BACTERIOLOGICAL SMEAR AND STAINING PROTOCOL

by David B. Fankhauser, Ph.D.,
Professor of Biology and Chemistry
University of Cincinnati Clermont College,
Batavia OH 45103
 Bacillus anthracis

11 February 1980, revised 29 June 1994, 28 June '96, 3 July '97, 30 June 98, 23 Feb 99, 26 July 00
This page has been accessed Counter times since 27 April 2005.
(counter reset, originally started 18 February 2002.)
Bacillus spores

Bacteria, like most cells, are essentially transparent, and must be stained in order to be easily visualized under the microscope. The specimen must be first spread out on a clean slide (preparation of a smear), heated gently to fix it to the slide, and then stained with an appropriate dye. Bacteria tend to be negatively charged, therefore positively-charged or basic dyes will bind to and stain them.

EQUIPMENT AND SUPPLIES:

clean microscope slide
soap and hot water
dH2O in dropper bottle
sample to be smeared
bacteriological loop (26 gauge Platinum as specified in Equipment for a Microbiological Work Station)
flame source
stains: 0.3% methylene blue or
Hucker's Crystal Violet
tap water
paper towels or bibulous paper
PREPARE 
THE SMEAR:
1. Secure a CLEAN microscope slide. The smear will not spread out properly if the slide is even slightly oily. If in doubt, wash slide well with soap and water, polish with clean paper towel or a Kimwipe (do not use brown recycled towels, they give off too much lint).
2. a. If the specimen is solid: place a small drop of dH20 on a clean slide. Pick up small sample with a sterile loop and suspend in the water. Spread to the diameter of a dime (1.8 cm). The suspension should appear very faintly cloudy.
2. b. If liquid: place small drop of sample on microscope slide, spread to the diameter of a dime. Dilute with small drop of water if more than faintly turbid.
FIX THE SMEAR:
3. Fix smear by lightly passing slide through a gentle flame. Do not overheat. The slide should not get too hot to comfortably hold. You are just trying to dry out the sample so that it will stick to the slide and not wash off in the next two steps.
STAIN THE 
FIXED SMEAR:
4. Add a drop or two of stain (for instance, 0.3% methylene blue or Hucker's Crystal Violet). Let sit 1 minute (or 30 seconds for Hucker's Stain, a more powerful stain).
5. Gently rinse off excess stain with tap water for a few seconds until no more stain is seen to flow off. Gently blot dry (do not rub) with clean white paper towel. (Bibulous paper should be used if lint is a problem.)
VIEW THE 
STAINED SMEAR:
6. Examine with 10x objective to locate a region which is well spread and not too heavily stained. View briefly with 40x objective to confirm a well-spread, well-stained section. Then use 100x oil immersion objective to study specimen (FOLLOW Oil Immersion Protocol CAREFULLY). Adjust light for maximum clarity and carefully draw individual bacteria with all structures seen. Title the drawing as to sample, give the stain used and, at lower right, indicate the magnification of the illustrated view.
7. If you are not saving your slide, wash it well in hot soapy water, air dry in a plastic rack.

Suggestions for specimens to view: Buccal smear, tooth scrapings, yogurt, buttermilk, yeast, fecal smear, vaginal smear, single colonies from agar plates, etc.


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