Literature DB >> 3129537

Evidence that the serum resistance genetic locus sac-3 of Neisseria gonorrhoeae is involved in lipopolysaccharide structure.

D S Stephens1, W M Shafer.   

Abstract

The gonococcal chromosome contains a sequence of closely linked genes (for example, sac-1, sac-3, nmp) known or presumed to affect cell envelope structure and which appear to influence susceptibility of gonococci to killing by normal human sera (NHS). Previous work has shown that the serum-resistant isolate FA19, and FA899, a serum-sensitive transformant of FA19, differ in outer membrane protein I (PI) and at the sac-3 genetic locus. However, the sac-3 locus is separable from changes determined by nmp-3, the gene determining PI species. We found that FA19 and FA899 differ in lipopolysaccharide (LPS) molecular size and in reactivity with a monoclonal antibody which recognizes an LPS (L8) epitope. To address the question of whether the changes in LPS were due to the sac-3 locus, we constructed new transformants of FA19 using donor DNA prepared from FA899. The new transformants could be divided into three groups: (1) those identical to FA19 in serum resistance (greater than 90% survival at 120 min), in LPS molecular size and in expression of the L8 epitope; (2) those identical to FA899 in serum sensitivity (100% killed at 30 min), in LPS molecular size and in lack of expression of the L8 epitope; (3) those significantly killed by 50% NHS at 120 min, whose LPS molecular size was greater than that of FA19 but less than that of FA899 and which did not express the L8 epitope. Except for PI there were no differences in other outer-membrane proteins (e.g. PII, PIII, H.8) among these transformants.(ABSTRACT TRUNCATED AT 250 WORDS)

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 3129537     DOI: 10.1099/00221287-133-9-2671

Source DB:  PubMed          Journal:  J Gen Microbiol        ISSN: 0022-1287


  7 in total

Review 1.  Genetic loci and linkage associations in Neisseria gonorrhoeae and Neisseria meningitidis.

Authors:  S E West; V L Clark
Journal:  Clin Microbiol Rev       Date:  1989-04       Impact factor: 26.132

Review 2.  Molecular basis for serum resistance in Neisseria gonorrhoeae.

Authors:  P A Rice
Journal:  Clin Microbiol Rev       Date:  1989-04       Impact factor: 26.132

Review 3.  Protein I: structure, function, and genetics.

Authors:  R C Judd
Journal:  Clin Microbiol Rev       Date:  1989-04       Impact factor: 26.132

4.  Comparison of isolates of Neisseria gonorrhoeae causing meningitis and report of gonococcal meningitis in a patient with C8 deficiency.

Authors:  C Del Rio; D S Stephens; J S Knapp; R J Rice; W O Schalla
Journal:  J Clin Microbiol       Date:  1989-05       Impact factor: 5.948

5.  The (alpha2-->8)-linked polysialic acid capsule and lipooligosaccharide structure both contribute to the ability of serogroup B Neisseria meningitidis to resist the bactericidal activity of normal human serum.

Authors:  C M Kahler; L E Martin; G C Shih; M M Rahman; R W Carlson; D S Stephens
Journal:  Infect Immun       Date:  1998-12       Impact factor: 3.441

6.  Phosphoethanolamine substitution of lipid A and resistance of Neisseria gonorrhoeae to cationic antimicrobial peptides and complement-mediated killing by normal human serum.

Authors:  Lisa A Lewis; Biswa Choudhury; Jacqueline T Balthazar; Larry E Martin; Sanjay Ram; Peter A Rice; David S Stephens; Russell Carlson; William M Shafer
Journal:  Infect Immun       Date:  2008-12-29       Impact factor: 3.441

7.  Tn916-generated, lipooligosaccharide mutants of Neisseria meningitidis and Neisseria gonorrhoeae.

Authors:  D S Stephens; C F McAllister; D Zhou; F K Lee; M A Apicella
Journal:  Infect Immun       Date:  1994-07       Impact factor: 3.441

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.