Antimicrobial Properties of a Peptide Derived from the Male Fertility Factor kl2 Protein of <i>Drosophila melanogaster</i>

Antimicrobial peptides (AMPs) are important components of innate immunity. Here, we report the antimicrobial properties of a peptide derived from the Male fertility factor kl2 (MFF-kl2) protein of <i>Drosophila melanogaster</i>, which was identified as a functional analog of the mammalia...

Full description

Bibliographic Details
Main Authors: Bernadetta Bilska, Urszula Godlewska, Milena Damulewicz, Krzysztof Murzyn, Mateusz Kwitniewski, Joanna Cichy, Elżbieta Pyza
Format: Article
Language:English
Published: MDPI AG 2022-02-01
Series:Current Issues in Molecular Biology
Subjects:
Online Access:https://www.mdpi.com/1467-3045/44/3/76
Description
Summary:Antimicrobial peptides (AMPs) are important components of innate immunity. Here, we report the antimicrobial properties of a peptide derived from the Male fertility factor kl2 (MFF-kl2) protein of <i>Drosophila melanogaster</i>, which was identified as a functional analog of the mammalian antibacterial chemerin-p4 peptide. The antimicrobial activity of multifunctional chemerin is mainly associated with a domain localized in the middle of the chemerin sequence, Val66-Pro85 peptide (chemerin-p4). Using bioinformatic tools, we found homologs of the chemerin-p4 peptide in the proteome of <i>D. melanogaster</i>. One of them is MFF-p1, which is a part of the MFF kl2 protein, encoded by the gene <i>male fertility factor kl2</i> (<i>kl-2</i>) located on the long arm of the Y chromosome. The second detected peptide (Z-p1) is a part of the Zizimin protein belonging to DOCK family, which is involved in cellular signaling processes. After testing the antimicrobial properties of both peptides, we found that only MFF-p1 possesses these properties. Here, we demonstrate its antimicrobial potential both in vitro and in vivo after infecting <i>D. melanogaster</i> with bacteria. MFF-p1 strongly inhibits the viable counts of <i>E. coli</i> and <i>B. subtilis</i> after 2 h of treatment and disrupts bacterial cells. The expression of <i>kl-2</i> is regulated by exposure to bacteria and by the circadian clock.
ISSN:1467-3037
1467-3045