M21: Disease Transmission IV: Biodefense Flashcards
Policies Against Bioweapons
- _ (1925): Prohibiting use of biological weapons in war
- _ (BWC, 1972): prevents development, production and stockpile of biological weapons
The Geneva Convention
The Biological Weapons Convention
Differences between biological agents vs. conventional weapons (5)
- Cheaper
- Ubiquitous
- Hard to detect
- Dual-use technology
- Potentially self-perpetuating
Components of the US plan include:
_ which capture particles from the air and are analyzed for the presence of bioagents
the strategic national stockpile of _
_ teams
Biowatch detectors
vaccines/antimicrobials
national disaster medical system
Epidemiologic clues:
The most likely scenario would be _ among people who are _.
The likely presenting symptoms would be _ because most infectious agents are distributed in _ form, but _ outbreaks through _ could also occur.
Another clue would be if an organism was identified that _.
Also _ around the country or organisms with an unusual pattern of _ would be suspicious.
a large epidemic with severe illness and high death rate
otherwise fairly healthy
respiratory
aerosolized
food borne
ingestion
wasn’t normally present in that part of the country or the world
multiple, simultaneous outbreaks
antibiotic resistance
Natural Events
There have been several natural events which would be managed in a fashion similar to an act of bioterrorism. This is an example of an “_” approach to preparedness. Because the principles are the same, these natural events are often discussed along with bioterrorism.
These include such diseases as (4)
The strengths needed to respond to natural outbreaks would be harnessed in the response to an unnatural outbreak.
all hazards
pandemic influenza
SARS
monkeypox
West Nile Virus.
Components
The first part of managing an outbreak is _. This can be done through laboratory and/or clinical reporting. This is important for containment but, most importantly, for better outcomes.
We generally rely on _ confirmation of the disease after which we focus on containing it through infection control measures.
This may involve (3) while monitoring for signs of infection.
early identification of it through surveillance
laboratory
isolating infected and contagious patients
finding close contacts
observing/quarantining individuals
Category A Agents
- _ (anthrax)
- _ (tularemia)
- _ (plague)
- _ (smallpox)
- _ and _ (Viral hemorrhagic fevers)
- _ (botulism)
- Bacillus anthracis (anthrax)
- Francisella tularensis (tularemia)
- Yersinia pestis (plague)
- Variola major (smallpox)
- Arenaviruses and filoviruses (Viral hemorrhagic fevers)
- Clostridium botulinum toxin (botulism)
Category A Agents
- Bacillus anthracis (_)
- Francisella tularensis (_)
- Yersinia pestis (_)
- Variola major (_)
- Arenaviruses and filoviruses (_)
- Clostridium botulinum toxin (_)
- Bacillus anthracis (anthrax)
- Francisella tularensis (tularemia)
- Yersinia pestis (plague)
- Variola major (smallpox)
- Arenaviruses and filoviruses (Viral hemorrhagic fevers)
- Clostridium botulinum toxin (botulism)
Category A Agents are considered to be high priority agents because (5)
– They can be easily spread from one person to another
– High mortality rates
– Major public health impact
– Public panic & social disruption
– Special action required for public health preparedness
Category B Agents
These are the 2nd highest priority. They are less likely to cause _ but they may be easier to _ and they are fairly easy to _.
fatal disease
obtain
disseminate
Category B Agents (7)
E. coli Salmonella Burkholderia mallei (glanders) Burkholderia pseaudomallei (melioidosis) Rickettsia prowazekii (typhus fever) ricin toxin
Category C Agents
These are the third highest priority. This group includes pathogens that could be _ because of availability and ease of production and dissemination.
These agents have the potential for high _ and _ and major health impact
engineered for mass dissemination
morbidity and mortality rates
Category C Agents (3)
Nipah virus
avian influenza virus
hantavirus
Category A Agents:
Anthrax:
Bacillus anthracis
- Gram (positive / negative) _
- Readily forms _ –> Can persist in the soil for years
- Non-_, _ colonies on blood agar
- Anthrax occurs worldwide
- Reservoirs (3)
- Gram positive rod
- spores
- Non-hemolytic, medusa’s head/comet’s tail colonies on blood agar
- Anthrax occurs worldwide
- Reservoirs: cattle, sheep, goats
Category A Agents:
Anthrax:
Naturally occurring anthrax is generally a disease of the _
Breakdown (? > ? >?): inhalational, gastrointestinal, cutaneous
skin
cutaneous > inhalational > gastrointestinal
Category A Agents:
Anthrax:
Anthrax Infection
In humans, anthrax is fairly (common / rare).
It usually occurs after exposure to _ or _.
In 2001, it was also associated with _ exposure.
Other recent outbreaks of note include cases in _ in Scotland through contaminated _ and people handling _.
rare
infected animals or animal products
intentional
injection drug users
heroin
drums made with animal skins
Category A Agents:
Anthrax:
Anthrax Infection
The infection begins with _ when it is in an environment conducive to vegetative growth.
It then _ and produces a _.
The organisms may stay contained in the _ or spread through both the _ and the _.
It causes severe inflammation of the _.
germination of the spore
multiplies
toxin
skin
bloodstream
lymphatics
lymph nodes
Category A Agents:
Anthrax:
Virulence Factors
- Capsule: The organism is protected from the immune system by an _ capsule (a _ capsule) encoded on a plasmid.
- Exotoxins (2) encoded on a plasmid
antiphagocytic polyglutamic acid (PGA)
Edema Toxin (protectiv eantigen + edema factor)
Lethal Toxin (protective antigen + lethal factor)
Category A Agents:
Anthrax:
Virulence Factors
a. Edema Toxin
i) an _ that increases intracellular _ concentrations and interferes with _
b. Lethal Toxin
i) _ that cleaves and inactivates multiple _ and interferes with _
adenylate cyclase
cyclic AMP
cell function
calmodulin-dependent zinc metalloprotease
mitogen-activated protein kinases
signal transduction
Category A Agents:
Anthrax in 2001
There were 22 cases diagnosed between October and November 2001. Eleven of these were _ infections and all survived. The others were _ anthrax and among these 11 cases; 7 were postal workers, 2 had known exposure to contaminated mail and 2 had presumed exposure to contaminated mail. These infections were all limited _ to Florida, Washington DC, New York, New Jersey and Connecticut. This was consistent with an intentional release in certain geographic areas. However the fear was widespread.
cutaneous
inhalational
geographically
Category A Agents:
Cutaneous (skin) anthrax
- Exposure _ to _ of anthrax
- Incubation period of _ days
- _ at site
- Vesicles –> _
- Lesion is usually (painful / painless)
- Enlarged _ in the region of the infection
- Exposure abraded/lacerated skin to spores of anthrax
- Incubation period of 1-7 days
- Pruritic papule at site
- VesiclesàBlack eschar
- Lesion is usually painless
- Enlarged lymph nodes in the region of the infection
Category A Agents:
Gastrointestinal Anthrax
- From _
- 40% mortality
- _ day incubation period
- _, _, and _, followed by severe _. Many cases will be associated with _, massive _, and _.
- From uncooked meat
- 40% mortality
- 1-5 day incubation period
- Nausea, vomiting, and fever, followed by severe abdominal pain. Many cases will be associated with hematemesis, massive ascites, and bloody diarrhea.
Category A Agents: Inhalational Anthrax (“_ Disease”)
- 45% mortality in 2001; Patients who survived were recognized and treated early in their course
- Incubation period of _ days
- _ illness (but no _)
- Does not cause _ but does cause _
- _ widening on chest x-ray (_)
- Dissemination from inhalational or GI anthrax can result in _ (“cardinal’s cap”)
Woolsorter’s
- 45% mortality in 2001; Patients who survived were recognized and treated early in their course
- Incubation period of 4-6 days
- Flu-like illness (but no rhinorrhea)
- Does not cause pneumonia but does cause bloody pleural effusions
- Mediastinal widening on chest x-ray (hemorrhagic mediastinitis)
- Dissemination from inhalational or GI anthrax can result in hemorrhagic meningitis (“cardinal’s cap”)
Category A Agents:
Anthrax:
Diagnosis
The easiest way to make the diagnosis is by _
– _ cultures turn positive in 6-24 hours
– _ cultures may be used for epidemiologic purposes to see if someone has been exposed
Other diagnostic tests include:
– _
– stains
– Anthrax _ test
– Looking for a 4-fold increase in _ antibody level—this requires follow up antibody levels ( diagnosis)
culture of blood, CSF, effusion
Blood
Nasal swab
– PCR
– Immunohistochemical stains
– Anthrax IgM test
– Looking for a 4-fold increase in IgG antibody level—this requires follow up antibody levels (retrospective diagnosis)