Evidence map›Paper›PMID 25547798›Full record

ArticleInfection and immunity2015

Role of BrnQ1 and BrnQ2 in branched-chain amino acid transport and virulence in Staphylococcus aureus.

Julienne C Kaiser, Sameha Omer, Jessica R Sheldon, Ian Welch, David E Heinrichs

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

40 citing papers in PubMed, 48 citations in OpenAlex.

  1. InJournal of bacteriology · 2026
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  4. InbioRxiv : the preprint server for biology · 2026
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  18. Mutations in a Membrane Permease orAntimicrobial agents and chemotherapy · 2021
    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

5 authors at 1 institution in 1 country.

Julienne C KaiserDepartment of Microbiology and Immunology, University of Western Ontario, London, Ontario, Canada.
Sameha OmerDepartment of Microbiology and Immunology, University of Western Ontario, London, Ontario, Canada.
Jessica R SheldonDepartment of Microbiology and Immunology, University of Western Ontario, London, Ontario, Canada.
Ian WelchDepartment of Animal Care and Veterinary Services, University of Western Ontario, London, Ontario, Canada.
David E HeinrichsDepartment of Microbiology and Immunology, University of Western Ontario, London, Ontario, Canada Centre for Human Immunology, University of Western Ontario, London, Ontario, Canada deh@uwo.ca.
Western University · CA

Funding

Canadian Institutes of Health Research MOP-38002
6 · The paper itself

Abstract

The branched-chain amino acids (BCAAs; Ile, Leu, and Val) not only are important nutrients for the growth of Staphylococcus aureus but also are corepressors for CodY, which regulates virulence gene expression, implicating BCAAs as an important link between the metabolic state of the cell and virulence. BCAAs are either synthesized intracellularly or acquired from the environment. S. aureus encodes three putative BCAA transporters, designated BrnQ1, BrnQ2, and BrnQ3; their functions have not yet been formally tested. In this study, we mutated all three brnQ paralogs so as to characterize their substrate specificities and their roles in growth in vitro and in vivo. We demonstrated that in the community-associated, methicillin-resistant S. aureus (CA-MRSA) strain USA300, BrnQ1 is involved in uptake of all three BCAAs, BrnQ2 transports Ile, and BrnQ3 does not have a significant role in BCAA transport under the conditions tested. Of the three, only BrnQ1 is essential for USA300 to grow in a chemically defined medium that is limited for Leu or Val. Interestingly, we observed that a brnQ2 mutant grew better than USA300 in media limited for Leu and Val, owing to the fact that this mutation leads to overexpression of brnQ1. In a murine infection model, the brnQ1 mutant was attenuated, but in contrast, brnQ2 mutants had significantly increased virulence compared to that of USA300, a phenotype we suggest is at least partially linked to enhanced in vivo scavenging of Leu and Val through BrnQ1. These data uncover a hitherto-undiscovered connection between nutrient acquisition and virulence in CA-MRSA.

Indexed as

Gene Expression Regulation, BacterialAnimalsBacterial ProteinsBiological TransportCarrier ProteinsCulture MediaHumansIsoleucineKidneyKineticsLeucineLiverMethicillin-Resistant Staphylococcus aureusMiceMice, Inbred BALB CMutationBacterial ProteinsCarrier ProteinsCodY protein, Staphylococcus aureusCulture MediaIsoleucineLeucineRepressor ProteinsValine

Identifiers

PMID25547798
PMCPMC4333469
OpenAlexW2163837366

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.