Evidence map›Paper›PMID 19324528›Full record

ArticleInternational journal of antimicrobial agents2009

sarA inactivation reduces vancomycin-intermediate and ciprofloxacin resistance expression by Staphylococcus aureus.

Reena Lamichhane-Khadka, Stephanie A Cantore, James T Riordan, Alejandro Delgado, Alesha E A Norman, Sarah Dueñas, Shahrear Zaman, Sonia Horan, Brian J Wilkinson, John E Gustafson

Abstract read
In one paragraph

Article in International journal of antimicrobial agents, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  3. Microorganisms · 2025
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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

10 authors at 3 institutions in 1 country.

Reena Lamichhane-KhadkaDepartment of Biology, New Mexico State University, Las Cruces, NM 88003-8001, USA.
Stephanie A Cantore
James T Riordan
Alejandro Delgado
Alesha E A Norman
Sarah Dueñas
Shahrear Zaman
Sonia Horan
Brian J Wilkinson
John E Gustafson
New Mexico State University · USIllinois State University · USLasen (United States) · US

Funding

ZUNI HEALTH INITIATIVE-PILOT STUDYP20RR016480 · NCRR · NEW MEXICO STATE UNIVERSITY LAS CRUCES · PI ZHANG, PENG F · 2001 to 2011
$33.7M
Translational Control in the Hepatitis C VirusS06GM008136 · NIGMS · NEW MEXICO STATE UNIVERSITY LAS CRUCES · PI KUEHN, GLENN D · 1989 to 2011
$23.2M
RISE PROGRAM AT NEW MEXICO STATE UNIVERSITYR25GM061222 · NIGMS · NEW MEXICO STATE UNIVERSITY LAS CRUCES · PI HOUSTON, JESSICA PEREA, REDDI, LAKSHMI · 2000 to 2022
$21.3M
Undergraduate Biomedical Research Training at New Mexico State Univ., Las CrucesT34GM007667 · NIGMS · NEW MEXICO STATE UNIVERSITY LAS CRUCES · PI UNGUEZ, GRACIELA ALEXANDRA · 1985 to 2022
$13.6M
Novel antibiotic resistance mechanisms in S. aureusR15AI054382 · NIAID · NEW MEXICO STATE UNIVERSITY LAS CRUCES · PI GUSTAFSON, JOHN E · 2002 to 2002
$143k
Howard Hughes Medical Institute 52005881NCRR NIH HHS P20 RR016480NCRR NIH HHS P20RR016480NIAID NIH HHS 1R15AI054382-01NIAID NIH HHS R15 AI054382NIGMS NIH HHS R25 GM061222NIGMS NIH HHS R25 GM07667-30NIGMS NIH HHS S06 GM008136NIGMS NIH HHS S06 GM008136-32NIGMS NIH HHS S06 GM61222-05NIGMS NIH HHS T34 GM007667
6 · The paper itself

Abstract

It is known that multiple genome-wide transcriptional changes often accompany the development of antimicrobial resistance and occur in response to challenge with antimicrobial agents. We now show that inactivation of the staphylococcal accessory gene regulator sarA, which controls at least tens of genes in Staphylococcus aureus, leads to dramatic reductions in vancomycin and ciprofloxacin resistance in vancomycin-intermediate and ciprofloxacin-resistant strains of S. aureus. This is particularly evident when judged by antimicrobial-gradient plate analysis or population analysis profiles. Whilst the intact sarA cistron is required for full vancomycin resistance expression by vancomycin-intermediate S. aureus (VISA), sarA expression as determined by quantitative real-time polymerase chain reaction was found to be VISA strain-dependent. Reductions in vancomycin resistance expression levels following sarA inactivation do not necessarily include an alteration in autolysis. Expression of sarR, the negative regulator of sarA, was downregulated in two VISA mutants, and transcription of the alternative sigma factor sigB was downregulated in one VISA strain. This study contributes to a growing body of evidence demonstrating the importance of loci previously identified to control virulence in the regulation of clinically relevant antibiotic resistance mechanisms.

Indexed as

Drug Resistance, BacterialAnti-Bacterial AgentsBacterial ProteinsCiprofloxacinGene DeletionGene Expression ProfilingGene Expression Regulation, BacterialMicrobial Sensitivity TestsStaphylococcus aureusVancomycinVancomycin ResistanceAnti-Bacterial AgentsBacterial ProteinsCiprofloxacinSarA protein, Staphylococcus aureusVancomycin

Identifiers

PMID19324528
PMCPMC3831611
OpenAlexW2029527849

What OpenQuestion holds

Textmetadata
LicenceTDM
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.