4.6 Article

Mining Amphibian and Insect Transcriptomes for Antimicrobial Peptide Sequences with rAMPage

Journal

ANTIBIOTICS-BASEL
Volume 11, Issue 7, Pages -

Publisher

MDPI
DOI: 10.3390/antibiotics11070952

Keywords

antimicrobial peptide; AMP discovery; genome mining; antimicrobial resistance

Funding

  1. Genome Canada
  2. Genome BC [291PEP, 281ANV]
  3. Canadian Agricultural Partnership, a federal-provincial-territorial initiative
  4. Investment Agriculture Foundation of BC [INV106]
  5. Office of the Vice President, Research and Innovation of the University of British Columbia

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Antibiotic resistance is a global health crisis, and alternative antimicrobial therapeutics are urgently needed. This study presents rAMPage, a bioinformatics discovery platform, to identify AMP sequences from RNA-seq datasets. The researchers used rAMPage on 84 publicly available RNA-seq datasets, identifying 1137 possible AMPs, with 1024 deemed novel. Testing 21 selected peptide sequences, seven of them showed high antimicrobial activity.
Antibiotic resistance is a global health crisis increasing in prevalence every day. To combat this crisis, alternative antimicrobial therapeutics are urgently needed. Antimicrobial peptides (AMPs), a family of short defense proteins, are produced naturally by all organisms and hold great potential as effective alternatives to small molecule antibiotics. Here, we present rAMPage, a scalable bioinformatics discovery platform for identifying AMP sequences from RNA sequencing (RNA-seq) datasets. In our study, we demonstrate the utility and scalability of rAMPage, running it on 84 publicly available RNA-seq datasets from 75 amphibian and insect species-species known to have rich AMP repertoires. Across these datasets, we identified 1137 putative AMPs, 1024 of which were deemed novel by a homology search in cataloged AMPs in public databases. We selected 21 peptide sequences from this set for antimicrobial susceptibility testing against Escherichia coli and Staphylococcus aureus and observed that seven of them have high antimicrobial activity. Our study illustrates how in silico methods such as rAMPage can enable the fast and efficient discovery of novel antimicrobial peptides as an effective first step in the strenuous process of antimicrobial drug development.

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