Exam 1 Flashcards

1
Q

Light Microscope Parts

A
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2
Q

Calculation of Total Magnification

A

Total magnification of the final image is a product of the separate magnifying powers of the two lens.

objective power x ocular power = total magnification

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3
Q

Bacterial Shapes

A
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4
Q

Bacterial Arrangements

A
  • Arrangement of cells is dependent on pattern of division and how cells remain attached after division:
    • Cocci:
      • Singles
      • Diplococci – in pairs
      • Tetrads – groups of four
      • Irregular clusters
      • Chains
      • Cubical packets (sarcina)
    • Bacilli:
      • Diplobacilli
      • Chains
      • Palisades
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5
Q

Simple Stain

Acidic Dyes

A
  • net negative charge
  • bind to components of cells and tissues that are positively charged.
  • Surface of bacterial cells are negatively charged (due to Teichoic acid)
    • basic dyes are most commonly used in bacteriology.
  • Examples:
    • Crystal Violet
    • Methylene Blue
    • Safranin
    • basic Fuchsin
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6
Q

Use for Simple Stain

A
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7
Q

Negative Stain

A
  • uses negative or acidic stains that do not bind to the test specimen
  • observe a clear specimen against a dark coloured background
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8
Q

Use for Negative Stain

A
  • determines the bacterial shape and arrangement.
  • helps us to stain the organisms that are too sensitive to be heat fixed.
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9
Q

Types of Stains

A
  • Simple Stains
    • Crystal violet
    • Methylene blue
    • Safranin
  • Differential Stains
    • Gram stain
    • Acid-fast stain
    • Endospore stain
    • Histological stain
  • Special Stains
    • Negative (capsule) stain
    • Flagellar stain
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10
Q

Heat Fixation

A
  • passing a slide of bacterial cells through a flame until the underside of the slide is warm to the touch.
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11
Q

Inoculating loops sterilized

A
  • passing it at an angle through the flame of a gas burner until the entire length of the wire becomes orange from the heat.
  • all contaminants on the wire are incinerated.
  • Never lay the loop down once it is sterilized
    • or it may again become contaminated.
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12
Q

Advantages of Simple Stains

A
  • simple method where one stain or reagent is used.
  • quick process.
  • determining the bacterial shape, size, arrangement.
  • difference between the living and the non-living structures.
  • morphological characteristics of the bacteria.
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13
Q

Disadvantages of Simple Stains

A
  • It only gives limited information about the morphological characteristics only.
  • It does not help in identifying the classification of bacteria.
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14
Q

Advantages of Negative Stains

A
  • Through negative staining, clear unstained cells are easily observable against the black coloured stained background.
  • A negative staining method does not involve the heat-fixing of the specimen. As a result, the cell will not deform by the heat.
  • It can also stain heat-sensitive microorganisms like Spirochetes, Yeasts etc.
  • The negative staining technique also permits examining a transparent capsule around the cell wall of various microorganisms like Cryptococcus neoformans.
  • It is quite an easy and rapid method that makes the use of a single acidic stain only.
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15
Q

Disadvantages of Negative Stains

A
  • Negative staining does not provide much information about the cell rather than the cell size, shape and arrangement.
  • By using this technique, we cannot examine a particular strain or a type of organism.
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16
Q

Aseptic Technique

A

Used to reduce the risk of post-procedure infections and to minimize the exposure of health care providers to potentially infectious microorganisms

17
Q

Pure Cultures Techniques

Streak Plate Method

A
18
Q

Fungi:

Molds and Yeast

A
19
Q

Protozoa

A
20
Q

Smear Preparation

A
21
Q

Simple Stains

A
22
Q

Simple Stain

Basic Dyes

A
  • net positive charge
  • bind to components of cells and tissues that are negatively charged
  • Basic stains
    • methylene blue
    • Gram safranin
    • Gram crystal violet
      • useful for staining most bacteria.
      • These stains will readily give up a hydroxide ion or accept a hydrogen ion, which leaves the stain positively charged.
23
Q

Gram Stain

A
  • Way to identify type of infectious bacteria
  • Treatment differs based on outcome
  1. Smear bacteria sample across glass slide
  2. Heat fix the bacteria to the slide
  3. Apply crystal violet to the bacteria
  4. Apply iodine to the bacteria
  5. Wash with alcohol (destaining)
  6. Apply safranin to the bacteria
  7. Results
    1. Gram positive = purple
    2. Gram negative = pink
24
Q

Gram-Positive

A
  • Innermost plasma membrane
  • Thick peptidoglycan cell wall
  • outer capsule
  • more easily treatable with antibiotics
  • stains purple/ violet after Gram Stain
25
Q

Gram-Negative

A
  • Innermost plasma membrane
  • Thin peptidoglycan cell wall
  • Another plasma membrane
  • Outer capsule
  • Harder to treat with antibiotics
  • Staines red/ pink after Gram Stain