Evidence map›Paper›PMID 11447163›Full record

ArticleInfection and immunity2001

Characterization of a stress-induced alternate sigma factor, RpoS, of Coxiella burnetii and its expression during the development cycle.

R Seshadri, J E Samuel

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

16 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Review
  3. Journal of bacteriology · 2019
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  7. Article
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  14. Complete genome sequence of the Q-fever pathogen Coxiella burnetii.Proceedings of the National Academy of Sciences of the United States of America · 2003
    Article
  15. Article
  16. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

R SeshadriDepartment of Medical Microbiology and Immunology, Texas A&M University System Health Science Center, College Station, Texas 77843-1114, USA.
J E Samuel
Texas A&M University System · US

Funding

Pathogenic Roles of Coxiella burnetti ProteinsR01AI037744 · NIAID · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI SAMUEL, JAMES EVANS · 2003 to 2007
$1.8M
PATHOGENIC ROLES OF COXIELLA BURNETTI SURFACE PROTEINSR21AI037744 · NIAID · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI SAMUEL, JAMES E · 2000 to 2000
$313k
PATHOGENIC ROLES OF COXIELLA BURNETII SURFACE PROTEINSR29AI037744 · NIAID · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI SAMUEL, JAMES E · 1995 to 1999
–
NIAID NIH HHS AI37744NIAID NIH HHS R01 AI037744NIAID NIH HHS R21 AI037744NIAID NIH HHS R29 AI037744
6 · The paper itself

Abstract

Coxiella burnetii is an obligate intracellular bacterium that resides in an acidified phagolysosome and has a remarkable ability to persist in the extracellular environment. C. burnetii has evolved a developmental cycle that includes at least two morphologic forms, designated large cell variants (LCV) and small cell variants (SCV). Based on differential protein expression, distinct ultrastructures, and different metabolic activities, we speculated that LCV and SCV are similar to typical logarithmic- and stationary-phase growth stages. We hypothesized that the alternate sigma factor, RpoS, a global regulator of genes expressed under stationary-phase, starvation, and stress conditions in many bacteria, regulates differential expression in life cycle variants of C. burnetii. To test this hypothesis, we cloned and characterized the major sigma factor, encoded by an rpoD homologue, and the stress response sigma factor, encoded by an rpoS homologue. The rpoS gene was cloned by complementation of an Escherichia coli rpoS null mutant containing an RpoS-dependent lacZ fusion (osmY::lacZ). Expression of C. burnetii rpoS was regulated by growth phase in E. coli (induced upon entry into stationary phase). A glutathione S-transferase-RpoS fusion protein was used to develop polyclonal antiserum against C. burnetii RpoS. Western blot analysis detected abundant RpoS in LCV but not in SCV. These results suggest that LCV and SCV are not comparable to logarithmic and stationary phases of growth and may represent a novel adaptation for survival in both the phagolysosome and the extracellular environment.

Indexed as

Alternative SplicingGene Expression Regulation, BacterialAmino Acid SequenceAnimalsBacterial ProteinsBase Sequencebeta-GalactosidaseCatalaseCloning, MolecularCoxiella burnetiiDNA, BacterialDNA-Directed RNA PolymerasesEscherichia coliMolecular Sequence DataRabbitsSequence Analysis, DNABacterial Proteinsbeta-GalactosidaseCatalaseDNA, BacterialDNA-Directed RNA PolymerasesRNA polymerase sigma 70Sigma Factorsigma factor KatF protein, Bacteria

Identifiers

PMID11447163
PMCPMC98577
OpenAlexW1973779126

What OpenQuestion holds

Textmetadata
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.