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The Hirudo Medicinalis Microbiome Is a Source of New Antimicrobial Peptides.


ABSTRACT: Antimicrobial peptides (AMPs) are considered a promising new class of anti-infectious agents. This study reports new antimicrobial peptides derived from the Hirudo medicinalis microbiome identified by a computational analysis method applied to the H. medicinalis metagenome. The identified AMPs possess a strong antimicrobial activity against Gram-positive and Gram-negative bacteria (MIC range: 5.3 to 22.4??M), including Staphylococcus haemolyticus, an opportunistic coagulase-negative pathogen. The secondary structure analysis of peptides via CD spectroscopy showed that all the AMPs except pept_352 have mostly disordered structures that do not change under different conditions. For peptide pept_352, the ?-helical content increases in the membrane environment. The examination of the mechanism of action of peptides suggests that peptide pept_352 exhibits a direct membranolytic activity. Furthermore, the cytotoxicity assay demonstrated that the nontoxic peptide pept_1545 is a promising candidate for drug development. Overall, the analysis method implemented in the study may serve as an effective tool for the identification of new AMPs.

SUBMITTER: Grafskaia E 

PROVIDER: S-EPMC7582656 | biostudies-literature | 2020 Sep

REPOSITORIES: biostudies-literature

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The <i>Hirudo Medicinalis</i> Microbiome Is a Source of New Antimicrobial Peptides.

Grafskaia Ekaterina E   Pavlova Elizaveta E   Babenko Vladislav V VV   Latsis Ivan I   Malakhova Maja M   Lavrenova Victoria V   Bashkirov Pavel P   Belousov Dmitrii D   Klinov Dmitry D   Lazarev Vassili V  

International journal of molecular sciences 20200927 19


Antimicrobial peptides (AMPs) are considered a promising new class of anti-infectious agents. This study reports new antimicrobial peptides derived from the <i>Hirudo medicinalis</i> microbiome identified by a computational analysis method applied to the <i>H. medicinalis</i> metagenome. The identified AMPs possess a strong antimicrobial activity against Gram-positive and Gram-negative bacteria (MIC range: 5.3 to 22.4 μM), including <i>Staphylococcus haemolyticus</i>, an opportunistic coagulase-  ...[more]

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