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Thayer Martin Medium Base Is Used For Selective Isolation
Thayer Martin Medium Base Is Used For Selective Isolation
INTENDED USE
For selective isolation of Gonococci from clinical samples
COMPOSITION
Ingredients Gm\Ltr.
Peptone, special 23.000
Agar 13.000
Sodium chloride 5.000
Starch 1.000
PRINCIPLE
Special peptone provides nutrients to the organisms while starch neutralizes the toxic fatty acids if
present in the agar. Haemoglobin provides the X factor whereas the V factor (N.A.D.) is provided by
the added supplement. Starch neutralizes the toxic fatty acids if present in the agar. Supplement (TS
22) also supplies vitamins, amino acids, coenzymes etc. which enhances the growth of pathogenic
Neisseria. Vancomycin and colistin inhibits gram-positive and gram-negative bacteria respectively.
Nystatin inhibits fungi. This medium may inhibit Haemophilus species. Some strains of
Capnocytophaga species may grow on this medium when inoculated with oropharyngeal specimens.
INTERPRETATION
Cultural characteristics observed with added sterile lysed blood/Haemoglobin solution (TS 021),
Vitamins Amino Growth Supplement (Vitamins & Amino Acids Mixture) (TS 022) and V.C.N.
Supplement (TS 038)/V.C.N.T. Supplement (TS 039) after incubation at 35-37°C for 18-48 hours.
Organism ATCC Inoculum Growth Recovery Colour of colony
(CFU)
Small, grayish white
Neisseria gonorrhoeae 19424 50 - 100 Good-Luxuriant ≥ 50%
to colourless, mucoid
Medium to large,
Neisseria meningitidis 13090 50 - 100 Good-Luxuriant ≥ 50%
blue gray, mucoid
Escherichia coli 25922 ≥ 10³ Inhibited 0% ---
Dehydrated powder, hygroscopic in nature, store in a dry place, in tightly-sealed containers below
25°C and protect from direct Sunlight. Under optimal conditions, the medium has a shelf life of 4
years. When the container is opened for the first time, note the time and date on the label space
provided on the container. After the desired amount of medium has been taken out replace the cap
tightly to protect from hydration.
1. Carpenter, C.M., and H.E. Morton. 1947. An improved medium for isolation of gonococcus in
24 hours. Proc. N.Y. State Assoc. Public Health Labs. 27:58–60.
2. Carpenter, C.M., M.A. Bucca, T.C. Buck, E.P. Casman, C.W. Christensen, E. Crowe, R. Drew, J.
Hill, C.E. Lankford, H.E. Morton, L.R. Peizer, C.I. Shaw, and J.D. Thayer. 1949. Evaluation of
twelve media for the isolation of the gonococcus. Am. J. Syphil. Gonorrh. Venereal diseases
33:164–176
3. Martin, J.E., T.E. Billings, J.F. Hackney, and J.D. Thayer. 1967. Primary isolation of N.
gonorrhoeae with a new commercial medium. Public Health Rep. 82:361–363
4. Thayer, J.D., and J.E. Martin, Jr. 1966. Improved medium selective for cultivation of N.
gonorrhoeae and N. meningitidis. Public Health Rep. 81:559–562.
5. Martin, J.E. Jr., and A. Lester. 1971. Transgrow, a medium for transport and growth of
Neisseria gonorrhoeae and Neisseria meningitidis. HSMHA Health Rep. 86:30–33.
6. MacFaddin J., 1985, Media for Isolation-Cultivation-Identification-Maintenance of Medical
Bacteria, Vol. I, Williams and Wilkins, Baltimore.
NOTE: Please consult the Material Safety Data Sheet for information regarding hazards and safe
handling practices.