The JI
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     
 


The Journal of Immunology, 1969, 103: 6-14.
Copyright © 1969 by The American Association of Immunologists, Inc.

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Smith, A. R.
Right arrow Articles by Ristic, M.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Smith, A. R.
Right arrow Articles by Ristic, M.

Identification of an Antigen and Specific Antibody in the Sera of Chickens Infected with Plasmodium Gallinaceum1

A. R. Smith2, J. D. Lykins2, E. W. Voss and M. Ristic

From the Department of Veterinary Pathology and Hygiene and the Department of Microbiology, University of Illinois, Urbana, Illinois 61803

Abstract

A study based on a double diffusion gel assay of pre- and post-infection sera with a standard antisoluble antigen serum pool demonstrated antigens in chicken sera during the acute phase of infection with Plasmodium gallinaceum. In a single chicken experiment, an antigen and specific antibody were demonstrated in one individual during the acute and convalescent phases of infection, respectively.

The antigen, designated soluble antigen one (SA 1), was a specific molecular entity associated with the descending portion of the macroglobulin peak. After Sephadex G-200 column chromatography, the purity of the antigen was ascertained by immuno- and disc-electrophoresis and analytical ultracentrifugation. The molecular weight of SA 1 was estimated at 500,000 to 700,000 on the basis of molecular sieve chromatography, ultracentrifugation and observations with disc-electrophoresis.

Specific antibody which reacted with SA 1 was precipitated from convalescent serum with 12.5% sodium sulfate and then eluted from DEAE in the 0.02 M and 0.10 M phosphate fractions. This antibody was identified as IgG.

Footnotes

This study was supported by National Institutes of Health Research Grant HE 10609, and in part by the Mark L. Morris Animal Research Foundation. Technical assistance of Mrs. Laurel Karr is gratefully acknowledged. This paper was presented in part at the 17th annual meeting of the American Society of Tropical Medicine and Hygiene, Atlanta, Georgia, November 1, 1968.

2 This article derives in part from the theses submitted by these authors in partial fulfillment of the requirements for the degree of Master of Science in Veterinary Medical Science.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
This Website Copyright © 1969 by The American Association of Immunologists, Inc. All rights reserved.
All Contents Copyright © 1969 by The American Association of Immunologists, Inc. All rights reserved.