Abstract
Mucin is a natural constituent of the intestinal contents; hence the assumption that it might be used as a culture medium for intestinal protozoa. So far as can be determined mucin has not been employed heretofore for this purpose. Samples of gastric mucin prepared by both Armour and Company and the Wilson Laboratories were used. These are dry powders, readily soluble in aqueous media and solutions may be sterilized in the autoclave.
A medium, composed of liver infusion agar slants 1 covered with a solution of 0.3% mucin in 0.7% aqueous NaCl with a 2 mm. loop of sterile rice starch to each tube, was used to isolate Endamoeba histolytica from one case of acute amoebiasis, from one human carrier and from 3 Macaca irus that were carriers. The amoeba grew in moderate numbers but cysts were not formed. Subcultures were made at 2 or 3 day intervals.
Trichomonas sp. from Pan niger, Cebus fatuellus, Macaca irus and Tapirus bairdii grew in abundance in a medium of 0.3% mucin in 0.7% NaCl solution. Subcultures were made at 3 to 4 day intervals. Trichomonas sp. and Eutrichomastix sp. from various reptiles have grown in abundance in 0.3% mucin in 0.5% aqueous NaCl solution, with subcultures every 7 days. A 2 mm. loop of rice starch to each tube seemed to increase the rate of growth of the flagellates from both mammals and reptiles. This medium, 0.3% mucin in 0.5% aqueous NaCl solution with rice starch, was used also to isolate 4 strains of Endamoeba sp. from Natrix sipedon and N. taxispilota. Growth and cyst formation was abundant. Subcultures were made every 7 days. Balantidium sp. from the intestine of Testuda galapogoensis has been cultured on this medium also, transfers being made every 7 days. The ciliates grew very well but did not encyst.
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