Literature DB >> 10644495

Evolutionary and molecular analyses of the Borrelia bdr super gene family: delineation of distinct sub-families and demonstration of the genus wide conservation of putative functional domains, structural properties and repeat motifs.

J A Carlyon1, D M Roberts, R T Marconi.   

Abstract

B. turicatae, a causative agent of relapsing fever, carries a polymorphic gene family that is homologous to the bdr gene family of the Lyme disease spirochetes (previously referred to as the rep+ or ORF-E gene family). Here we demonstrate that bdr related genes are widely distributed among pathogenic Borrelia species and exist as large, polymorphic, plasmid carried, gene families. Twenty distinct bdr alleles were identified in isolates of the relapsing fever spirochete, B. hermsii, and were localized to linear plasmids. Cloning and sequence analyses demonstrate that the putative Bdr functional domains (i.e. the phosphorylation motifs and the transmembrane C-terminal domain) are conserved across the genus while other regions of these proteins exhibit variability. An assessment of the evolutionary relationships among all known Bdr protein sequences obtained from five pathogenic Borrelia species revealed that there are distinct Bdr sub-families. The recognition of distinct phyletic clusters serves as the basis of a revised and simplified nomenclature for the bdr proteins that can be applied genus wide. At the biological level the delineation of multiple bdr sub-families within isogeneic populations raises the possibility that there may be functional partitioning among alleles. In summary, the distribution and conservation of the Bdr proteins suggests that they are important in the biology/pathogenesis of the Borrelia at the genus wide level. Copyright 2000 Academic Press.

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Year:  2000        PMID: 10644495     DOI: 10.1006/mpat.1999.0326

Source DB:  PubMed          Journal:  Microb Pathog        ISSN: 0882-4010            Impact factor:   3.738


  10 in total

1.  Molecular and immunological analyses of the Borrelia turicatae Bdr protein family.

Authors:  J A Carlyon; D M Roberts; M Theisen; C Sadler; R T Marconi
Journal:  Infect Immun       Date:  2000-04       Impact factor: 3.441

2.  Long-term microclimatic stress causes rapid adaptive radiation of kaiABC clock gene family in a cyanobacterium, Nostoc linckia, from "Evolution Canyons" I and II, Israel.

Authors:  Volodymyr Dvornyk; Oxana Vinogradova; Eviatar Nevo
Journal:  Proc Natl Acad Sci U S A       Date:  2002-02-12       Impact factor: 11.205

3.  Rrp1, a cyclic-di-GMP-producing response regulator, is an important regulator of Borrelia burgdorferi core cellular functions.

Authors:  Elizabeth A Rogers; Darya Terekhova; Hong-Ming Zhang; Kelley M Hovis; Ira Schwartz; Richard T Marconi
Journal:  Mol Microbiol       Date:  2009-01-23       Impact factor: 3.501

4.  Phylogenetic analysis of the spirochetes Borrelia parkeri and Borrelia turicatae and the potential for tick-borne relapsing fever in Florida.

Authors:  Tom G Schwan; Sandra J Raffel; Merry E Schrumpf; Paul F Policastro; Julie A Rawlings; Robert S Lane; Edward B Breitschwerdt; Stephen F Porcella
Journal:  J Clin Microbiol       Date:  2005-08       Impact factor: 5.948

5.  The relapsing fever spirochete Borrelia hermsii contains multiple, antigen-encoding circular plasmids that are homologous to the cp32 plasmids of Lyme disease spirochetes.

Authors:  B Stevenson; S F Porcella; K L Oie; C A Fitzpatrick; S J Raffel; L Lubke; M E Schrumpf; T G Schwan
Journal:  Infect Immun       Date:  2000-07       Impact factor: 3.441

6.  Environmental regulation and differential production of members of the Bdr protein family of Borrelia burgdorferi.

Authors:  David M Roberts; Melissa Caimano; John McDowell; Michael Theisen; Arne Holm; Edward Orff; David Nelson; Stephen Wikel; Justin Radolf; Richard T Marconi
Journal:  Infect Immun       Date:  2002-12       Impact factor: 3.441

7.  Analysis of the cellular localization of Bdr paralogs in Borrelia burgdorferi, a causative agent of lyme disease: evidence for functional diversity.

Authors:  D M Roberts; M Theisen; R T Marconi
Journal:  J Bacteriol       Date:  2000-08       Impact factor: 3.490

8.  bdrF2 of Lyme disease spirochetes is coexpressed with a series of cytoplasmic proteins and is produced specifically during early infection.

Authors:  Hongming Zhang; Abayami Raji; Michael Theisen; Paul R Hansen; Richard T Marconi
Journal:  J Bacteriol       Date:  2005-01       Impact factor: 3.490

9.  Analysis of mechanisms associated with loss of infectivity of clonal populations of Borrelia burgdorferi B31MI.

Authors:  J V McDowell; S Y Sung; M Labandeira-Rey; J T Skare; R T Marconi
Journal:  Infect Immun       Date:  2001-06       Impact factor: 3.441

10.  Genome stability of Lyme disease spirochetes: comparative genomics of Borrelia burgdorferi plasmids.

Authors:  Sherwood R Casjens; Emmanuel F Mongodin; Wei-Gang Qiu; Benjamin J Luft; Steven E Schutzer; Eddie B Gilcrease; Wai Mun Huang; Marija Vujadinovic; John K Aron; Levy C Vargas; Sam Freeman; Diana Radune; Janice F Weidman; George I Dimitrov; Hoda M Khouri; Julia E Sosa; Rebecca A Halpin; John J Dunn; Claire M Fraser
Journal:  PLoS One       Date:  2012-03-14       Impact factor: 3.240

  10 in total

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