Literature DB >> 9746562

Genetic divergence and evolutionary instability in ospE-related members of the upstream homology box gene family in Borrelia burgdorferi sensu lato complex isolates.

S Y Sung1, C P Lavoie, J A Carlyon, R T Marconi.   

Abstract

A series of related genes that are flanked at their 5' ends by a conserved upstream sequence element called the upstream homology box (UHB) have been identified in Borrelia burgdorferi. These genes have been referred to as the UHB or erp gene family. We previously demonstrated that among a limited number of B. burgdorferi isolates, the UHB gene family is variable in composition and organization. Prior to this report the UHB gene family in other species of the B. burgdorferi sensu lato complex had not been studied, and if this family is important in the pathogenesis or biology of the Lyme disease spirochetes, then a wide distribution among species and isolates of the B. burgdorferi sensu lato complex would be expected. To assess this, we screened for the UHB element by Southern hybridization and determined its restriction fragment length polymorphism (RFLP) patterns. The UHB element was found to be carried by all B. burgdorferi sensu lato complex species tested (B. burgdorferi, B. garinii, B. afzelii, B. japonica, B. valaisiana sp. nov., and B. andersonii), but the RFLP patterns varied widely at both the inter- and intraspecies levels. Variation in both the number and size of the hybridizing restriction fragments was evident. PCR analyses also revealed the presence of polymorphic, ospE-related alleles in many isolates. Sequence analyses identified the molecular basis of the polymorphisms as being primarily insertions and deletions. Sequence variation and the insertions and deletions were found to be clustered in two distinct domains (variable domains 1 and 2). In many isolates variable domain 1 is flanked by direct repeat elements, some as long as 38 bp. Computer analyses of the deduced amino acid sequences encoded within variable domain 1 predict them to be hydrophilic, surface exposed, and antigenic. The analyses conducted here suggest that the UHB gene family, as evidenced by the variable UHB RFLP patterns, is not evolutionarily stable and that the polymorphic ospE alleles are derived from a common ancestral gene which has been modified through mutation or recombination events. The characterization of ospE-related genes of the UHB gene family among B. burgdorferi sensu lato species will prove important in attempts to construct a model for UHB gene family organization and in deciphering the role of the UHB gene family in the biology and pathogenesis of the Lyme disease spirochetes.

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Year:  1998        PMID: 9746562      PMCID: PMC108573     

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


  29 in total

1.  Analysis of supercoiled circular plasmids in infectious and non-infectious Borrelia burgdorferi.

Authors:  W J Simpson; C F Garon; T G Schwan
Journal:  Microb Pathog       Date:  1990-02       Impact factor: 3.738

2.  Identification of a third genomic group of Borrelia burgdorferi through signature nucleotide analysis and 16S rRNA sequence determination.

Authors:  R T Marconi; C F Garon
Journal:  J Gen Microbiol       Date:  1992-03

3.  The antigenic index: a novel algorithm for predicting antigenic determinants.

Authors:  B A Jameson; H Wolf
Journal:  Comput Appl Biosci       Date:  1988-03

4.  Analysis of the organization of multicopy linear- and circular-plasmid-carried open reading frames in Borrelia burgdorferi sensu lato isolates.

Authors:  J A Carlyon; C LaVoie; S Y Sung; R T Marconi
Journal:  Infect Immun       Date:  1998-03       Impact factor: 3.441

5.  Prediction of protein antigenic determinants from amino acid sequences.

Authors:  T P Hopp; K R Woods
Journal:  Proc Natl Acad Sci U S A       Date:  1981-06       Impact factor: 11.205

6.  Transcriptional start and MetR binding sites on the Escherichia coli metH gene.

Authors:  R Marconi; J Wigboldus; H Weissbach; N Brot
Journal:  Biochem Biophys Res Commun       Date:  1991-03-29       Impact factor: 3.575

7.  rRNA gene organization in the Lyme disease spirochete, Borrelia burgdorferi.

Authors:  J J Schwartz; A Gazumyan; I Schwartz
Journal:  J Bacteriol       Date:  1992-06       Impact factor: 3.490

8.  Linear plasmids of Borrelia burgdorferi have a telomeric structure and sequence similar to those of a eukaryotic virus.

Authors:  J Hinnebusch; A G Barbour
Journal:  J Bacteriol       Date:  1991-11       Impact factor: 3.490

9.  Delineation of Borrelia burgdorferi sensu stricto, Borrelia garinii sp. nov., and group VS461 associated with Lyme borreliosis.

Authors:  G Baranton; D Postic; I Saint Girons; P Boerlin; J C Piffaretti; M Assous; P A Grimont
Journal:  Int J Syst Bacteriol       Date:  1992-07

10.  Phylogenetic analysis of the genus Borrelia: a comparison of North American and European isolates of Borrelia burgdorferi.

Authors:  R T Marconi; C F Garon
Journal:  J Bacteriol       Date:  1992-01       Impact factor: 3.490

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  18 in total

1.  Molecular and evolutionary characterization of the cp32/18 family of supercoiled plasmids in Borrelia burgdorferi 297.

Authors:  M J Caimano; X Yang; T G Popova; M L Clawson; D R Akins; M V Norgard; J D Radolf
Journal:  Infect Immun       Date:  2000-03       Impact factor: 3.441

2.  Mutation and recombination in the upstream homology box-flanked ospE-related genes of the Lyme disease spirochetes result in the development of new antigenic variants during infection.

Authors:  S Y Sung; J V McDowell; J A Carlyon; R T Marconi
Journal:  Infect Immun       Date:  2000-03       Impact factor: 3.441

3.  Molecular and evolutionary analysis of Borrelia burgdorferi 297 circular plasmid-encoded lipoproteins with OspE- and OspF-like leader peptides.

Authors:  D R Akins; M J Caimano; X Yang; F Cerna; M V Norgard; J D Radolf
Journal:  Infect Immun       Date:  1999-03       Impact factor: 3.441

4.  Demonstration of the genetic stability and temporal expression of select members of the lyme disease spirochete OspF protein family during infection in mice.

Authors:  J V McDowell; S Y Sung; G Price; R T Marconi
Journal:  Infect Immun       Date:  2001-08       Impact factor: 3.441

5.  Evidence that the BBA68 protein (BbCRASP-1) of the Lyme disease spirochetes does not contribute to factor H-mediated immune evasion in humans and other animals.

Authors:  John V McDowell; Kelley M Hovis; Hongming Zhang; Emily Tran; Justin Lankford; R T Marconi
Journal:  Infect Immun       Date:  2006-05       Impact factor: 3.441

6.  Serologic proteome analysis of Borrelia burgdorferi membrane-associated proteins.

Authors:  Andrew J Nowalk; Robert D Gilmore; James A Carroll
Journal:  Infect Immun       Date:  2006-07       Impact factor: 3.441

7.  Selective binding of Borrelia burgdorferi OspE paralogs to factor H and serum proteins from diverse animals: possible expansion of the role of OspE in Lyme disease pathogenesis.

Authors:  Kelley M Hovis; Emily Tran; Christina M Sundy; Eric Buckles; John V McDowell; Richard T Marconi
Journal:  Infect Immun       Date:  2006-03       Impact factor: 3.441

8.  Borrelia burgdorferi B31 Erp proteins that are dominant immunoblot antigens of animals infected with isolate B31 are recognized by only a subset of human lyme disease patient sera.

Authors:  J C Miller; N El-Hage; K Babb; B Stevenson
Journal:  J Clin Microbiol       Date:  2000-04       Impact factor: 5.948

9.  Antigenic and genetic heterogeneity of Borrelia burgdorferi populations transmitted by ticks.

Authors:  J Ohnishi; J Piesman; A M de Silva
Journal:  Proc Natl Acad Sci U S A       Date:  2001-01-16       Impact factor: 11.205

10.  Stability of erp loci during Borrelia burgdorferi infection: recombination is not required for chronic infection of immunocompetent mice.

Authors:  N El Hage; L D Lieto; B Stevenson
Journal:  Infect Immun       Date:  1999-06       Impact factor: 3.441

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