Evidence map›Paper›PMID 25487798›Full record

Trial reportAntimicrobial agents and chemotherapy2015

Microbiome changes in healthy volunteers treated with GSK1322322, a novel antibiotic targeting bacterial peptide deformylase.

Seda Arat, Aaron Spivak, Stephanie Van Horn, Elizabeth Thomas, Christopher Traini, Ganesh Sathe, George P Livi, Karen Ingraham, Lori Jones, Kelly Aubart and 3 more

Open access · bronzeAbstract readClinical Trial, Phase IRandomized Controlled Trial
In one paragraph

Trial report in Antimicrobial agents and chemotherapy, 2015. 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
0.6field-weighted citation impact, top 30% 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, 25 citations in OpenAlex.

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

13 authors at 4 institutions in 1 country.

Seda AratComputational Biology, GSK R&D, Collegeville, Pennsylvania, USA Department of Mathematics, Virginia Tech, Blacksburg, Virginia, USA.
Aaron SpivakComputational Biology, GSK R&D, Collegeville, Pennsylvania, USA.
Stephanie Van HornTarget and Pathway Validation, GSK R&D, Collegeville, Pennsylvania, USA.
Elizabeth ThomasTarget and Pathway Validation, GSK R&D, Collegeville, Pennsylvania, USA.
Christopher TrainiTarget and Pathway Validation, GSK R&D, Collegeville, Pennsylvania, USA.
Ganesh SatheTarget and Pathway Validation, GSK R&D, Collegeville, Pennsylvania, USA.
George P LiviTarget and Pathway Validation, GSK R&D, Collegeville, Pennsylvania, USA.
Karen IngrahamAntibacterial Discovery Performance Unit, GSK R&D, Collegeville, Pennsylvania, USA.
Lori JonesAntibacterial Discovery Performance Unit, GSK R&D, Research Triangle Park, North Carolina, USA.
Kelly AubartAntibacterial Discovery Performance Unit, GSK R&D, Collegeville, Pennsylvania, USA.
David J HolmesAntibacterial Discovery Performance Unit, GSK R&D, Collegeville, Pennsylvania, USA.
Odin NadererAntibacterial Discovery Performance Unit, GSK R&D, Research Triangle Park, North Carolina, USA.
James R BrownComputational Biology, GSK R&D, Collegeville, Pennsylvania, USA james.r.brown@gsk.com.
Target (United States) · USGlaxoSmithKline (United States) · USResearch Triangle Park Foundation · USVirginia Tech · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

GSK1322322 is a novel antibacterial agent under development, and it has known antibacterial activities against multidrug-resistant respiratory and skin pathogens through its inhibition of the bacterial peptide deformylase. Here, we used next-generation sequencing (NGS) of the bacterial 16S rRNA genes from stool samples collected from 61 healthy volunteers at the predosing and end-of-study time points to determine the effects of GSK1322322 on the gastrointestinal (GI) microbiota in a phase I, randomized, double-blind, and placebo-controlled study. GSK1322322 was administered either intravenously (i.v.) only or in an oral-i.v. combination in single- and repeat-dose-escalation infusions. Analysis of the 16S rRNA sequence data found no significant changes in the relative abundances of GI operational taxonomic units (OTUs) between the prestudy and end-of-study samples for either the placebo- or i.v.-only-treated subjects. However, oral-i.v. treatment resulted in significant decreases in some bacterial taxa, the Firmicutes and Bacteroidales, and increases in others, the Betaproteobacteria, Gammaproteobacteria, and Bifidobacteriaceae. Microbiome diversity plots clearly differentiated the end-of-study oral-i.v.-dosed samples from all others collected. The changes in genome function as inferred from species composition suggest an increase in bacterial transporter and xenobiotic metabolism pathways in these samples. A phylogenetic analysis of the peptide deformylase protein sequences collected from the published genomes of clinical isolates previously tested for GSK1322322 in vitro susceptibility and GI bacterial reference genomes suggests that antibiotic target homology is one of several factors that influences the response of GI microbiota to this antibiotic. Our study shows that dosing regimen and target class are important factors when considering the impact of antibiotic usage on GI microbiota. (This clinical trial was registered at the GlaxoSmithKline Clinical Study Register under study identifier PDF 113376.).

Indexed as

AmidohydrolasesAnti-Bacterial AgentsBetaproteobacteriaBifidobacteriumBridged Bicyclo Compounds, HeterocyclicDouble-Blind MethodGammaproteobacteriaHealthy VolunteersHigh-Throughput Nucleotide SequencingHumansHydroxamic AcidsMicrobiotaRNA, Ribosomal, 16SAmidohydrolasesAnti-Bacterial AgentsBridged Bicyclo Compounds, HeterocyclicGSK1322322Hydroxamic Acidspeptide deformylaseRNA, Ribosomal, 16S

Identifiers

PMID25487798
PMCPMC4335841
OpenAlexW2147026737

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.