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46 Cards in this Set
- Front
- Back
Temperature Lethal Effects |
Thermal Death Point Thermal Death Time |
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TDP |
Thermal Death Point: The temperature at which the organism dies in 10 minutes |
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TDT |
Thermal Death Time: The time of death for an organism at a given temperature |
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Evaluate Data on a Chart |
Chart Example |
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Selective Media |
The media has 1 or more ingredients that only allow certain organisms to grow by inhibiting other kinds. Manital Salt ager: 10% MaConkey agar for Gr- Hektoen agar for Salmonella and Shigella |
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Mannitol Salt Agar |
A selective media that contains a high (10%) concentration of salt which thereby inhibits most organisms except Staph. Therefore Mannitol Salt Agar selects for Staph. Also a differential media that can be fermented by certain organisms. If fermentation occurs, then acid is produced which lowers the pH. When the pH drops, it causes a chemical indicator in the media to change color from pink to yellow. This change means we have grown S. aureus. |
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Differential Media |
Means that there is a characteristic of the media which allows us to differentiate among the organisms which do grow on a plate. Two different colors on the same media. MSA: Colors (Yellow or Fuschia) occur when bacteria can metabolize the media. Blood Agar |
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Kirbey Bauer |
Zones of inhibition Measure the diameter of zones in mm to determine if it is Resistant intermediate of Sensitive (p. 121) |
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Staph and strep Identification |
Use Flow Chart (ditto) |
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API Strips |
To Identify Gram - Bacteria Fermentation (Yellow) Citrate (Blue) H2S (Black) Memorize chart p. 175 |
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Antiseptic |
Can be put on the skin, living organisms |
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Disinfectant |
Only put on inatimate objects |
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Gram Stain |
Review slides |
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Acid Fast |
The acid-fast stain is a differential stain used to identify acid-fastorganisms such as members of the genus Mycobacterium . Acid-fast organisms are characterized by wax-like, nearly impermeable cell walls; they contain mycolic acidand large amounts of fatty acids, waxes, and complex lipids. |
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Schaffer Fulton Spore Stain |
Mature spores stain green whether free or still inside the vegetative sporangium. Vegetative cells and sporangia stain red. The Schaeffer-Fulton stain technique was applied. The primary stain, malachite green, is forced into the spores by heating the prepared slide to boiling for 4-5 minutes. After washing, the vegetative cells are counterstained with safranine. |
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Hemolysis |
Alpha, Beta, Gamma |
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Graph |
Which bacteria grew the best at a pH, Temperature |
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Know all Micro vocabulary |
Hello |
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Fomite |
An inanimate object |
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Rapid ID Method for Staphylococcus |
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Gram Positive |
Peptidoclycan Layer captures the violet stain |
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Gram Negative |
There is no Paptidoglyan to capture the violet stain so it washes away and is replaced by a red stain. |
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Rapid ID for staphylococcus Aureus entails what? |
1. Gram + (Purple) 2. + H2O2 (Bubbles) 3. + Coagulase (Clot forms) |
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ID for Micrococcus and other Staph Species |
1. Gram + (Purple) 2. + H2O2 (Bubbles) 3. - Coagulase (Clot does not form) |
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ID for Streptococcus |
1. Gram + (Purple) Chains 2. - H2O2 (No Bubbles) (Many other tests to differentiate Streptococcus species) |
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Beta Hemolysis |
Complete Breakdown of Red Blood Cells |
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Alpha Hemolysis |
Partial Breakdown of hemoglobin inside of RBC in a blood agar plate producing greenish discoloration around the colonies. |
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Gamma Hemolysis |
No hemolysis is exhibited on the blood plate. |
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Physiological Tests for Streptococci and Enterococci Differentiation: Group A Streptococci: S. Pyogenes |
Beta Hemolysis + for Bacitracin Susceptibility |
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Physiological Tests for Streptococci and Enterococci Differentiation: Group B Streptococci: s. algalactiae |
Beta Hemolysis + for CAMP Reaction |
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Camp Reaction |
Group B Strept (s. agalaciae) produces an extracellular substance that increases the beta hemolysis production of certain strains of staph aureus. The CAMP test will detect this production. |
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Physiological Tests for Streptococci and Enterococci Differentiation: Group C Streptococci: s. dysgalactiae |
Beta Hemolysis (S) SXT Sensitivity |
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Bile esculin hydrolysis |
Right: Black agar = Bile Esculin + Left: Unchanged Agar = Bile Esculin - |
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Physiological Tests for Streptococci and Enterococci Differentiation: Group D Streptococci: E. Faecalis E. Faecium S. Bovis |
+ Bile Esculin Hydrolysis |
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Physiological Tests for Streptococci and Enterococci Differentiation: Group D Streptococci: E. Faecalis E. Faecium |
+ Bile Esculin Hydrolysis and + Tolerance to 6.5% NaCl |
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API Test |
Gram Negative Boxed reagents filled to top Underlined reagents: add mineral oil to create anaerobic conditions Allow to incubate Develop with developing agents as needed Generate a 7 figure number Look up the 7 figure number to identify GR- bacteria |
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Kirby-Bauer Antimicrobic Test |
The KB test is a test of the antibiotic sensitivity of bacteria. It uses antibiotic-impregnated wafers to test the extent to which bacteria are affected by those antibiotics (zones of inhibition). |
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Kirby-Bauer Procedure |
1. Use a panel of 12 Antibiotics on organism lawn 2. Pure Culture on Mueller-Hinton Agar 3. Standardized test A. Must innoculate with pure culture B. The strength of innoculum must be of certain turbudity (McFarland std, 0.5) C. Antibiotic disc = standard dosages 4. Measure the zones of inhibition in mm |
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Kirby-Bauer Procedure: Factors which influence Zone Size |
1. Type of organism 2. Amount of inoculum on the agar plate 3. Type of medium 4. Diffusibility of the chemical Too much bacteria = false negative Too little bacteria = false positive |
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Broad Spectrum Antibiotic |
KIlls both gr- and gr+ bacteria (most, not all) |
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Narrow Spectrum Antibiotic |
Kills most Gr+ only |
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Drug fastness |
Resistance to Antibiotics |
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Thermophilic |
Thrives in heat |
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Thermoduric |
Can survive/ is durable with high temperatures |
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Antiseptic |
An antiseptic is used on living tissues and cells to destroy any types of infections which may be living on the tissue. |
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Disinfectant |
Disinfectants are meant to destroy microorganisms which can infect nonliving objects. |