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MICROSCOPY AND STAINING

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Presentation on theme: "MICROSCOPY AND STAINING"— Presentation transcript:

1 MICROSCOPY AND STAINING
CHAPTER 3

2 Metric Units Microbe sizes – μm to nm

3 Light Properties (λ) Wavelength Electromagnetic spectrum
Shorter wavelength Higher energy More resolution

4 Light Properties (RP) Resolving Power (Resolution)
Distance between 2 points that can be distinguished

5 Light Travel Reflection Waves are bounced off some materials
Transmission Waves pass through Absorption Energy modification

6 Light Travel Refraction Altered angle of movement

7 Compound Light Microscopy
Condenser Iris diaphragm Objective lenses Ocular lens(es) Stage Focusing knobs Total Magnification

8 Light Microscopy Types
Bright Field Dark Field Spirochaetes T. pallidum B. burgdorferi

9 Dual Beam Microscopy 2 light beams Phase Contrast
Interference creates areas of contrast Internal cellular structures Nomarski Higher resolution Shallow depth of field

10 Fluorescence Microscopy
Ultraviolet light Excited electrons emit light after UV absorption Natural fluorescence versus flouorochromes FAb staining Antibodies tagged with flourescent dyes Specific for molecules

11 Imaging Techniques Confocal Microscopy (UV) Digital Microscopy

12 Electron Microscopy (EM)
Uses X-rays Focused by electromagnets Transmission (TEM) Thin tissue slices Heavy metal staining Scanning (SEM) Gold/Carbon coating Profiles or fractures

13 EM Images

14 EM Images

15 Light Microscope Specimen Preparation
Wet Mounts Thick liquid preparation Smears Placement of cells Air drying Heat fixation

16 Staining Principles Acidic (-ve) / Basic (+ve) Simple Stains
Differential Stains Special Stains

17 Gram Stain Differential Stain CV-I complex Alcohol wash
2 colors for Gram +ve and Gram –ve Developed by Hans Gram Distinguishes microbes based on peptidoglycan content in cell wall CV-I complex Crystal violet + iodine forms a large molecular complex Alcohol wash Cannot wash out of the Gram +ve cell wall Gram –ve wall is easily disrupted by alcohol wash Saffranin counterstain Gram +ve cells stay purple Gram –ve cells stain pink Diagnostic importance Peptidoglycan is a target for many antibiotics when present in a thick layer Penicillins Monobactams Carbapenems

18 Appearance After Each Step
Crystal violet Addition of Iodine Alcohol rinse step Safranin Counterstain

19 Ziehl-Neelsen Acid Fast Stain
Acid Fast Bacteria Mycobacterium genus identification Waxy lipid mycolic acid repels most dye chemicals Genus is one of few that stain pink Diagnosis Tuberculosis Leprosy

20 Negative (Capsule) Stain
Visualizes the Capsule Thick glycocalyx around cell Negatively charged dyes Repelled by –ve charge on glycocalyx Halo effect is seen Cells are counterstained with positively charged dye Virulence factor Repels phagocytic WBC May prevent antibiotic entry into cells

21 Endospore Stain (Schaefer-Fulton)
Endospores are hard to see with Gram stain Waxy dipicolinic acid Visualizes pathogens Clostridium tetani C. botulinum C. perfringens Bacillus anthracis Vegetative cells vs. Endospores Sterilization challenge Heat and dessication-resisitant


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