JB
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
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 Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Deeb, B. J.
Right arrow Articles by Kenny, G. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Deeb, B. J.
Right arrow Articles by Kenny, G. E.
J Bacteriol. 1967 April; 93(4): 1425-1429
Copyright © 1967 American Society for Microbiology. All Rights Reserved.

Characterization of Mycoplasma pulmonis Variants Isolated from Rabbits II. Basis for Differentiation of Antigenic Subtypes1

Barbara J. Deeb2 and George E. Kenny

a Department of Preventive Medicine, University of Washington School of Medicine, Seattle, Washington

ABSTRACT

The antigen composition of Mycoplasma pulmonis variants was studied by complement-fixation, agar-gel diffusion, and growth-inhibition tests. Two classes of complement-fixing antigens were demonstrated for M. pulmonis strains 47 and 63: (i) cross-related, heat-labile, water-soluble antigens, and (ii) high-titered, subtype-specific, heat-stable, water-soluble antigens. Lipid antigens prepared by organic solvent fractionation were low-titered antigens and showed little specificity. With the aid of agar-gel double-diffusion plates, the subtype-specific antigens were found to be precipitated by trichloroacetic acid and to be stable to periodate, but they were inactivated by pronase. Pronase-stable, periodate-labile precipitating antigens were observed as common components between the two variants. Antisera prepared with boiled antigens were found to be serologically active on gel diffusion but lacked neutralizing ability in growth-inhibition tests. Each of three strains of M. pulmonis (47, 63, ATCC 14267) could be identified as a variant because each strain possessed immunologically distinct heat-stable subtype-specific antigen(s).


FOOTNOTES

2 Present address: Department of Biology, American University of Beirut, Beirut, Lebanon.

1 Some of the data in this paper were presented in a preliminary communication: Bacteriol. Proc., p. 48, 1966. This paper is part of a thesis submitted by B. J. D. in partial fulfillment of the requirements for the M.S. degree in Preventive Medicine, University of Washington, Seattle.


J Bacteriol. 1967 April; 93(4): 1425-1429
Copyright © 1967 American Society for Microbiology. All Rights Reserved.







Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
Appl. Environ. Microbiol. Infect. Immun. Eukaryot. Cell
Mol. Cell. Biol. J. Virol. Microbiol. Mol. Biol. Rev.
ALL ASM JOURNALS

Copyright © 1967 by the American Society for Microbiology. All rights reserved.