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Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

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Page 1: Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

Anthraxthe “agent of doom”Anthrax

the “agent of doom”

By Molly McMahon and Katelynn Johnson

By Molly McMahon and Katelynn Johnson

Page 2: Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

Basic InfoBasic Info

• Anthrax is an acute disease in animals caused by the bacteria Bacillus Anthracis.

• Anthrax bacillus has the unique ability to form long-lived spores, they become inactive dormat spores and can remain this way for many decades maybe even centuries! This can be caused by:

• The death of a host• Extremes in temperature

• Anthrax is an acute disease in animals caused by the bacteria Bacillus Anthracis.

• Anthrax bacillus has the unique ability to form long-lived spores, they become inactive dormat spores and can remain this way for many decades maybe even centuries! This can be caused by:

• The death of a host• Extremes in temperature

Page 3: Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

Basic InfoBasic Info

• Anthrax is found on all of the continents except Antarctica.

• It most commonly infects wild and domesticate herbivorous mammals

• Usually the mammals become infected by inhaling the bacteria while eating

• Anthrax is found on all of the continents except Antarctica.

• It most commonly infects wild and domesticate herbivorous mammals

• Usually the mammals become infected by inhaling the bacteria while eating

Page 4: Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

InfectionInfection

• Ingestion is assumed to be the most common way animals are infected, however it is yet to be proven.

• Carnivores are infected by feeding on infected animals.

• Anthrax can infect humans by being exposed to infected blood or tissues, eat tissues of an infected organism, or are exposed to high densities of anthrax spores.

• Ingestion is assumed to be the most common way animals are infected, however it is yet to be proven.

• Carnivores are infected by feeding on infected animals.

• Anthrax can infect humans by being exposed to infected blood or tissues, eat tissues of an infected organism, or are exposed to high densities of anthrax spores.

Page 5: Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

Forms of InfectionForms of Infection

• Cutaneous anthrax• Bacteria enters through cut or

abrasion• Contact with affected animals• Easily treatable through antibiotics• Symptoms:

• Raised bump• Painless ulcer with a necrotic (cell death) center• Swollen lymph nodes locally

• Cutaneous anthrax• Bacteria enters through cut or

abrasion• Contact with affected animals• Easily treatable through antibiotics• Symptoms:

• Raised bump• Painless ulcer with a necrotic (cell death) center• Swollen lymph nodes locally

Page 6: Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

Forms of InfectionForms of Infection

• Gastointestinal Anthrax• Infected meat is ingested • Mortality rate 25-60%• Symptoms

• Loss of appetite • Nausea    • Abdominal pain • Vomiting of blood • Severe diarrhea

• Gastointestinal Anthrax• Infected meat is ingested • Mortality rate 25-60%• Symptoms

• Loss of appetite • Nausea    • Abdominal pain • Vomiting of blood • Severe diarrhea

Page 7: Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

Forms of InfectionForms of Infection

• Inhalation Anthrax• Begins in lungs• Incubation time of 7 days• Mortality rate of 100% with 1-2 days of

symptoms• Symptoms:

• Unremarkable upper-respiratory infection• Dyspnea (uncomftorable breathing) , diaphoresis

(perspiring profusely), myalgia (muscle pain)• Septic shock

• Inhalation Anthrax• Begins in lungs• Incubation time of 7 days• Mortality rate of 100% with 1-2 days of

symptoms• Symptoms:

• Unremarkable upper-respiratory infection• Dyspnea (uncomftorable breathing) , diaphoresis

(perspiring profusely), myalgia (muscle pain)• Septic shock

Page 8: Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

InfectionInfection

• Anthrax does not spread directly from one infected organism to another, it’s the spores that are transferred from one organism to another.

• There are 89 known strains of anthrax documented in the world today.

• The most widely recognized is the Ames strain. It was the strain used in the 2001 Athrax attacks on the US.

• Anthrax does not spread directly from one infected organism to another, it’s the spores that are transferred from one organism to another.

• There are 89 known strains of anthrax documented in the world today.

• The most widely recognized is the Ames strain. It was the strain used in the 2001 Athrax attacks on the US.

Page 9: Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

InfectionInfection• Once the spores are inhaled they are

transported through the air passages of the body, and into the lungs. Macrophages pick up the spores and transport them to the lymph nodes.

• Here the bacilli and spores cause damage to the lymph nodes and cause chest pain and difficulty breathing.

• The spores germinate into active bacilli and burst the macrophages, multiplying and and infecting the body with more bacilli which are carried in the blood to the entire body.

• Once the spores are inhaled they are transported through the air passages of the body, and into the lungs. Macrophages pick up the spores and transport them to the lymph nodes.

• Here the bacilli and spores cause damage to the lymph nodes and cause chest pain and difficulty breathing.

• The spores germinate into active bacilli and burst the macrophages, multiplying and and infecting the body with more bacilli which are carried in the blood to the entire body.

Page 10: Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

How anthrax infectsHow anthrax infects

Page 11: Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

InfectionInfection

• To enter the cells the lethal factors use another protein produced by B. anthracis, protective antigen. Edema factor inactivates a type of phagocytic cell so that they lose the ability to phagocytose bacteria, meaning that it cannot destroy the matter

• To enter the cells the lethal factors use another protein produced by B. anthracis, protective antigen. Edema factor inactivates a type of phagocytic cell so that they lose the ability to phagocytose bacteria, meaning that it cannot destroy the matter

Page 12: Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

InfectionInfection

• Recent evidence indicates that anthrax targets endothelial cells and cause vascular leakage of fluid and cells in the body. This leads to hypovolemic shock which is basically low blood volume and septic shock.

• Recent evidence indicates that anthrax targets endothelial cells and cause vascular leakage of fluid and cells in the body. This leads to hypovolemic shock which is basically low blood volume and septic shock.

Page 13: Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

InfectionInfection

Page 14: Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

InfectionInfection

• The severity of a strain of Anthrax depends on many factors, however the poly-D-glutamic acid capsule that protects the bacterium from phagocytosis by the specific host cell and its toxins are a primary factor.

• The severity of a strain of Anthrax depends on many factors, however the poly-D-glutamic acid capsule that protects the bacterium from phagocytosis by the specific host cell and its toxins are a primary factor.

Page 15: Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

Anthrax & Biological Warfare

Anthrax & Biological Warfare

• The Ames strain was used in the 2001 Anthrax attacks on the US in a series of mailed letters.

• The Vollum strain was isolated in 1935, developed as a biological weapon for WWII, it was never used.

• The Vollum strain was also used during the Gruinard bioweapons trials.

• The Vollum 1B strain was used during the 1960’s in US and UK bioweapon programs.

• The Ames strain was used in the 2001 Anthrax attacks on the US in a series of mailed letters.

• The Vollum strain was isolated in 1935, developed as a biological weapon for WWII, it was never used.

• The Vollum strain was also used during the Gruinard bioweapons trials.

• The Vollum 1B strain was used during the 1960’s in US and UK bioweapon programs.

Page 16: Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

Anthrax & Biological Warfare

Anthrax & Biological Warfare

• 220 pounds of powdered anthrax material, seeded into the air of a city, could kill more than 1 million people.

• In contrast, 80,000 would die in the explosion of a 12.5-kiloton atomic bomb.

• 220 pounds of powdered anthrax material, seeded into the air of a city, could kill more than 1 million people.

• In contrast, 80,000 would die in the explosion of a 12.5-kiloton atomic bomb.

Page 17: Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

Why Anthrax?Why Anthrax?

• It is easily grown• Easy to spread when spores are

‘healthy’• High Mortality • Stores for long periods of time• Non-transmissible• Does not need ‘food’ to stay alive

and reproduce

• It is easily grown• Easy to spread when spores are

‘healthy’• High Mortality • Stores for long periods of time• Non-transmissible• Does not need ‘food’ to stay alive

and reproduce

Page 18: Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

ReplicationReplication

• Plasmid pXO1 is involved in the growth of B.anthracis

• Anthrax spores enter the body through macrophages and are transported via the lymphatic system to the lymph nodes where germination occurs

• As replication occurs the anthrax organisms release distinct toxins causing tissue edema, hemorrhage, and host cell death

• Plasmid pXO1 is involved in the growth of B.anthracis

• Anthrax spores enter the body through macrophages and are transported via the lymphatic system to the lymph nodes where germination occurs

• As replication occurs the anthrax organisms release distinct toxins causing tissue edema, hemorrhage, and host cell death

Page 19: Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

Factor proteins of AnthraxFactor proteins of Anthrax

• Lethal Factor (LF):• Adheres to enzymes important to cell division• Stimulates macrophages and causes inflammation, which is

normally a protective mechanism. But the LF enzyme is so active that the hormone and inflammation become lethal to the cells.

• Edema Factor (EF):• Leads to water unbalance, diarrhea, pneumonia, swelling• This enzyme stimulates production of a normal cellular hormone, so

much so that the hormone levels immobilize the cellular immune system. The cell becomes defenseless.

• Protective Antigen (PA):• Promotes endocytosis (cell drinking) of itself• Escape route from the endosome

• Lethal Factor (LF):• Adheres to enzymes important to cell division• Stimulates macrophages and causes inflammation, which is

normally a protective mechanism. But the LF enzyme is so active that the hormone and inflammation become lethal to the cells.

• Edema Factor (EF):• Leads to water unbalance, diarrhea, pneumonia, swelling• This enzyme stimulates production of a normal cellular hormone, so

much so that the hormone levels immobilize the cellular immune system. The cell becomes defenseless.

• Protective Antigen (PA):• Promotes endocytosis (cell drinking) of itself• Escape route from the endosome

Page 20: Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

ReproductionReproduction

• Anthrax reproduces asexually• While this is not rare, the spores

that anthrax produces are “super”• This means that the have an

extremely thick outer wall which allows it to survive in many different kinds of environments

• Anthrax reproduces asexually• While this is not rare, the spores

that anthrax produces are “super”• This means that the have an

extremely thick outer wall which allows it to survive in many different kinds of environments

Page 21: Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

More on factor proteinsMore on factor proteins

• Neither the Edema factor protein or the Lethal Factor protein can enter cells without Protective Antigen

• Alone, the Protective Antigen is not harmful• The lysis of macrophages and other cells

leads to release of:• Pro-inflammatory mediators• Reactive O2 and N2 species• Lysomal enzymes which can attempt to protect the cell

• Anthrax proteins inhibit cell replication

• Neither the Edema factor protein or the Lethal Factor protein can enter cells without Protective Antigen

• Alone, the Protective Antigen is not harmful• The lysis of macrophages and other cells

leads to release of:• Pro-inflammatory mediators• Reactive O2 and N2 species• Lysomal enzymes which can attempt to protect the cell

• Anthrax proteins inhibit cell replication

Page 22: Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

TreatmentTreatment

• The first effective vaccine that was developed for anthrax was developed in 1881 by French scientist Louis Pasteur.

• Australia, New Zealand, Russia, Europe, North American and parts of Africa and Asia have all contributed to more than 100 years of animal vaccination programs.

• These programs have made Anthax a very rare disease in animals with only a few dozen cases reported each year.

• The first effective vaccine that was developed for anthrax was developed in 1881 by French scientist Louis Pasteur.

• Australia, New Zealand, Russia, Europe, North American and parts of Africa and Asia have all contributed to more than 100 years of animal vaccination programs.

• These programs have made Anthax a very rare disease in animals with only a few dozen cases reported each year.

Page 23: Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

Side Effects of VaccineSide Effects of Vaccine

• 30% report minor reactions: soreness, redness, itching, swelling and lumps at the injection site

• 35% experience muscle or joint aches, chills, fever, headaches, nausea, loss of appetite, feeling on unease

• Serious reactions requiring hospitalization are rare, occurring about once per 50,000 doses.

• Severe allergic reactions can occur after any vaccination less than one per 100,000 doses

• 30% report minor reactions: soreness, redness, itching, swelling and lumps at the injection site

• 35% experience muscle or joint aches, chills, fever, headaches, nausea, loss of appetite, feeling on unease

• Serious reactions requiring hospitalization are rare, occurring about once per 50,000 doses.

• Severe allergic reactions can occur after any vaccination less than one per 100,000 doses

Page 24: Anthrax the “agent of doom” By Molly McMahon and Katelynn Johnson

AntibioticsAntibiotics

• Most antibiotics are effective against B.anthracis: • Doxycycline• Penicillin• Amoxicillin

• If inhaled or ingested, medications through an IV reach the bacteria quickly

• Treatment can last for up to 60 days

• Most antibiotics are effective against B.anthracis: • Doxycycline• Penicillin• Amoxicillin

• If inhaled or ingested, medications through an IV reach the bacteria quickly

• Treatment can last for up to 60 days