Evidence map›Paper›PMID 22081606›Full record

ArticleThe Journal of biological chemistry2011

Serine/threonine phosphatase Stp1 mediates post-transcriptional regulation of hemolysin, autolysis, and virulence of group B Streptococcus.

Kellie Burnside, Annalisa Lembo, Maria Isabel Harrell, Michael Gurney, Liang Xue, Nguyen-Thao BinhTran, James E Connelly, Kelsea A Jewell, Byron Z Schmidt, Melissa de Los Reyes and 3 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

27 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Analysis of serotype distribution and characteristics of nonhemolytic and nonpigmented strains among group B Streptococcus isolates in a southern Taiwan local hospital.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2025
    Article
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  12. ¡vIVA la DivIVA!Journal of bacteriology · 2019
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  14. The Cell Wall ofMicrobiology spectrum · 2019
    Review
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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

13 authors at 4 institutions in 1 country.

Kellie BurnsideDepartment of Pediatric Infectious Diseases, University of Washington School of Medicine and Seattle Children's Hospital Research Institute, Seattle, Washington 98101.
Annalisa LemboDepartment of Pediatric Infectious Diseases, University of Washington School of Medicine and Seattle Children's Hospital Research Institute, Seattle, Washington 98101.
Maria Isabel HarrellDepartment of Pediatric Infectious Diseases, University of Washington School of Medicine and Seattle Children's Hospital Research Institute, Seattle, Washington 98101.
Michael GurneyDepartment of Biology and Center for Microbial Sciences, San Diego State University, San Diego, California 92182.
Liang XueDepartment of Biochemistry, Purdue University, West Lafayette, Indiana 47907.
Nguyen-Thao BinhTranDepartment of Pediatric Infectious Diseases, University of Washington School of Medicine and Seattle Children's Hospital Research Institute, Seattle, Washington 98101.
James E ConnellyDepartment of Pediatric Infectious Diseases, University of Washington School of Medicine and Seattle Children's Hospital Research Institute, Seattle, Washington 98101.
Kelsea A JewellDepartment of Pediatric Infectious Diseases, University of Washington School of Medicine and Seattle Children's Hospital Research Institute, Seattle, Washington 98101.
Byron Z SchmidtDepartment of Pediatric Infectious Diseases, University of Washington School of Medicine and Seattle Children's Hospital Research Institute, Seattle, Washington 98101.
Melissa de Los ReyesDepartment of Pediatric Infectious Diseases, University of Washington School of Medicine and Seattle Children's Hospital Research Institute, Seattle, Washington 98101.
Weiguo Andy TaoDepartment of Biochemistry, Purdue University, West Lafayette, Indiana 47907.
Kelly S DoranDepartment of Biology and Center for Microbial Sciences, San Diego State University, San Diego, California 92182.
Lakshmi RajagopalDepartment of Pediatric Infectious Diseases, University of Washington School of Medicine and Seattle Children's Hospital Research Institute, Seattle, Washington 98101. Electronic address: lakshmi.rajagopal@seattlechildrens.org.
University of Washington · USSeattle Children's Hospital · USPurdue University West Lafayette · USSan Diego State University · US

Funding

ACADEMIC PEDIATRIC INFECTIOUS DISEASET32HD007233 · NICHD · SEATTLE CHILDREN'S HOSPITAL · PI KEVIN B URDAHL · 1985 to 2026
$6.7M
Blood-brain barrier in bacterial meningitisR01NS051247 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DORAN, KELLY S · 2006 to 2015
$3.2M
Eukaryotic-type signaling mediates two-component regulation of GBS virulenceR01AI070749 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI RAJAGOPAL, LAKSHMI · 2007 to 2011
$2.0M
New Proteomic Technologies for the Analysis of Tyrosine Kinase Signaling PathwaysR01GM088317 · NIGMS · PURDUE UNIVERSITY · PI TAO, W. ANDY · 2010 to 2014
$1.6M
NIAID NIH HHS R01 AI070749NIAID NIH HHS R01AI070749NICHD NIH HHS 5 T32 HD007233-29NICHD NIH HHS T32 HD007233NIGMS NIH HHS GM088317NIGMS NIH HHS R01 GM088317NINDS NIH HHS R01 NS051247NINDS NIH HHS R01NS051247
6 · The paper itself

Abstract

Elucidating how serine/threonine phosphatases regulate kinase function and bacterial virulence is critical for our ability to combat these infections. Group B streptococci (GBS) are β-hemolytic Gram-positive bacteria that cause invasive infections in humans. To adapt to environmental changes, GBS encodes signaling mechanisms comprising two component systems and eukaryotic-like enzymes. We have previously described the importance of the serine/threonine kinase Stk1 to GBS pathogenesis. However, how the presence or absence of the cognate serine/threonine phosphatase Stp1 affects Stk1 function and GBS virulence is not known. Here, we show that GBS deficient only in Stp1 expression are markedly reduced for their ability to cause systemic infections, exhibit decreased β-hemolysin/cytolysin activity, and show increased sensitivity to autolysis. Although transcription of genes important for β-hemolysin/cytolysin expression and export is similar to the wild type (WT), 294 genes (excluding stp1) showed altered expression in the stp1 mutant and included autolysin genes. Furthermore, phosphopeptide enrichment analysis identified that 35 serine/threonine phosphopeptides, corresponding to 27 proteins, were unique to the stp1 mutant. This included phosphorylation of ATP synthase, DNA and RNA helicases, and proteins important for cell division and protein synthesis. Collectively, our results indicate that Stp1 is important for appropriate regulation of Stk1 function, hemolysin activity, autolysis, and GBS virulence.

Indexed as

Gene Expression RegulationVirulenceAnimalsAnimals, NewbornArylsulfotransferaseBrainHemolysin ProteinsHumansMicrocirculationPhosphoprotein PhosphatasesPhosphorylationProtein Serine-Threonine KinasesProteomicsRatsRNA Processing, Post-TranscriptionalStreptococcus agalactiaeArylsulfotransferaseHemolysin ProteinsPhosphoprotein PhosphatasesProtein Serine-Threonine KinasesStk1 protein, Streptococcus agalactiaeSULT1A1 protein, humanSult1a1 protein, rat

Identifiers

PMID22081606
PMCPMC3243546
OpenAlexW2089172583

What OpenQuestion holds

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Registered trials

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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.