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10.3390/biom11050745

http://scihub22266oqcxt.onion/10.3390/biom11050745
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34067685!8156702!34067685
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suck abstract from ncbi


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pmid34067685      Biomolecules 2021 ; 11 (5): ä
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  • Antimicrobial Activity of Cyclic-Monomeric and Dimeric Derivatives of the Snail-Derived Peptide Cm-p5 against Viral and Multidrug-Resistant Bacterial Strains #MMPMID34067685
  • Gonzalez-Garcia M; Morales-Vicente F; Pico ED; Garay H; Rivera DG; Grieshober M; Raluca Olari L; Gross R; Conzelmann C; Kruger F; Zech F; Prelli Bozzo C; Muller JA; Zelikin A; Raber H; Kubiczek D; Rosenau F; Munch J; Stenger S; Spellerberg B; Franco OL; Rodriguez Alfonso AA; Standker L; Otero-Gonzalez AJ
  • Biomolecules 2021[May]; 11 (5): ä PMID34067685show ga
  • Cm-p5 is a snail-derived antimicrobial peptide, which demonstrated antifungal activity against the pathogenic strains of Candida albicans. Previously we synthetized a cyclic monomer as well as a parallel and an antiparallel dimer of Cm-p5 with improved antifungal activity. Considering the alarming increase of microbial resistance to conventional antibiotics, here we evaluated the antimicrobial activity of these derivatives against multiresistant and problematic bacteria and against important viral agents. The three peptides showed a moderate activity against Pseudomonas aeruginosa, Klebsiella pneumoniae Extended Spectrum beta-Lactamase (ESBL), and Streptococcus agalactiae, with MIC values > 100 microg/mL. They exerted a considerable activity with MIC values between 25-50 microg/mL against Acinetobacter baumanii and Enterococcus faecium. In addition, the two dimers showed a moderate activity against Pseudomonas aeruginosa PA14. The three Cm-p5 derivatives inhibited a virulent extracellular strain of Mycobacterium tuberculosis, in a dose-dependent manner. Moreover, they inhibited Herpes Simplex Virus 2 (HSV-2) infection in a concentration-dependent manner, but had no effect on infection by the Zika Virus (ZIKV) or pseudoparticles of Severe Acute Respiratory Syndrome Corona Virus 2 (SARS-CoV-2). At concentrations of >100 microg/mL, the three new Cm-p5 derivatives showed toxicity on different eukaryotic cells tested. Considering a certain cell toxicity but a potential interesting activity against the multiresistant strains of bacteria and HSV-2, our compounds require future structural optimization.
  • |Amino Acid Sequence[MESH]
  • |Animals[MESH]
  • |Anti-Bacterial Agents/chemistry/*pharmacology[MESH]
  • |Antimicrobial Cationic Peptides/*chemistry/pharmacology[MESH]
  • |Antiviral Agents/chemistry/*pharmacology[MESH]
  • |Candida albicans/drug effects[MESH]
  • |Cell Line[MESH]
  • |Cell Survival/drug effects[MESH]
  • |Dimerization[MESH]
  • |Drug Resistance, Multiple, Bacterial/*drug effects[MESH]
  • |Gram-Negative Bacteria/drug effects[MESH]
  • |Gram-Positive Bacteria/drug effects[MESH]
  • |Herpesvirus 2, Human/*drug effects[MESH]
  • |Humans[MESH]
  • |Microbial Sensitivity Tests[MESH]


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