ch 3: observing microorganisms through a microscope
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Ch 3: Observing Microorganisms Through a Microscope. Q&A. Acid-fast staining of a patient’s sputum is a rapid, reliable, and inexpensive method to diagnose tuberculosis. What color would bacterial cells appear if the patient has tuberculosis?. Objectives - PowerPoint PPT PresentationTRANSCRIPT
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Ch 3:
Observing Microorganisms
Through a Microscope
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Q&A
Acid-fast staining of a patient’s sputum is a rapid, reliable, and inexpensive method to diagnose tuberculosis. What color would bacterial cells appear if the patient has tuberculosis?
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ObjectivesReview the metric units of measurementDefine total magnification and resolution Explain how electron and light microscopy differDifferentiate between acidic and basic dyes Compare simple, differential, and special stains List the steps in preparing a Gram stain. Describe the
appearance of Gram-positive and Gram-negative cells after each step
Compare and contrast Gram stain and acid-fast stainExplain why endospore and capsule stains are used
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Units of Measurement
Review Table 3.1
• 1 µm = ______ m = ______ mm
• 1 nm = ______ m = ______ mm
• 1000 nm = ______ µm
• 0.001 µm = ______ nm
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Sizes Among Microorganisms
• Protozoa: 100 µm
• Yeasts: 8 µm
• Bacteria: 1 - 5 µm (some much longer than wide)
• Rickettsia: 0.4 µm = _________ nm
• Chlamydia and Mycoplasma: 0.25 µm
• Viruses: 20 – 250 nm
Cells Alive – How big is a . . .?
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Principles of the Compound Light Microscope
Fig 3.1
Magnification: Ocular and objective lenses of compound microscope (total mag.?)
Resolution: Ability of lens to . . . Maximum resolving power ___ m
Contrast: Stains change refractive index contrast between bacteria and surrounding medium
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Refractive Index
• Measures light-bending ability of a medium
• Light may bend in air so much that it misses the small high-magnification lens.
• Immersion oil is used to keep light from bending.
Fig 3.3
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Brightfield Microscopy• Simplest of all the
optical microscopy illumination. techniques
• Dark objects are visible against a bright background.
Darkfield Microscopy• Light objects visible
against dark background.• used to enhance the
contrast in unstained samples.
• Instrument of choice for spirochetes
Microscopy: The Instruments
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Spirochetes (Treponema pallidum) viewed with darkfield microscope
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Fluorescence Microscopy• Uses UV light.
• Fluorescent substances absorb UV light and emit visible light.
• Cells may be stained with fluorescent chemicals (fluorochromes).
• Immunofluorescence
Fig 3.6; T. pallidum
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Figure 3.6a
Fig 3.6bPrinciple of Immunofluorescence
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Electron Microscopy: Detailed Images of Cell Parts
Uses electrons, electromagnetic lenses, and fluorescent screens
Electron wavelength ~ 100,000 x smaller than visible light wavelength
Specimens may be stained with heavy metal salts
Two types of EMs:?
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Bacterial division
Leaf surface
SEM or TEM?
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Rod-shaped Mycobacterium avium
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Preparation of Specimens for Light Microscopy
• Staining Techniques Provide Contrast
• Smear air-dry heat-fix • Basic dyes: cationic chromophore
• Acidic dyes: anionic chromophore negative staining (good for capsules)
• Three types of staining techniques: Simple, differential, and special
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Simple Stains
• Use a single basic dye.
• A mordant may be used to hold the stain or coat the specimen to enlarge it.
React differently with different bacteria
• Gram stain
• Acid fast stain
Differential Stains
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Important Staining Reactions in MicrobiologyReview of different staining techniques
For Gram stain technique compare to Fig 3-12
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Gram Stain
safranin
crystal violet
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Acid Fast Stain
• Cells that retain a basic stain in the presence of acid-alcohol are called acid-fast.
• Non–acid-fast cells lose the primary stain when rinsed with acid-alcohol, and are counterstained with a different color basic stain
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Special Stains
• Endospore stain: Heat is required to drive a stain into the endospore.
• Flagella staining: requires a mordant to make the flagella wide enough to see.
• Capsule stain uses basic stain and negative stain
See Fig 3.14