Presentation Transcript

1. Bacterial motility

2. Objectives: • To gain expertise in determining the motility of living bacteria. • To learn about the different methods of motilty determination. Principle: • The ability of an organism to move by itself is called motility. • Motility is closely linked with chemotaxis, the ability to orientate along certain chemical gradients. • Eucaryotic cells can move by means of different  locomotor organelles such as cilia, flagella, or pseudopods. • Procaryotes move by means of propeller-like flagella unique to bacteria or by special fibrils that produce a gliding form of motility. • Almost all spiral bacteria and about half of the bacilli are motile, whereas essentially none of the cocci are motile.

3. Peritrichous (E.coli) Monotrichous ( Vibrio cholerae) Site of flagella

4. Lophotrichous (pseudomonas) amphitrichous (Spirillum volutans) Site of flagella

5. Flagella compose from: • Filament – Composed of a protein called flagellin • Hook – Base of filament near cell wall • Basal Body - Anchors filament & hook to cell wall Types of movement : • Run : straight line movement occurs when the flagella rotates couterclockwise • Tumbles : turning the direction by clockwise movement of the flagella

6. Motility testing • Motility could be detected by: • Wet mount slide • Hanging Drop technique. • Flagella stain. • Semi-Solid media Inoculation.

7. 1. Wet Mount slideWhen working with non-pathogens, the simplest way to determine motility is to place a few loopfuls of the organism on a clean slide and cover it with a cover glass.  Organisms are observed in a drop that is suspended under a cover glass in a concave depression slide 2. Hanging Drop slide The slide for a hanging drop is ground with a concave well in the centre; the cover glass holds a drop of the suspension. • When the cover glass is inverted over the well of the slide, the drop hangs from the glass in the hollow concavity of the slide. • Since the drop lies within an enclosed glass chamber, drying out occurs very slowly. A ring of Vaseline around the edge of the cover slip keeps the slide from drying out.

8. 3. Flagella stain • Flagella are too thin to be seen by the ordinary light microscope. • Flagella should be amplified (enlarged). Use a stain that is specifically deposited on Flagella thus increasing diameter. • Some flagellar stains employ rosaniline dyes and a mordant, applied to a bacterial suspension fixed in formalin and spread across a glass slide. The formalin links to, or “fixes,” the flagellar and other surface protein of the cells. The dye and mordant then precipitate around these “fixed” surfaces, enlarging their diameters, and making flagella visible when viewed under the microscope. • Another method, a ferric-tannatemordant and a silver nitrate solution are applied to a bacterial suspension. The resulting dark precipitate that forms on the bacteria and their flagella allows them to be easily visualized under the microscope. This silver-plating technique is also used to stain the very slender spirochetes.

9. Rosanalin dye silver nitrate + ferric tannate

10. 4. Semi-Solid media Inoculation • The most commonly used test for motility in microbiology lab. • It depends on the ability of motile bacteria to move through semi-solid media. • Ordinary solid media contain 1.5-2.0% Agar • Semi solid media contain about 0.4% Agar

11. Procedure of Motility Test • How to Perform Test: • Using a sterile bacteriological needle, pick a colony of the test organism • Stab quickly a tube of semi solid media. (avoid using bent needles). • Incubate the semi solid media for 24 hours

12. Reading Results: • If bacteria is motile, there will be growth going out away from the stab line, and test is positive. • If bacteria is not motile, there will only be growth along the stab line. • A colored indicator can be used to make the results easier to see.

13. Semi solid media with tetrazolium chloride (color indicator) + – +