Previous Article | Next Article ![]()
J. Bacteriol., 12 1995, 7275-7279, Vol 177, No. 24
RJ Danaher, JC Levin, D Arking, CL Burch, R Sandlin and DC Stein
Neisseria gonorrhoeae lipooligosaccharide (LOS) undergoes antigenic
variation at a high rate, and this variation can be monitored by changes in
a strain's ability to bind LOS-specific monoclonal antibodies. We report
here the cloning and identification of a gene, lsi-2, that can mediate this
variation. The DNA sequence of lsi-2 has been determined for N. gonorrhoeae
1291, a strain that expresses a high- molecular-mass LOS, and a derivative
of this strain, RS132L, that produces a truncated LOS. In the parental
strain, lsi-2 contains a string of 12 guanines in the middle of its coding
sequence. In cells that had antigenically varied to produce a truncated
LOS, the number of guanines in lsi-2 was altered. Site-specific deletions
were constructed to verify that expression of a 3.6-kDa LOS is due to
alterations in lsi- 2.
Copyright © 1995, American Society for Microbiology
Genetic basis of Neisseria gonorrhoeae lipooligosaccharide antigenic variation
Department of Microbiology, University of Maryland, College Park 20742, USA.
This article has been cited by other articles:
| Appl. Environ. Microbiol. | Infect. Immun. | Eukaryot. Cell |
|---|---|---|
| Mol. Cell. Biol. | J. Virol. | Microbiol. Mol. Biol. Rev. |
| ALL ASM JOURNALS |