1 / 18

MICROBIOLOGY – ALCAMO

MICROBIOLOGY – ALCAMO. LECTURE: SPECIMEN PREPARATION AND STAINING . 1. INTRODUCTION. Why? --- MOs are small and transparent --- Cytoplasm of bacteria lacks color --- Stains enhance visibility. 2. WET SPECIMEN PREPARATIONS. ORGANISMS ARE NOT DRIED BEFORE HANDLING. WET MOUNT.

fawzi
Download Presentation

MICROBIOLOGY – ALCAMO

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. MICROBIOLOGY – ALCAMO LECTURE: SPECIMEN PREPARATION AND STAINING

  2. 1. INTRODUCTION Why? --- MOs are small and transparent --- Cytoplasm of bacteria lacks color --- Stains enhance visibility

  3. 2. WET SPECIMEN PREPARATIONS ORGANISMS ARE NOT DRIED BEFORE HANDLING

  4. WET MOUNT • Quick and easy • Since no stain is used only large dense organisms are visible • TECHNIQUE: • Place drop of specimen on clean slide • Place cover slip over it

  5. Simple Staining • Positively and negatively charged molecules are attracted to each other • MO cytoplasmhas (-) charge • Basic stains have (+) charge • Crystal Violet • Methylene Blue • Therefore: Use (+) stains to color MOs

  6. Bacterial cocci stained with crystal violet

  7. NEGATIVE STAIN • EASY, FAST, GOOD FOR SIZE EVALUATION • STAIN BACKGROUND, NOT MO CHARGE OF STAIN IS (-) • TECHNIQUE: • PLACE DROP OF STAIN AT END OF SLIDE • DROP OF MOs ½ INCH BEFORE STAIN • WITH 2ND SLIDE HELD AT 45*, DRAW ACROSS MOs, THEN ACROSS STAIN • REVERSE DIRECTION, SMEAR FORWARD

  8. TECHNIQUE: • PLACE DROP OF STAIN AT END OF SLIDE • DROP OF MOs ½ INCH BEFORE STAIN • WITH 2ND SLIDE HELD AT 45*, DRAW ACROSS MOs, THEN ACROSS STAIN • REVERSE DIRECTION, SMEAR FORWARD

  9. 3. DRY PREPARATIONS • MOs ARE DRIED (AND KILLED) BY “FIXING • FIXING – FLAME QUICKLY 3X Differential Simple

  10. SIMPLE STAIN • ONE COLOR DYE ONLY • EX: CRYSTAL VIOLET, METHYLENE BLUE • EASY, FAST STAIN METHOD, GOOD RESULTS • TECHNIQUE: • MO TO SLIDE • AIR DRY MO (OR WARM, NOT HOT) • FIX – THROUGH FLAME (3X) • STAIN • RINSE • DRY FOR MICROSCOPIC EXAMINATION

  11. DIFFERENTIAL STAIN • TWO DIFFERENT DYES, TWO COLORS SOMEWHAT DIFFICULT, VARIABLE • EX: GRAM STAIN – IDENTIFIES DIFFERENCE IN CELL WALLS • GRAM + ‘PEPTIDOGLYCAN’ IN CELL WALL • RETAINS PURPLE STAIN • GRAM – ‘LIPID’ IN CELL WALL, • PURPLE COLORED FAT DISSOLVED, • CELL NOW COLORLESS, MUST USE 2nd STAIN TO COLOR THESE MOs

  12. DIFFERENTIAL STAIN • TECHNIQUE: • CRYSTAL VIOLET (ALL MO PURPLE) • DECOLORIZE • G+ STAY PURPLE • G- WILL LOSE PURPLE DYE • SAFRANIN DYE (G- MO NOW RED)

  13. SPECIAL STAINS • INVOLVES SPECIAL COMPLICATED METHODS NOT FOR AMATEURS • INVOLVES SPECIAL STRUCTURES: • ENDOSPORES • FLAGELLA • CAPSULES

  14. Penicillin

  15. Gram Stain

More Related