Evidence map›Paper›PMID 31723175›Full record

ArticleScientific reports2019

Development of a Staphylococcus aureus reporter strain with click beetle red luciferase for enhanced in vivo imaging of experimental bacteremia and mixed infections.

Robert J Miller, Heidi A Crosby, Katrin Schilcher, Yu Wang, Roger V Ortines, Momina Mazhar, Dustin A Dikeman, Bret L Pinsker, Isabelle D Brown, Daniel P Joyce and 12 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

32 citing papers in PubMed, 42 citations in OpenAlex.

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  20. Evaluating the Targeting of aInternational journal of molecular sciences · 2023
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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

22 authors at 4 institutions in 1 country.

Robert J MillerDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Heidi A CrosbyDepartment of Immunology & Microbiology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, 80045, USA.
Katrin SchilcherDepartment of Immunology & Microbiology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, 80045, USA.
Yu WangDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Roger V OrtinesDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Momina MazharDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Dustin A DikemanDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Bret L PinskerDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Isabelle D BrownDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Daniel P JoyceDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Jeffrey ZhangDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Nathan K ArcherDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.ORCID http://orcid.org/0000-0002-8212-8985
Haiyun LiuDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Martin P AlphonseDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.ORCID http://orcid.org/0000-0003-3447-1284
Julie CzuprynaPerkinElmer, Hopkinton, Massachusetts, USA.
William R AndersonPerkinElmer, Hopkinton, Massachusetts, USA.
Nicholas M BernthalDepartment of Orthopaedic Surgery, David Geffen School of Medicine at UCLA, Santa Monica, California, USA.
Lea Fortuno-MirandaRussell H. Morgan Department of Radiology and Radiological Science, Division of MR Research, Johns Hopkins University School of Medicine, Baltimore, Maryland, 21205, USA.
Jeff W M BulteRussell H. Morgan Department of Radiology and Radiological Science, Division of MR Research, Johns Hopkins University School of Medicine, Baltimore, Maryland, 21205, USA.
Kevin P FrancisPerkinElmer, Hopkinton, Massachusetts, USA.
Alexander R HorswillDepartment of Immunology & Microbiology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, 80045, USA.ORCID http://orcid.org/0000-0002-5568-0096
Lloyd S MillerDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA. lloydmiller@jhmi.edu.ORCID http://orcid.org/0000-0002-8332-2210
Johns Hopkins University · USPerkinElmer (United States) · USUniversity of Colorado Anschutz Medical Campus · USDenver VA Medical Center · US

Funding

IL-36 responses in Staphylococcus aureus driven skin inflammationR01AR073665 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI ARCHER, NATHAN K. · 2018 to 2022
$1.8M
STAT3-mediated immunity to Staphylococcus aureus in skinR01AR069502 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI ARCHER, NATHAN K. · 2016 to 2020
$1.8M
Combined Optical/Micro-CT ScannerS10OD010744 · OD · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI BULTE, JEFF W. · 2012 to 2012
$599k
Quorum Sensing Dependent Interactions with Biofilms and Innate Immunity DefensesI01BX002711 · VA · VA EASTERN COLORADO HEALTH CARE SYSTEM · PI ALEXANDER R HORSWILL · 2015 to 2026
–
BLRD VA I01 BX002711NIAMS NIH HHS R01 AR069502NIAMS NIH HHS R01 AR073665NIH HHS S10 OD010744
6 · The paper itself

Abstract

In vivo bioluminescence imaging has been used to monitor Staphylococcus aureus infections in preclinical models by employing bacterial reporter strains possessing a modified lux operon from Photorhabdus luminescens. However, the relatively short emission wavelength of lux (peak 490 nm) has limited tissue penetration. To overcome this limitation, the gene for the click beetle (Pyrophorus plagiophtalamus) red luciferase (luc) (with a longer >600 emission wavelength), was introduced singly and in combination with the lux operon into a methicillin-resistant S. aureus strain. After administration of the substrate D-luciferin, the luc bioluminescent signal was substantially greater than the lux signal in vitro. The luc signal had enhanced tissue penetration and improved anatomical co-registration with infected internal organs compared with the lux signal in a mouse model of S. aureus bacteremia with a sensitivity of approximately 3 × 10

Indexed as

AnimalsBacteremiaCoinfectionColeopteraDiagnostic ImagingFemaleGenes, ReporterLuciferasesLuminescent MeasurementsMaleMiceMice, Inbred C57BLPseudomonas aeruginosaPseudomonas InfectionsRabbitsStaphylococcal InfectionsLuciferases

Identifiers

PMID31723175
PMCPMC6853927
OpenAlexW2987375379

What OpenQuestion holds

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LicenceCC BY
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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.