IMMUNOCHEMICAL STUDY OF RECEPTION OF PLAGUE BACTERIOPHAGE POKROVSKY
- Authors: Byvalov A.A.1, Dudina L.G.2, Litvinets S.G.2, Martinson E.A.2
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Affiliations:
- Vyatsky State University, institute of Physiology
- Vyatsky State University
- Issue: Vol 93, No 4 (2016)
- Pages: 16-21
- Section: ORIGINAL RESEARCHES
- Submitted: 10.04.2019
- Published: 28.08.2016
- URL: https://microbiol.crie.ru/jour/article/view/64
- DOI: https://doi.org/10.36233/0372-9311-2016-4-16-21
- ID: 64
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Abstract
Aim. Study of mechanism of reception of plague bacteriophage Pokrovsky to cells of Yersinia pestis using a panel of monoclonal antibodies. Materials and methods. Using a method of competitive inhibition, the ability of monoclonal antibodies against antigenic epitopes of outer membrane of Yersinia genus bacteria to inhibit adhesion of the studied bacteriophage to cells of Y. pestis EV strain, was evaluated. Results. A key role of structure of carbohydrate nature in reception of Pokrovsky bacteriophage was confirmed. Among 5 lines of monoclonal antibodies against protein epitopes 2 were established to cause significant inactivation of bacteriophage adhesion to bacterial cells. Conclusion. An assumption is proposed regarding participation of a structure of polypeptide nature in reception of Pokrovsky bacteriophage by cells of plague microbe.
Keywords
About the authors
A. A. Byvalov
Vyatsky State University, institute of Physiology
Author for correspondence.
Email: noemail@neicon.ru
Россия
L. G. Dudina
Vyatsky State University
Email: noemail@neicon.ru
Россия
S. G. Litvinets
Vyatsky State University
Email: noemail@neicon.ru
Россия
E. A. Martinson
Vyatsky State University
Email: noemail@neicon.ru
Россия
References
- Анисимов А.П. Факторы Yersinia pestis, обеспечивающие циркуляцию и сокранение возбудителя чумы в экосистемах природных очагов. Молекул, генетика. 2002, 3: 3-23.
- Вывалов А.А., Дудина Л.Г., Литвинец С.Г., Новикова О. Д., Хоменко В. А., Портнягина О. Ю., Оводов Ю. С. Исследование поверхностных антигенных эпитопов Yersinia pseudotuberculosis с помощью моноклональных антител. Прикладная биохимия и микробиология. 2014, 50 (2): 203-210.
- Вывалов. А. А., Дудина Л. Г., Чернядьев А. В., Конышев И. В., Литвинец С. Г., Оводов Ю.С. Иммунохимическая активность Б-антигена Yersinia pseudotuberculosis. Молекул, генетика. 2015, 2: 32-38.
- Лабинская А.С. Титрование бактериофага. В кн.: Лабинская А.С. Микробиология с техникой микробиологических исследований. М., Медицина, 1978, с. 77-79.
- СидоринЕ.В.,ЗиганшинР.Х.,НабережныхГ.А.,ЛихацкаяГ.Н.,ТрифоновЕ.В.,Анастюк С.Д., Черников О.В., Соловьева Т.Ф. Белок шаперон Skp из Yersinia pseudotuberculosis обладает способностью связывать иммуноглобулины G. Биохимия. 2009, 74 (4): 501 -514.
- Achtman М., Zurth К., Morelli G. et al. Yersinia pestis, the cause of plague, is a resently emerged clone of Yersinia pseudotuberculosis. Proc. Natl. Acad. Sci. USA. 1999, 96: 14043-14048.
- Anisimov A. P, Amoako K.K. Treatment of plague: promising alternatives to antibiotics. J. Med. Microbiol. 2006, 55: 1461-1475.
- Beczala A., Ovchinnikova O.G., Datta N. et al. Structure and genetic basis of Yersinia similis serotype 0:9 О-specific polysaccharide. Innate Immunity. 2015, 21 (1): 3-16.
- Filippov A.A., Sergueev K.V., He Y. et al. Bacteriophage-resistant mutants in Yersinia pestis: identification of phage receptors and attenuation for mice. PLoS One. 2011, 6 (9): E25486.
- Golkar Z., Bagasra O., Pace D.G. Bacteriophage therapy: a potential solution for the antibiotic resistance crisis. J. Infect. Dev. Ctries. 2014, 8 (2): 129-136.
- Marraffmi L.A. CRISPR-Cas immunity in prokaryotes. Nature. 2015, 1; 526 (7571): 55-61.
- Montag D., Hashemolhosseini S., Henning U. The receptor-recognition area of protein 37 of phage T4 Tula and Tulb. Receptor-recognition proteins ofT-even type bacteriophages. J. Mol. Biol. 1990, 216 (2): 327-334.
- Welch T.J., Fricke W.F., McDermott P.F. et al. Multiple antimicrobial resistance in plague: an emerging public health risk. PLoS One. 2007, 2 (3): E309.
- Summers W.C. Bacteriophage therapy. Annu. Rev. Microbiol. 2001, 55: 437-453.
- Zhao X., Cui Y., Yan Y. et al. Outer membrane proteins Ail and OmpF of Yersinia pestis are involved in the adsorption of T7-related bacteriophage Yep-phi.J. Virol. 2013, 87 (22): 12260-12269.