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Bacteria

Gram Churukian–Schenk for Gram Positive & Negative Bacteria

By Bacteria, Gram Staining, Protocols, Stain Target, Stain Type

Gram Churukian–Schenk

for Gram Positive & Negative Bacteria

14
steps
15
materials

Materials

  • Stock basic fuchsin
    MaterialAmount
    Basic fuchsin0.5g
    Distilled water100mL
  • Solution A
    Crystal violet 10% in 2mL ethanol

    MaterialAmount
    Ammonium oxalate 1% aqueous98mL
  • Solution B
    MaterialAmount
    Iodine2g
    Potassium iodide4g
    Distilled water400mL
  • Solution C
    MaterialAmount
    Absolute ethanol1volume
    Acetone1volume
  • Solution D
    MaterialAmount
    Stock basic fuchsin5mL
    Distilled water45mL
  • Solution E
    MaterialAmount
    Picric acid0.1g
    Acetone100mL
  • Solution F
    MaterialAmount
    Acetone1Volume
    Xylene1volume

Tissue Sample

5µ paraffin sections of neutral buffered formalin fixed tissue are suitable. Other fixatives are likely to be satisfactory.

Protocol

  1. Bring sections to water via xylene and ethanol.
  2. Place in solution A for 2 minutes.
  3. Rinse with tap water.
  4. Place in solution B for 1 minute.
  5. Rinse well with tap water.
  6. Blot the slide, but not the tissue.
  7. Decolorise with solution C until no more blue floods off.
  8. Wet section with solution D then apply for 1 minute.
  9. Rinse with distilled water.
  10. Blot the slide, but not the tissue.
  11. Place in acetone for 3 seconds.
  12. Differentiate in solution E for 10 seconds.
  13. Quickly dip a few times in solution F.
  14. Clear with xylene and mount with a resinous medium.

Expected Results

  • Gram positive bacteria  –  blue
  • Nocardia and actinomyces  –  blue, or blue and red
  • Gram negative bacteria  –  red
  • Nuclei, Elastic, Paneth cells  –  red
  • Background  –  yellow

Notes

  • Picric acid should be handled with care. Solution E may be made by taking 12 mL of a saturated solution of picric acid in ethanol and diluting to 1 liter with acetone.
  • Basic fuchsin homologues with CI numbers of 42500 (pararosanilin) or 42510 (rosanilin) were specified. It was also noted that new fuchsin (CI 42520) was satisfactory, but not recommended because it was not certified by the Biological Stain Commission.
  • The authors note that sections must not be allowed to dry out after being stained with basic fuchsin. Doing so makes it difficult or impossible to properly differentiate the red counterstain.

Safety Note

Prior to handling any chemical, consult the Safety Data Sheet (SDS) for proper handling and safety precautions.

References

  1. Churukian, C. J. & Schenk, E. A. (1982)
    A method for demonstrating Gram-positive and Gram-negative bacteria.
    Journal of Histotechnology, v.5, No.3, p.127

Gram Weigert for Fibrin and Gram Positive Bacteria

By Bacteria, Fibrin, Gram Staining, Protocols, Stain Target, Stain Type

Gram Weigert

for Fibrin and Gram Positive Bacteria

11
steps
9
materials

Materials

Eosin

MaterialAmount
Eosin Y ws5g
Distilled water100mL

Crystal violet

MaterialAmount
Crystal violet1g
Distilled water100mL

Gram’s iodine

MaterialAmount
Iodine2g
Potassium iodide4g
Distilled water400mL

Aniline-Xylene

MaterialAmount
Aniline1volume
Xylene1volume

Tissue Sample

5µ paraffin sections of neutral buffered formalin fixed tissue are suitable. Other fixatives are likely to be satisfactory.

Protocol

  1. Bring sections to water via xylene and ethanol.
  2. Place in eosin solution for 5 minutes.
  3. Rinse with tap water.
  4. Place in crystal violet 1 minute.
  5. Rinse with tap water.
  6. Flood with Gram’s iodine for 1 minute.
  7. Rinse with tap water.
  8. Gently blot the section, being careful not to damage it.
  9. Decolorise the section with aniline-xylene.
  10. Rinse with several changes of xylene to remove all aniline.
  11. Mount with a resinous medium.

Expected Results

  • Gram positive bacteria  –  blue
  • Fibrin  –  blue
  • Background  –  pink

Notes

  • Control the differentiation with aniline-xylene microscopically. To examine, place the section in xylene to stop dye removal. Return to aniline-xylene if more differentiation is needed. Stop differentiation when the target element has good contrast.
  • Increasing the aniline content of the aniline-xylene will increase the speed of dye removal. Decreasing it will slow dye removal.
  • If the background is not pink enough, increase the time in eosin, stain in eosin at elevated temperature, or increase the eosin concentration.
  • The eosin counterstain may be omitted entirely if wished.

Safety Note

Prior to handling any chemical, consult the Safety Data Sheet (SDS) for proper handling and safety precautions.

References

  1. Culling, C.F.A., (1963)
    Handbook of histopathological techniques, 2nd ed.
    Butterworths, London.
  2. McManus, J.F.A. and Mowry, R.W., (1960),
    Staining methods, histologic and histochemical,
    Harper & Row, New York, NY, USA.