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Dissemination and serotype modification potential of pSFxv_2, an O-antigen PEtN modification plasmid in Shigella flexneri.

Authors :
Sun, Qiangzheng
Knirel, Yuriy A
Lan, Ruiting
Wang, Jianping
Senchenkova, Sof'ya N
Shashkov, Alexander S
Wang, Yan
Wang, Yiting
Luo, Xia
Xu, Jianguo
Source :
Glycobiology. Mar2014, Vol. 24 Issue 3, p305-313. 9p.
Publication Year :
2014

Abstract

The O-antigens of all Shigella flexneri serotypes, except serotype 6, share a linear tetrasaccharide repeat composed of one N-acetylglucosamine and three l-rhamnose residues, and differences between the serotypes are due to modification of various monosaccharide residues with glucosyl and/or O-acetyl and/or phosphoethanolamine (PEtN) groups. Plasmid-borne opt (formerly lpt-O) gene encoding a PEtN transferase which modifies the O-antigens of S. flexneri serotype X, 4a and Y strains and converts the hosts into MASF IV-1 (E1037) positive “variant” (v) Xv, 4av and Yv serotypes, respectively. In this study, we showed that the opt-carrying plasmid pSFxv_2 can transform strains of all S. flexneri serotypes (1–6) to confer them with the MASF IV-1 epitope recognized by monoclonal antibody MASF IV-1 and typing antiserum IV. The transformants possessed modified O-antigens with a PEtN group(s) at position 3 of one or two rhamnose residues. In some serotypes, the PEtN modification competed or/and interfered with glucosylation and O-acetylation at the same or its neighboring sugar residue. We also showed that the plasmid pSFxv_2 is mobilizable to other S. flexneri strains by conjugation. Although pSFxv_2-harboring S. flexneri strains found in clinical infections are restricted to serotypes Xv, 4av, Yv and, possibly, 6v, our results demonstrate a high potential of dissemination of this plasmid in S. flexneri and emergence of new S. flexneri serotypes. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09596658
Volume :
24
Issue :
3
Database :
Academic Search Index
Journal :
Glycobiology
Publication Type :
Academic Journal
Accession number :
94393468
Full Text :
https://doi.org/10.1093/glycob/cwt115