Evidence map›Paper›PMID 18310032›Full record

ArticleMicrobiology (Reading, England)2008

Wall teichoic acids are dispensable for anchoring the PNAG exopolysaccharide to the Staphylococcus aureus cell surface.

Marta Vergara-Irigaray, Tomas Maira-Litrán, Nekane Merino, Gerald B Pier, José R Penadés, Iñigo Lasa

Open access · greenAbstract read
In one paragraph

Article in Microbiology (Reading, England), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

54 citing papers in PubMed, 98 citations in OpenAlex.

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  14. Using Knock-Out Mutants to Investigate the Adhesion ofInternational journal of molecular sciences · 2021
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  16. AFrontiers in molecular biosciences · 2021
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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

6 authors at 6 institutions in 2 countries.

Marta Vergara-IrigarayLaboratory of Microbial Biofilms, Instituto de Agrobiotecnología, Universidad Pública de Navarra-CSIC-Gobierno de Navarra, 31006 Pamplona, Spain.
Tomas Maira-LitránChanning Laboratory, Department of Medicine, Brigham Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Nekane MerinoLaboratory of Microbial Biofilms, Instituto de Agrobiotecnología, Universidad Pública de Navarra-CSIC-Gobierno de Navarra, 31006 Pamplona, Spain.
Gerald B PierChanning Laboratory, Department of Medicine, Brigham Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
José R PenadésCentro de Investigación y Tecnología Animal, Instituto Valenciano de Investigaciones Agrarias (CITA-IVIA), Apdo 187, 12400 Segorbe, Castellón, Spain.
Iñigo LasaLaboratory of Microbial Biofilms, Instituto de Agrobiotecnología, Universidad Pública de Navarra-CSIC-Gobierno de Navarra, 31006 Pamplona, Spain.
Agrobiotechnology Institute · ESBrigham and Women's Hospital · USGobierno de Navarra · ESHarvard University · USInstituto Valenciano de Investigaciones Agrarias · ESUniversidad Publica de Navarra · ES

Funding

Virulence and Immunity to StaphylcocciR01AI046706 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI PIER, GERALD B · 2001 to 2010
$4.1M
VIRULENCE AND IMMUNITY TO STAPHYLOCOCCIR21AI046706 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI PIER, GERALD B · 2000 to 2000
$418k
NIAID NIH HHS AI-46706NIAID NIH HHS R01 AI046706NIAID NIH HHS R21 AI046706
6 · The paper itself

Abstract

Biofilm formation in Staphylococcus aureus is usually associated with the production of the poly-N-acetylglucosamine (PNAG) exopolysaccharide, synthesized by proteins encoded by the icaADBC operon. PNAG is a linear beta-(1-6)-linked N-acetylglucosaminoglycan that has to be partially deacetylated and consequently positively charged in order to be associated with bacterial cell surfaces. Here, we investigated whether attachment of PNAG to bacterial surfaces is mediated by ionic interactions with the negative charge of wall teichoic acids (WTAs), which represent the most abundant polyanions of the Gram-positive bacterial envelope. We generated WTA-deficient mutants by in-frame deletion of the tagO gene in two genetically unrelated S. aureus strains. The DeltatagO mutants were more sensitive to high temperatures, showed a higher degree of cell aggregation, had reduced initial adherence to abiotic surfaces and had a reduced capacity to form biofilms under both steady-state and flow conditions. However, the levels as well as the strength of the PNAG interaction with the bacterial cell surface were similar between DeltatagO mutants and their corresponding wild-type strains. Furthermore, double DeltatagO DeltaicaADBC mutants displayed a similar aggregative phenotype to that of single DeltatagO mutants, indicating that PNAG is not responsible for the aggregative behaviour observed in DeltatagO mutants. Overall, the absence of WTAs in S. aureus had little effect on PNAG production or anchoring to the cell surface, but did affect the biofilm-forming capacity, cell aggregative behaviour and the temperature sensitivity/stability of S. aureus.

Indexed as

Bacterial AdhesionBacteriolysisbeta-GlucansBiofilmsBiosynthetic PathwaysGene DeletionHot TemperatureMicroscopy, Electron, ScanningMicroscopy, ImmunoelectronStaphylococcus aureusTeichoic Acidsbeta-Glucanspoly-N-acetyl-1-6-glucosamineTeichoic Acids

Identifiers

PMID18310032
PMCPMC2292800
OpenAlexW2116749466

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.