Evidence map›Paper›PMID 24865555›Full record

ArticlemBio2014

AB5075, a Highly Virulent Isolate of Acinetobacter baumannii, as a Model Strain for the Evaluation of Pathogenesis and Antimicrobial Treatments.

Anna C Jacobs, Mitchell G Thompson, Chad C Black, Jennifer L Kessler, Lily P Clark, Christin N McQueary, Hanan Y Gancz, Brendan W Corey, Jay K Moon, Yuanzheng Si and 16 more

Open access · goldAbstract read
In one paragraph

Article in mBio, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 243 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
243citing papers in PubMed, 1 pooled it
6.5field-weighted citation impact, top 2% 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

243 citing papers in PubMed, 1 synthesis or guideline pooled it, 334 citations in OpenAlex.

  1. Pooled it
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  17. Characterization of the role of putativeJournal of bacteriology · 2026
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183 more citing papers are in PubMed but not listed here.

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

26 authors at 4 institutions in 1 country.

Anna C JacobsDepartment of Wound Infections, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Mitchell G ThompsonDepartment of Wound Infections, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Chad C BlackDepartment of Wound Infections, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Jennifer L KesslerDepartment of Wound Infections, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Lily P ClarkDepartment of Wound Infections, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Christin N McQuearyDepartment of Wound Infections, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Hanan Y GanczDepartment of Wound Infections, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Brendan W CoreyDepartment of Wound Infections, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Jay K MoonDepartment of Wound Infections, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Yuanzheng SiDepartment of Wound Infections, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Matthew T OwenDivision of Orthopaedics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Justin D HallockDivision of Orthopaedics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Yoon I KwakMultidrug-resistant Organism and Surveillance Network, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Amy SummersDepartment of Wound Infections, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Charles Z LiDepartment of Wound Infections, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
David A RaskoInstitute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland, USA.
William F PenwellDepartment of Microbiology, Miami University, Oxford, Ohio, USA.
Cary L HonnoldDepartment of Pathology, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Matthew C WiseDepartment of Pathology, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Paige E WatermanMultidrug-resistant Organism and Surveillance Network, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Emil P LeshoMultidrug-resistant Organism and Surveillance Network, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Rena L StewartDivision of Orthopaedics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Luis A ActisDepartment of Microbiology, Miami University, Oxford, Ohio, USA.
Thomas J PalysDepartment of Wound Infections, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
David W CraftDepartment of Wound Infections, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Daniel V ZurawskiDepartment of Wound Infections, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA daniel.v.zurawski.ctr@mail.mil.
Walter Reed Army Institute of Research · USUniversity of Alabama at Birmingham · USMiami University · USUniversity of Maryland, Baltimore · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledAcinetobacter baumannii is recognized as an emerging bacterial pathogen because of traits such as prolonged survival in a desiccated state, effective nosocomial transmission, and an inherent ability to acquire antibiotic resistance genes. A pressing need in the field of A. baumannii research is a suitable model strain that is representative of current clinical isolates, is highly virulent in established animal models, and can be genetically manipulated. To identify a suitable strain, a genetically diverse set of recent U.S. military clinical isolates was assessed. Pulsed-field gel electrophoresis and multiplex PCR determined the genetic diversity of 33 A. baumannii isolates. Subsequently, five representative isolates were tested in murine pulmonary and Galleria mellonella models of infection. Infections with one strain, AB5075, were considerably more severe in both animal models than those with other isolates, as there was a significant decrease in survival rates. AB5075 also caused osteomyelitis in a rat open fracture model, while another isolate did not. Additionally, a Tn5 transposon library was successfully generated in AB5075, and the insertion of exogenous genes into the AB5075 chromosome via Tn7 was completed, suggesting that this isolate may be genetically amenable for research purposes. Finally, proof-of-concept experiments with the antibiotic rifampin showed that this strain can be used in animal models to assess therapies under numerous parameters, including survival rates and lung bacterial burden. We propose that AB5075 can serve as a model strain for A. baumannii pathogenesis due to its relatively recent isolation, multidrug resistance, reproducible virulence in animal models, and genetic tractability. IMPORTANCE: The incidence of A. baumannii infections has increased over the last decade, and unfortunately, so has antibiotic resistance in this bacterial species. A. baumannii is now responsible for more than 10% of all hospital-acquired infections in the United States and has a >50% mortality rate in patients with sepsis and pneumonia. Most research on the pathogenicity of A. baumannii focused on isolates that are not truly representative of current multidrug-resistant strains isolated from patients. After screening of a panel of isolates in different in vitro and in vivo assays, the strain AB5075 was selected as more suitable for research because of its antibiotic resistance profile and increased virulence in animal models. Moreover, AB5075 is susceptible to tetracycline and hygromycin, which makes it amenable to genetic manipulation. Taken together, these traits make AB5075 a good candidate for use in studying virulence and pathogenicity of this species and testing novel antimicrobials.

Indexed as

Acinetobacter baumanniiAcinetobacter InfectionsAnimalsAnti-Infective AgentsDisease Models, AnimalElectrophoresis, Gel, Pulsed-FieldFemaleGenome, BacterialMiceMothsPhylogenyRifampinVirulenceAnti-Infective AgentsRifampin

Identifiers

PMID24865555
PMCPMC4045072
OpenAlexW2102749349

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.