Evidence map›Paper›PMID 32291307›Full record

ArticlemBio2020

Romo1-Derived Antimicrobial Peptide Is a New Antimicrobial Agent against Multidrug-Resistant Bacteria in a Murine Model of Sepsis.

Hye-Ra Lee, Deok-Gyun You, Hong Kyu Kim, Jang Wook Sohn, Min Ja Kim, Jong Kuk Park, Gi Young Lee, Young Do Yoo

Open access · goldAbstract read
In one paragraph

Article in mBio, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

23 citing papers in PubMed, 54 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Anti-inflammatory effect of ApoE23 onOpen medicine (Warsaw, Poland) · 2023
    Article
  10. A Novel Antimicrobial Peptide SpampcinInternational journal of molecular sciences · 2022
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. New Scabimycins A-C Isolated fromMolecules (Basel, Switzerland) · 2021
    Article
  18. Antimicrobial Peptides: A Potent Alternative to Antibiotics.Antibiotics (Basel, Switzerland) · 2021
    Review
  19. Article
  20. Article
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

8 authors at 3 institutions in 1 country.

Hye-Ra LeeLaboratory of Molecular Cell Biology, Graduate School of Medicines, Korea University College of Medicine, Korea University, Seoul, Republic of Korea.
Deok-Gyun YouLaboratory of Molecular Cell Biology, Graduate School of Medicines, Korea University College of Medicine, Korea University, Seoul, Republic of Korea.
Hong Kyu KimDepartment of Surgery, Seoul National University College of Medicine, Seoul, Republic of Korea.
Jang Wook SohnDivision of Infectious Diseases, Department of Internal Medicine, Korea University College of Medicine, Seoul, Republic of Korea.
Min Ja KimDivision of Infectious Diseases, Department of Internal Medicine, Korea University College of Medicine, Seoul, Republic of Korea.ORCID 0000-0002-2125-7521
Jong Kuk ParkDivision of Radiation Biomedical Research, Korea Institute of Radiological and Medical Sciences, Seoul, Republic of Korea.
Gi Young LeeLaboratory of Molecular Cell Biology, Graduate School of Medicines, Korea University College of Medicine, Korea University, Seoul, Republic of Korea gylative@gmail.com ydy1130@korea.ac.kr.
Young Do YooLaboratory of Molecular Cell Biology, Graduate School of Medicines, Korea University College of Medicine, Korea University, Seoul, Republic of Korea gylative@gmail.com ydy1130@korea.ac.kr.
Korea University · KRKorea Institute of Radiological and Medical Sciences · KRSeoul National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To overcome increasing bacterial resistance to conventional antibiotics, many antimicrobial peptides (AMPs) derived from host defense proteins have been developed. However, there are considerable obstacles to their application to systemic infections because of their low bioavailability. In the present study, we developed an AMP derived from Romo1 (AMPR-11) that exhibits a broad spectrum of antimicrobial activity. AMPR-11 showed remarkable efficacy against sepsis-causing bacteria, including multidrug-resistant strains, with low toxicity in a murine model of sepsis after intravenous administration. It seems that AMPR-11 disrupts bacterial membranes by interacting with cardiolipin and lipid A. From the results of this study, we suggest that AMPR-11 is a new class of agent for overcoming low efficacy in the intravenous application of AMPs and is a promising candidate to overcome multidrug resistance.

Indexed as

Drug Resistance, Multiple, BacterialAdministration, IntravenousAnimalsAnti-Infective AgentsAntimicrobial Cationic PeptidesBacteriaBacterial Outer MembraneBiofilmsDisease Models, AnimalHeLa CellsHumansMaleMembrane ProteinsMiceMice, Inbred C57BLMicrobial Sensitivity TestsAnti-Infective AgentsAntimicrobial Cationic PeptidesMembrane ProteinsMitochondrial ProteinsROMO1 protein, humanAMPR-11antimicrobial peptidedrug resistancemultidrug-resistant bacteriapeptide antibioticssepsis

Identifiers

PMID32291307
PMCPMC7157825
OpenAlexW3015617138

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.