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Microbiology 1 Lab Practical 1

front 1

MPN

back 1

(Most Probable Number) indirect/viable method, live cells. Make statistical estimates numbers of cells by their patterns of growth in liq. culture media

front 2

Standard plate count (SPC)

back 2

Direct/viable, live cells, good for patients. Dilute a sample in saline, spread on solid media & count colonies. Calculate the # of cells in original sample from counts & dilution. *most common*

front 3

Spectroscopy

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Indirect/total live & dead, not good for patients. Cells dead & alive. Measure the amount of light that passes thru a liq. culture using a spectrophotometer & est. the # of cells/mL based on amount of light that passes through the culture. * most common *

front 4

DAPI or AODC staining & microscopy

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Direct/total. Live/dead. Stain the cells w/fluorescent dyes, which make them visible in raw samples (ie soil). Count the # of cells using a fluorescent microscope.

front 5

# of colonies needed on media to give accurate counting results

back 5

30-300

front 6

Spectroscopy method of counting (how it works)

back 6

based on turbidity. Optical density used to describe the turbidity of a culture. The Spec 20 can quantify the OD of a culture indirectly by measuring the amount of light that can pass through a a culture (percent transmittance %T). The higher the OD the lower the %T (indirectly proportional, the higher the OD the higher the turbidity (directly proportional)

front 7

If you were given a stock culture that was really old, would you expect the SPC to be higher or lower?

back 7

Lower because most bacteria in death phase

front 8

With SPC/dilution, why bother doing 3 replicates?

back 8

To normalize & standardie counts

front 9

Why shouldn't you use a plate that has 10 colonies to calulate the number of cells in the starting culture?

back 9

Not enough to get statisical validity. NETC

front 10

Which counting method would you use if you need isolated colonies from a soil sample and why?

back 10

DAPI or AODC staining. You can apply flourescent stain to bacteria you want to to see and use fluoresent microsope.

front 11

Kirby-Bauer Technique

back 11

Using paper disks impregnated w/different antibacterial medicines on Mueller-Hinton agar plate to determine the sensitivity of a bacterium to serveral antibacterial medicines. No growth or halo around disk = sensitive (zone of inhabition--use whole diameter). Grows right up to the disk = resistant.

front 12

Robert Kock

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In the 1880s he developed streaking for isolation.

front 13

Aseptic technique

back 13

Lab technique used to exclude contaminants.

front 14

Why is it desirable that microscope objectives be parfocal?

back 14

So you can focus it once, then switch objectives and refocus only using fine adjustment knob.

front 15

Which objective focuses closest to the slide?

back 15

100x Oil immersion

front 16

What controls the amount of light reaching the oculars?

back 16

Iris diaphragm (opens/closes)and condensor (up/down)

front 17

What effect does increased magnification have on the field of vision?

back 17

Raise magnification lowers field of view

front 18

What does the "ubiquity of microorganisms" refer to ?

back 18

The concept that microorganisms are everywhere

front 19

Fastidious organisms

back 19

Live in body and have "finicky" nutrient requirements

front 20

What are the objective powers and names?

back 20

4x scanning, 10x low power, 40x high powerh(high dry), 100x oil immersion

front 21

Primary purpose of: deeps, slants, broths?

back 21

Deeps= ovservie O2 requirements and motility. Slants = surface growth and pattern. Broths = large numbers of bacterial growth.

front 22

Resolution (or resolving power)

back 22

The ability of lenses to reveal fine detail or 2 points distinctly separated.

front 23

When using low-power lense, the iris diaphragm should be...?

back 23

Barely open so that good contrast is achieved. More light is needed w/higher magnification.

front 24

Darkfield microscopy is valuable for observing...?

back 24

Bacterium that are not stainable with conventional stains, but can be observed in directd smears (ex. Treponema pallidum - syphilis).

front 25

Brownian movement

back 25

Not true motility but rather the movement caused by molecules in the liquid striking an object. Vibrates or quivers.

front 26

Shape of most bacteria grown in the lab

back 26

Cocci or rods

front 27

What is the usual % agar and what is a lower % used for?

back 27

1.5% agar is normal. Semisolid deeps 0.5-o.7% agar can be used to determine motility.

front 28

Slants vs. plates

back 28

Slants also provide a solid growth surface, but are easier to store and transport.

front 29

The 6 patterns of growth on agar slants

back 29

Arborescent (branched-looks like tree
Beaded
Echinulate (pointed)
Filiform (even)
Rhizoid (rootlike)
Spreading

front 30

CFU

back 30

Colony forming unit

front 31

Where is isolation of bacteria frequently used?

back 31

On selective media

front 32

Selective Media

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Designed to encourage growth of certain types of organisms

front 33

Differential Media

back 33

Contain indicators that expose differences between organisms (i.e. pH)

front 34

Enteric

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Gut bacteria, usually Enterobacteriaceae. Coliforms are enteros & lactosefermentators, noncoliform do not ferment lactose

front 35

Bacteroides fragilis

back 35

The most abudnand bacteria in the human colon. 10^11 cells per gram of feces. Also the most common anerobic pathogen. Used in BBE AGar

front 36

Growth patterns in agar & broth

back 36

-Colony shape--circular, irregular, punctiform (tiny)
-Margin--entire(smooth, undulate, lobated, filamentous, rhizoid (branched root)
-Elevation--flat, raised, convex, pulvincate (very convex_, umbonate (raised in center)
-Texture--moist, dry, mucoid
-Pigment--opaque, translucent, shiny, dull
-BROTH--pellicles (dots), sediment (at bottom), uniform fine turbidity, flocculent (clump)

front 37

Aerotolerance determined in what media?

back 37

Agar deep stabs and shakes

front 38

Obligate aerobes

back 38

Require O2, grow at top

front 39

Facultatvie anearobes

back 39

Grow with or without O2, grow throughout media but more dense on top

front 40

Aerotolerant anaerobes

back 40

Don't require O2, but not aversely affected by it. Uniform growth throughout media

front 41

Microaerophiles

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Survive only in lower than atmospheric levels of O2, middle or upper middle growth in media.

front 42

Capnophiles

back 42

Are microaerophiles that must have elevated CO2

front 43

What type of agar used in agar deep stabs?

back 43

Tryptic soy agar

front 44

Bile salts

back 44

Used in selective media, selects against organisms incapable of surviving gut (especially gram +)

front 45

Lactose

back 45

Helps distinguish between fermtors and nonfermentors

front 46

Thiosulfate

back 46

Used to id organisms cable of reducing sulfure to H2S

front 47

Ferric Iron

back 47

Inicator of sulfur reducers, black precip