Abstract
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.
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CITATION STYLE
Danaher, R. J., Levin, J. C., Arking, D., Burch, C. L., Sandlin, R., & Stein, D. C. (1995). Genetic basis of Neisseria gonorrhoeae lipooligosaccharide antigenic variation. Journal of Bacteriology, 177(24), 7275–7279. https://doi.org/10.1128/jb.177.24.7275-7279.1995
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