Acipensins - Novel Antimicrobial Peptides from Leukocytes of the Russian Sturgeon Acipenser gueldenstaedtii
- Authors: Shamova O.V.1,2, Orlov D.S.1,2, Balandin S.V.3,4, Shramova E.I.3, Tsvetkova E.V.2, Panteleev P.V.3, Leonova Y.F.3, Tagaev A.A.3, Kokryakov V.N.1,2, Ovchinnikova T.V.3,4
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Affiliations:
- Institute of Experimental Medicine, Northwest Branch of the Russian Academy of Medical Sciences
- Saint-Petersburg State University
- Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences
- Moscow Institute of Physics and Technology (State University)
- Issue: Vol 6, No 4 (2014)
- Pages: 99-109
- Section: Research Articles
- Submitted: 17.01.2020
- Published: 15.12.2014
- URL: https://actanaturae.ru/2075-8251/article/view/10532
- DOI: https://doi.org/10.32607/20758251-2014-6-4-99-109
- ID: 10532
Cite item
Abstract
Antimicrobial peptides (AMPs) play an important role in the innate defense mechanisms in humans and animals. We have isolated and studied a set of antimicrobial peptides from leukocytes of the Russian sturgeon Acipenser gueldenstaedtii belonging to a subclass of chondrosteans, an ancient group of bony fish. Structural analysis of the isolated peptides, designated as acipensins (Ac), revealed in leukocytes of the Russian sturgeon six novel peptides with molecular masses of 5336.2 Da, 3803.0 Da, 5173.0 Da, 4777.5 Da, 5449.4 Da, and 2740.2 Da, designated as Ac1-Ac6, respectively. Complete primary structures of all the isolated peptides were determined, and the biological activities of three major components - Ac1, Ac2, and Ac6 - were examined. The peptides Ас1, Ас2, Ас3, Ас4, and Ac5 were found to be the N-terminal acetylated fragments 1-50, 1-35, 1-49, 1-44, and 1-51 of the histone Н2А, respectively, while Ас6 was shown to be the 62-85 fragment of the histone Н2А. The peptides Ac1 and Ac2 displayed potent antimicrobial activity towards Gram-negative and Gram-positive bacteria (Escherichia coli ML35p, Listeria monocytogenes EGD, MRSA ATCC 33591) and the fungus Candida albicans 820, while Ac6 proved effective only against Gram-negative bacteria. The efficacy of Ac 1 and Ac2 towards the fungus and MRSA was reduced upon an increase in the ionic strength of the solution. Ac1, Ac2, and Ac6, at concentrations close to their minimum inhibitory concentrations, enhanced the permeability of the E.coli ML35p outer membrane to the chromogenic marker, but they did not affect appreciably the permeability of the bacterial inner membrane in comparison with a potent pore-forming peptide, protegrin 1. Ac1, Ac2, and Ac6 revealed no hemolytic activity against human erythrocytes at concentrations of 1 to 40 μM and had no cytotoxic effect (1 to 20 μM) on K-562 and U-937 cells in vitro. Our findings suggest that histone-derived peptides serve as important anti-infective host defense molecules.
About the authors
O. V. Shamova
Institute of Experimental Medicine, Northwest Branch of the Russian Academy of Medical Sciences; Saint-Petersburg State University
Author for correspondence.
Email: ovch@ibch.ru
Russian Federation
D. S. Orlov
Institute of Experimental Medicine, Northwest Branch of the Russian Academy of Medical Sciences; Saint-Petersburg State University
Email: ovch@ibch.ru
Russian Federation
S. V. Balandin
Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences; Moscow Institute of Physics and Technology (State University)
Email: ovch@ibch.ru
Russian Federation
E. I. Shramova
Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences
Email: ovch@ibch.ru
Russian Federation
E. V. Tsvetkova
Saint-Petersburg State University
Email: ovch@ibch.ru
Russian Federation
P. V. Panteleev
Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences
Email: ovch@ibch.ru
Russian Federation
Yu. F. Leonova
Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences
Email: ovch@ibch.ru
Russian Federation
A. A. Tagaev
Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences
Email: ovch@ibch.ru
Russian Federation
V. N. Kokryakov
Institute of Experimental Medicine, Northwest Branch of the Russian Academy of Medical Sciences; Saint-Petersburg State University
Email: ovch@ibch.ru
Russian Federation
T. V. Ovchinnikova
Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences; Moscow Institute of Physics and Technology (State University)
Email: ovch@ibch.ru
Russian Federation
References
- Kokryakov V.N. // Ocherki o vrozhdennom immunutete (Essays on the innate immunity). St-Petersburg: Nauka. 2006, P.261
- Rieger A.M., Barreda D.R. // Dev. Comp. Immunol. 2011, V.35, №12, P.1238-1245
- Cole A.M., Weis P., Diamond G. // J. Biol. Chem. 1997, V.272, №18, P.12008-12013
- Douglas S.E., Gallant J.W., Gong Z., Hew C. // Dev. Comp. Immunol. 2001, V.25, №2, P.137-147
- Shai Y., Fox J., Caratsch C., Shih Y.L., Edwards C., Lazarovici I.O., P. I.O. // FEBS Lett. 1988, V.242, P.161-166
- Shike H., Lauth X., Westerman M.E., Ostland V.E., Carlberg J.M., Van Olst J.C., Shimizu C., Bulet P., Burns J.C. // Eur. J. Biochem. 2002, V.269, P.2232-2237
- Park C., Lee J., Park I., Kim M., Kim S. // FEBS Lett. 1997. V. 411. № 2-3. 1997, V.411, №2-3, P.173-178
- Wang G., Li J., Zou P., Xie H., Huang B., Nie P., Chang M. // Fish Shellfish Immunol. 2012, V.33, №3, P.522-531
- Guo M., Wei J., Huang X., Huang Y., Qin Q. // Fish Shellfish Immunol. 2012, V.32, №5, P.828-838
- Marel Mv., Adamek M., Gonzalez S.F., Frost P., Rombout J.H., Wiegertjes G.F., Savelkoul H.F., Steinhagen D. // Fish Shellfish Immunol. 2012, V.32, №3, P.494-501
- Maier V.H., Dorn K.V., Gudmundsdottir B.K., Gudmundsson G.H. // Molecular Immunology. 2008, V.45, P.3723-3730
- Chang C., Pleguezuelos O., Zhang Y., Zou J., Secombes C. // Infection and Immunity. 2005, V.73, P.5053-5064
- Chang C., Zhang Y., Zou J., Nie P., Secombes C. // Antimicrobial Agents and Chemotherapy. 2006, V.50, P.185-195
- Scocchi M., Pallavicini A., Salgaro R., Bociek K., Gennaro R. // Comp. Biochem. Physiol. B Biochem. Mol. Biol. 2009, V.152, №4, P.376-381
- Bridle A., Nosworthy E., Polinski M., Nowak B. // PLoS One. 2011, V.6, №8, P.e23417
- Birkemo G. A., Lüders T., Andersen Ø., Nes I.F., Nissen-Meyer J. // Hipposin, a histone-derived antimicrobial peptide in Atlantic halibut (Hippoglossus hippoglossus). // Biochimica et Biophisica Acta. 2003, V.1646, P.207-215
- Park I.Y., Park C.B., Kim M.S., Kim S.C. // FEBS Lett. 1998, V.437, P.258-262
- Richards R.C., O’Neil D.B., Thibault P., Ewart K.V. // Biochem. Biophis. Res. Commun. 2001, V.284, P.549-555
- Shamova O., Orlov D., Stegemann C., Czihal P., Hoffmann R., Brogden K., Kolodkin N., Sakuta G., Tossi A., Sahl H.G. // International Journal of Peptide Research and Therapeutics. 2009, V.15, №1, P.31-35
- Harwig S.S., Chen N.P., Park A.S.K., Lehreer R.I. // Anal. Biochem. 1993, V.208, P.382-346
- Schagger H., von Jagow G. // Anal. Biochem. 1987, V.166, P.368-379
- Wolf P. // Anal. Biochem. 1983, V.129, №1, P.145-155
- Lehrer R.I., Rosenman M., Harwig S.S., Jackson R., Eisenhauer P. // J. Immunol. Methods. 1991, V.137, №2, P.167-73
- Lehrer R., Barton A., Ganz T. // J. Immunol. Methods. 1988, V.108, P.153-158
- Artamonov A.Yu., Shamova O.V., Kokryakov V.N., Orlov D.S. // Vestnik Sankt-Peterburgskogo Universiteta. 2008, V.3, №2, P.139-142
- Mosmann T. // Journal of Immunological Methods. 1983, V.65, P.55-63
- Wellner D., Panneerselvam C., Horecker B.L. // Proc. Nat. Acad. Sci. 1990, V.87, P.1947-1949
- Sambrook J., Fritsch E.F., Maniatis T. // Molecular Cloning: a laboratory manuals. 2nd ed. New York: Cold Spring Harbor Laboratory Press, 1989. 1989, P.1626
- Shamova O.V., Orlov D.S., Ovchinnikova T.V., Sal Kh.G., Tver’yanovich I.A., Popova V.A., Dyubin V.A., Kokryakov V.N. // Fundamentalnye Issledovaniya. 2006, V.1, P.10-13
- Marzluff W.F., Wagner E.J., Duronio R.J. // Nat. Rev. Genet. 2008, V.9, №11, P.843-54
- Kim H.S., Park C.B., Kim M.S., Kim S.C. // Biochem. Biophys. Res. Commun. 1996, V.229, №2, P.381-7
- Kawasaki H., Iwamuro S. // Infect. Disord. Drug Targets. 2008, V.8, №3, P.195-205
- Parseghian M., Luhrs K. // Biochem. Cell Biol. 2006, V.84, №4, P.589-604
- Rose F.R., Bailey K., Keyte J.W., Chan W.C., Greenwood D., Mahida Y.R.. // Infect. Immun. 1998, V.66, P.3255-3263
- Brix K., Summa W., Lottspeich F., Herzog V. // J. Clin. Invest. 1998, V.102, P.283-293
- Hiemstra P.S., Eisenhauer P.B., Harwig S.S., van den Barselaar M.T., van Furth R., Lehrer R.I. // Infect. Immun. 1993, V.61, P.3038-3046
- Bolton S.J., Perry V.H. // J. Neurocytol. 1997, V.26, P.823-831
- Holers V.M., Kotzin B.L. // J. Clin. Invest. 1985, V.76, P.991-998
- Evans D.L., Kaur H., Leary J. 3rd., Praveen K., Jaso-Friedmann L. // Dev Comp Immunol. 2005, V.29, №12, P.1049-64
- Nauseef W.M., Borregaard N. // Nat. Immunol. 2014, V.15, №7, P.602-11
- Zawrotniak M., Rapala-Kozik M. // Acta Biochim Pol. 2013, V.60, №3, P.277-84
- Brinkmann V., Reichard U., Goosmann C., Fauler B., Uhlemann Y., Weiss D.S., Weinrauch Y., Zychlinsky A. // Science. 2004, V.303, №5663, P.1532-5
- De Zoysa M., Nikapitiya C., Whang I., Lee J.S., Lee J. // Fish Shellfish Immunol. 2009, V.27, №5, P.639-46
- Nagaoka I., Hirota S., Yomogida S., Ohwada A., Hirata M. // Inflamm Res. 2000, V.49, №2, P.73-9
- Park C.B., Kim H.S., Kim S.C. // Biochem Biophys Res Commun 1998, V.244, №1, P.253-257
- Cho J.H., Sung B.H., Kim S.C. // Biochim Biophys Acta. 2009, V.1788, №8, P.1564-9
- Koo Y.S., Kim J.M., Park I.Y., Yu B.J., Jang S.A., Kim K.S., Park C.B., Cho J.H., Kim S.C. // Peptides. 2008, V.29, P.1102-1108
- Bustillo M.E., Fischer A. L., LaBouyer M.A., Klaips J. A., Webb A.C., Elmore D.E. // Biochim. Biophys. Acta. 2014, V.1838, №9, P.2228-2233
- Podda E., Benincasa M., Pacor S., Micali F., Mattiuzzo M., Gennaro R., Scocchi M. // Biochim. Biophysi. Acta. 2006, V.1760, P.1732-1740