IJSEM Applied and Environmental Microbiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Int J Syst Bacteriol 42 (1992), 127-132; DOI 10.1099/00207713-42-1-127
© 1992 Society for General Microbiology
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 Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Shankarappa, B.
Right arrow Articles by Mattingly-Napier, B. L.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Shankarappa, B.
Right arrow Articles by Mattingly-Napier, B. L.
Agricola
Right arrow Articles by Shankarappa, B.
Right arrow Articles by Mattingly-Napier, B. L.

Antigenic and Genomic Relatedness among Ehrlichia risticii, Ehrlichia sennetsu, and Ehrlichia canis{dagger}

Basavaraju Shankarappa{ddagger}, Sukanta K. Dutta* and Bonnie L. Mattingly-Napier

1Virginia-Maryland Regional College of Veterinary Medicine, University of Maryland, College Park, Maryland 20742

* Corresponding author.

ABSTRACT

Antigenic and genomic relatedness among Ehrlichia risticii, E. sennetsu, and E. canis was analyzed by enzyme-linked immunosorbent assay, Western blotting (immunoblotting) and DNA-DNA hybridization. E. risticii and E. sennetsu were serologically related, and their Western blot antigen profiles were nearly identical. Two antigens of E. sennetsu corresponding to the 28- and 51-kDa antigens of E. risticii were apparently larger than the E. risticii antigens, and the 55-kDa antigen of E. risticii appeared to be unique to this species. The 110-, 70-, and 44-kDa antigens of these two species were identical, as determined by the use of monospecific antibodies. DNA homology between these two species was high. On the other hand, E. canis was antigenically least reactive with the antisera to E. risticii and E. sennetsu. However, a dog convalescent-stage E. canis antiserum recognized antigens in the other two species which were different from those recognized by their homologous antisera. Similarly, homology between the DNA of E. canis and the DNAs of the other two species was very minimal. These results indicate that E. risticii and E. sennetsu are closely related both at the genomic and antigenic levels and that the relationship of these two species with E. canis is minimal.


{ddagger} Present address: Department of Pathology, School of Medicine, University of Pittsburgh, Pittsburgh, PA 15261.

{dagger} Published as scientific article no. A6252. contribution no. 8421 of the Maryland Agricultural Experiment Station.




This article has been cited by other articles:


Home page
J. Clin. Microbiol.Home page
A. R. Alleman, L. J. McSherry, A. F. Barbet, E. B. Breitschwerdt, H. L. Sorenson, M. V. Bowie, and M. Belanger
Recombinant Major Antigenic Protein 2 of Ehrlichia canis: a Potential Diagnostic Tool
J. Clin. Microbiol., July 1, 2001; 39(7): 2494 - 2499.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Microbiol.Home page
X.-J. Yu, J. W. McBride, and D. H. Walker
Genetic Diversity of the 28-Kilodalton Outer Membrane Protein Gene in Human Isolates of Ehrlichia chaffeensis
J. Clin. Microbiol., April 1, 1999; 37(4): 1137 - 1143.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 1992 by the International Union of Microbiological Societies.