Evidence map›Paper›PMID 31586049›Full record

ArticleNature communications2019

Integrated evolutionary analysis reveals antimicrobial peptides with limited resistance.

Réka Spohn, Lejla Daruka, Viktória Lázár, Ana Martins, Fanni Vidovics, Gábor Grézal, Orsolya Méhi, Bálint Kintses, Mónika Számel, Pramod K Jangir and 12 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 186 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
186citing papers in PubMed, 2 pooled it
25.3field-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

186 citing papers in PubMed, 2 syntheses or guidelines pooled it, 337 citations in OpenAlex.

  1. Pooled it
  2. BioprospectingFrontiers in fungal biology · 2021
    Pooled it
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Adaptive Response ofAntibiotics (Basel, Switzerland) · 2026
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Antimicrobial Potential of Defensin-DerivedInternational journal of molecular sciences · 2026
    Article
  18. Article
  19. Article
  20. Article

126 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

22 authors at 4 institutions in 3 countries.

Réka SpohnSynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
Lejla DarukaSynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
Viktória LázárSynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
Ana MartinsSynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
Fanni VidovicsSynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
Gábor GrézalSynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.ORCID http://orcid.org/0000-0003-1685-4791
Orsolya MéhiSynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
Bálint KintsesSynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
Mónika SzámelSynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
Pramod K JangirSynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
Bálint CsörgőSynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
Ádám GyörkeiSynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
Zoltán BódiSynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
Anikó FaragóDoctoral School of Biology, Faculty of Science and Informatics, University of Szeged, Szeged, Hungary.
László BodaiDepartment of Biochemistry and Molecular Biology, University of Szeged, Szeged, Hungary.ORCID http://orcid.org/0000-0001-8411-626X
Imre FöldesiDepartment of Laboratory Medicine, University of Szeged, Szeged, Hungary.
Diána KataDepartment of Laboratory Medicine, University of Szeged, Szeged, Hungary.
Gergely MarótiInstitute of Plant Biology, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary.
Bernadett PapInstitute of Plant Biology, Biological Research Centre, Hungarian Academy of Sciences, Szeged, Hungary.
Roland WirthDepartment of Biotechnology, University of Szeged, Szeged, Hungary.
Balázs PappSynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
Csaba PálSynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary. cpal@brc.hu.ORCID http://orcid.org/0000-0002-5187-9903
HUN-REN Szegedi Biológiai Kutatóközpont · HUUniversity of Szeged · HUTechnion – Israel Institute of Technology · ILUniversity of California, San Francisco · US

Funding

Wellcome Trust
6 · The paper itself

Abstract

Antimicrobial peptides (AMPs) are promising antimicrobials, however, the potential of bacterial resistance is a major concern. Here we systematically study the evolution of resistance to 14 chemically diverse AMPs and 12 antibiotics in Escherichia coli. Our work indicates that evolution of resistance against certain AMPs, such as tachyplesin II and cecropin P1, is limited. Resistance level provided by point mutations and gene amplification is very low and antibiotic-resistant bacteria display no cross-resistance to these AMPs. Moreover, genomic fragments derived from a wide range of soil bacteria confer no detectable resistance against these AMPs when introduced into native host bacteria on plasmids. We have found that simple physicochemical features dictate bacterial propensity to evolve resistance against AMPs. Our work could serve as a promising source for the development of new AMP-based therapeutics less prone to resistance, a feature necessary to avoid any possible interference with our innate immune system.

Indexed as

Anti-Infective AgentsAntimicrobial Cationic PeptidesBacteriaBacterial InfectionsDirected Molecular EvolutionDrug DevelopmentDrug Resistance, Multiple, BacterialGenome, BacterialHumansMetagenomicsMicrobial Sensitivity TestsPlasmidsPoint MutationSoil MicrobiologyAnti-Infective AgentsAntimicrobial Cationic Peptides

Identifiers

PMID31586049
PMCPMC6778101
OpenAlexW2979238556

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.