Evidence map›Paper›PMID 34516248›Full record

ArticleAntimicrobial agents and chemotherapy2021

Simultaneous Exposure to Intracellular and Extracellular Photosensitizers for the Treatment of Staphylococcus aureus Infections.

Sydney L Drury, Anderson R Miller, Clare L Laut, Alec B Walter, Monique R Bennett, Meng Su, Mingfeng Bai, Bingwen Jing, Scott B Joseph, Edward J Metzger and 11 more

Open access · greenAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
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

21 authors at 3 institutions in 1 country.

Sydney L Drury *Department of Pathology, Microbiology and Immunology, Vanderbilt Universitygrid.152326.1grid.412807.8grid.152326.1grid.412807.8 Medical Center, Nashville, Tennessee, USA.
Anderson R Miller *Department of Pathology, Microbiology and Immunology, Vanderbilt Universitygrid.152326.1grid.412807.8grid.152326.1grid.412807.8 Medical Center, Nashville, Tennessee, USA.
Clare L LautDepartment of Pathology, Microbiology and Immunology, Vanderbilt Universitygrid.152326.1grid.412807.8grid.152326.1grid.412807.8 Medical Center, Nashville, Tennessee, USA.
Alec B WalterDepartment of Biomedical Engineering, Vanderbilt Universitygrid.152326.1grid.412807.8grid.152326.1grid.412807.8, Nashville, Tennessee, USA.
Monique R BennettDepartment of Pathology, Microbiology and Immunology, Vanderbilt Universitygrid.152326.1grid.412807.8grid.152326.1grid.412807.8 Medical Center, Nashville, Tennessee, USA.
Meng SuVanderbilt University Institute of Imaging Science, Vanderbilt Universitygrid.152326.1grid.412807.8grid.152326.1grid.412807.8Vanderbilt University Institute of Imaging Science, grid.152326.1grid.412807.8grid.152326.1grid.412807.8, Nashville, Tennessee, USA.
Mingfeng BaiVanderbilt University Institute of Imaging Science, Vanderbilt Universitygrid.152326.1grid.412807.8grid.152326.1grid.412807.8Vanderbilt University Institute of Imaging Science, grid.152326.1grid.412807.8grid.152326.1grid.412807.8, Nashville, Tennessee, USA.
Bingwen JingWalter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Scott B JosephWalter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Edward J MetzgerWalter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Charles E BaneWalter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Chad C BlackWalter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Mary T MacdonaldWalter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Brendan F DutterDepartment of Chemical Biology, Vanderbilt Universitygrid.152326.1grid.412807.8grid.152326.1grid.412807.8, Nashville, Tennessee, USA.
Ian M RomaineDepartment of Chemical Biology, Vanderbilt Universitygrid.152326.1grid.412807.8grid.152326.1grid.412807.8, Nashville, Tennessee, USA.
Alex G WatersonDepartment of Chemical Biology, Vanderbilt Universitygrid.152326.1grid.412807.8grid.152326.1grid.412807.8, Nashville, Tennessee, USA.
Gary A SulikowskiDepartment of Chemical Biology, Vanderbilt Universitygrid.152326.1grid.412807.8grid.152326.1grid.412807.8, Nashville, Tennessee, USA.
E Duco JansenDepartment of Biomedical Engineering, Vanderbilt Universitygrid.152326.1grid.412807.8grid.152326.1grid.412807.8, Nashville, Tennessee, USA.
James E CroweDepartment of Pathology, Microbiology and Immunology, Vanderbilt Universitygrid.152326.1grid.412807.8grid.152326.1grid.412807.8 Medical Center, Nashville, Tennessee, USA.ORCID 0000-0002-0049-1079
Richard J SciottiWalter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Eric P SkaarDepartment of Pathology, Microbiology and Immunology, Vanderbilt Universitygrid.152326.1grid.412807.8grid.152326.1grid.412807.8 Medical Center, Nashville, Tennessee, USA.ORCID 0000-0001-5094-8105
Vanderbilt University · USWalter Reed Army Institute of Research · USVanderbilt University Medical Center · US

Funding

Chemistry-Biology Interface Training GrantT32GM065086 · NIGMS · VANDERBILT UNIVERSITY · PI BACHMANN, BRIAN O, SULIKOWSKI, GARY ALLEN · 2002 to 2022
$7.0M
Mechanism and function of heme-iron utilization in staphylococcal pathogenesisR01AI069233 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI SKAAR, ERIC P · 2006 to 2020
$5.6M
HHS | National Institutes of Health (NIH) R0169233HHS | National Institutes of Health (NIH) T32GM065086NIAID NIH HHS R01 AI069233NIGMS NIH HHS T32 GM065086U.S. Department of Defense (DOD) W81XWH-17-2-0003
6 · The paper itself

Abstract

Staphylococcus aureus is a serious threat to public health due to the rise of antibiotic resistance in this organism, which can prolong or exacerbate skin and soft tissue infections (SSTIs). Methicillin-resistant S. aureus is a Gram-positive bacterium and a leading cause of SSTIs. As such, many efforts are under way to develop therapies that target essential biological processes in S. aureus. Antimicrobial photodynamic therapy is an effective alternative to antibiotics; therefore we developed an approach to simultaneously expose S. aureus to intracellular and extracellular photosensitizers. A near infrared photosensitizer was conjugated to human monoclonal antibodies (MAbs) that target the S. aureus iron-regulated surface determinant (Isd) heme acquisition proteins. In addition, the compound VU0038882 was developed to increase photoactivatable porphyrins within the cell. Combinatorial photodynamic treatment of drug-resistant S. aureus exposed to VU0038882 and conjugated anti-Isd MAbs proved to be an effective antibacterial strategy

Indexed as

Methicillin-Resistant Staphylococcus aureusSoft Tissue InfectionsStaphylococcal InfectionsAnimalsAnti-Bacterial AgentsHumansMicePhotosensitizing AgentsStaphylococcus aureusAnti-Bacterial AgentsPhotosensitizing Agentsantibodiesantimicrobial photodynamic therapyiron-regulated surface determinant systemphotosensitizersmall moleculesStaphylococcus aureus

Identifiers

PMID34516248
PMCPMC8597735
OpenAlexW3199952541

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.