Evidence map›Paper›PMID 30625152›Full record

ArticlePLoS computational biology2019

A computational knowledge-base elucidates the response of Staphylococcus aureus to different media types.

Yara Seif, Jonathan M Monk, Nathan Mih, Hannah Tsunemoto, Saugat Poudel, Cristal Zuniga, Jared Broddrick, Karsten Zengler, Bernhard O Palsson

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.7field-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

31 citing papers in PubMed, 61 citations in OpenAlex.

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  10. Genome-scale model ofMicrobiology spectrum · 2024
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  18. Adaptive laboratory evolution and independent component analysis disentangle complex vancomycin adaptation trajectories.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
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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

9 authors at 1 institution in 1 country.

Yara SeifDepartment of Bioengineering, University of California, San Diego, La Jolla, CA, United States of America.
Jonathan M MonkDepartment of Bioengineering, University of California, San Diego, La Jolla, CA, United States of America.
Nathan MihDepartment of Bioengineering, University of California, San Diego, La Jolla, CA, United States of America.ORCID 0000-0002-4302-9052
Hannah TsunemotoDivision of Biological Sciences, University of California San Diego, La Jolla, CA, United States of America.ORCID 0000-0002-1546-097X
Saugat PoudelDepartment of Bioengineering, University of California, San Diego, La Jolla, CA, United States of America.ORCID 0000-0002-3732-2463
Cristal ZunigaDepartment of Bioengineering, University of California, San Diego, La Jolla, CA, United States of America.ORCID 0000-0002-0135-7429
Jared BroddrickDepartment of Bioengineering, University of California, San Diego, La Jolla, CA, United States of America.ORCID 0000-0003-4871-4822
Karsten ZenglerDepartment of Bioengineering, University of California, San Diego, La Jolla, CA, United States of America.
Bernhard O PalssonDepartment of Bioengineering, University of California, San Diego, La Jolla, CA, United States of America.ORCID 0000-0003-2357-6785
University of California San Diego · US

Funding

Systems Biology Approach to Redefine Susceptibility Testing and Treatment of MDR Pathogens in the Context of Host ImmunityU01AI124316 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI PALSSON, BERNHARD O · 2016 to 2020
$10.2M
NIAID NIH HHS U01 AI124316
6 · The paper itself

Abstract

S. aureus is classified as a serious threat pathogen and is a priority that guides the discovery and development of new antibiotics. Despite growing knowledge of S. aureus metabolic capabilities, our understanding of its systems-level responses to different media types remains incomplete. Here, we develop a manually reconstructed genome-scale model (GEM-PRO) of metabolism with 3D protein structures for S. aureus USA300 str. JE2 containing 854 genes, 1,440 reactions, 1,327 metabolites and 673 3-dimensional protein structures. Computations were in 85% agreement with gene essentiality data from random barcode transposon site sequencing (RB-TnSeq) and 68% agreement with experimental physiological data. Comparisons of computational predictions with experimental observations highlight: 1) cases of non-essential biomass precursors; 2) metabolic genes subject to transcriptional regulation involved in Staphyloxanthin biosynthesis; 3) the essentiality of purine and amino acid biosynthesis in synthetic physiological media; and 4) a switch to aerobic fermentation upon exposure to extracellular glucose elucidated as a result of integrating time-course of quantitative exo-metabolomics data. An up-to-date GEM-PRO thus serves as a knowledge-based platform to elucidate S. aureus' metabolic response to its environment.

Indexed as

Culture MediaStaphylococcus aureusGene Expression Regulation, BacterialGenome, BacterialKnowledge BasesMetabolic Networks and PathwaysMetabolomeMetabolomicsModels, BiologicalSystems BiologyCulture Media

Identifiers

PMID30625152
PMCPMC6326480
OpenAlexW2910511306

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.