Evidence map›Paper›PMID 29642590›Full record

ArticleViruses2018

Characterizing Phage Genomes for Therapeutic Applications.

Casandra W Philipson, Logan J Voegtly, Matthew R Lueder, Kyle A Long, Gregory K Rice, Kenneth G Frey, Biswajit Biswas, Regina Z Cer, Theron Hamilton, Kimberly A Bishop-Lilly

Open access · goldAbstract readValidation Study
In one paragraph

Article in Viruses, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 106 papers.

0numbers the graph read from it
0cells of the map it votes in
106citing papers in PubMed
14.4field-weighted citation impact, top 1% 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

106 citing papers in PubMed, 177 citations in OpenAlex.

  1. Bacteriophage vB_SalS_KY05 controlsThe veterinary quarterly · 2026
    Article
  2. Escherichia coli bacteriophage vB_EcoS_MS2 effectively prevents biofilm formation but shows limited activity against mature biofilms.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2026
    Article
  3. Article
  4. Article
  5. Bacteriophages AgainstViruses · 2026
    Review
  6. Characterization of a novel phage-plasmid vB_EcoM_ED targeting multidrug-resistant Escherichia coli isolates.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026
    Article
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46 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

10 authors at 2 institutions in 1 country.

Casandra W PhilipsonDefense Threat Reduction Agency, Fort Belvoir, VA 22060, USA. casandra.w.philipson.civ@mail.mil.
Logan J VoegtlyBiological Defense Research Directorate, Naval Medical Research Center, Fort Detrick, MD 21702, USA. logan.j.voegtly.ctr@mail.mil.
Matthew R LuederBiological Defense Research Directorate, Naval Medical Research Center, Fort Detrick, MD 21702, USA. matthew.r.lueder.ctr@mail.mil.
Kyle A LongBiological Defense Research Directorate, Naval Medical Research Center, Fort Detrick, MD 21702, USA. kyle.a.long8.ctr@mail.mil.
Gregory K RiceBiological Defense Research Directorate, Naval Medical Research Center, Fort Detrick, MD 21702, USA. gregory.k.rice.ctr@mail.mil.
Kenneth G FreyBiological Defense Research Directorate, Naval Medical Research Center, Fort Detrick, MD 21702, USA. kenneth.g.frey4.civ@mail.mil.
Biswajit BiswasBiological Defense Research Directorate, Naval Medical Research Center, Fort Detrick, MD 21702, USA. biswajit.biswas.civ@mail.mil.
Regina Z CerBiological Defense Research Directorate, Naval Medical Research Center, Fort Detrick, MD 21702, USA. regina.z.cer.ctr@mail.mil.
Theron HamiltonBiological Defense Research Directorate, Naval Medical Research Center, Fort Detrick, MD 21702, USA. theron.c.hamilton.mil@mail.mil.
Kimberly A Bishop-LillyBiological Defense Research Directorate, Naval Medical Research Center, Fort Detrick, MD 21702, USA. kimberly.a.bishop-lilly.civ@mail.mil.
Leidos (United States) · USNaval Medical Research Command · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multi-drug resistance is increasing at alarming rates. The efficacy of phage therapy, treating bacterial infections with bacteriophages alone or in combination with traditional antibiotics, has been demonstrated in emergency cases in the United States and in other countries, however remains to be approved for wide-spread use in the US. One limiting factor is a lack of guidelines for assessing the genomic safety of phage candidates. We present the phage characterization workflow used by our team to generate data for submitting phages to the Federal Drug Administration (FDA) for authorized use. Essential analysis checkpoints and warnings are detailed for obtaining high-quality genomes, excluding undesirable candidates, rigorously assessing a phage genome for safety and evaluating sequencing contamination. This workflow has been developed in accordance with community standards for high-throughput sequencing of viral genomes as well as principles for ideal phages used for therapy. The feasibility and utility of the pipeline is demonstrated on two new phage genomes that meet all safety criteria. We propose these guidelines as a minimum standard for phages being submitted to the FDA for review as investigational new drug candidates.

Indexed as

BacteriophagesGenome, ViralGenomicsGuidelines as TopicHumansPhage TherapyPhylogenyReproducibility of ResultsWorkflowbest practiceshigh-throughput sequencingINDphage therapyviral genomes

Identifiers

PMID29642590
PMCPMC5923482
OpenAlexW2798058122

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.