Resistance to Human Serum of Gonococci in Urethral Exudates is Reduced by Neuraminidase

• Published in: Proceedings of the Royal Society. B, Biological sciences Vol. 241; no. 1300; pp. 3 - 5
• Main Authors: Parsons, N. J, Cole, J. A., Smith, Harry
• Format: Journal Article
• Language: English
• Published: London The Royal Society 23.07.1990
• Subjects: Blood Bactericidal Activity; Clostridium perfringens - enzymology; Cytidine Monophosphate N-Acetylneuraminic Acid - pharmacology; Erythrocytes; Exudates and Transudates - drug effects; Exudates and Transudates - microbiology; Humans; Integration host factors; Lipopolysaccharides; Neisseria gonorrhoeae; Neisseria gonorrhoeae - drug effects; Neisseria gonorrhoeae - growth & development; Neuraminidase - pharmacology; Pathogens; Phagocytes; Secretion; Subcultures; Urethra - microbiology; Virulence
• ISSN: 0962-8452; 1471-2954
• DOI: 10.1098/rspb.1990.0056

Gonococci examined directly from urethral exudates are resistant to killing by human serum, but most strains become susceptible on subculture. Previous work with gonococci grown in vitro indicates that resistance in vivo is due to sialylation of gonococcal lipopolysaccharide (LPS) by a host factor, cytidine 5'- monophospho- N-acetylneuraminic acid (CMP-NANA) or a related compound present in urogenital secretions and blood cells including phagocytes, which exude during inflammation. This sialylation inhibits the reaction between bactericidal IgM in serum and its target LPS sites. Here, we confirm the indication by using gonococci grown in vivo. Crucial to the above conclusions was the marked reduction of CMP-NANA-conferred serum resistance when gonococci were treated with neuraminidase to remove sialyl groups from their LPS. We now show that the serum resistance of gonococci in urethral exudates was reduced by treatment with neuraminidase from more than 95% (calculated in relation to controls incubated with heated serum) to 2-11% according to sample and incubation time. Subculture of the gonococci also reduced resistance to 9-11% but resistance was restored to more than 95% by incubation with CMP-NANA. This work is the culmination of an investigation that underlines the need to identify specific host factors and the virulence determinants they induce in vivo in future studies of pathogenicity.