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G T DIMOPOULLOS

Publications and source records attributed to G T DIMOPOULLOS.

At least 19 recordsLinked to original sources
PubMed1965

CATALASE ACTIVITY IN ANAPLASMA MARGINALE.

Wallace, W. R. (Louisiana State University, Baton Rouge), and G. T. Dimopoullos. Catalase activity in Anaplasma marginale. J. Bacteriol. 91:309-311. 1965.-Extracts of erythrocytes infected with Anaplasma marginale were found to contain more catalase activity than normal erythrocytic preparations. The increase in catalase activity appeared concurrently with increases in the number of erythrocytes containing Anaplasma bodies. Antisera against normal bovine erythrocytes and Anaplasma-infected erythrocytes were prepared in rabbits to test the source of increased catalase activity during anaplasmosis. Antiserum against normal erythrocytes decreased the catalase activity of extracts of normal erythrocytes by 271 units per ml and of partially purified Anaplasma bodies by only 120 units. Rabbit antiserum against Anaplasma-infected bovine erythrocytes removed only 73 units of activity from normal erythrocytes, but decreased the activity of the partially purified Anaplasma bodies by 260 units, indicating the association of catalase with the marginal body.

Anaplasma↗
PubMed1964

IMMUNOLOGY AND SEROLOGY OF ANAPLASMA MARGINALE. I. FRACTIONATION OF THE COMPLEMENT-FIXING ANTIGEN.

Rogers, Thomas E. (Louisiana State University, Baton Rouge), Richard J. Hidalgo, and George T. Dimopoullos. Immunology and serology of Anaplasma marginale. I. Fractionation of the complement-fixing antigen. J. Bacteriol. 88:81-86. 1964.-Studies were conducted to fractionate and purify the complement-fixation (CF) antigen of Anaplasma marginale in infected erythrocytes of cattle. Initial attempts were made to resolve the antigen from crude stromatal preparations by various chemical and physical methods. Fractionation procedures involving partial and total lipid extraction suggested that the CF antigen was lipoprotein in nature. Fluorocarbon deproteinization of stromatal antigens was also attempted. A method was developed for the preparation of a desirable Anaplasma CF antigen which involved disintegration of infected erythrocytes by sonic vibration and separation of the antigen by differential centrifugation. Antigens prepared by this method were highly specific, colorless, did not exhibit anticomplementary activity, and possessed higher titers than standard Anaplasma antigens. When density-gradient sedimentation was applied to sonic extracts of infected cells, it was demonstrated that the CF antigen could also be fractionated by this method.

Anaplasma↗