Evidence map›Paper›PMID 31170282›Full record

ArticleThe Journal of antimicrobial chemotherapy2019

Adjunctive transferrin to reduce the emergence of antibiotic resistance in Gram-negative bacteria.

Brian M Luna, Ksenia Ershova, Jun Yan, Amber Ulhaq, Travis B Nielsen, Sarah Hsieh, Paul Pantapalangkoor, Brian Vanscoy, Paul Ambrose, Sue Rudin and 5 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of antimicrobial chemotherapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.6field-weighted citation impact, top 41% 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

15 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
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  5. Ceftazidime retainsmSphere · 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

15 authors at 5 institutions in 1 country.

Brian M LunaDepartment of Medicine, Keck School of Medicine at the University of Southern California (USC), Los Angeles, CA, USA.
Ksenia ErshovaDepartment of Medicine, Keck School of Medicine at the University of Southern California (USC), Los Angeles, CA, USA.
Jun YanDepartment of Medicine, Keck School of Medicine at the University of Southern California (USC), Los Angeles, CA, USA.
Amber UlhaqDepartment of Medicine, Keck School of Medicine at the University of Southern California (USC), Los Angeles, CA, USA.
Travis B NielsenDepartment of Medicine, Keck School of Medicine at the University of Southern California (USC), Los Angeles, CA, USA.
Sarah HsiehDepartment of Medicine, Keck School of Medicine at the University of Southern California (USC), Los Angeles, CA, USA.
Paul PantapalangkoorDepartment of Medicine, Keck School of Medicine at the University of Southern California (USC), Los Angeles, CA, USA.
Brian VanscoyInstitute for Clinical Pharmacodynamics, Schenectady, NY, USA.
Paul AmbroseInstitute for Clinical Pharmacodynamics, Schenectady, NY, USA.
Sue RudinLouis Stokes Cleveland Department of Veterans Affairs Medical Center, Cleveland, OH, USA.
Kristine HujerLouis Stokes Cleveland Department of Veterans Affairs Medical Center, Cleveland, OH, USA.
Robert A BonomoLouis Stokes Cleveland Department of Veterans Affairs Medical Center, Cleveland, OH, USA.
Luis ActisDepartment of Microbiology, Miami University, Oxford, OH, USA.
Eric P SkaarDepartment of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN, USA.
Brad SpellbergDepartment of Medicine, Keck School of Medicine at the University of Southern California (USC), Los Angeles, CA, USA.
University of Southern California · USLouis Stokes Cleveland VA Medical Center · USInstitute for Clinical Pharmacodynamics (United States) · USMiami University · USVanderbilt University Medical Center · US

Funding

Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
MAb Passive Vaccination against Acinetobacter baumanniiR01AI130060 · NIAID · UNIVERSITY OF SOUTHERN CALIFORNIA · PI BRAD J SPELLBERG · 2017 to 2026
$6.7M
Understanding B-Lactam Resistance in Acinetobacter baumanniiR01AI072219 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI ROBERT A. BONOMO, Philip N. Rather · 2007 to 2026
$6.6M
Mechanism and function of heme-iron utilization in staphylococcal pathogenesisR01AI069233 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI SKAAR, ERIC P · 2006 to 2020
$5.6M
Transferrin Combination Therapy to Address Antimicrobial ResistanceR01AI117211 · NIAID · UNIVERSITY OF SOUTHERN CALIFORNIA · PI SPELLBERG, BRAD J · 2016 to 2019
$2.7M
Humanized Monoclonal Antibodies to Treat Acinetobacter InfectionsR41AI106375 · NIAID · BIOLOGICAL ANTI-INFECTIVE MEDICINES, LLC · PI SPELLBERG, BRAD J · 2013 to 2014
$574k
Diabetes and Inflammation During InfectionR21AI127954 · NIAID · UNIVERSITY OF SOUTHERN CALIFORNIA · PI SPELLBERG, BRAD J · 2017 to 2018
$454k
NIAID NIH HHS R01 AI069233NIAID NIH HHS R01 AI072219NIAID NIH HHS R01 AI117211NIAID NIH HHS R01 AI130060NIAID NIH HHS R21 AI127954NIAID NIH HHS R41 AI106375NIDDK NIH HHS P30 DK058404
6 · The paper itself

Abstract

backgroundNew strategies are needed to slow the emergence of antibiotic resistance among bacterial pathogens. In particular, society is experiencing a crisis of antibiotic-resistant infections caused by Gram-negative bacterial pathogens and novel therapeutics are desperately needed to combat such diseases. Acquisition of iron from the host is a nearly universal requirement for microbial pathogens-including Gram-negative bacteria-to cause infection. We have previously reported that apo-transferrin (lacking iron) can inhibit the growth of Staphylococcus aureus in culture and diminish emergence of resistance to rifampicin.

objectivesTo define the potential of apo-transferrin to inhibit in vitro growth of Klebsiella pneumoniae and Acinetobacter baumannii, key Gram-negative pathogens, and to reduce emergence of resistance to antibiotics.

methodsThe efficacy of apo-transferrin alone or in combination with meropenem or ciprofloxacin against K. pneumoniae and A. baumannii clinical isolates was tested by MIC assay, time-kill assay and assays for the selection of resistant mutants.

resultsWe confirmed that apo-transferrin had detectable MICs for all strains tested of both pathogens. Apo-transferrin mediated an additive antimicrobial effect for both antibiotics against multiple strains in time-kill assays. Finally, adding apo-transferrin to ciprofloxacin or meropenem reduced the emergence of resistant mutants during 20 day serial passaging of both species.

conclusionsThese results suggest that apo-transferrin may have promise to suppress the emergence of antibiotic-resistant mutants when treating infections caused by Gram-negative bacteria.

Indexed as

Acinetobacter baumanniiAnti-Bacterial AgentsApoproteinsCiprofloxacinDrug Resistance, BacterialGram-Negative BacteriaGram-Negative Bacterial InfectionsHumansKlebsiella pneumoniaeMeropenemMicrobial Sensitivity TestsMutationTransferrinAnti-Bacterial AgentsApoproteinsapotransferrinCiprofloxacinMeropenemTransferrin

Identifiers

PMID31170282
PMCPMC6736376
OpenAlexW2969364911

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.