Culture technique
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This document describes various culture methods used to isolate and grow bacteria. It discusses streak culture, lawn culture, stroke culture, stab culture, pour plate culture, and liquid culture. It also covers different techniques for culturing anaerobic bacteria, including vacuum production, gas displacement, chemical and biological methods, medium reduction, and use of anaerobic chambers.
Culture technique
- 2. • Isolate bacteria in pure culture from the clinical specimens and their identification by various tests • Determine antibiotics susceptibility • Prepare antigen for serodiagnosis of infective diseases • Maintain stock culture
- 3. Method of culture • Streak culture • Lawn culture • Stroke culture • Stab culture • Pour plate culture • Liquid culture
- 4. Streak culture • Used for the isolation of bacteria in pure culture from clinical specimens. • Nichrome wire loop is used due to high cost of platinum wire. • One loop full of the specimen is transferred onto the surface of a well dried plate. • Spread over a small area at the periphery. • The inoculum is then distributed thinly over the plate by streaking it with a loop in a series of parallel lines in different segments of the plate. • On incubation, separated colonies are obtained over the last series of streaks.
- 5. Lawn culture • Provides a uniform surface growth of the bacterium. • Uses – For bacteriophage typing. – Antibiotic sensitivity testing. – In the preparation of bacterial antigens and vaccines. • Lawn cultures are prepared by flooding the surface of the plate with a liquid suspension of the bacterium.
- 6. Stroke culture • Stroke culture is made in tubes containing agar slope/ slant. • Uses: Provides a pure growth of bacterium for slide agglutination and other diagnostic tests.
- 7. Stab culture • Prepared by puncturing a suitable medium – gelatin or glucose agar with a long, straight, charged wire. • Uses – Demonstration of gelatin liquefaction. – Oxygen requirements of the bacterium under study. – Maintenance of stock cultures.
- 8. Pour Plate Culture • Tubes contaning 15 ml of agar medium in each are melted and kept to cool in a water bath at 45-50 ° C. • The inoculum to be tested is diluted in serial dilutions. • 1 ml of the inoculum is added to the each tube of molten agar, mix well and pour to a sterile Petri dish and allow it to set. • Uses: – Gives an estimate of the viable bacterial count in a suspension. – • To quantitate bacteria in urine cultures.
- 9. LIQUID CULTURES • Liquid cultures are inoculated by touching with a charged loop or by adding the inoculum with pipettes or syringes. • Uses – • Blood culture • Sterility tests • Continuous culture methods • Disadvantage – It does not provide a pure culture from mixed inocula.
- 11. • Anaerobic bacteria differ in their requirement and sensitivity to oxygen. • Cl. tetani is a strict anaerobe - grows at an oxygen tension < 2 mm Hg. • Methods: – • Production of vacuum • Displacement of oxygen with other gases • Chemical method • Biological method • Reduction of medium • Anaerobic chambers
- 12. Production of vacuum • Incubate the cultures in a vacuum desiccators
- 13. Displacement of oxygen with other gases • Displacement of oxygen with hydrogen, nitrogen, helium or CO2. • Eg: Candle jar • Mclntosh filde jar
- 14. • McIntosh – Fildes’ anaerobic jar • Methylene blue is used as indicator, it remain colourless in anerobic condition but turn blue on exposure to oxygen. • Consists of a metal jar or glass jar with a metal lid which can be clamped air tight. • The lid has 2 tubes – gas inlet and gas outlet • The lid has two terminals – connected to electrical supply. • Under the lid – small grooved porcelain spool, wrapped with a layer of palladinised asbestos.
- 15. •Working: •Inoculated plates are placed inside the jar and the lid clamped air tight. •The outlet tube is connected to a vacuum pump and the air inside is evacuated. •The outlet tap is then closed and the inlet tube is connected to a hydrogen supply. •After the jar is filled with hydrogen, the electric terminals are connected to a current supply, so that the palladinised asbestos is heated. •catalyst helps to combine hydrogen and residual oxygen to form water.
- 16. Chemical method • Alkaline pyrogallol absorbs oxygen. • Chromium and Sulphuric acid
- 17. • Gaspak • Commercially available disposable envelope. • Contains chemicals which generate H2 and CO2 on addition of water. • Cold catalyst – permits combination of Hydrogen & Oxygen • Indicator is used – reduced methylene blue. – Colourless – anaerobically – Blue colour – on exposure to oxygen
- 18. • Biological method • Absorption of oxygen by incubation with aerobic bacteria, germinating seeds or chopped vegetables. • Reduction of oxygen • By using reducing agents – 1% glucose, 0.1% Thioglycolate
- 19. • Cooked meat broth- • It is also known as robertson’s cooked meat medium. • It contains nutrient broth and pieces of fat free minced cooked meat of ox heart
- 20. • Principal • Unsatturated fatty acids present in meat utilise oxygen for autooxidation , this reaction is catalysed by hematin in the meat. • Glutathione and cystine present in meat also utilize oxygen. • Sulphydryl compounds also contribute for a reduced oxidation reduction potential.
- 21. • Procedure • Before inoculation the medium is boiled in water bath at 80° C for 30 mnt to make it oxygen free. • For strict anerobiosis the surface of CMB medium maybe covered with a layer of sterile liquid peraffin.
- 22. • Anerobic chamber • It is an anerobic incubation system • It provides oxygen free environment for inoculating culture media and for the incubation. • It is fitted with airtight rubber gloves to insert hands for working with specimens. • These anaerobic chamber contains a catalyst , hydrogen gas Co2 and nitrogen gas.