iCN718, an updated and improved genome-scale metabolic network reconstruction of Acinetobacter baumannii AYE

Charles J. Norsigian, Erol Kavvas, Yara Seif, Bernhard O. Palsson, Jonathan M. Monk

Research output: Contribution to journalArticlepeer-review

Abstract

Acinetobacter baumannii has become an urgent clinical threat due to the recent emergence of multi-drug resistant strains. There is thus a significant need to discover new therapeutic targets in this organism. One means for doing so is through the use of high-quality genome-scale reconstructions. Well-curated and accurate genome-scale models (GEMs) of A. baumannii would be useful for improving treatment options. We present an updated and improved genome-scale reconstruction of A. baumannii AYE, named iCN718, that improves and standardizes previous A. baumannii AYE reconstructions. iCN718 has 80% accuracy for predicting gene essentiality data and additionally can predict large-scale phenotypic data with as much as 89% accuracy, a new capability for an A. baumannii reconstruction. We further demonstrate that iCN718 can be used to analyze conserved metabolic functions in the A. baumannii core genome and to build strain-specific GEMs of 74 other A. baumannii strains from genome sequence alone. iCN718 will serve as a resource to integrate and synthesize new experimental data being generated for this urgent threat pathogen.

Original languageEnglish
Article number121
JournalFrontiers in Genetics
Volume9
Issue numberAPR
DOIs
Publication statusPublished - 10 Apr 2018

Bibliographical note

Funding Information: We thank J. T. Yurkovich for critical comments on the manuscript. This work was supported by the NIH Grant: 1-U01-AI124316-01 Publisher Copyright: © 2018 Norsigian, Kavvas, Seif, Palsson and Monk.

Other keywords

  • Acinetobacter baumannii
  • Antibiotic resistance
  • Constraint-based modeling
  • Genome-scale reconstruction
  • Metabolism

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