Identification and characterization of novel cecropins from the Oxysternon conspicillatum neotropic dung beetle.
Lily Johanna Toro SegoviaGermán Alberto Téllez RamírezDiana Carolina Henao AriasJuan David Rivera DuranJuan Pablo BedoyaJhon Carlos Castaño OsorioPublished in: PloS one (2017)
Dung beetles are exposed to a complex microbiological ecosystem during their life cycle. Characterization of novel host-defense peptides (HDP) is essential to understanding the host innate immune response in insects. It constitutes a promising alternative to look for new therapeutic agents against pathogenic microbes. We identified four new HDP, Oxysterlins 1, 2, 3, and 4 from the transcriptome of the Oxysternon conspicillatum dung beetle. These HDP display a highly conserved signal peptide and a mature peptide, characterized by an overall positive charge (cationic) (pI: 10.23-11.49), a hydrophobic ratio (ΦH: 35-41), and amphipathicity. Oxysterlins 1, 2, and 3 have a linear α-helix structure, whilst Oxysterlin 4 has a mixture of both α-helix and β-sheet structures without disulfide bonds through bioinformatics prediction and circular dichroism. Oxysterlins are part of the cecropin family group in an exclusive clade related to beetle cecropins. They have predominant antimicrobial activity against Gram-negative bacteria, including multidrug resistant strains (3.12-50 μg/mL) measured by plate microdilution. Their kinetics, in a time-killing curve showed concentration-dependent bactericidal activity. Furthermore, these HDP have low toxicity against human erythrocytes (62.5-500 μg/mL) and Vero cells (250-500 μg/mL). This article describes new HDP of the cecropin family from the Oxysternon conspicillatum dung beetle, with antimicrobial activity against multidrug resistant bacteria and low toxicity.
Keyphrases
- multidrug resistant
- immune response
- life cycle
- drug resistant
- acinetobacter baumannii
- gram negative
- oxidative stress
- induced apoptosis
- endothelial cells
- klebsiella pneumoniae
- climate change
- gene expression
- cell cycle arrest
- high resolution
- dna binding
- rna seq
- genome wide
- transcription factor
- single cell
- dendritic cells
- ionic liquid
- toll like receptor
- mass spectrometry
- cell death
- human health
- dna methylation
- pi k akt
- endoplasmic reticulum stress
- cystic fibrosis
- solar cells
- innate immune
- oxide nanoparticles