Evidence map›Paper›PMID 19943896›Full record

ArticleMolecular microbiology2009

Who is the BosR around here anyway?

D Scott Samuels, Justin D Radolf

Open access · bronzeAbstract readComment
In one paragraph

Article in Molecular microbiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.8field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 47 citations in OpenAlex.

  1. TheInfection and immunity · 2026
    Article
  2. The BosR Is Back!Molecular microbiology · 2026
    Article
  3. Review
  4. Article
  5. Gene Regulation and Transcriptomics.Current issues in molecular biology · 2021
    Article
  6. Article
  7. The CXXC Motifs Are Essential for the Function of BosR inFrontiers in cellular and infection microbiology · 2019
    Article
  8. The Stringent Response-Regulated sRNA Transcriptome ofFrontiers in cellular and infection microbiology · 2018
    Article
  9. Article
  10. Small RNAs ofThe Yale journal of biology and medicine · 2017
    Review
  11. Article
  12. Investigation ofFrontiers in cellular and infection microbiology · 2017
    Article
  13. Article
  14. Review
  15. Review
  16. Gene Regulation During the Enzootic Cycle of the Lyme Disease Spirochete.Forum on immunopathological diseases and therapeutics · 2016
    Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

D Scott SamuelsDivision of Biological Sciences and Center for Biomolecular Structure and Dynamics, The University of Montana, Missoula, MT 59812-4824, USA. scott.samuels@umontana.edu
Justin D Radolf
University of Montana · US

Funding

RpoS Regulation of Borrelia burgdorferi Genes in vivoR01AI029735 · NIAID · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI CAIMANO, MELISSA J, RADOLF, JUSTIN D · 1990 to 2022
$10.7M
Regulation of Gene Expression in Borrelia burgdorferiR01AI051486 · NIAID · UNIVERSITY OF MONTANA · PI SAMUELS, D. SCOTT · 2003 to 2018
$5.1M
RpoS Regulation of Borrelia burgdorferi Genes in vivoR56AI029735 · NIAID · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI RADOLF, JUSTIN D · 2012 to 2012
$536k
NIAID NIH HHS AI051486NIAID NIH HHS AI29735NIAID NIH HHS R01 AI029735NIAID NIH HHS R01 AI051486NIAID NIH HHS R56 AI029735
6 · The paper itself

Abstract

Borrelia burgdorferi encodes a novel DNA-binding protein in the Fur/PerR family of transcriptional regulators termed BosR (BB0647). This issue of Molecular Microbiology contains two molecular genetic studies that help to clarify the function of BB0647 and resolve longstanding controversies. Loss of BB0647 appears to have a pronounced effect on borrelial gene expression and, in one study, caused significant in vitro growth defects. BB0647 was also found to be essential for infection of the mammalian host but not the tick vector. Both Ouyang et al. and Hyde et al. also demonstrate, quite unexpectedly, that BB0647 is required for induction of RpoS, an alternative sigma factor that controls a cadre of B. burgdorferi genes, most notably ospC, which enable the spirochetes to establish mammalian infection following tick inoculation. There are still many unanswered questions regarding the precise physiological role of BB0647, the most important of which relate to its homologues Fur and PerR: to what extent does it regulate either the response to oxidative stress and/or transition metal uptake? The mechanism(s) whereby BB0647 interfaces with the Rrp2-RpoN-RpoS pathway also remains to be discerned. However, these two seminal papers establish BB0647 (BosR) as a central player in the molecular biology and physiology of B. burgdorferi as well as the pathogenesis of Lyme disease.

Indexed as

Gene Expression Regulation, BacterialAnimalsBacterial ProteinsBorrelia burgdorferiDNA-Binding ProteinsGene DeletionHumansSigma FactorBacterial ProteinsDNA-Binding ProteinsSigma Factorsigma factor KatF protein, Bacteria

Identifiers

PMID19943896
PMCPMC3005592
OpenAlexW1550355855

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.