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.
Highlights
Analysis of the DNA sequence indicated that these two ORFs overlap and that each contains a string of guanines
When the DNA sequence of this region was amplified from N. gonorrhoeae 1291 by PCR and the DNA sequence of the amplicon was determined, this region was found to contain 12 guanines
This differed from the DNA sequence found in pREV2, which has 13 guanines
Summary
The region responsible for the alteration of LOS expression in N. gonorrhoeae 1291 was mapped to lsi-2, which contains two ORFs instead of the expected single ORF encoding a protein similar to lgtA. Analysis of the DNA sequence indicated that these two ORFs overlap and that each contains a string of guanines.
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