Literature DB >> 7927790

A family of phase- and size-variant membrane surface lipoprotein antigens (Vsps) of Mycoplasma bovis.

A Behrens1, M Heller, H Kirchhoff, D Yogev, R Rosengarten.   

Abstract

A set of strain- and size-variant highly immunogenic membrane surface protein antigens of Mycoplasma bovis, which has been identified by a monoclonal antibody, is shown in this report to make up a family of antigenically and structurally related lipid-modified proteins, designated Vsps (variable surface proteins). By systematic analysis of several isogenic clonal lineages of the type strain PG45, three members of this family have been identified, VspA, VspB, and VspC, each of which was shown to undergo independent high-frequency changes in size as well as noncoordinate phase variation between ON and OFF expression states. The monoclonal antibody-defined epitope common to VspA, VspB, and VspC was accessible on the cell surface in most, but not all, of the clonal populations analyzed and was present on a C-terminal limit tryptic fragment of each Vsp variant that was released from the membrane surface. VspA and VspC were distinguished from VspB by their selective detection with colloidal gold and by their distinctive reaction with a polyclonal antibody against M. bovis D490. VspA, VspB, and VspC were further distinguishable from one another by their characteristic patterns of degradation at carboxypeptidase Y pause sites. While these Vsp-specific structural fingerprints with an irregular periodic spacing were constant for similarly sized variants of a defined Vsp product, they showed distinct differences among variants differing in size. This variability included gain or loss of individual bands within distinct subsets of bands, as well as shifts of the entire banding patterns up- or downwards, indicating that insertions or deletions underlying Vsp size variation can occur at various locations either within the C-terminal domain or within other regions of these proteins. This was similarly confirmed by comparative epitope mapping analysis of tryptic cleavage products generated from different Vsp size variants. The Vsp family of M. bovis described in this study represents a newly discovered system of surface antigenic variation in mycoplasmas displaying features which closely resemble but are also different from the characteristics reported for the Vlp (variable lipoprotein) system of M. hyorhinis. The isogenic lineages established here provide key populations for subsequent analysis of corresponding genes to further elucidate Vsp structure and variation, which may have important relevance for a better understanding of the pathogenicity of this agent.

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Year:  1994        PMID: 7927790      PMCID: PMC303228          DOI: 10.1128/iai.62.11.5075-5084.1994

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  29 in total

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Authors:  R Rosengarten; K S Wise
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Review 4.  Genetic diversity in Plasmodium falciparum.

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Authors:  S K Hollingshead; V A Fischetti; J R Scott
Journal:  Mol Gen Genet       Date:  1987-05

6.  Lipid-modified surface protein antigens expressing size variation within the species Mycoplasma hyorhinis.

Authors:  M J Boyer; K S Wise
Journal:  Infect Immun       Date:  1989-01       Impact factor: 3.441

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Authors:  R Hayashi; S Moore; W H Stein
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8.  Molecular cloning of a member of the gene family that encodes pMGA, a hemagglutinin of Mycoplasma gallisepticum.

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9.  Reacquisition of specific proteins confers virulence in Mycoplasma pneumoniae.

Authors:  D C Krause; D K Leith; J B Baseman
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10.  Mechanisms of attachment of Mycoplasma arthritidis to host cells in vitro.

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  43 in total

1.  The vsp locus of Mycoplasma bovis: gene organization and structural features.

Authors:  I Lysnyansky; K Sachse; R Rosenbusch; S Levisohn; D Yogev
Journal:  J Bacteriol       Date:  1999-09       Impact factor: 3.490

2.  P48 major surface antigen of Mycoplasma agalactiae is homologous to a malp product of Mycoplasma fermentans and belongs to a selected family of bacterial lipoproteins.

Authors:  S Rosati; S Pozzi; P Robino; B Montinaro; A Conti; M Fadda; M Pittau
Journal:  Infect Immun       Date:  1999-11       Impact factor: 3.441

3.  Characterization of a multigene family undergoing high-frequency DNA rearrangements and coding for abundant variable surface proteins in Mycoplasma agalactiae.

Authors:  M D Glew; L Papazisi; F Poumarat; D Bergonier; R Rosengarten; C Citti
Journal:  Infect Immun       Date:  2000-08       Impact factor: 3.441

4.  Extended repertoire of genes encoding variable surface lipoproteins in Mycoplasma bovis strains.

Authors:  Sarit Nussbaum; Inessa Lysnyansky; Konrad Sachse; Sharon Levisohn; David Yogev
Journal:  Infect Immun       Date:  2002-04       Impact factor: 3.441

5.  Juxtaposition of an active promoter to vsp genes via site-specific DNA inversions generates antigenic variation in Mycoplasma bovis.

Authors:  I Lysnyansky; Y Ron; D Yogev
Journal:  J Bacteriol       Date:  2001-10       Impact factor: 3.490

6.  Surface diversity in Mycoplasma agalactiae is driven by site-specific DNA inversions within the vpma multigene locus.

Authors:  Michelle D Glew; Marc Marenda; Renate Rosengarten; Christine Citti
Journal:  J Bacteriol       Date:  2002-11       Impact factor: 3.490

Review 7.  Phase and antigenic variation in bacteria.

Authors:  Marjan W van der Woude; Andreas J Bäumler
Journal:  Clin Microbiol Rev       Date:  2004-07       Impact factor: 26.132

8.  Molecular epidemiological analysis of Mycoplasma bovis isolates from the United Kingdom shows two genetically distinct clusters.

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Journal:  J Clin Microbiol       Date:  2004-10       Impact factor: 5.948

9.  Epitope mapping of immunogenic and adhesive structures in repetitive domains of Mycoplasma bovis variable surface lipoproteins.

Authors:  K Sachse; J H Helbig; I Lysnyansky; C Grajetzki; W Müller; E Jacobs; D Yogev
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10.  Association of a major protein antigen of Mycoplasma arthritidis with virulence.

Authors:  A-H T Tu; B Clapper; T R Schoeb; A Elgavish; J Zhang; L Liu; H Yu; K Dybvig
Journal:  Infect Immun       Date:  2005-01       Impact factor: 3.441

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