SlideShare a Scribd company logo
DR.PRINCE C P
Associate Professor , Department of Microbiology
Mother Theresa Post Graduate & Research Institute of Health Sciences
(Government of Puducherry Institution)
Botulism
 Clostridium botulinum, which produces the condition
known as botulism
 Category A toxin.
 It is an anaerobic, Gram-positive bacterium commonly
found in soil that works by blocking acetylcholine
release and inhibiting nerve conduction.
Botulinum toxin
 Botulinum toxin is the most lethal toxin known,
approximately 15,000 times more toxic than nerve gas
or chemical exposure.
 There are seven types of botulism toxins, A through G.
 The most naturally occurring of these are A, B and G,
and the only types that cause botulism or other illness
in humans are A, B, E and F.
Weapon of terror
 Botulism has been used as a weapon of terror in the past.
During World War II, the infamous Unit 731, the Japanese
biological warfare group, fed cultures of Clostridium botulinum
to prisoners during the Japanese occupation of Manchuria,
killing them.
 It was suspected that Germany had weaponized botulism as
well, and several other countries were suspected to have done
research into the use of botulism as a weapon.
 More recently, between 1990 and 1995, aerosols were dispersed
on at least three occasions by the Japanese cult Aum Shinrikyo,
who would later go on to release sarin gas in the Tokyo subway,
to disastrous effect. These releases of botulism failed for various
reasons, but the ease with which Aum Shinrikyo was able to
culture Clostridium botulinum from the soil is one reason that
this toxin would make an excellent bioweapon.
.
 After the Persian Gulf War, Iraq admitted that it had
put concentrated botulinum into missiles during the
war, although had not used them.
 These weapons have not yet been found, and the
amount of botulinum contained in them constitute
over 3 times the amount needed to kill the entire
current human population if it were aerosolized
Botox
 The commercially available product known as Botox
contains Type A of the Botulinum toxin, but only in very
small quantities.
 Botox would therefore make a poor bioterrorist weapon
because prohibitively large amounts of botox would be
necessary to cause even a single death.
 However, in January 2005, it appeared that there were a
number of cases of botulism poisonings resulting from
administration of Botox injections.
 After investigation, it was discovered that instead of the
costlier Botox, the physicians or clinical medical personnel
involved in these cases were actually injecting raw botulism
or botulinum bacteria into patients, which could be fatal in
high enough doses.
There are three forms of botulism
 These are foodborne botulism, infant botulism, and wound botulism.
 Foodborne botulism is the most well-known form of botulism, and it
occurs when an individual eats food contaminated with the toxin
produced by C. botulinum. Although not usually due to terrorism,
foodborne botulism is considered a public health emergency because
more than one person has the potential to eat the same food before it is
identified as the source of the botulism outbreak.
 Heating of food generally inactivates the toxin.
 Infant botulism occurs in a small number of infants each year who
have C. botulinum in their intestinal tract from ingesting botulism
spores. These spores are very common and can be found in food such
as honey.
 Wound botulism occurs when wounds are infected with soil
containing C. botulinum.
 A final form of botulism, aerosolized botulism, is man-made, and
occurs when the toxin is inhaled into the lungs.
 Routes of infection for botulinum used as a biological
weapon include dispersion by aerosolization and deliberate
contamination of food, water or beverages.
 Contamination of water, although it is feasible, is unlikely.
 The most likely route of terroristic dissemination is
through aerosolization of the toxin, which would be
extremely lethal.
 It is estimated that 1 gram of aerosolized botulinum toxin
could kill up to 1.5 million people. Despite its potential
lethality, botulism is not capable of being spread person-
to-person.
 Since botulism is naturally occurring, there are several signs you
can look for that may indicate that an outbreak of botulism is
not natural, but may in fact be the result of a biological attack.
 Any outbreak of a large number of cases of flaccid, descending
paralysis has the potential to be a terrorist attack.
 A particularly telling sign is if the outbreak occurs with an
unusual botulinum toxin type, such as Type C, D, F or G.
 An outbreak that has a common geographic factor, such as
location, but no common dietary exposure, is likely to be an
aerosolized, and thus biological attack.
 Finally, multiple simultaneous outbreaks with no common
source is also a potential sign of attack.
 In any case of botulism encountered, it is important to take a
careful travel, activity and dietary history to look both for signs
of intentional exposure, as well as to identify the source of the
outbreak, and other individuals who might have been exposed.
 Symptoms usually begin 12 to 72 hours after ingestion of
botulism, although symptoms may begin as early as 2 hours
or as late as 8 days later.
 It is not known how soon symptoms would begin after an
aerosolized attack, because there are so few recorded cases,
but it is likely that the incubation period would be similar.
 Symptoms include double or blurred vision, drooping
eyelids, slurred speech, difficulty swallowing, dry mouth
and muscle weakness.
 Infants with botulism poisoning appear lethargic, feed
poorly, are constipated, and have a weak cry and poor
muscle tone.
 Pets and farm animals can also get botulism from eating
contaminated food or inhaling the toxin. However, they
cannot transmit the disease to humans.
 The symmetric descending flaccid paralysis seen in patients with
botulism is the hallmark of this type of poisoning.
 Paralysis begins in the muscles of the head and neck, and if
untreated, continue down to the arms, legs, and eventually
respiratory muscles.
 The botulinum toxin does not penetrate the brain parenchyma,
so patients are not confused. However, the lack of a gag reflex
produced by botulism may require intubation.
 Untreated patients with botulism may eventually die of upper
airway obstruction produced by the paralysis of the respiratory
muscles. Currently, only about 8% of patients with botulism die.
 There are several other conditions that may look similar to
botulism in presentation, such as Guillan Barre syndrome,
stroke and myasthenia gravis.
 These conditions can be excluded through testing such as
brain scans, spinal fluid examinations, nerve conduction
tests and tensilon tests.
 However, the best way to confirm a diagnosis of botulism is
to inject serum or stool from the infected patient into mice
and look for signs of botulism in the mice.
 These sorts of tests can be performed at most state health
laboratories, but a physician making an on-the-spot
diagnosis does not have immediate access to this kind of
testing.
 Once botulism is diagnosed, treatment for botulism is
mainly supportive, such as enteral and parenteral feeding,
ventilation, and treatment of secondary infections in an
intensive care setting.
 Respiratory failure may require that patients be put on a
ventilator, or breathing machine for extended periods.
 Timely administration of equine antitoxin provides passive
immunization of the botulinum toxin, and prevents
patients from worsening. While it stops the further
progression of paralysis, it does NOT reverse the paralysis
that has already occurred, so the sooner the antitoxin can
be administered, the better.
 The antitoxin is not usually given for treatment of infant
botulism.
Thank you

More Related Content

Similar to Botulism/ Clostridium botulinum.ppt prepared by Dr PRINCE C P.

mycrobial presentation (Basoz).pptx. .
mycrobial presentation (Basoz).pptx.    .mycrobial presentation (Basoz).pptx.    .
mycrobial presentation (Basoz).pptx. .
d64jq2vryw
 
Biological disasters
Biological disastersBiological disasters
Biological disasters
PRISHA SOUN
 
botulismgshsbdvdbdbebehejz-161205091721.pdf
botulismgshsbdvdbdbebehejz-161205091721.pdfbotulismgshsbdvdbdbebehejz-161205091721.pdf
botulismgshsbdvdbdbebehejz-161205091721.pdf
w7t4bztj2q
 

Similar to Botulism/ Clostridium botulinum.ppt prepared by Dr PRINCE C P. (16)

Clinical Cases in Infectious Diseases - sample chapter
Clinical Cases in Infectious Diseases - sample chapterClinical Cases in Infectious Diseases - sample chapter
Clinical Cases in Infectious Diseases - sample chapter
 
Botulism
Botulism Botulism
Botulism
 
Botulism
BotulismBotulism
Botulism
 
Botulism
BotulismBotulism
Botulism
 
Polio Virus
Polio VirusPolio Virus
Polio Virus
 
mycrobial presentation (Basoz).pptx. .
mycrobial presentation (Basoz).pptx.    .mycrobial presentation (Basoz).pptx.    .
mycrobial presentation (Basoz).pptx. .
 
Botulism; Toxicology - February 2017
Botulism; Toxicology - February 2017Botulism; Toxicology - February 2017
Botulism; Toxicology - February 2017
 
Botulism-Epi.pptx
Botulism-Epi.pptxBotulism-Epi.pptx
Botulism-Epi.pptx
 
Food borne illness (TOPIC: Food borne Disease and Food Intoxication)
Food borne illness (TOPIC: Food borne Disease and Food Intoxication)Food borne illness (TOPIC: Food borne Disease and Food Intoxication)
Food borne illness (TOPIC: Food borne Disease and Food Intoxication)
 
Botulism Foodborne Disease.pptx
Botulism Foodborne Disease.pptxBotulism Foodborne Disease.pptx
Botulism Foodborne Disease.pptx
 
Botulism
BotulismBotulism
Botulism
 
Biological disasters
Biological disastersBiological disasters
Biological disasters
 
botulismgshsbdvdbdbebehejz-161205091721.pdf
botulismgshsbdvdbdbebehejz-161205091721.pdfbotulismgshsbdvdbdbebehejz-161205091721.pdf
botulismgshsbdvdbdbebehejz-161205091721.pdf
 
Botulism 1
Botulism 1Botulism 1
Botulism 1
 
Botulism
BotulismBotulism
Botulism
 
Botulism
BotulismBotulism
Botulism
 

More from DR.PRINCE C P

Spauldings classification ppt by Dr C P PRINCE
Spauldings classification ppt by Dr C P PRINCESpauldings classification ppt by Dr C P PRINCE
Spauldings classification ppt by Dr C P PRINCE
DR.PRINCE C P
 

More from DR.PRINCE C P (20)

Herpes viruses ppt prepared by DR. PRINCE C P
Herpes viruses ppt prepared by DR. PRINCE C PHerpes viruses ppt prepared by DR. PRINCE C P
Herpes viruses ppt prepared by DR. PRINCE C P
 
Polio viruses and polio immunisation ppt by Dr Prince C P
Polio viruses and polio immunisation ppt by Dr Prince C PPolio viruses and polio immunisation ppt by Dr Prince C P
Polio viruses and polio immunisation ppt by Dr Prince C P
 
Higher education for Science students by Dr. PRINCE C P
Higher education for Science students by Dr. PRINCE C PHigher education for Science students by Dr. PRINCE C P
Higher education for Science students by Dr. PRINCE C P
 
Spauldings classification ppt by Dr C P PRINCE
Spauldings classification ppt by Dr C P PRINCESpauldings classification ppt by Dr C P PRINCE
Spauldings classification ppt by Dr C P PRINCE
 
Emergence of Drug resistant microbes PPT By DR.C.P.Prince
Emergence of Drug resistant microbes PPT By DR.C.P.PrinceEmergence of Drug resistant microbes PPT By DR.C.P.Prince
Emergence of Drug resistant microbes PPT By DR.C.P.Prince
 
Biomarkers for early diagnosis ppt by Dr C P PRINCE
Biomarkers for early diagnosis ppt by Dr C P PRINCEBiomarkers for early diagnosis ppt by Dr C P PRINCE
Biomarkers for early diagnosis ppt by Dr C P PRINCE
 
VIRUSES structure and classification ppt by Dr.Prince C P
VIRUSES structure and classification ppt by Dr.Prince C PVIRUSES structure and classification ppt by Dr.Prince C P
VIRUSES structure and classification ppt by Dr.Prince C P
 
Protozoa and Helminth Parasites ppt by Dr.Prince.C.P
Protozoa and Helminth Parasites ppt by Dr.Prince.C.PProtozoa and Helminth Parasites ppt by Dr.Prince.C.P
Protozoa and Helminth Parasites ppt by Dr.Prince.C.P
 
Fungal Infections/ Mycoses ppt by Dr.C.P.PRINCE
Fungal Infections/ Mycoses ppt by Dr.C.P.PRINCEFungal Infections/ Mycoses ppt by Dr.C.P.PRINCE
Fungal Infections/ Mycoses ppt by Dr.C.P.PRINCE
 
CSSD- Central Sterile Supply Department ppt by DR.PRINCE.C.P
CSSD- Central Sterile Supply Department ppt by DR.PRINCE.C.PCSSD- Central Sterile Supply Department ppt by DR.PRINCE.C.P
CSSD- Central Sterile Supply Department ppt by DR.PRINCE.C.P
 
Autoimmunity & disorders ppt by DR.C P. PRINCE
Autoimmunity & disorders ppt by  DR.C P. PRINCEAutoimmunity & disorders ppt by  DR.C P. PRINCE
Autoimmunity & disorders ppt by DR.C P. PRINCE
 
Hypersensitivity/ Allergy ppt by DR.C.P.PRINCE
Hypersensitivity/ Allergy ppt by DR.C.P.PRINCEHypersensitivity/ Allergy ppt by DR.C.P.PRINCE
Hypersensitivity/ Allergy ppt by DR.C.P.PRINCE
 
Antigen ,Antibody and Ag-Ab reactions ppt by DR.C.P.PRINCE
Antigen ,Antibody and Ag-Ab reactions ppt by DR.C.P.PRINCEAntigen ,Antibody and Ag-Ab reactions ppt by DR.C.P.PRINCE
Antigen ,Antibody and Ag-Ab reactions ppt by DR.C.P.PRINCE
 
Immune system and immunity ppt by DR.C.P.PRINCE
Immune system and immunity ppt by DR.C.P.PRINCEImmune system and immunity ppt by DR.C.P.PRINCE
Immune system and immunity ppt by DR.C.P.PRINCE
 
STERILITY TESTING OF PHARMACEUTICALS ppt by DR.C.P.PRINCE
STERILITY TESTING OF PHARMACEUTICALS ppt by DR.C.P.PRINCESTERILITY TESTING OF PHARMACEUTICALS ppt by DR.C.P.PRINCE
STERILITY TESTING OF PHARMACEUTICALS ppt by DR.C.P.PRINCE
 
Introduction to Microbiology & Microorganisms PPT by DR.C.P.Pince
Introduction to Microbiology & Microorganisms PPT by DR.C.P.PinceIntroduction to Microbiology & Microorganisms PPT by DR.C.P.Pince
Introduction to Microbiology & Microorganisms PPT by DR.C.P.Pince
 
Bacterial growth curve ppt by Dr.C.P.PRINCE
Bacterial growth curve ppt by  Dr.C.P.PRINCEBacterial growth curve ppt by  Dr.C.P.PRINCE
Bacterial growth curve ppt by Dr.C.P.PRINCE
 
Culture media and Cultivation of Bacteria DR.C.P.PRINCE
Culture media and Cultivation of Bacteria DR.C.P.PRINCECulture media and Cultivation of Bacteria DR.C.P.PRINCE
Culture media and Cultivation of Bacteria DR.C.P.PRINCE
 
Antibiotic sensitivity test PPT by Dr.C.P.PRINCE
Antibiotic sensitivity test PPT by Dr.C.P.PRINCEAntibiotic sensitivity test PPT by Dr.C.P.PRINCE
Antibiotic sensitivity test PPT by Dr.C.P.PRINCE
 
Classification and mechanism of action of ANTIMICROBIALS by DR.PRINCE.C.P
Classification and mechanism of action of ANTIMICROBIALS  by DR.PRINCE.C.PClassification and mechanism of action of ANTIMICROBIALS  by DR.PRINCE.C.P
Classification and mechanism of action of ANTIMICROBIALS by DR.PRINCE.C.P
 

Recently uploaded

Urinary Elimination BY ANUSHRI SRIVASTAVA.pptx
Urinary Elimination BY ANUSHRI SRIVASTAVA.pptxUrinary Elimination BY ANUSHRI SRIVASTAVA.pptx
Urinary Elimination BY ANUSHRI SRIVASTAVA.pptx
AnushriSrivastav
 
Demystifying-Gene-Editing-The-Promise-and-Peril-of-CRISPR.pdf
Demystifying-Gene-Editing-The-Promise-and-Peril-of-CRISPR.pdfDemystifying-Gene-Editing-The-Promise-and-Peril-of-CRISPR.pdf
Demystifying-Gene-Editing-The-Promise-and-Peril-of-CRISPR.pdf
SasikiranMarri
 
Benefits of Dentulu's Salivary Testing.pptx
Benefits of Dentulu's Salivary Testing.pptxBenefits of Dentulu's Salivary Testing.pptx
Benefits of Dentulu's Salivary Testing.pptx
Dentulu Inc
 
Antibiotic Stewardship by Anushri Srivastava.pptx
Antibiotic Stewardship by Anushri Srivastava.pptxAntibiotic Stewardship by Anushri Srivastava.pptx
Antibiotic Stewardship by Anushri Srivastava.pptx
AnushriSrivastav
 
CHAPTER 1 SEMESTER V - ROLE OF PEADIATRIC NURSE.pdf
CHAPTER 1 SEMESTER V - ROLE OF PEADIATRIC NURSE.pdfCHAPTER 1 SEMESTER V - ROLE OF PEADIATRIC NURSE.pdf
CHAPTER 1 SEMESTER V - ROLE OF PEADIATRIC NURSE.pdf
Sachin Sharma
 

Recently uploaded (20)

Best Erectile Dysfunction Treatment In Narela
Best Erectile Dysfunction Treatment In NarelaBest Erectile Dysfunction Treatment In Narela
Best Erectile Dysfunction Treatment In Narela
 
Valle Egypt Illustrates Consequences of Financial Elder Abuse
Valle Egypt Illustrates Consequences of Financial Elder AbuseValle Egypt Illustrates Consequences of Financial Elder Abuse
Valle Egypt Illustrates Consequences of Financial Elder Abuse
 
R3 Stem Cells and Kidney Repair A New Horizon in Nephrology.pptx
R3 Stem Cells and Kidney Repair A New Horizon in Nephrology.pptxR3 Stem Cells and Kidney Repair A New Horizon in Nephrology.pptx
R3 Stem Cells and Kidney Repair A New Horizon in Nephrology.pptx
 
Urinary Elimination BY ANUSHRI SRIVASTAVA.pptx
Urinary Elimination BY ANUSHRI SRIVASTAVA.pptxUrinary Elimination BY ANUSHRI SRIVASTAVA.pptx
Urinary Elimination BY ANUSHRI SRIVASTAVA.pptx
 
💃Joint ❤89011-83002❤ #ℂALL #gIRLS Ludhiana Escorts by ✔️🍑💃Hotel #cALL #gIRLS...
💃Joint ❤89011-83002❤ #ℂALL #gIRLS Ludhiana Escorts  by ✔️🍑💃Hotel #cALL #gIRLS...💃Joint ❤89011-83002❤ #ℂALL #gIRLS Ludhiana Escorts  by ✔️🍑💃Hotel #cALL #gIRLS...
💃Joint ❤89011-83002❤ #ℂALL #gIRLS Ludhiana Escorts by ✔️🍑💃Hotel #cALL #gIRLS...
 
Navigating Healthcare with Telemedicine
Navigating Healthcare with  TelemedicineNavigating Healthcare with  Telemedicine
Navigating Healthcare with Telemedicine
 
Demystifying-Gene-Editing-The-Promise-and-Peril-of-CRISPR.pdf
Demystifying-Gene-Editing-The-Promise-and-Peril-of-CRISPR.pdfDemystifying-Gene-Editing-The-Promise-and-Peril-of-CRISPR.pdf
Demystifying-Gene-Editing-The-Promise-and-Peril-of-CRISPR.pdf
 
Contact mE 👙👨‍❤️‍👨 (89O1183OO2) 💘ℂall Girls In MOHALI By MOHALI 💘ESCORTS GIRL...
Contact mE 👙👨‍❤️‍👨 (89O1183OO2) 💘ℂall Girls In MOHALI By MOHALI 💘ESCORTS GIRL...Contact mE 👙👨‍❤️‍👨 (89O1183OO2) 💘ℂall Girls In MOHALI By MOHALI 💘ESCORTS GIRL...
Contact mE 👙👨‍❤️‍👨 (89O1183OO2) 💘ℂall Girls In MOHALI By MOHALI 💘ESCORTS GIRL...
 
Management of psoriasis.pptx (Recent advances)
Management of psoriasis.pptx (Recent advances)Management of psoriasis.pptx (Recent advances)
Management of psoriasis.pptx (Recent advances)
 
QA Paediatric dentistry department, Hospital Melaka 2020
QA Paediatric dentistry department, Hospital Melaka 2020QA Paediatric dentistry department, Hospital Melaka 2020
QA Paediatric dentistry department, Hospital Melaka 2020
 
Storage_of _Bariquin_Components_in_Storage_Boxes.pptx
Storage_of _Bariquin_Components_in_Storage_Boxes.pptxStorage_of _Bariquin_Components_in_Storage_Boxes.pptx
Storage_of _Bariquin_Components_in_Storage_Boxes.pptx
 
Benefits of Dentulu's Salivary Testing.pptx
Benefits of Dentulu's Salivary Testing.pptxBenefits of Dentulu's Salivary Testing.pptx
Benefits of Dentulu's Salivary Testing.pptx
 
Enhancing-Patient-Centric-Clinical-Trials.pdf
Enhancing-Patient-Centric-Clinical-Trials.pdfEnhancing-Patient-Centric-Clinical-Trials.pdf
Enhancing-Patient-Centric-Clinical-Trials.pdf
 
Antibiotic Stewardship by Anushri Srivastava.pptx
Antibiotic Stewardship by Anushri Srivastava.pptxAntibiotic Stewardship by Anushri Srivastava.pptx
Antibiotic Stewardship by Anushri Srivastava.pptx
 
Virtual Health Platforms_ Revolutionizing Patient Care.pdf
Virtual Health Platforms_ Revolutionizing Patient Care.pdfVirtual Health Platforms_ Revolutionizing Patient Care.pdf
Virtual Health Platforms_ Revolutionizing Patient Care.pdf
 
CHAPTER 1 SEMESTER V - ROLE OF PEADIATRIC NURSE.pdf
CHAPTER 1 SEMESTER V - ROLE OF PEADIATRIC NURSE.pdfCHAPTER 1 SEMESTER V - ROLE OF PEADIATRIC NURSE.pdf
CHAPTER 1 SEMESTER V - ROLE OF PEADIATRIC NURSE.pdf
 
Jesse Jhaj: Building Relationships with Patients as a Doctor or Healthcare Wo...
Jesse Jhaj: Building Relationships with Patients as a Doctor or Healthcare Wo...Jesse Jhaj: Building Relationships with Patients as a Doctor or Healthcare Wo...
Jesse Jhaj: Building Relationships with Patients as a Doctor or Healthcare Wo...
 
#cALL# #gIRLS# In Chhattisgarh ꧁❤8901183002❤꧂#cALL# #gIRLS# Service In Chhatt...
#cALL# #gIRLS# In Chhattisgarh ꧁❤8901183002❤꧂#cALL# #gIRLS# Service In Chhatt...#cALL# #gIRLS# In Chhattisgarh ꧁❤8901183002❤꧂#cALL# #gIRLS# Service In Chhatt...
#cALL# #gIRLS# In Chhattisgarh ꧁❤8901183002❤꧂#cALL# #gIRLS# Service In Chhatt...
 
Overcome Your Phobias with Hypnotherapy.pptx
Overcome Your Phobias with Hypnotherapy.pptxOvercome Your Phobias with Hypnotherapy.pptx
Overcome Your Phobias with Hypnotherapy.pptx
 
Navigating Women's Health: Understanding Prenatal Care and Beyond
Navigating Women's Health: Understanding Prenatal Care and BeyondNavigating Women's Health: Understanding Prenatal Care and Beyond
Navigating Women's Health: Understanding Prenatal Care and Beyond
 

Botulism/ Clostridium botulinum.ppt prepared by Dr PRINCE C P.

  • 1. DR.PRINCE C P Associate Professor , Department of Microbiology Mother Theresa Post Graduate & Research Institute of Health Sciences (Government of Puducherry Institution)
  • 2. Botulism  Clostridium botulinum, which produces the condition known as botulism  Category A toxin.  It is an anaerobic, Gram-positive bacterium commonly found in soil that works by blocking acetylcholine release and inhibiting nerve conduction.
  • 3. Botulinum toxin  Botulinum toxin is the most lethal toxin known, approximately 15,000 times more toxic than nerve gas or chemical exposure.  There are seven types of botulism toxins, A through G.  The most naturally occurring of these are A, B and G, and the only types that cause botulism or other illness in humans are A, B, E and F.
  • 4. Weapon of terror  Botulism has been used as a weapon of terror in the past. During World War II, the infamous Unit 731, the Japanese biological warfare group, fed cultures of Clostridium botulinum to prisoners during the Japanese occupation of Manchuria, killing them.  It was suspected that Germany had weaponized botulism as well, and several other countries were suspected to have done research into the use of botulism as a weapon.  More recently, between 1990 and 1995, aerosols were dispersed on at least three occasions by the Japanese cult Aum Shinrikyo, who would later go on to release sarin gas in the Tokyo subway, to disastrous effect. These releases of botulism failed for various reasons, but the ease with which Aum Shinrikyo was able to culture Clostridium botulinum from the soil is one reason that this toxin would make an excellent bioweapon. .
  • 5.  After the Persian Gulf War, Iraq admitted that it had put concentrated botulinum into missiles during the war, although had not used them.  These weapons have not yet been found, and the amount of botulinum contained in them constitute over 3 times the amount needed to kill the entire current human population if it were aerosolized
  • 6. Botox  The commercially available product known as Botox contains Type A of the Botulinum toxin, but only in very small quantities.  Botox would therefore make a poor bioterrorist weapon because prohibitively large amounts of botox would be necessary to cause even a single death.  However, in January 2005, it appeared that there were a number of cases of botulism poisonings resulting from administration of Botox injections.  After investigation, it was discovered that instead of the costlier Botox, the physicians or clinical medical personnel involved in these cases were actually injecting raw botulism or botulinum bacteria into patients, which could be fatal in high enough doses.
  • 7. There are three forms of botulism  These are foodborne botulism, infant botulism, and wound botulism.  Foodborne botulism is the most well-known form of botulism, and it occurs when an individual eats food contaminated with the toxin produced by C. botulinum. Although not usually due to terrorism, foodborne botulism is considered a public health emergency because more than one person has the potential to eat the same food before it is identified as the source of the botulism outbreak.  Heating of food generally inactivates the toxin.  Infant botulism occurs in a small number of infants each year who have C. botulinum in their intestinal tract from ingesting botulism spores. These spores are very common and can be found in food such as honey.  Wound botulism occurs when wounds are infected with soil containing C. botulinum.  A final form of botulism, aerosolized botulism, is man-made, and occurs when the toxin is inhaled into the lungs.
  • 8.  Routes of infection for botulinum used as a biological weapon include dispersion by aerosolization and deliberate contamination of food, water or beverages.  Contamination of water, although it is feasible, is unlikely.  The most likely route of terroristic dissemination is through aerosolization of the toxin, which would be extremely lethal.  It is estimated that 1 gram of aerosolized botulinum toxin could kill up to 1.5 million people. Despite its potential lethality, botulism is not capable of being spread person- to-person.
  • 9.  Since botulism is naturally occurring, there are several signs you can look for that may indicate that an outbreak of botulism is not natural, but may in fact be the result of a biological attack.  Any outbreak of a large number of cases of flaccid, descending paralysis has the potential to be a terrorist attack.  A particularly telling sign is if the outbreak occurs with an unusual botulinum toxin type, such as Type C, D, F or G.  An outbreak that has a common geographic factor, such as location, but no common dietary exposure, is likely to be an aerosolized, and thus biological attack.  Finally, multiple simultaneous outbreaks with no common source is also a potential sign of attack.  In any case of botulism encountered, it is important to take a careful travel, activity and dietary history to look both for signs of intentional exposure, as well as to identify the source of the outbreak, and other individuals who might have been exposed.
  • 10.  Symptoms usually begin 12 to 72 hours after ingestion of botulism, although symptoms may begin as early as 2 hours or as late as 8 days later.  It is not known how soon symptoms would begin after an aerosolized attack, because there are so few recorded cases, but it is likely that the incubation period would be similar.  Symptoms include double or blurred vision, drooping eyelids, slurred speech, difficulty swallowing, dry mouth and muscle weakness.  Infants with botulism poisoning appear lethargic, feed poorly, are constipated, and have a weak cry and poor muscle tone.  Pets and farm animals can also get botulism from eating contaminated food or inhaling the toxin. However, they cannot transmit the disease to humans.
  • 11.  The symmetric descending flaccid paralysis seen in patients with botulism is the hallmark of this type of poisoning.  Paralysis begins in the muscles of the head and neck, and if untreated, continue down to the arms, legs, and eventually respiratory muscles.  The botulinum toxin does not penetrate the brain parenchyma, so patients are not confused. However, the lack of a gag reflex produced by botulism may require intubation.  Untreated patients with botulism may eventually die of upper airway obstruction produced by the paralysis of the respiratory muscles. Currently, only about 8% of patients with botulism die.
  • 12.  There are several other conditions that may look similar to botulism in presentation, such as Guillan Barre syndrome, stroke and myasthenia gravis.  These conditions can be excluded through testing such as brain scans, spinal fluid examinations, nerve conduction tests and tensilon tests.  However, the best way to confirm a diagnosis of botulism is to inject serum or stool from the infected patient into mice and look for signs of botulism in the mice.  These sorts of tests can be performed at most state health laboratories, but a physician making an on-the-spot diagnosis does not have immediate access to this kind of testing.
  • 13.  Once botulism is diagnosed, treatment for botulism is mainly supportive, such as enteral and parenteral feeding, ventilation, and treatment of secondary infections in an intensive care setting.  Respiratory failure may require that patients be put on a ventilator, or breathing machine for extended periods.  Timely administration of equine antitoxin provides passive immunization of the botulinum toxin, and prevents patients from worsening. While it stops the further progression of paralysis, it does NOT reverse the paralysis that has already occurred, so the sooner the antitoxin can be administered, the better.  The antitoxin is not usually given for treatment of infant botulism.