Acipensins - Novel Antimicrobial Peptides from Leukocytes of the Russian Sturgeon Acipenser gueldenstaedtii

Cover Page

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
Россия

D. S. Orlov

Institute of Experimental Medicine, Northwest Branch of the Russian Academy of Medical Sciences; Saint-Petersburg State University

Email: ovch@ibch.ru
Россия

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
Россия

E. I. Shramova

Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences

Email: ovch@ibch.ru
Россия

E. V. Tsvetkova

Saint-Petersburg State University

Email: ovch@ibch.ru
Россия

P. V. Panteleev

Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences

Email: ovch@ibch.ru
Россия

Yu. F. Leonova

Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences

Email: ovch@ibch.ru
Россия

A. A. Tagaev

Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences

Email: ovch@ibch.ru
Россия

V. N. Kokryakov

Institute of Experimental Medicine, Northwest Branch of the Russian Academy of Medical Sciences; Saint-Petersburg State University

Email: ovch@ibch.ru
Россия

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
Россия

References

  1. Kokryakov V.N. // Ocherki o vrozhdennom immunutete (Essays on the innate immunity). St-Petersburg: Nauka. 2006, P.261
  2. Rieger A.M., Barreda D.R. // Dev. Comp. Immunol. 2011, V.35, №12, P.1238-1245
  3. Cole A.M., Weis P., Diamond G. // J. Biol. Chem. 1997, V.272, №18, P.12008-12013
  4. Douglas S.E., Gallant J.W., Gong Z., Hew C. // Dev. Comp. Immunol. 2001, V.25, №2, P.137-147
  5. 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
  6. 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
  7. 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
  8. Wang G., Li J., Zou P., Xie H., Huang B., Nie P., Chang M. // Fish Shellfish Immunol. 2012, V.33, №3, P.522-531
  9. Guo M., Wei J., Huang X., Huang Y., Qin Q. // Fish Shellfish Immunol. 2012, V.32, №5, P.828-838
  10. 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
  11. Maier V.H., Dorn K.V., Gudmundsdottir B.K., Gudmundsson G.H. // Molecular Immunology. 2008, V.45, P.3723-3730
  12. Chang C., Pleguezuelos O., Zhang Y., Zou J., Secombes C. // Infection and Immunity. 2005, V.73, P.5053-5064
  13. Chang C., Zhang Y., Zou J., Nie P., Secombes C. // Antimicrobial Agents and Chemotherapy. 2006, V.50, P.185-195
  14. Scocchi M., Pallavicini A., Salgaro R., Bociek K., Gennaro R. // Comp. Biochem. Physiol. B Biochem. Mol. Biol. 2009, V.152, №4, P.376-381
  15. Bridle A., Nosworthy E., Polinski M., Nowak B. // PLoS One. 2011, V.6, №8, P.e23417
  16. 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
  17. Park I.Y., Park C.B., Kim M.S., Kim S.C. // FEBS Lett. 1998, V.437, P.258-262
  18. Richards R.C., O’Neil D.B., Thibault P., Ewart K.V. // Biochem. Biophis. Res. Commun. 2001, V.284, P.549-555
  19. 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
  20. Harwig S.S., Chen N.P., Park A.S.K., Lehreer R.I. // Anal. Biochem. 1993, V.208, P.382-346
  21. Schagger H., von Jagow G. // Anal. Biochem. 1987, V.166, P.368-379
  22. Wolf P. // Anal. Biochem. 1983, V.129, №1, P.145-155
  23. Lehrer R.I., Rosenman M., Harwig S.S., Jackson R., Eisenhauer P. // J. Immunol. Methods. 1991, V.137, №2, P.167-73
  24. Lehrer R., Barton A., Ganz T. // J. Immunol. Methods. 1988, V.108, P.153-158
  25. Artamonov A.Yu., Shamova O.V., Kokryakov V.N., Orlov D.S. // Vestnik Sankt-Peterburgskogo Universiteta. 2008, V.3, №2, P.139-142
  26. Mosmann T. // Journal of Immunological Methods. 1983, V.65, P.55-63
  27. Wellner D., Panneerselvam C., Horecker B.L. // Proc. Nat. Acad. Sci. 1990, V.87, P.1947-1949
  28. 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
  29. 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
  30. Marzluff W.F., Wagner E.J., Duronio R.J. // Nat. Rev. Genet. 2008, V.9, №11, P.843-54
  31. Kim H.S., Park C.B., Kim M.S., Kim S.C. // Biochem. Biophys. Res. Commun. 1996, V.229, №2, P.381-7
  32. Kawasaki H., Iwamuro S. // Infect. Disord. Drug Targets. 2008, V.8, №3, P.195-205
  33. Parseghian M., Luhrs K. // Biochem. Cell Biol. 2006, V.84, №4, P.589-604
  34. Rose F.R., Bailey K., Keyte J.W., Chan W.C., Greenwood D., Mahida Y.R.. // Infect. Immun. 1998, V.66, P.3255-3263
  35. Brix K., Summa W., Lottspeich F., Herzog V. // J. Clin. Invest. 1998, V.102, P.283-293
  36. 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
  37. Bolton S.J., Perry V.H. // J. Neurocytol. 1997, V.26, P.823-831
  38. Holers V.M., Kotzin B.L. // J. Clin. Invest. 1985, V.76, P.991-998
  39. Evans D.L., Kaur H., Leary J. 3rd., Praveen K., Jaso-Friedmann L. // Dev Comp Immunol. 2005, V.29, №12, P.1049-64
  40. Nauseef W.M., Borregaard N. // Nat. Immunol. 2014, V.15, №7, P.602-11
  41. Zawrotniak M., Rapala-Kozik M. // Acta Biochim Pol. 2013, V.60, №3, P.277-84
  42. 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
  43. De Zoysa M., Nikapitiya C., Whang I., Lee J.S., Lee J. // Fish Shellfish Immunol. 2009, V.27, №5, P.639-46
  44. Nagaoka I., Hirota S., Yomogida S., Ohwada A., Hirata M. // Inflamm Res. 2000, V.49, №2, P.73-9
  45. Park C.B., Kim H.S., Kim S.C. // Biochem Biophys Res Commun 1998, V.244, №1, P.253-257
  46. Cho J.H., Sung B.H., Kim S.C. // Biochim Biophys Acta. 2009, V.1788, №8, P.1564-9
  47. 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
  48. 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
  49. Podda E., Benincasa M., Pacor S., Micali F., Mattiuzzo M., Gennaro R., Scocchi M. // Biochim. Biophysi. Acta. 2006, V.1760, P.1732-1740

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2014 Shamova O.V., Orlov D.S., Balandin S.V., Shramova E.I., Tsvetkova E.V., Panteleev P.V., Leonova Y.F., Tagaev A.A., Kokryakov V.N., Ovchinnikova T.V.

Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.

This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies