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GUIDENCE :
Dr. Banumathi
Lecture
PG Dept of Biotechnology
Sahyadri Science College,
Shivamoga
PRESENTED BY
RANJITHA SL
1ST YEAR Msc Biotechnology
Sahyadri Science College,
Shivamoga
KUVEMPU UNIVERSITY
SAHYADRI SCIENCE COLLEGE,
SHIVAMOGA
SEMINAR TOPIC
CHOLERA
CONTENTS
•INTRODUCTION
•EPIDEMIOLOGY
•CULTURAL CHARACTERSSSS
•BIOCHEMICAL REACTIONS
•ANTIGENIC CHARACTERS
•SENSITIVITY
•PATHOGENICITY
•SYMPTOMS
•LABORATORY DIAGNOSIS
•TREATMENT
•PREVENTION
•SUMMARY
•CONCULSION
•REFERENCE
INTRODUCTION
CHOLERA
Cholera is an infection in the small intestine
caused by the bacterium called Vibrio
Cholerae
The word cholera is from greek : kholera from
khole “bile”and the word 𝓥𝓲𝓫𝓻𝓲𝓸 -Filippo pacini
isolated micro organism and he called it as
Vibrions from cholera patient
The main symptoms are watery diarrhea and
vomiting
Transmission occurs primarily by drinking water
or eating food that has been contaminated by the
TAXONOMY
ITS BELONGS TO
1. KINGDOM : BACTERIA
2. PHYLUM:PROTECBACTERIA
3. CLASS:GAMMAPROTEOBACTERIA
4. ORDER:VIBRIONALES
5. FAMILY: VIBRIONACEAE
6. GENUS: VIBRIO
7. SPECIES: VIBRIO CHOLERA
MORPHOLOGY
• The vibrio cholera resembling letter “V”
• Its measures from : length -1.5 to 3.0 μm
breadth - 0.5 μm .
• It’s a curved or “comma – shaped” rod with rounded or
slightly pointed ends.
• Gram negative, non- sporing and non-capsulated .
•The vibrio is actively motile, and the movement is of a
“darting” type due to a single long terminal flagellum
• In liquid cultures the vibrios occur singly, in pairs, or in chains
end to end with the curves alternating presenting S-shaped
arrangement.
EPIDEMIOLOGY
According to WHO, During 19th Century, cholera spread across the
world from its original reservoir in the Ganges Delt in India.
Six subsequent pandemics killed million of people across all
contients.
The current (seventh) pandemic started in South Asia in 1971 and
the America in 1991
Cholera is now endemic in many countries.
HISTORY
The germ responisble for cholera was
discovered :
John Snow conducted pioneering investing on cholera
epidemics in england and particulary in london in 1854 in
which he demonstrated that contaminated water was the
key sources of the epidemics
 The Italian physican, Filippo Pacini,work independtly in
Italy,in 1854,first observed comma shaped forms under a
microscope in cholera stools
In 1884,Robert Koch first isolated Vibrio Cholera in pure
culture in work that began in epypt and continued
Calcutta in India has favoring the germ theory over the
miasma theory of disease
CULTURE CHARACTERS
VIBRIO CHOLERAE IS AN AEROBIC
 It grow at a temperature range of 16 ͦ-40 ͦ C, but the optimum temperature is 37 ͦ C
It grow on ordinary media having the Ph of 7.6 to 8 & will also grow at a Ph of 9 to 9.5
Colonies on agar occur after 12-24 hours of incubation
The colonies are moist ,translucent, regular discs,1-2mm in diameter, showing a
characteristics bluish colour in transmitted light
CONTINUED…..
MEDIA Uses
Alkaline peptone water Enrichment media for Vibrio cholerae
Alkaline Salt Transport
Medium
Taurocholate Peptone
Transport Medium
Liquid media by addition of
* Glucose (0.5 % to 1%)
* Ascorbic Acid (0.1%)
*Cysteine (0.1)%
*Sodium Merceptoacetate (0.1%)
* Thioglycollate ( 0.1%)
* Particles of cooked meat broth
Transport media for diarrheal diseases suspected of
being caused by V.cholerae
Anaerobic Media
CONTINUED…..
MEDIA Colony Morphology
Nutrient Agar The colonies are moist ,translucent
round disks(1-2mm in
diameter)with a blush tinge in
transmitted
Mac Conkey Agar The colonies are colorless at first
but become reddish on prolonged
incubation due to late
fermentation of lactose
Thiosulphate citrate bile sucrose
agar(Ph 8.6)
It is used as a selective medium for
isolation of vibrios.it produces
large yellow convex due to sucrose
fermentation.
BIOCHEMICAL REACTIONS
The cholera vibrios form acid without gas in glucose,maltose,sucrose and mannose in
1-2 days,but don’t ferment arabinose.
Indole is produed and nitrates are reduced to nitrate
Gelatin and serum are rapidly reduced
NH3 & H2S are formed
Reaction in the Voges Proskauer test are variable

ANTIGENIC CHARACTERS
 The organism possesses both H and O antigens
Common heat labile flagellar H – antigen
O –lipopolysaccharide confers serlogic specificity
More than 150 O antigen serogroups
Only O-1 & 0139(polysaccharide capulse)
serogroups causes ,asiatic cholera
There serotypes ; Ogawa,Inaba,Hikojima
Two biovars ; Classic and EI T or hemolysin
SENSITIVITY
 V - cholerae is killed at 56 ͦ C within 30 minutes.
 On drying in sunlight , the organism dies within two or three hours.
 In stagnant water with an alkaline reaction the organism may survive for a considerable
period . E.g., 5 -10 days or longer, but it probably does not multiply to any extent in such
water .
 it is sensitive to sulphonamides, streptomycins chloramphenicol and the tetracyclines.
PATHOGENICITY
 Cholera is an exclusively human disease acquired through contamination of water with V.cholerae.
 This is in acute disease of sudden onset characterised by pofuse watery diarrhoea(rice watery stools),Vomitting, muscular cramps
and extreme collapse.
The vibrios multiply freely in the lumen of the small intestine and are present in large numbers in the intestial contents and dejecta.
The stools contain many white flakes consisting mostly and some epithelial cells,the “rice water stools”.
The organsims does not pentrate deeply in the bowel wall and practically never invades the blood stream .
The gall – bladder may be infected.
PATHOGENICITY
SYMPTOMS

LABORATORY DIAGNOSIS

TREATMENT

Antibiotics Ageofpatient Recommendeddoes
Adult 2cap4timesadayfor3days
Children 12.5mg|kgbodyweight4timesadayfor3days
Erythromycintab.(250mg)Adult 2tab4timesadayfor3days
Erythromycinsyr. Children 12.5mg|kgbodyweight4timesadayfor3days
Adult Twiceadayfor3days
Children 1.25mg|kgbodyweight
Tetracyclinecap.(200mg)
Furazolidine(100mg)
ORS
PREVENTION

SUMMARY
Cholera is an extremly virulent disease transmitted through ingestion of contamission of food and wate
Cholera can cause sever acute watery diarrhoea and the severe forms of the disease can kill within
hours is left untreated
Prevention is mainly based on basic santiary and hygiene measures,newly developed oral vaccines
are under consideration for their use in public health

REFERENCE
 Dr. CHANDRAKANTH KELMANI Ph.D.,Text of microbiology vol. IV, Edited by
Prof. S.B.SULLIA (PAGE NO 79 - 81).
 Retrived from – https://www.cdc.gov/cholera/preventionsteps.html
https://www.slideshare.net/NikilVaishnav3/cholera-ppts


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Vibrio cholera disease presentation slide

  • 1. GUIDENCE : Dr. Banumathi Lecture PG Dept of Biotechnology Sahyadri Science College, Shivamoga PRESENTED BY RANJITHA SL 1ST YEAR Msc Biotechnology Sahyadri Science College, Shivamoga KUVEMPU UNIVERSITY SAHYADRI SCIENCE COLLEGE, SHIVAMOGA SEMINAR TOPIC CHOLERA
  • 2. CONTENTS •INTRODUCTION •EPIDEMIOLOGY •CULTURAL CHARACTERSSSS •BIOCHEMICAL REACTIONS •ANTIGENIC CHARACTERS •SENSITIVITY •PATHOGENICITY •SYMPTOMS •LABORATORY DIAGNOSIS •TREATMENT •PREVENTION •SUMMARY •CONCULSION •REFERENCE
  • 3. INTRODUCTION CHOLERA Cholera is an infection in the small intestine caused by the bacterium called Vibrio Cholerae The word cholera is from greek : kholera from khole “bile”and the word 𝓥𝓲𝓫𝓻𝓲𝓸 -Filippo pacini isolated micro organism and he called it as Vibrions from cholera patient The main symptoms are watery diarrhea and vomiting Transmission occurs primarily by drinking water or eating food that has been contaminated by the
  • 4. TAXONOMY ITS BELONGS TO 1. KINGDOM : BACTERIA 2. PHYLUM:PROTECBACTERIA 3. CLASS:GAMMAPROTEOBACTERIA 4. ORDER:VIBRIONALES 5. FAMILY: VIBRIONACEAE 6. GENUS: VIBRIO 7. SPECIES: VIBRIO CHOLERA
  • 5. MORPHOLOGY • The vibrio cholera resembling letter “V” • Its measures from : length -1.5 to 3.0 μm breadth - 0.5 μm . • It’s a curved or “comma – shaped” rod with rounded or slightly pointed ends. • Gram negative, non- sporing and non-capsulated . •The vibrio is actively motile, and the movement is of a “darting” type due to a single long terminal flagellum • In liquid cultures the vibrios occur singly, in pairs, or in chains end to end with the curves alternating presenting S-shaped arrangement.
  • 6. EPIDEMIOLOGY According to WHO, During 19th Century, cholera spread across the world from its original reservoir in the Ganges Delt in India. Six subsequent pandemics killed million of people across all contients. The current (seventh) pandemic started in South Asia in 1971 and the America in 1991 Cholera is now endemic in many countries.
  • 7. HISTORY The germ responisble for cholera was discovered : John Snow conducted pioneering investing on cholera epidemics in england and particulary in london in 1854 in which he demonstrated that contaminated water was the key sources of the epidemics  The Italian physican, Filippo Pacini,work independtly in Italy,in 1854,first observed comma shaped forms under a microscope in cholera stools In 1884,Robert Koch first isolated Vibrio Cholera in pure culture in work that began in epypt and continued Calcutta in India has favoring the germ theory over the miasma theory of disease
  • 8. CULTURE CHARACTERS VIBRIO CHOLERAE IS AN AEROBIC  It grow at a temperature range of 16 ͦ-40 ͦ C, but the optimum temperature is 37 ͦ C It grow on ordinary media having the Ph of 7.6 to 8 & will also grow at a Ph of 9 to 9.5 Colonies on agar occur after 12-24 hours of incubation The colonies are moist ,translucent, regular discs,1-2mm in diameter, showing a characteristics bluish colour in transmitted light
  • 9. CONTINUED….. MEDIA Uses Alkaline peptone water Enrichment media for Vibrio cholerae Alkaline Salt Transport Medium Taurocholate Peptone Transport Medium Liquid media by addition of * Glucose (0.5 % to 1%) * Ascorbic Acid (0.1%) *Cysteine (0.1)% *Sodium Merceptoacetate (0.1%) * Thioglycollate ( 0.1%) * Particles of cooked meat broth Transport media for diarrheal diseases suspected of being caused by V.cholerae Anaerobic Media
  • 10. CONTINUED….. MEDIA Colony Morphology Nutrient Agar The colonies are moist ,translucent round disks(1-2mm in diameter)with a blush tinge in transmitted Mac Conkey Agar The colonies are colorless at first but become reddish on prolonged incubation due to late fermentation of lactose Thiosulphate citrate bile sucrose agar(Ph 8.6) It is used as a selective medium for isolation of vibrios.it produces large yellow convex due to sucrose fermentation.
  • 11. BIOCHEMICAL REACTIONS The cholera vibrios form acid without gas in glucose,maltose,sucrose and mannose in 1-2 days,but don’t ferment arabinose. Indole is produed and nitrates are reduced to nitrate Gelatin and serum are rapidly reduced NH3 & H2S are formed Reaction in the Voges Proskauer test are variable 
  • 12. ANTIGENIC CHARACTERS  The organism possesses both H and O antigens Common heat labile flagellar H – antigen O –lipopolysaccharide confers serlogic specificity More than 150 O antigen serogroups Only O-1 & 0139(polysaccharide capulse) serogroups causes ,asiatic cholera There serotypes ; Ogawa,Inaba,Hikojima Two biovars ; Classic and EI T or hemolysin
  • 13. SENSITIVITY  V - cholerae is killed at 56 ͦ C within 30 minutes.  On drying in sunlight , the organism dies within two or three hours.  In stagnant water with an alkaline reaction the organism may survive for a considerable period . E.g., 5 -10 days or longer, but it probably does not multiply to any extent in such water .  it is sensitive to sulphonamides, streptomycins chloramphenicol and the tetracyclines.
  • 14. PATHOGENICITY  Cholera is an exclusively human disease acquired through contamination of water with V.cholerae.  This is in acute disease of sudden onset characterised by pofuse watery diarrhoea(rice watery stools),Vomitting, muscular cramps and extreme collapse. The vibrios multiply freely in the lumen of the small intestine and are present in large numbers in the intestial contents and dejecta. The stools contain many white flakes consisting mostly and some epithelial cells,the “rice water stools”. The organsims does not pentrate deeply in the bowel wall and practically never invades the blood stream . The gall – bladder may be infected.
  • 18. TREATMENT  Antibiotics Ageofpatient Recommendeddoes Adult 2cap4timesadayfor3days Children 12.5mg|kgbodyweight4timesadayfor3days Erythromycintab.(250mg)Adult 2tab4timesadayfor3days Erythromycinsyr. Children 12.5mg|kgbodyweight4timesadayfor3days Adult Twiceadayfor3days Children 1.25mg|kgbodyweight Tetracyclinecap.(200mg) Furazolidine(100mg) ORS
  • 20. SUMMARY Cholera is an extremly virulent disease transmitted through ingestion of contamission of food and wate Cholera can cause sever acute watery diarrhoea and the severe forms of the disease can kill within hours is left untreated Prevention is mainly based on basic santiary and hygiene measures,newly developed oral vaccines are under consideration for their use in public health
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  • 22. REFERENCE  Dr. CHANDRAKANTH KELMANI Ph.D.,Text of microbiology vol. IV, Edited by Prof. S.B.SULLIA (PAGE NO 79 - 81).  Retrived from – https://www.cdc.gov/cholera/preventionsteps.html https://www.slideshare.net/NikilVaishnav3/cholera-ppts
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