Reversible synthesis of colanic acid and O-antigen polysaccharides in Salmonella Typhimurium enhances induction of cross-immune responses and provides protection against heterologous Salmonella challenge. Issue 21 (15th May 2017)
- Record Type:
- Journal Article
- Title:
- Reversible synthesis of colanic acid and O-antigen polysaccharides in Salmonella Typhimurium enhances induction of cross-immune responses and provides protection against heterologous Salmonella challenge. Issue 21 (15th May 2017)
- Main Title:
- Reversible synthesis of colanic acid and O-antigen polysaccharides in Salmonella Typhimurium enhances induction of cross-immune responses and provides protection against heterologous Salmonella challenge
- Authors:
- Li, Pei
Liu, Qing
Huang, Chun
Zhao, Xinxin
Roland, Kenneth L.
Kong, Qingke - Abstract:
- Highlights: The products of cps G and rfb K in Salmonella are isozymes for mannose synthesis. The Δ cpsG Δ rfbK mutant produces full length O-antigen in the presence of mannose. Salmonella with two mutations enhance induction of IgG cross-reactive with OMPs. Abstract: Colanic Acid (CA) and lipopolysaccharide (LPS) are two major mannose-containing extracellular polysaccharides of Salmonella . Their presence on the bacterial surface can mask conserved protective outer membrane proteins (OMPs) from the host immune system. The mannose moiety in these molecules is derived from GDP-mannose, which is synthesized in several steps. The first two steps require the action of phosphomannose isomerase, encoded by pmi ( manA ), followed by phosphomannomutase, encoded by manB . There are two copies of manB present in the Salmonella chromosome, one located in the cps gene cluster ( cpsG ) responsible for CA synthesis, and the other in the rfb gene cluster ( rfbK ) involved in LPS O-antigen synthesis. In this study, it was demonstrated that the products of cpsG and rfbK are isozymes. To evaluate the impact of these genes on O-antigen synthesis, virulence and immunogenicity, single mutations (Δ pmi, Δ rfbK or Δ cpsG ) and a double mutation (Δ rfbK Δ cpsG ) were introduced into both wild-type Salmonella enterica and an attenuated Δ cya Δ crp vaccine strain. The Δ pmi, Δ rfbK and Δ cpsG Δ rfbK mutants were defective in LPS synthesis and attenuated for virulence. In orally inoculated mice,Highlights: The products of cps G and rfb K in Salmonella are isozymes for mannose synthesis. The Δ cpsG Δ rfbK mutant produces full length O-antigen in the presence of mannose. Salmonella with two mutations enhance induction of IgG cross-reactive with OMPs. Abstract: Colanic Acid (CA) and lipopolysaccharide (LPS) are two major mannose-containing extracellular polysaccharides of Salmonella . Their presence on the bacterial surface can mask conserved protective outer membrane proteins (OMPs) from the host immune system. The mannose moiety in these molecules is derived from GDP-mannose, which is synthesized in several steps. The first two steps require the action of phosphomannose isomerase, encoded by pmi ( manA ), followed by phosphomannomutase, encoded by manB . There are two copies of manB present in the Salmonella chromosome, one located in the cps gene cluster ( cpsG ) responsible for CA synthesis, and the other in the rfb gene cluster ( rfbK ) involved in LPS O-antigen synthesis. In this study, it was demonstrated that the products of cpsG and rfbK are isozymes. To evaluate the impact of these genes on O-antigen synthesis, virulence and immunogenicity, single mutations (Δ pmi, Δ rfbK or Δ cpsG ) and a double mutation (Δ rfbK Δ cpsG ) were introduced into both wild-type Salmonella enterica and an attenuated Δ cya Δ crp vaccine strain. The Δ pmi, Δ rfbK and Δ cpsG Δ rfbK mutants were defective in LPS synthesis and attenuated for virulence. In orally inoculated mice, strain S122 (Δ crp Δ cya Δ cpsG Δ rfbK ) and its parent S738 (Δ crp Δ cya ) were both avirulent and colonized internal tissues. Strain S122 elicited higher levels of anti- S . Typhimurium OMP serum IgG than its parent strain. Mice immunized with S122 were completely protected against challenge with wild-type virulent S. Typhimurium and partially protected against challenge with either wild-type virulent S. Choleraesuis or S. Enteritidis. These data indicate that deletions in rfbK and cpsG are useful mutations for inclusion in future attenuated Salmonella vaccine strains to induce cross-protective immunity. … (more)
- Is Part Of:
- Vaccine. Volume 35:Issue 21(2017)
- Journal:
- Vaccine
- Issue:
- Volume 35:Issue 21(2017)
- Issue Display:
- Volume 35, Issue 21 (2017)
- Year:
- 2017
- Volume:
- 35
- Issue:
- 21
- Issue Sort Value:
- 2017-0035-0021-0000
- Page Start:
- 2862
- Page End:
- 2869
- Publication Date:
- 2017-05-15
- Subjects:
- Colanic acid -- O-antigen -- Mannose -- manB -- Live attenuated Salmonella vaccine -- Cross-immunity
Vaccines -- Periodicals
615.372 - Journal URLs:
- http://www.sciencedirect.com/science/journal/0264410X ↗
http://www.clinicalkey.com/dura/browse/journalIssue/0264410X ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/0264410X ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.vaccine.2017.04.002 ↗
- Languages:
- English
- ISSNs:
- 0264-410X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9138.628000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 1538.xml