Antiviral Activity of a Turbot (Scophthalmus maximus) NK-Lysin Peptide by Inhibition of Low-pH Virus-Induced Membrane Fusion

Global health is under attack by increasingly-frequent pandemics of viral origin. Antimicrobial peptides are a valuable tool to combat pathogenic microorganisms. Previous studies from our group have shown that the membrane-lytic region of turbot (Scophthalmus maximus) NK-lysine short peptide (Nkl71–...

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Bibliographic Details
Published in:Marine Drugs
Main Authors: Falcó, Alberto, Medina-Gali, Regla María, Poveda, José Antonio, Bello Pérez, Melissa, Novoa, Beatriz, Encinar, José Antonio
Other Authors: Consejo Superior de Investigaciones Científicas (España), Ministerio de Economía y Competitividad (España), Xunta de Galicia, Generalitat Valenciana
Format: Article in Journal/Newspaper
Language:unknown
Published: Multidisciplinary Digital Publishing Institute 2019
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Online Access:http://hdl.handle.net/10261/177043
https://doi.org/10.3390/md17020087
https://doi.org/10.13039/501100003329
https://doi.org/10.13039/501100003359
https://doi.org/10.13039/501100003339
https://doi.org/10.13039/501100010801
Description
Summary:Global health is under attack by increasingly-frequent pandemics of viral origin. Antimicrobial peptides are a valuable tool to combat pathogenic microorganisms. Previous studies from our group have shown that the membrane-lytic region of turbot (Scophthalmus maximus) NK-lysine short peptide (Nkl71–100) exerts an anti-protozoal activity, probably due to membrane rupture. In addition, NK-lysine protein is highly expressed in zebrafish in response to viral infections. In this work several biophysical methods, such as vesicle aggregation, leakage and fluorescence anisotropy, are employed to investigate the interaction of Nkl71–100 with different glycerophospholipid vesicles. At acidic pH, Nkl71–100 preferably interacts with phosphatidylserine (PS), disrupts PS membranes, and allows the content leakage from vesicles. Furthermore, Nkl71–100 exerts strong antiviral activity against spring viremia of carp virus (SVCV) by inhibiting not only the binding of viral particles to host cells, but also the fusion of virus and cell membranes, which requires a low pH context. Such antiviral activity seems to be related to the important role that PS plays in these steps of the replication cycle of SVCV, a feature that is shared by other families of virus-comprising members with health and veterinary relevance. Consequently, Nkl71–100 is shown as a promising broad-spectrum antiviral candidate. This research was funded by the Spanish Ministry of Science and Innovation, grant numbers AGL2014-51773-C3-1-R, AGL2015-67995-C3-1-R, BIO2017-82851-C3-1-R and PIE 201230E057; Xunta de Galicia (GAIN), grant number IN607B 2016/12, and Generalitat Valenciana, grant numbers ACIF/2016/207 and PROMETEO/2016/006. We acknowledge support by the CSIC Open Access Publication Initiative through its Unit of Information Resources for Research (URICI) Peer reviewed