Evidence map›Paper›PMID 27375107›Full record

ReviewCurrent opinion in microbiology2016

Antisense antimicrobial therapeutics.

Erin K Sully, Bruce L Geller

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in microbiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
8.9field-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

55 citing papers in PubMed, 122 citations in OpenAlex.

  1. Oligonucleotide genetics forbioRxiv : the preprint server for biology · 2026
    Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. High-Throughput Tiling of Essential mRNAs Increases Potency of Antisense Antibiotics.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  7. Review
  8. Article
  9. Parallel and Automated PNA Synthesis in μSPOT Format.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  10. Chemical strategies for antisense antibiotics.Chemical Society reviews · 2024
    Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

2 authors at 1 institution in 1 country.

Erin K SullyDepartment of Microbiology, 226 Nash Hall, Oregon State University, Corvallis, OR 97331-3804, USA.
Bruce L GellerDepartment of Microbiology, 226 Nash Hall, Oregon State University, Corvallis, OR 97331-3804, USA. Electronic address: gellerb@oregonstate.edu.
Oregon State University · US

Funding

Circumventing Antibiotic Resistance with Novel Gene-Silencing TherapeuticsR33AI111753 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI GELLER, BRUCE L, GREENBERG, DAVID ELIHU · 2016 to 2018
$1.4M
Novel gene-silencing therapeutics for multidrug-resistant gram-negative pathogensR33AI098724 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI GREENBERG, DAVID ELIHU · 2014 to 2016
$1.1M
Gene silencing therapeutics for chronic infections in cystic fibrosisR33AI105980 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI GREENBERG, DAVID ELIHU · 2015 to 2017
$1.1M
Gene silencing therapeutics for chronic infections in cystic fibrosisR21AI105980 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI GREENBERG, DAVID ELIHU · 2013 to 2014
$416k
Circumventing Antibiotic Resistance with Novel Gene-Silencing TherapeuticsR21AI111753 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI GELLER, BRUCE L, GREENBERG, DAVID ELIHU · 2014 to 2015
$415k
Novel gene-silencing therapeutics for multidrug-resistant gram-negative pathogensR21AI098724 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI GREENBERG, DAVID ELIHU · 2012 to 2013
$354k
NIAID NIH HHS R21 AI098724NIAID NIH HHS R21 AI105980NIAID NIH HHS R21 AI111753NIAID NIH HHS R33 AI098724NIAID NIH HHS R33 AI105980NIAID NIH HHS R33 AI111753
6 · The paper itself

Abstract

Antisense antimicrobial therapeutics are synthetic oligomers that silence expression of specific genes. This specificity confers an advantage over broad-spectrum antibiotics by avoiding unintended effects on commensal bacteria. The sequence-specificity and short length of antisense antimicrobials also pose little risk to human gene expression. Because antisense antimicrobials are a platform technology, they can be rapidly designed and synthesized to target almost any microbe. This reduces drug discovery time, and provides flexibility and a rational approach to drug development. Recent work has shown that antisense technology has the potential to address the antibiotic-resistance crisis, since resistance mechanisms for standard antibiotics apparently have no effect on antisense antimicrobials. Here, we describe current reports of antisense antimicrobials targeted against viruses, parasites, and bacteria.

Indexed as

AnimalsAnti-Bacterial AgentsAntiviral AgentsBacteriaBacterial InfectionsDrug DiscoveryOligodeoxyribonucleotides, AntisenseOligoribonucleotides, AntisenseParasitesParasitic DiseasesPhosphorothioate OligonucleotidesVirus DiseasesVirusesAnti-Bacterial AgentsAntiviral AgentsOligodeoxyribonucleotides, AntisenseOligoribonucleotides, AntisensePhosphorothioate Oligonucleotides

Identifiers

PMID27375107
PMCPMC5069135
OpenAlexW2462548304

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.