WK 2 Flashcards

1
Q

methods of studying bacteria

A
  1. Microscopic
  2. Cultural
  3. Serological
  4. Animal inoculation
  5. Molecular techniques
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2
Q

Two types of preparations for microscopic exams:

A

wet mount and bacterial smear

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3
Q

for living cells to see motility tissue
sections

A

wet mount

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4
Q

ovement seen is
due to molecules of the solvent medium
bombarding with the organism’s surface;
occurs in all microscopic bodies
suspended in water.

A

brownian motility

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5
Q

movement of a bacteria
in a given direction.

A

true motility

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6
Q

be best
obsserved during wet mounttechnique.

A

Features which may be particulate, such as spores
of fungi and ferns, and pollen grains may be best
obsserved during this technique

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7
Q

2 methods in wet mount

A

normal wet mount and hanging drop metjhod

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8
Q

the best smears are made from

A

he best smears are made from bacteria that have
grown on a solid surface such as an agar slant or
plate.

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9
Q

Basic Cultural Techniques

A
  1. Grow bacteria
  2. Isolate bacteria
  3. Grow bacteria in pure culture
  4. Observe bacteria
  5. Identify bacteria
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10
Q

5 I’s following specimen collection

A
  • Inoculation – producing a culture
  • Incubation – creating the proper temperature and other
    conditions to promote the growth of microbes
  • Isolation – separating microbes from one another, grow
    colonies (pure cultures).
  • Inspection – observing characteristics of colonies and
    cultures (color, texture, size, shape, motility).
  • Identification – main purpose is to determine the type of
    microbe using biochemical, immunologic, serologic tests,
    and DNA analysis
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11
Q

It provides rapid and accurate data when it comes to dealing
with results.

A

Molecular techniques

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12
Q

– bacteria possess diverse proteins and RNA that
can sense change to their intracellular and extracellular
movement. The signals received by these macromolecules
are transmitted to key genes or proteins which alter their
activities to suit the new conditions

A

signalnig

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13
Q

for stain typing of
epidemiologically related organisms.

A

Pulsified gel electrophoresis

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14
Q

how bacteria evolves.

A

Phylogenetic studies

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15
Q

– to detect genetic
material from a specific organism such as virus, to amplify
DNA sequences.

A

pcr

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16
Q

separate double-stranded DNA

A

Denutration

17
Q

complementary sequence is attached

A

Annealing

18
Q

extending the gene to amplify the
genes

A

Extension

19
Q

specificity and quantification
of the targer organism.

A

Quantitative PCR

20
Q

sed routinely in microbiology to
separate DNA, RNA, or protein molecules using an electric
field by virtue of their size, shape, or electric charge

A

gel electrophoresis

21
Q

molecular techniques for
detecting the presence of microbial:
o DNA sequences (Southern)

A

Southern blotting, northern blotting, western blotting,
and eastern blotting

22
Q

used in microbiology as the modern
alternative to the “blotting” techniques

permit the exploration of thousands
of sequences at one time.

Used in molecular microbiology to detect the
presence of pathogens in a sample (air, water,
organ tissue, etc.)

sed to determine the genetic differences
between two microbial stains

A

dna microassays

23
Q

first to be completely analysed by DNA
Sequencing

A

viral genomes

24
Q

) was discovered as a cellular
gene regulation mechanism in 1998, but several RNAibased applications for gene silencing have already made it
into clinical trials

A

rna interferencew

25
Q

Transfer tools or Inoculating tools

A
  1. Serological pipette – putting a autoclave tape at the
    end of the pipette, so when it is aspirated, it won’t reach
    the aspirator. It should be individually wrapped using a
    paper, and put them in canister when placed in a
    autoclave. It has volume markings.
  2. Pasteur pipet – putting a cotton plugs so that when it
    overflows when aspirated too much, the liquid won’t
    reach the aspirator but will be absored by the cotton.
  3. Disposable transfer pipet – plastic and has various
    sizes.
  4. Inoculating loop – it has a circle in the tip, comes into
    two sizes: 1ul and 10 ul loop.
  5. Inoculating needle
  6. Cotton Swab – it must be individually wrapped, not in
    packed to avoid contamination.
  7. Glass spreading rod – spreads the specimens in the
    culture medium.
  8. Loop sterilizer – sterilizes the inoculating loop and
    needle. If not available, Bunsen burner can be used
26
Q

Aseptic technique is the process of:

A
  • Preventing contamination of a culture with environmental
    microbes.
  • Preventing contamination of yourself or the environment
    with the organism in the culture.
  • Remember everything is contaminated with a variety of
    environmental microbes.
  • Remember microbes are visible, you must “see with your
    minds eye” during these procedures
27
Q

types of aseptic transfer

A

Types:
o Plate to broth or broth to plate
o Plate to plate
o Broth to broth
o Broth to slide
o Plate to slide

28
Q

Bacterial colony on LIQUID MEDIUM

A
  1. Degree of growth: absence, scanty, moderate,
    abundant, etc.
  2. Present of turbidity and its nature: the more turbid it
    is, the more bacteria are present.
  3. Presence of deposit and its character
  4. Nature of surface growth
  5. Ease and disintegration and odor
29
Q

Observe bacterial colony on a SOLID MEDIUM

A
  1. Shape: circular, irregular, radiate, or rhizoid.
  2. Size: diamete in mm.
  3. Elevation: this describes the “side view” of a colony.
    These are the most common.
    o Flat, raised, low convex, dome shaped.
  4. Margin: the margin or edge of a colony (or any growth)
    may be an important characteristic in identifying
    organisms.
    o Entire, wavy, lobate, filiform
  5. Surface: smooth, wavy, rough, granular, papillate,
    glistening, etc.
  6. Texture: dry, moist, mucoid, brittle, viscous, butyrous
    (buttery).
  7. Color: colorless, pink, black, red, bluish-green.
30
Q

producing a culture

A

inoculation

31
Q

creating the proper temperature and other
conditions to promote the growth of microbes

A

incubation

32
Q

separating microbes from one another, grow
colonies (pure cultures

A

isolation

33
Q

observing characteristics of colonies and
cultures (color, texture, size, shape, motility)

A

inspection

34
Q

main purpose is to determine the type of
microbe using biochemical, immunologic, serologic tests,
and DNA analysis.

A

identification

35
Q
A