Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
21 Cards in this Set
- Front
- Back
Three enteric gram negs with disease
|
Aggregatibacter (Actinobacillus)
A. actinomycetemcomitans Periodontitis, endocarditis, Bite wound infections Bordetella B. pertussis and B. parapertussis Whooping cough B. bronchiseptica Brucella and Francisella Zoonotic diseases Brucellosis Tularemia |
|
AA
|
Gram-negative, facultative anaerobic coccobacillus
present in patients with chronic periodontitis causative agent for other serious systemic infections (endocarditis) |
|
virulence factors of AA
|
leukotoxin encoded by lktA gene - kills neutrophils and monocytes
Fimbriae EmaA - mediates the adhesion to collagen |
|
Bordatella
|
small, Gram-negative, aerobic coccobacilli
encapsulated no spores produced |
|
B. Pertussin
|
whooping cough
Transmission is by droplets Begins with the catarrhal phase (1-2 weeks) paroxysmal phase (2-4wks) convalescent phase (1-3wks) |
|
Virulence factors of Pertussis toxin
|
toxin reacts with different cell types, including T lymphocytes, and acts on different cellular regulatory processes
ADP-ribosylating bacterial toxins. |
|
virulence factors of Bordetella
|
Filamentous hemagglutinin
Heat-Labile Toxin Adenylate Cyclase Toxin Tracheal Cytotoxin Lipopolysaccharide Agglutinogens |
|
Virulence in B. Pertussi
|
B. pertussis organisms undergo antigenic variation
Pertussis toxin is produced solely by B. pertussis. |
|
Epidemiology of Bordetella Disease
|
mucous membranes of the human respiratory tract are the natural habitat for B. pertussis and B. parapertussis
patient is most infectious during the early catarrhal phase |
|
Treatment and prevention of Pertussis
|
tetracycline, erythromycin, and chloramphenicol
Pertussis vaccine was originally produced from smooth forms (phase I) Acellular pertussis vaccine |
|
Brucella and Francisella
|
Zoonotic diseases
Brucellosis - category B bioweapon Tularemia - Category A bioweapon |
|
Bioterrorism agents
|
Brucellosis (Brucella species) is a Category B bioterrorism agent
Tularemia (Francisella tularensis) is a Category A bioterrorism agent |
|
Category A bioterrorism
|
High-priority agents include organisms that pose a risk to national security because they
can be easily disseminated or transmitted from person to person; result in high mortality rates and have the potential for major public health impact; might cause public panic and social disruption; and require special action for public health preparedness. |
|
Category B bioterrorism
|
Second highest priority agents include those that
are moderately easy to disseminate; result in moderate morbidity rates and low mortality rates; and require specific enhancements of CDC's diagnostic capacity and enhanced disease surveillance. |
|
Category C bioterrorism
|
Third highest priority agents include emerging pathogens that could be engineered for mass dissemination in the future because of
availability; ease of production and dissemination; and potential for high morbidity and mortality rates and major health impact. |
|
Brucella characteristics
|
Gram-negative coccobacilli; non-spore-forming and non-motile; aerobic, but may need added CO2
Two different O chains occur in the LPS Brucellosis is a zoonosis, acquired from handling of infected animals or consuming contaminated milk or milk products |
|
Brucellosis symptoms
|
Symptoms are variable.
influenza-like with fever. Limb and back pains are unusually severe, and sweating and fatigue are marked. recover entirely within 3 to 12 months but some will develop complications marked by involvement of various organs, and a few may enter an ill-defined chronic syndrome. |
|
Treatment and prevention of Brucellosis
|
doxycycline, streptomycin and rifampin for 4 to 6 weeks
prevented by pasteurizing milk, eradicating infection from herds and flocks, and observing safety precautions |
|
Francisella
|
Very small Gram negative coccobacili, strict aerobe
Polysaccharide-rich Capsule (antiphagocytic) Grows intracellularly , survives inside macrophages Tularemia (glandular fever, rabbit fever, tick fever or deer fly fever |
|
Tularemia diseases
|
Ulceroglandular tularemia (painful papule)
Oculograndular tularemia (eye infection) Pneumonic tularemia (sepsis) |
|
Treatment and prevention of Tularemia
|
treated with Streptomycin (not always available and has toxicity), gentamicin, fluoroquinolones and doxycycline
Avoidance of the reservoirs of infection Vaccine is available |