Fourth postulate –
        HAV grows in primate cell cultures. After serial passage, strains may
  lose virulence for the liver.
BOIL
• Sub-epidermal collection of
  pus
• Usually arises around a hair
  follicle
• This is caused by a bacteria
  called staphylococcus
  aureus


                                 Staphylococcus aureus
Koch’s postulates - Proved
1. The Koch saw -must be presentpusall cases of
1878 – organism staphylococci in in from
   disease.        boils .
2. The bacteria must be isolated from culture
 1884 – Rosenbach studied through pure the
 and identified Staphylococcusin pure culture.
   diseased host and grown aureus
3. The Garre rubbed Staphylococcus aureus on the
1885 –
         specific disease must be reproduced
skin of hisa pure culture of bacteria is inoculated
   when arm and was able to produce boils.
   into a healthy susceptible host.
4. The bacteria must be recoverable from the
   experimentally infected host.
Leprosy
(Hanson’s disease)
Koch’s Postulates               Evidence/Exceptions


1. The micro-organism must            1. 1873- Dr.Gerhard Hansen
   regularly be isolated from cause      discovered Mycobacterium
   of the illness.                       leprae.
2. It must be grown in pure culture   2. 1968- Research started on in vivo
   in vitro.                             culturing of the bacterium, in
3. When such a pure culture is           Armadillos.
   inoculated in to susceptible       3. When such an in vivo-cultured
   animal species, the typical           organism is inoculated into
   disease must result.                  susceptible species the particular
4. From such experimentally              disease results.
   induced disease, the micro-        4. The particular microbe can be
   organism must again be isolated.      isolated from such a diseased
                                         animal.
Disease :- Tetanus
Name of Microbe :- Clostridium tetani
Genus of the microbe :- Genus Clotridium


                                          Spores (cultivated fields)
Common Features                                                 Contamination
(Genus - Clostridum )
                                Necrotic & Poorly
                                                                Colonization
                                perfused wounds
• Widely distributed
• Rod shaped                                                      Infection

• Spore forming                              Vegetative microbe
• Gram-positive
• Anaerobic
                                           Toxin – tetanospasmin
                                           (Tetanospasmin toxemia)
Postulate 01 :- agree
              - Not included in ‘Normal Microbiota’ (Primary pathogen)
              - Production of Highly toxic Tetanospasmin
              - When colonized always cause Tetanus

Postulate 02 :- agree
             - Can be grown in ‘Pure Culture’ – Needs special conditions
             - Very little number of organisms
             - Difficulty to locate the place of colonization


Postulate 03 :- agree
              Should be inoculated under special conditions


                  Well perfused and
                  living tissue
                                                 tissue   O2      No Colonization
Postulate 04 :- agree
               - Can be grown again by specimens taken from experimentally
.                inoculated patients
               - (same principles apply as postulate 02)


    Postulate 05 :- Does not agree
                 Very small amount of toxin                Disease or death

                    Little or Inadequate                       No immune response
                    production of the                          when inoculated again
                    antigen
Typhoid Fever (Salmonella typhi)
• Characterised by           • Number of organisms
  –   Sustained fever          needed - 103
  –   Headache               • Transmitted by
  –   Malaise                   – Faecally contaminated water
  –   Anorexia                    and food
  –   Constipation              – Via the fecal-oral route
  –   Diarrhea               • Affects the
  –   Non productive cough      – Reticuloendothelial system
  –   Rose spots

                     Typhoid Mary !
Koch’s Postulates & Typhoid
Koch’s Postulate         Agree/     Reason
                         Disagree
1. Presence of           (Agree)    Typhoid Mary
microbe at the lesion               Tony Labella
site and absent in all
healthy animals
2. Ability to isolate    Agree      HEK agar
from the site and                   MacConkey’s agar
culture                             Red slant and yellow butt in TSI
3. Ability to reproduce Agree       Chimpanzee’s throat
the disease in a                    By Elie Metchnikoff (1911)
susceptible
experimental animal
4. Ability to recover -             -
from the experimental
animal
•   Introduction
•   History
•   Virus & vector          KOCH

•   How it affects humans
•   Clinical features
Virus:

  •   Found in both affected & unaffected people
  •   Is grown in a variety of cultures.
  •   May or may not produce disease.
  •   Isolated from diseased persons.
Can it be proved by Koch's postulates?
Can't.........
Why cannot it   be proved by Koch's postulates?
   Is  the organism (Streptococcus pyogenes) present in
   all the affected sites (joints, heart, CNS)?

   Can   the organism be isolated from the affected sites
   (joints, heart, CNS)?
   If the isolated and cultured organism inoculated
   in to a susceptible person or animal, does it always
   cause rheumatic fever?
How was causation proved?

  Epidemiological studies
   1960 – Stollerman noted
     Outbreak of type A streptococcal upper respiratory
     tract infection followed by outbreak of Rheumatic fever ¹
     Another observation:
           Streptococcus is not resistant to penicillin and
           it has not developed into resistant forms!
     But...
     Penicillin has clearly failed to eradicate Rheumatic fever ²
  Pathogenesis of Rheumatic fever?
  Is Streptococcus pyogenes the only causative agent?
Reference: 1 & 2 http://www.heart.bmjjournals.com/cgi/content/full/91/1/3

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Proof of causation of the disease by koch’s postulates

  • 1.
  • 2. 1843-1910 • Discriminating between organisms and associating organisms with particular diseases • formulated a set of conditions that needed to be met in order to ‘prove’ a causal relationship
  • 3. Koch's postulates 1. The microorganism must be found in abundance in all organisms suffering from the disease, but not in healthy organisms. 2. The microorganism must be isolated from a diseased organism and grown in pure culture 3. The cultured microorganism should cause disease when introduced into a healthy organism. 4. The microorganism must be re-isolated from the inoculated, diseased experimental host and identified as being identical to the original specific causative agent.
  • 5. Why may it be difficult to prove causation using Koch’s postulates ? 1. chronic or minor conditions 2. multiple causes 3. pathogen can't be grown 4. no suitable animal model 5. Long incubation period
  • 6. "Molecular Koch's Postulates": Stanley Falklow (1988) 1. Identify gene (or gene product) responsible for virulence determinant 2. Show gene present in strains of bacteria that cause the disease 3. Not present in avirulent strains 4. Disrupting the gene reduces virulence 5. Introduction of cloned gene into avirulent strain confers virulence. 6. The gene is expressed in vivo 7. Specific immune response to gene protects
  • 7. Guillain Barre Syndrome • Hepatitis A • Boil • Leprosy (Hanson’s disease) • Tetanus • Typhoid fever • Yellow fever • Rheumatic Fever
  • 8. Guillain Barre Syndrome & Campylobacter jejuni Scanning electron microscope image of Blood-free, charcoal-based selective Campylobacter jejuni, illustrating its corkscrew medium agar (CSM) for isolation of appearance and bipolar flagella. Campylobacter jejuni at 42 C Evidence of link between campylobacter jejuni and GBS •For more than 100 years, a variety of preceding infectious diseases have been described in association with GBS. •But the relation with Campylobacter jejuni was discovered recently. •However gastrointestinal illnesses occurring in up to 20% of GBS patients were recognized many decades ago. •Campylobacter infection was first reported as a potential cause of GBS in 1982 in a 45- year-old man who developed severe GBS with irreversible neurologic damage 2 weeks after a gastrointestinal illness caused by Campylobacter infection .
  • 9. Guillain Barre Syndrome & Koch’s postulates Koch’s postulates can not be applied to prove the etiological relationship between GBS and Campylobacter jejuni Koch's postulates 01 In GBS only 40 % of the cases Campylobacter jejuni can be isolated as an antecedent event But in the other cases no such association is found. Campylobacter can be found in patients with no evidence of GBS and in patients with gastroenteritis. Koch's postulates 02 Only 40% of cases this can be done. It requires special culture media for culture and special conditions. (E.g. Blood-free, charcoal-based selective medium agar (CSM) at 420C) Organism will also be absent in stool by the time the patient gets the disease. Koch's postulates 03 It does not cause GBS in all cases only few cases progress in to Guillan Barre syndrome. Only 1:1000 cases will get GBS from C.jejuni infection. Koch's postulates 04 Development of GBS can be related to the inoculation of C. jejuni in to a healthy individual or it can be a purely an incidental cause. So organism isolation is not always definite.
  • 10. Robert Koch Blood-free, charcoal-based selective medium agar (CSM) for isolation of Campylobacter jejuni at 42 C Scanning electron microscope image of A patient with Guillain Barre Campylobacter jejuni, illustrating its syndrome showing acute flaccid corkscrew appearance and bipolar paralysis of lower limbs with areflexia
  • 11. Koch’s postulates can not be applied to prove the etiological relationship between GBS and Campylobacter jejuni 1. Koch's postulates 01 The microorganism must be found in abundance in all organisms suffering from the disease, but should not be found in healthy animals. In GBS only 40 % of the cases Campylobacter jejuni can be isolated as an antecedent event but in the other cases no such association is found. Campylobacter can be found in patients with no evidence of GBS and in patients with gastroenteritis 2. Koch's postulates 02 The microorganism must be isolated from a diseased organism and grown in pure culture. Only 40% of cases this can be done. It requires special culture media for culture and special conditions. E.g. Blood-free, charcoal-based selective medium agar (CSM) at 42 C 3. Koch's postulates 03 The cultured microorganism should cause disease when introduced into a healthy organism. It does not cause GBS in all cases only few cases progress in to Guillan Barre syndrome. 4. Koch's postulates 04 The microorganism must be reisolated from the inoculated, diseased experimental host and identified as being identical to the original specific causative agent Development of GBS can be related to the inoculation of C. jejuni in to a healthy individual or it can be a purely an incidental cause. So organism isolation is not always definite.
  • 12.  HAV is a Heat stable, Picornavirus (ssRNA)  Mode of transmission by Fecal-oral route  Water & food borne disease  HAV causes inflammation of the liver  Signs & symptoms Jaundice, Fever, Abdominal pain, Nausea ,Diarrhoea, Sharp pain in right upper quadrant of the abdomen.  During Hippocrates's era - Infectious icterus  1956, Dr. Saul Krugmann - Labelled the of two forms of hepatitis By their aetiological agents (In 1956 Dr. Krugman conduct a study among mentally retarded, disabled children in Willow brook State School (New York), and he fed & injected infected serum to the children. And ethics of his experiment aroused controversy & it was censured by NY senate.)  1973, Feinstone & Purcell - identified Hepatitis A virus – 1st visualized by Immune electron microscopy
  • 13. HAV & Koch’s postulates • First postulate – 90% of infected children <= 5 yrs are Asymptomatic Not all the subjects who have infected get the symptoms, infants • Second postulate – Pure cultures for the viruses were not available during that time. Nowadays HAV grows in primate cell cultures. (chimpanzees/marmosets) • Third postulate – No evidence of disease by Pure cultured virus. BUT ; 1944, McCollam, Transmission of the infected serum to volunteers 1956, Dr.Saul Krugman, feed & inject infected serum to the mentally retarded, disabled children in Willow brook State School (New York) and they developed the hepatitis • Fourth postulate – HAV grows in primate cell cultures. After serial passage, strains may lose virulence for the liver.
  • 14. BOIL • Sub-epidermal collection of pus • Usually arises around a hair follicle • This is caused by a bacteria called staphylococcus aureus Staphylococcus aureus
  • 15. Koch’s postulates - Proved 1. The Koch saw -must be presentpusall cases of 1878 – organism staphylococci in in from disease. boils . 2. The bacteria must be isolated from culture 1884 – Rosenbach studied through pure the and identified Staphylococcusin pure culture. diseased host and grown aureus 3. The Garre rubbed Staphylococcus aureus on the 1885 – specific disease must be reproduced skin of hisa pure culture of bacteria is inoculated when arm and was able to produce boils. into a healthy susceptible host. 4. The bacteria must be recoverable from the experimentally infected host.
  • 17. Koch’s Postulates Evidence/Exceptions 1. The micro-organism must 1. 1873- Dr.Gerhard Hansen regularly be isolated from cause discovered Mycobacterium of the illness. leprae. 2. It must be grown in pure culture 2. 1968- Research started on in vivo in vitro. culturing of the bacterium, in 3. When such a pure culture is Armadillos. inoculated in to susceptible 3. When such an in vivo-cultured animal species, the typical organism is inoculated into disease must result. susceptible species the particular 4. From such experimentally disease results. induced disease, the micro- 4. The particular microbe can be organism must again be isolated. isolated from such a diseased animal.
  • 18. Disease :- Tetanus Name of Microbe :- Clostridium tetani Genus of the microbe :- Genus Clotridium Spores (cultivated fields) Common Features Contamination (Genus - Clostridum ) Necrotic & Poorly Colonization perfused wounds • Widely distributed • Rod shaped Infection • Spore forming Vegetative microbe • Gram-positive • Anaerobic Toxin – tetanospasmin (Tetanospasmin toxemia)
  • 19.
  • 20. Postulate 01 :- agree - Not included in ‘Normal Microbiota’ (Primary pathogen) - Production of Highly toxic Tetanospasmin - When colonized always cause Tetanus Postulate 02 :- agree - Can be grown in ‘Pure Culture’ – Needs special conditions - Very little number of organisms - Difficulty to locate the place of colonization Postulate 03 :- agree Should be inoculated under special conditions Well perfused and living tissue tissue O2 No Colonization
  • 21. Postulate 04 :- agree - Can be grown again by specimens taken from experimentally . inoculated patients - (same principles apply as postulate 02) Postulate 05 :- Does not agree Very small amount of toxin Disease or death Little or Inadequate No immune response production of the when inoculated again antigen
  • 22. Typhoid Fever (Salmonella typhi) • Characterised by • Number of organisms – Sustained fever needed - 103 – Headache • Transmitted by – Malaise – Faecally contaminated water – Anorexia and food – Constipation – Via the fecal-oral route – Diarrhea • Affects the – Non productive cough – Reticuloendothelial system – Rose spots Typhoid Mary !
  • 23. Koch’s Postulates & Typhoid Koch’s Postulate Agree/ Reason Disagree 1. Presence of (Agree) Typhoid Mary microbe at the lesion Tony Labella site and absent in all healthy animals 2. Ability to isolate Agree HEK agar from the site and MacConkey’s agar culture Red slant and yellow butt in TSI 3. Ability to reproduce Agree Chimpanzee’s throat the disease in a By Elie Metchnikoff (1911) susceptible experimental animal 4. Ability to recover - - from the experimental animal
  • 24. Introduction • History • Virus & vector KOCH • How it affects humans • Clinical features
  • 25. Virus: • Found in both affected & unaffected people • Is grown in a variety of cultures. • May or may not produce disease. • Isolated from diseased persons.
  • 26. Can it be proved by Koch's postulates? Can't......... Why cannot it be proved by Koch's postulates? Is the organism (Streptococcus pyogenes) present in all the affected sites (joints, heart, CNS)? Can the organism be isolated from the affected sites (joints, heart, CNS)? If the isolated and cultured organism inoculated in to a susceptible person or animal, does it always cause rheumatic fever?
  • 27. How was causation proved? Epidemiological studies 1960 – Stollerman noted Outbreak of type A streptococcal upper respiratory tract infection followed by outbreak of Rheumatic fever ¹ Another observation: Streptococcus is not resistant to penicillin and it has not developed into resistant forms! But... Penicillin has clearly failed to eradicate Rheumatic fever ² Pathogenesis of Rheumatic fever? Is Streptococcus pyogenes the only causative agent? Reference: 1 & 2 http://www.heart.bmjjournals.com/cgi/content/full/91/1/3