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Family : mycobacteriaceae Genus : mycobacterium Species : 1. mycobacterium tuberculosis in human causes tuberculosis . 2. mycobacterium leprae in human causes Leprosy . 3. mycobacterium bovis produce disease in cattle & other animals,spread to Human by raw milk ingestion. Disease in human similar to that caused by TB. 4. mycobacterium avium also known as mycobacterium avium complex (MAC) May develop into pulmonary infection. Morphology & staining : The mycobacteria are thin straight rods or slightly curved rods of varying lengths & sometimes branching filamentous forms occure . The mycobacteria don’t take up the dyes of the gram stain because the cell wall are rich in lipid that called mycolic acid . mycobacteria cells are not easily decolourised even by acid- alcohol so it have acid-fast stain (Ziehl-Neelsen). The cells take red color (carbol fuchsin) by using mild heat or heatless method by addition of a wetting agent (Turgitol)& back ground is blue (methylene blue). 1 Natural habitat : The source of pathogenic mycobacteria is usually infected animals. M. bovis is excreted in respiratory discharge, faeces, milk,urine & semen. M. avium & M.paratuberculosis are shed in faeces . M. tuberculosis mainly in respiratory discharge . Cultural characteristics : The mycobacteria are aerobic & oxidative & non motile bacteria .They don’t have capsules, and most don’t form spore . Many Mycobacterium species adapt readily to growth on very simple substrates, using ammonia or amino acids as nitrogen sources and glycerol as a carbon source in the presence of mineral salts. Optimum growth temperatures vary widely according to the species and range from 25 °C to over 50 °C. Some species can be very difficult to culture (they are fastidious) . Decontaminating agents such as : oxalic acid 5% , NaoH 2-4% can be used on specimens before culture . Media for mycobacteria : 1. The egg-based Lowenstein- Jensen medium 2. Stone brinks media 3. Middle brook broth & media 2 They are most commonly used for culture of Mycobacterium, notably Mycobacterium tuberculosis. Composition of these media are includ e : Malachite green Glycerol Asparagine Potato starch Coagulated eggs Mineral salt solution Potassium dihydrogen phosphate Magnesium sulfate Sodium citrate These media are prepared as a solid slants in screw capped bottles. Malachite green dye is commonly used as the selective agent Low levels of penicillin and nalidixic acid are also present in LJ medium to inhibit growth of gram positive and gram negative bacteria, in order to limit growth to Mycobacteria species only. Presence of malachite green in the medium inhibits most other bacteria . Presence of glycerol enhances the growth of Mycobacterium tuberculosis & M. avium & many of the typical mycobacteria but glycerol is inhibitory to M. bovis while sodium pyruvate enhances its growth . The medium appears green, opaque and opalescent. Colony morphology on media : M. tuberculosis on glycerol- containing media giving the characteristic dry, rough, tough& buff colonies, hard to break up, is known as Eugonic . the growth of M. avium in the same media also called Eugonic . M. bovis has sparse thin growth on glycerol- containing media that is called dysgenic. (white,small,moist,flat colonies ) . M. bovis grow well on pyruvate containing media without glycerol . 3 Pigment production : *M. that produce yellowish- orange pigments are called chromogenic . *The term photo chromogenic is applied to those M. that produce pigment only if exposed to light. *Scoto chromogenic M. produce pigment when incubated either in the light or in the dark. 4 Niacin test: All species of mycobacterium produces Niacin (nicotinic acid) and the Mycobacterium tuberculosis accumulates the most. A positive niacin test provides preliminary evidence that an organism that exhibits a buff-colored, slow-growing rough colony may be M. tuberculosis. Nitrate Reduction test: Mycobacterium tuberculosis is a strongly nitrate positive organism. This test is valuable for the identification of M. tuberculosis, M. kansasii, M. szulgai and M. fortuitum. Rapid growers such as M. fortuitum can be tested within 2 weeks, but slow growers should be tested after 3-4 weeks of luxuriant growth. Both chemical procedure and commercially available nitrate strips are available . Catalase test: Semiquantitative catalase test is used for the identification of Mycobacteria. Catalase is an enzyme which splits Hydrogen peroxide to water and oxygen and positive catalase test is indicated by formation of gas bubbles. Most species of Mycobacteria, except strains of M. tuberculosis complex and M. gastri, produce catalase enzyme. Tween 80 hydrolysis test: Tween 80 hydrolysis test is used to separate the species of Photochromogens, scotochromogens and nonchromogens. Non pathogenic slow growing scotochromogens and nonchromogens produce a lipase that is able to hydrolyze Tween 80 into oleic acid and polyoxyethylated sorbitol, where as pathogenic species do not. Tellurite reduction test: The ability of mycobacterial species to reduce tellurite in 3 to 4 days is used to distinguish members of M. avium complex from most other non-chromogenic species. All rapid growers reduce tellurite in 3 days. Arylsulfatase test: Arylsulfatase enzyme is present in most mycobacteria. The rate by which arylsulfatase enzyme breaks down phenolphthalein disulfate into phenolphthalein (which forms a red color in the presence of sodium bicarbonate) and other salts is used to differentiate certain strains of Mycobacteria. 3 day arylsulfatase test is used to identify rapid growers such as M. fortuitum and M. chelonae. Slow growing M. marinum and M. szulgai . 5 Growth type Colony form on media with glycerol M. Tb Eugenic Rough,tough&buff , dry&hard tobreak up Growth time Glycerol for growth Na pyruvate for growth Niacin production Urease Nitrate reduction Pyrazin amidase Growth on TCH 3-8 week + enhanced - Inhibited + + + + + M. bovis Dysgenic Small,moistsheen,breakup easily 3-8 week - Inhibited + enhanced + - Dr. Ban sahib Abed Al-Nabi Zoonotic disease unit Post graduate lecture 6 M. avium Eugenic White,stickey, breakup easily 2-6 week + enhanced + enhanced + + -