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MicroLabPrac

Lab Practical On

QuestionAnswer
Epidemiology study of disease transmission including what,where and when.
Disease any change from a normal healthy state.
Infection colonization and replication of potential pathogens in a hose
Reservoir constant source of infection that gives pathogen place to survive and replicate.
Carriers human reservoirs who do not show signs of disease.
Chronic Carrier shed pathogens all their life.
Casual(transient) Carrier shed temporarily and do not get disease themselves.
Incubactory Carrier show no symptoms in communicable period; shed temporarily.
Convalescent carrier show no sign of disease because they have recovered; shed temporarily.
Vectors animals that carry pathogens from one host to another.
Arthropod Vector (most common) insects
Biological Vector vector bites one host and then another.
Mechanical Vector vector carries pathogen on its feet/other body parts.
Direct Transmission passed from one person to another by direct body contact, sexual, or close personal contact.
Indirect Transmission passed person to person by other objects like food, water, dust, soil, animals, or inanimate objects.
Fomites inanimate objects that transmit disease (spoons, cups, bedding, etc.)
Droplet Transmission microorganisms carried in small drops of liquid.
Droplet Nuclei organisms encased in dried mucus (protective covering)
Aerosol formation suspension of microorganisms w/particle in the air.
Aseptic Objectives prevent contamination of clinical specimen, worker, and maintains known standard control cultures w/o contaminates.
Septic presence of pathogenic microbes in living tissue.
Aseptic absence of pathogenic microbes.
Broth Medium solution containing nutrients required by microbes for growth.
Agar seaweed polysaccharide (D and L galactose). It makes broth solid.
Solid Medium broth that has agar in it to make it hard.
Petri Plates flat plastic plates w/lid; filled w/solid medium.
Pour Plate organisms spread throughout plate (partial liquid)
4 Quadrant Streak Plate used for colony isolation.
Form(from top,naked eye) circular, irregular, filamentous,rhizoid
Elevation(lateral view) raised, convex, flat, umbonate,crateriform
Margin(edges) Entire, Undulate Filiform, Curled, Lobate
Sediment Growth at the bottom. IE. STAPHYLOCOCCUS EPIDERMIDIS
Pellicle Growth at the top. Obligate aerobes, motile IE BACILLUS SUBTILIS
Turbidity(cloudy) Growth throughout. Facultative anaerobes, motile IE E. coli or Serratia marcescens(cloudy and red in color)
Dark Field dark background, bright (non-stained) living organisms
Simple Microscope one lens
Compound Microscope two lenses: Ocular and Objective
Ocular Lens closest to the eye 10x
Objective Lens Closest to the specimen 4x low, 10x, 40x, 100x high
Condenser group of lenses below the stage which functions as a light gathering system which sends light to the specimen from the light source.
Diaphragm iris-like closure system below the stage below the stage which regulates the amount of light passing through the condenser.
Resolving Power the ability to distinguish 2 points as distinct, seperate objects rather than as one blurred image. It depends on wave length of light(shorter=better), design of the condenser and use of oil immersion.
Numercial Aperture relates to the size of the cone of light entering the objective and the medium surrounding the objective (usually air)
Immersion Oil prevents loss of light rays due to diffraction because the oil has the same refractive index as glass and improves resolution.
Total Magnification ocular magnification multiplied by the objective magnification.
Parfocalism once the specimen has been focused under low power(10x)the microscope is parfocal if you are able to switch to a highter magnification with a minimum of focal adjustment.
Working Distance distance between the bottom of the objective lens and the slide. As the magnification increases, the working distance decreases.
Light intensity less light is required at low magnifications. As the magnification increases, the need for light increases. Too much light can cause burn out.
Diameter of field as the magnification increases the diameter of the field decreases.
Real Image image passing into the objective lens from the specimen
Virtual image real image is further magnified by the ocular lens and passes to the retina of the eye. It is upside down and reversed left to right.
Coarse Focus used to bring the specimen into approximate focus.
Fine Focus used to bring the specimen into clear focus
Rheostat electrical adjustment for the light bulb.
Light field Uses visible/white light, bright background, stained organisms.
Fluorescent emit light when light of different wavelength strikes them(UV rays)
Electron Microscopy uses beam of electrons guided by strong magnets; increase RP
Scanning(SEM) magnify objects 50,000 x actual size; 3-D image, color
Transmission(TEM) magnify 500,000x; black and white; granular
Heat Fix to keep the bacteria from washing off during the staining procedure.
Basic dyes (+) attracted to (-) structures in cell. Blue,green, violet, red.
Simple stains attracted to plasma membrane
Acidic dyes(-) repel by negative charge of organism: don't stain organism but stains background.
Smears and Simple Stains Heat fix; Basic dyes; Acidic dyes
Gram Stain Separate organisms based on cell wall construction. Peptidoglycan(layer); Primary stain(crystal violet); Counterstain(Safranin);Mordant iodine(binds crystal violet and intensifies stain); decolorizer (alcohol or acetone) (+)purple (-)pink
Spore stain Stains spores. IE Bacillus subtlilus(anthrax) and Clostridium(botulism) Primary stain (Malachite green) Counterstain (safranin); no decolorizer; Spores(green) vegetative cells (pink or red)
Direct Motility Looking a flagella
Monotrichous single flagella on one end
Amphitrichous one flagella on each end.
Lophotrichous multiple flagella on one or both ends.
Peritrichous flagella cover entire surface.
Indirect motility evidence(hanging drop), SIM tube, Motility test medium or half strength agar.
Acid-fast stain Difficult to stain, diagnostic test for Mycobacterium, short rod. Primary stain(carbolfuschin); Decolorizer(5% acid alcohol); Counterstain methylene blue
Negative Stain Transparent organisms with stained background. Negative acidic dyes(Nigrosin-purple);congo red(pink) or India Ink(not based on charge) Drop dye one end, smear across slide, air dry and view. Not heat fixed/ and specimen is alive.
Capsule stain Protective, sticky glycopolysaccharide layer. It protects from phagocytosis b/c non Ag capsule. Use negative stain technique plus addition of crystal violet at end.
Carbohydrate test PH indicator Phenol Red; sugar broth; neutral pH, durham tube capture gas.
Acid only yellow, no gas bubble.
Acid and gas Yellow and gas bubble
Negative acid red/pink
Neutral orange
Starch Hydrolysis complex carb. Testing for amylase(saliva). Add iodine and should see the halo
Catalase production Peroxide converts to H2O and oxygen. It will bubble when it is positive.
DNA digestion Halo around organism when viewed on white background. Touleudine blue migrates away, leaving clear halo. Any color change=+ test.
Hydrogen Sulfide production(cysteine metabolism) Gas: cysteine (trying to make pyruvic acid) clips off sulfur(alanine)etc...generate energy. Sulfur bound to H and will make Ferrous iron(replace H ion on sulfur) and Iron Sulfate=black precipitate(ppt=desulfurase) Must have cysteine to ppt.
Indole/Trytophane Metabolism Makes pyruvic acid, indole, and ammonia. Use Kovak's reagent and a positive test will have a red ring at the top.
Kovak's Reagent paraaminobenzalidehyde and binds to indole.
Blood agar plates Used for streptococcus. Alpha(Olive Green) Beta(total hemolysis) clear; Gama(no hemolysis) and has no changes in color
Urea Digestion. Test changes pH. Conducive for growth (Proteus, Helicobacter pylori); urease +. Breaks it down CO2 and ammonia (HOT PINK, alkalyline
Obligate aerobes(strict) requires mine 21%oxygen. Both SOD and catalase(free radicals)
Obligate anaerobes(no enzymes) 0% oxygen
Facultative Anaerobe grow w/out oxygen 0-21% only SOD, no catylase
Microaerophils grow just below surface 2-10% Myeloperoxidase
Created by: DixieDoll
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