Nouvelles et mises à jour

de la SCSLM
16 mars, 2012
De bonnes affaires, des trucs gratuits et une nouvelle vidéo – SNLM2012
en lire plus
16 mars, 2012
Promotion d’hiver en formation : Vous pourriez gagner une inscription à LABCON2012!
en lire plus
07 février, 2012
CSMLS Workforce Integration Project Report
en lire plus

Fastidious Gram Negative Bacilli

 Fastidious Gram Negative Bacilli (9820-11) Learn about the classification and nomenclature, morphology and growth requirements, identification and susceptibility, pathogenicity and relationship to differentiation strategies for Haemophilus, Bordetella, Pasteurella, Gardnerella and Capnocytophaga.

Code 9820-11
Niveau Supérieur

Prix membres

$0

Prix non-membres

$135

 

Renseignements additionnels

PEP hours: 11
CPS/ART credits: 0
 
Learning Outcomes:
·       State the criteria originally used to place an organism in the genus Haemophilus.
Haemophilus influenzae
·       Describe the cellular morphology.
·       Describe the growth requirements:
·       Describe colonial morphology on blood agar with a staph streak and on chocolate agar.
·       State the criteria necessary to establish the genus Haemophilus.
·       State how to differentiate the different species of Haemophilus.using hemolysis, growth factor requirements and porphyrin test.
·       Explain why biotyping and serotyping would be carried out and state which serotype is the most virulent.
·       State the approximate rate of resistance to ampicillin, describe the two mechanisms responsible for the resistance and how each is detected.
·       Name a rapid test for chloramphenicol resistance.
·       Explain why childhood infections due to this organism are decreasing in number.
·       Name the two invasive infections found in children and describe typical findings in spinal fluid from a case of meningitis.
Haemophilus aegyptius
·       Explain the taxonomic relationship with H. influenzae.
·       Describe two acute infections caused by H. aegyptius.
Other Haemophilus species
·       Describe the clinical significance of H. parainfluenzae, H. haemolyticus and H. parahaemolyticus.
·       State the atmosphere required for isolation of H. aphrophilus and the type of specimen where it may be found as a pathogen.
·       Describe the cellular morphology of H. ducreyi in direct smears and in cultures.
·       State the pathogenicity of H. ducreyi.
X and V Growth Factor Requirements
·       State the criteria the test medium must meet and name the recommended medium.
·       State how the test medium should be inoculated, how carryover of growth factors in the inoculum would affect results and how to avoid this.
·       Describe how to interpret results.
Porphyrin Test
·       State the principle of the test including the substrate used.
·       State how the test is inoculated and describe two methods of detecting porphyrins.
·       State how to interpret test results.
·       Explain how the test interpretation is affected by:
·        Testing bacteria belonging to another genus
·        Using non-viable bacteria
·        Using too light an inoculum
Bordetella
·       Name the species most commonly infecting man.
 
Bordetella pertussis
·       Describe typical cellular morphology.
·       Describe how diagnosis may be made using direct smears.
·       Name the site that should be sampled for culture and explain how the specimen is obtained.
·       Name and describe a suitable transport medium.
·       Describe the growth requirements. Name two media used for isolation of B. pertussis, compare the shelf life and name the antibiotic recommended for these media.
·       State the usual time required for visible colonies to form.
·       State the criteria indicating the genus Bordetella.
·       State how to differentiate B. pertussis from B. parapertussis and B. bronchiseptica.
·       Name the disease caused by B. pertussis and describe the symptoms.
·       Describe the clinical significance of B. parapertussis and B. bronchiseptica.
Capnocytophaga
·      Describe typical cellular morphology.
·      State suitable media and atmosphere for growth.
·      Describe typical colonies.
·      Describe laboratory findings that indicate Capnocytophaga.
·      State how complete species identification is carried out.
·      Describe the pathogenicity of C. canimorsus and state the usual source of the bacteria.
Actinobacillus
·      Describe typical cellular morphology.
·      State suitable media and atmosphere for growth.
·      Describe typical colonies.
·      Describe laboratory findings that indicate Actinobacillus
·      Describe the pathogenicity of Actinobacillus and state the usual source of the bacteria.
Eikenella
·      Describe typical cellular morphology.
·      State suitable media and atmosphere for growth.
·      Describe typical colonies.
·      Describe laboratory findings that indicate Eikenella
·      Describe the pathogenicity of Eikenella and state the usual source of the bacteria.
Kingella
·      Describe typical cellular morphology.
·      State suitable media and atmosphere for growth.
·      Describe typical colonies.
·      Describe laboratory findings that indicate Kingella.
·      Describe the pathogenicity of Kingella and state the usual source of the bacteria.
Cardibacterium
  • Describe typical cellular and colonial morphology.
  • Describe pathogenicity
Pasteurella
·       Name the species most commonly isolated from man.
·       Name the genus to which some Pasteurella species are being moved.
Pasteurella multocida
·       Describe typical cellular morphology.
·       Describe growth requirements:
·       Describe typical colonies on blood agar.
·       State criteria that indicate a possible P. multocida.State the usual source of the bacteria infecting man and describe clinical infection.
 
Instructor: Helen Smith, MLT
Prerequisites: None
Textbook: N/A
Equipment: Computer with Internet is required
Start Date: Upon registration
Completion: Up to 52 weeks
Version Date: December 2011