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Integrated evolutionary analysis reveals antimicrobial peptides with limited resistance.
Spohn, Réka; Daruka, Lejla; Lázár, Viktória; Martins, Ana; Vidovics, Fanni; Grézal, Gábor; Méhi, Orsolya; Kintses, Bálint; Számel, Mónika; Jangir, Pramod K; Csörgo, Bálint; Györkei, Ádám; Bódi, Zoltán; Faragó, Anikó; Bodai, László; Földesi, Imre; Kata, Diána; Maróti, Gergely; Pap, Bernadett; Wirth, Roland; Papp, Balázs; Pál, Csaba.
Afiliação
  • Spohn R; Synthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
  • Daruka L; Synthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
  • Lázár V; Doctoral School of Biology, Faculty of Science and Informatics, University of Szeged, Szeged, Hungary.
  • Martins A; Synthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
  • Vidovics F; Faculty of Biology, Technion - Israel Institute of Technology, Haifa, Israel.
  • Grézal G; Synthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
  • Méhi O; Synthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
  • Kintses B; Synthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
  • Számel M; HCEMM-BRC Metabolic Systems Biology Lab, Szeged, Hungary.
  • Jangir PK; Synthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
  • Csörgo B; Synthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
  • Györkei Á; Department of Biochemistry and Molecular Biology, University of Szeged, Szeged, Hungary.
  • Bódi Z; Synthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
  • Faragó A; Doctoral School of Biology, Faculty of Science and Informatics, University of Szeged, Szeged, Hungary.
  • Bodai L; Synthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
  • Földesi I; Doctoral School of Biology, Faculty of Science and Informatics, University of Szeged, Szeged, Hungary.
  • Kata D; Synthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
  • Maróti G; University of California, San Francisco, Department of Microbiology and Immunology, San Francisco, CA, USA.
  • Pap B; Synthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
  • Wirth R; HCEMM-BRC Metabolic Systems Biology Lab, Szeged, Hungary.
  • Papp B; Synthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Centre, Szeged, Hungary.
  • Pál C; Doctoral School of Biology, Faculty of Science and Informatics, University of Szeged, Szeged, Hungary.
Nat Commun ; 10(1): 4538, 2019 10 04.
Article em En | MEDLINE | ID: mdl-31586049
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Genoma Bacteriano / Peptídeos Catiônicos Antimicrobianos / Farmacorresistência Bacteriana Múltipla / Anti-Infecciosos Limite: Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Hungria País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Genoma Bacteriano / Peptídeos Catiônicos Antimicrobianos / Farmacorresistência Bacteriana Múltipla / Anti-Infecciosos Limite: Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Hungria País de publicação: Reino Unido