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Lipopolysaccharide core components of Rhizobium etli reacting with a panel of monoclonal antibodies

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Book cover Current Issues in Symbiotic Nitrogen Fixation

Part of the book series: Developments in Plant and Soil Sciences ((DPSS,volume 72))

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Abstract

Monoclonal antibodies that react with Rhizobium leguminosarum lipopolysaccharide core antigens (LPS-2) have been used to investigate LPS-2 structure in Rhizobium etli. The panel of antibodies (JIM 32 - JIM 35, JIM 37, JIM 38) specific for LPS-2 of R. leguminosarum strain 3841 and its core components displays similar reactivities towards isolated LPS-2 from R. etli CE109 (a mutant of wild-type strain R. etli CE3 that displays LPS-2 as its main LPS form on the cell surface). This result suggests the antibodies bind to similar epitopes on both strains and, hence, that R. leguminosarum and R. etli have very similar LPS core and lipid A antigen structures. More detailed analysis of the antibody binding sites with isolated LPS-2 and lipid A from R. etli suggests that some of the antibodies (JIM 32, 33, 34, and MASM-I) bind some part of the core oligosaccharides, while others (JIM 35 and JIM 38) involve lipid A. These antibodies have already proven useful in the biochemical analysis of the LPS antigen forms. For example, the loss of reactivity of certain LPS forms with antibody JIM 37 has led to the discovery of a hitherto unnoticed form of the LPS antigen in a precipitate formed during the phenol/water extraction procedure. This new form reacts with the JIM 37 antibody. Furthermore, the positive reaction of some of the antibodies with only sonicated wild-type R. etli cells suggests that either an effective way of masking the display of core antigens on whole bacterial cells is occurring or that core forms of the LPSs are never displayed on the surface of the bacterial cells. Either possibility, once confirmed, could be important for our picture of the Rhizobium cell surface and could also have some bearing on symbiotic nodule infection and development.

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Abbreviations

LPS:

lipopolysaccharide

References

  • Bhat U R, Bhagyalakshmi S K and Carlson R W 1991a Re-examination of the structures of the lipopolysaccharide core oligosaccharides from Rhizobium leguminosarum biovar phase-oli. Carbohydr. Res. 220, 219–227.

    Article  PubMed  CAS  Google Scholar 

  • Bhat U R, Mayer H, Yokota A, Hollingsworth R I and Carlson R W 1991b Occurrence of lipid A variants with 27-hydroxyoctacosanoic acid in lipopolysaccharides from membranes of the family Rhizobiaceae. J. Bacteriol. 173, 2155–2159.

    PubMed  CAS  Google Scholar 

  • Bhat U R, Forsberg L S and Carlson R W 1994 Structure of lipid A component of Rhizobium leguminosarum bv. phaseoli lipopolysaccharide. J. Biol. Chem. 269, 14402–14410.

    PubMed  CAS  Google Scholar 

  • Carlson R W, Kalembasa S, Turowski D, Pachori P and Noel, K D 1987 Characterization of the lipopolysaccharide from a Rhi-zobium phaseoli mutant that is defective in infection thread development. J. Bacteriol. 169, 4923–4928.

    PubMed  CAS  Google Scholar 

  • Carlson R W, Forsberg S L, Price N P J, Bhat U R, Kelly T M and Raetz R H 1995 The structure and biosynthesis of Rhizobium leguminosarum lipid A. In Bacterial Endotoxins: Lipopolysac-charides; From Genes to Therapy. Eds. J Levin, C R Alving, R S Munford and H Redl. pp 25–31. Wiley-Liss, Inc., New York, USA.

    Google Scholar 

  • Hollingsworth R I, Carlson R W, Garcia F and Gage D A 1990 A new core tetrasaccharide component from the lipopolysaccharide of Rhizobium trifolii ANU 843. J. Biol. Chem. 264, 9294–9299 (Erratum 265, 12752).

    Google Scholar 

  • Kannenberg E L and Brewin N J 1989 Expression of a cell surface antigen from Rhizobium leguminosarum3841 is regulated by oxygen and pH. J. Bacteriol. 171, 4543–4548.

    PubMed  CAS  Google Scholar 

  • Kannenberg E L, Rathbun E A and Brewin N J 1992 Molecular dissection of structure and function in the lipopolysaccharide of Rhizobium leguminosarum strain 3841 using monoclonal antibodies and genetic analysis. Mol. Microbiol. 6, 2477–2487.

    Article  PubMed  CAS  Google Scholar 

  • Kannenberg E L, Perotto S, Vianciotto V, Rathbun E A and Brewin N J 1994 Lipopolysaccharide epitope expression of Rhizobium bacteroids as revealed by in situ immunolabelling of pea root nodule sections. J. Bacteriol. 176, 2021–2032.

    PubMed  CAS  Google Scholar 

  • Lind S M, Carlin N I A and Lomdberg A A 1985 Production and characterisation of KDO-specific monoclonal antibodies recognising lipopolysaccharides from heptoseless mutants of Salmonella. FEMS Microbiol. Lett. 28, 45–49.

    Article  CAS  Google Scholar 

  • Lucas M M, Peart J L, Brewin N J and Kannenberg E L 1996 Isolation of monoclonal antibodies reacting with the core component of lipopolysaccharide from Rhizobium leguminosarum strain 3841 and mutant derivatives. J. Bacteriol. 178, 2727–2733.

    PubMed  CAS  Google Scholar 

  • Noel K D, Vanden Bosch K A and Kulpaca B 1986 Mutations in Rhizobium phaseoli that lead to arrested development of infection threads. J. Bacteriol. 168, 1392–1401.

    PubMed  CAS  Google Scholar 

  • Noel K D 1992 Rhizobial polysaccharides required in symbiosis with legumes. In The Molecular Signals in Plant-Microbe Communication. Ed. D P S Verma. pp 341–357. CRC Press, Boca Raton, USA.

    Google Scholar 

  • Perotto S, Brewin N J and Kannenberg E L 1994 Cytological evidence for a host defence response that reduces cell and tissue invasion in pea nodules by lipopolysaccharide-defective mutants of Rhizobium leguminosarum strain 3841. Mol. Plant-Microbe Interact. 7, 99–112.

    Article  CAS  Google Scholar 

  • Tao H, Brewin N J and Noel K D 1992 Rhizobium leguminosarum CFN42 lipopolysaccharide antigenic changes induced by environmental conditions. J. Bacteriol. 174, 2222–2229.

    PubMed  CAS  Google Scholar 

  • Wood E A, Butcher G W, Brewin N J and Kannenberg E L 1989 Genetic derepression of a developmentally regulated lipopolysaccharide antigen from Rhizobium leguminosarum3841. J. Bacteriol. 171, 4549–4555.

    PubMed  CAS  Google Scholar 

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G. H. Elkan R. G. Upchurch

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© 1996 Springer Science+Business Media Dordrecht

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Kannenberg, E.L., Forsberg, L.S., Carlson, R.W. (1996). Lipopolysaccharide core components of Rhizobium etli reacting with a panel of monoclonal antibodies. In: Elkan, G.H., Upchurch, R.G. (eds) Current Issues in Symbiotic Nitrogen Fixation. Developments in Plant and Soil Sciences, vol 72. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-5700-1_22

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  • DOI: https://doi.org/10.1007/978-94-011-5700-1_22

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-010-6404-0

  • Online ISBN: 978-94-011-5700-1

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