Identification And Differentiation Of Microorganisms

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IDENTIFICATION AND DIFFERENTIATION OF MICROORGANISMS Microbiology

Transcript of Identification And Differentiation Of Microorganisms

Page 1: Identification And Differentiation Of Microorganisms

IDENTIFICATION AND DIFFERENTIATION OF

MICROORGANISMSMicrobiology

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Processes InvolvedStainingMicroscopyMicrobial CultureColony MorphologyBiochemical CharacteristicsImmunological MethodsUltrastructure Studies

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MicroscopyThe human eye cannot resolve objects much

less than 0.1 – 0.2 mm.It cannot detect objects with diameters less

that about one thousandths of an inch (30 µm).

Bacterial size range from 0.2 – 2 µm.Much of what we know today about

microorganisms was made possible with the aid of the microscope.

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Parts of a Microscope

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Types of MicroscopesBright-Field MicroscopeDark-Field MicroscopePhase-Contrast MicroscopeFluorescent MicroscopeDissection MicroscopeScanning Electron MicroscopeTransmission Electron Microscope

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StainingUsed to increase visibility of microorganisms

being studiedUsed to identify the shape of bacteriaUsed to determine the morphological

features of microorganismsUsed to detect contamination Used to differentiate and classify

microorganisms (differential stains)Used to detect bacterial parts such as

capsule, spores, flagella or inclusion bodies (special stains)

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FixationThe process by which the internal and

external structures of microorganisms are preserved and fixed in place.

Heat fixation – fixation by means of application of heatThe prepared smear of microorganisms is

gently heated and air-dried.Chemical fixation – involves the use of

chemicals such as ethanol and formaldehyde.

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Simple Staining TechniqueOnly one stain is usedCrystal Violet, Carbol Fuchsin, and

Methylene Blue are examples of basic dyes used in simple staining technique.

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Differential StainingUsed to classify bacteria into separate groups

based on their distinct staining propertiesMakes use of a primary stain, a decolorizer,

and a counterstainGram Stain and Acid-Fast Stain are examples

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Gram StainDifferentiates bacteria into two groups: Gram

positive and Gram negativeStain mechanism is generally related to the

thickness of the cell wall, pore size and permeability properties of intact cell envelope

Makes use of a primary stain (Crystal Violet), a mordant (Gram’s Iodine) a decolorizer (Alcohol or Acetone) and a counterstain (Safranin).

Gram positive organisms stain blue while gram negative organisms stain red.

Most cocci are gram positive; a third of all cocci, half of the bacilli, and all the spiral bacteria are gram negative.

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Examples of Gram Positive BacteriaStaphylococcus aureus

Streptococcus pyogenes

Clostridium perfringens

Listeria monocytogenes

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Examples of Gram Negative BacteriaEscherichia coli

Haemophilus influenzae

Vibrio cholerae

Neisseria meningitidis

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Acid-Fast StainUsed to differentiate Mycobacteria (M.

tuberculosis) from other bacteriaMycobacteria are lipophilic or difficult to

stain.Once stained, Mycobacteria are resistant to

counterstain.Nocardia are partially acid fastMakes use of a primary stain (Kinyoun Carbol

Fuchsin), decolorizer (Acid Alcohol), and counterstain (Methylene Blue).

Acid fast bacteria appear as bright red bacilli against a light blue background.

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Special Staining TechniquesNegative Staining using India Ink or

Negrosine is used to reveal the presence of capsule

Schaefer-Fulton using Malachite Green and Safranin is used to stain endospores

The Leifson Method (pararosalanine), and Gray Method (basic fuchsin) are used to stain flagella.

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Microbial CultureMakes use of a growth environment called

culture mediumMicroorganisms form culture when

inoculated in or on the medium.May be purely chemical (defined or

synthetic), may contain organic materials, or may consist of living organisms.

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Types of Culture MediumNutrient broth and Nutrient agar – used to

cultivate bacteria. Both contain proteins, salts, and growth enhancers.

Selective Medium – enhances the growth of a desired organism while retards the growth of unwanted organisms.

Differential Medium – does not retard growth but provides environment where different bacteria can be differentiated from each other.

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Selective Medium

MacConkey Agar retards the growth of Gram + bacteria and enhances the growth of Gram - bacteria

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Selective Medium

Thayer-Martin Medium favors the growth of Neisseria gonorrhea only

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Selective MediumLowenstein-Jensen medium is used for the detection of M. tuberculosis

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Differential Medium

BLOOD AGAR PLATE (BAP)

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Differential Medium

MacConkey Agar is used to differentiate lactose fermenters from non-lactose fermenters

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Colony MorphologyS. Pneumoniae in BAP P. aeroginosa

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Colony Morphology

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Biochemical CharacteristicsRefers to the characteristic patterns of

substrate utilization, metabolic product formation and sugar formation.

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