Abstract
We cloned and characterized the Neisseria meningitidis rfaC gene which encodes an enzyme, α-1,5 heptosyltransferase 1, involved in the synthesis of the deep-core of the lipooligosaccharide. The N. meningitidis rfaC mutant, obtained by an allelic exchange, produced lipooligosaccharide which migrated faster in sodium dodecyl sulfate-polyacrylamide gel electrophoresis than the lipooligosaccharide isolated from the wild-type N. meningitidis. The N. meningitidis rfaC mutant was not affected by growth in a rich microbiological medium and did not show any defect in adhesion to epithelial cell lines. Conversely, the rfaC mutant was attenuated in the infant rat model of meningococcemia, thus confirming the importance of intact lipooligosaccharide in the virulence of N. meningitidis.
Original language | English (US) |
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Pages (from-to) | 41-49 |
Number of pages | 9 |
Journal | FEMS Microbiology Letters |
Volume | 151 |
Issue number | 1 |
DOIs | |
State | Published - Jun 1 1997 |
Externally published | Yes |
Keywords
- Lipooligosaccharide
- Neisseria meningitidis
- rfaC
ASJC Scopus subject areas
- General Medicine