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Lipopolysaccharide-Linked Enterobacterial Common Antigen (ECALPS) Occurs in Rough Strains of Escherichia coli R1, R2, and R4.
- Source :
- International Journal of Molecular Sciences; Sep2020, Vol. 21 Issue 17, p6038-6038, 1p
- Publication Year :
- 2020
-
Abstract
- Enterobacterial common antigen (ECA) is a conserved surface antigen characteristic for Enterobacteriaceae. It is consisting of trisaccharide repeating unit, →3)-α-d-Fucp4NAc-(1→4)-β-d-ManpNAcA-(1→4)-α-d-GlcpNAc-(1→, where prevailing forms include ECA linked to phosphatidylglycerol (ECA<subscript>PG</subscript>) and cyclic ECA (ECA<subscript>CYC</subscript>). Lipopolysaccharide (LPS)-associated form (ECA<subscript>LPS</subscript>) has been proved to date only for rough Shigella sonnei phase II. Depending on the structure organization, ECA constitutes surface antigen (ECA<subscript>PG</subscript> and ECA<subscript>LPS</subscript>) or maintains the outer membrane permeability barrier (ECA<subscript>CYC</subscript>). The existence of LPS was hypothesized in the 1960–80s on the basis of serological observations. Only a few Escherichia coli strains (i.e., R1, R2, R3, R4, and K-12) have led to the generation of anti-ECA antibodies upon immunization, excluding ECA<subscript>PG</subscript> as an immunogen and conjecturing ECA<subscript>LPS</subscript> as the only immunogenic form. Here, we presented a structural survey of ECA<subscript>LPS</subscript> in E. coli R1, R2, R3, and R4 to correlate previous serological observations with the presence of ECA<subscript>LPS</subscript>. The low yields of ECA<subscript>LPS</subscript> were identified in the R1, R2, and R4 strains, where ECA occupied outer core residues of LPS that used to be substituted by O-specific polysaccharide in the case of smooth LPS. Previously published observations and hypotheses regarding the immunogenicity and biosynthesis of ECA<subscript>LPS</subscript> were discussed and correlated with presented herein structural data. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 16616596
- Volume :
- 21
- Issue :
- 17
- Database :
- Complementary Index
- Journal :
- International Journal of Molecular Sciences
- Publication Type :
- Academic Journal
- Accession number :
- 145669316
- Full Text :
- https://doi.org/10.3390/ijms21176038