Assessing efficiency of synthetic peptide-containing spray in combination therapy of chronic generalized periodontitis

Cover Page


Cite item

Full Text

Abstract

Antibacterial drugs are routinely used in therapy of periodontal diseases. However, increasing incidence of antibiotics resistance necessitates development of novel therapeutic approaches for oral diseases. Currently, newly designed antibacterial agents based on natural, semi-synthetic and synthetic peptides is the most promising approach in dentistry. Among them is a product containing synthetic peptide (ZP2) replicating active site of granulocyte-macrophage colonystimulating factor (GM-CSF) as the main active ingredient in Atsegram-spray (manufactured by Academic Innovation Research Center, Chelyabinsk). Our study was aimed at assessing efficacy of a combination therapy of inflammatory periodontal diseases by introducing Atsegram-spray as well as examining potential relationship between peptide ZP2-related biological properties, physicochemical properties of the spray and mechanism of antibacterial and immunotropic action for substantiating its application on oral mucosa. During the first stage experiments, it was found that the peptide ZP2 was able to trigger lymphocyte blast transformation in vitro indicating that it might influence cell proliferation and exhibit marked immunotropic activity. Next, we assessed potential effects of the peptide ZP2 on biofilm formation mediated by staphylococcal clinical isolates. It was shown that peptide ZP2 inhibited biofilm formation in 75.0±9.0% of S. aureus and 50.0±15.1% of S. epidermidis strains, with mean inhibition index of biofilm formation reaching 25.1±3.8 and 50.4±6.0%, respectively. However, peptide ZP2 in 8.3–25.0% of staphylococcal clinical isolates was found to stimulate/lack effect on biofilm formation by 14.9–48.5 and 16.7–25.0% cultures, respectively. Thus, the synthetic peptide ZP2 exerts divergent, but mainly inhibitory effects on biofilm formation with staphylococcal clinical strains, which are characterized by inter- and intraspecific (strain) variability. Use of a synthetic peptide-based spray in antibacterial therapy of mild chronic generalized periodontitis (main group) one month after the onset was found to improve oral hygiene by 28.5% as well as decrease PMA index and gum bleeding index by 82.8 and 100%, respectively. In contrast, such parameters in patients receiving basic therapy (comparison group) were lower on average by 2-fold. While analyzing physicochemical properties of the spray such as pH, buffer capacity and solution osmotic pressure, it was found that they were related to the antibacterial mechanism of drug activity and efficacy in treatment of inflammatory periodontal diseases. Thus, assessing peptide ZP2-related biological properties and physicochemical parameters of the spray allows to evaluate their role in mechanism of previously unknown antibacterial and immunotropic activity. These findings confirm feasibility and efficacy of using Atsegram-spray in dentistry as an alternative means to antimicrobial agents, such as antibacterial drugs.

About the authors

N. G. Sarkisian

Ural State Medical University of the Ministry of Health of the Russian Federation, Yekaterinburg
Institute of Immunology and Physiology Ural detachment of the Russian Academy of Sciences, Yekaterinburg

Email: narine_25@mail.ru

PhD (Medicine), Associate Professor, Department of Therapeutic Dentistry and Propaedeutics of Dental Diseases;

Professor of Postgraduate Studies, Institute of Immunology and Physiology,

620028, Yekaterinburg, Repin str., 3

Russian Federation

N. N. Kataeva

Ural State Medical University of the Ministry of Health of the Russian Federation

Author for correspondence.
Email: kataeva.nn@mail.ru

PhD (Chemistry), Associate Professor, Department of General Chemistry,

Yekaterinburg

Russian Federation

I. A. Tuzankina

Institute of Immunology and Physiology Ural detachment of the Russian Academy of Sciences

Email: fake@neicon.ru

PhD, MD (Medicine), Professor, Honored Worker of Science, Head Researcher, Laboratory of Immunology of Inflammation, 

Yekaterinburg

Russian Federation

S. G. Melikyan

Ural State Medical University of the Ministry of Health of the Russian Federation

Email: fake@neicon.ru

3rd Year Student, Faculty of Dentistry,

Yekaterinburg

Russian Federation

V. A. Zurochka

Institute of Immunology and Physiology Ural detachment of the Russian Academy of Sciences;
South Ural State University (National Research University)

Email: fake@neicon.ru

PhD, MD (Medicine), Senior Researcher, Institute of Immunology and Physiology, Yekaterinburg;

Professor of the Department of Food Technology and Biotechnology, Chelyabinsk

A. V. Zurochka

Institute of Immunology and Physiology Ural detachment of the Russian Academy of Sciences;
South Ural State University (National Research University)

Email: fake@neicon.ru

PhD, MD (Medicine), Professor, Leading Researcher, Institute of Immunology and Physiology, Yekaterinburg;

Professor of the Department of Food Technology and Biotechnology, Chelyabinsk

Russian Federation

References

  1. Борисов Л.Б. Медицинская микробиология, вирусология, иммунология. Учебник для вузов. М.: Медицинское информационное агентство, 2005. 734 с.
  2. Бухарин О.В. Инфекционная симбиология // Журнал микробиологии, эпидемиологии и иммунобиологии. 2015. № 4. С. 4–9.
  3. Вавилова Т.П., Янушевич О.О., Островская И.Г. Слюна. Аналитические возможности и перспективы. М.: Бином, 2014. 312 с.
  4. Гриценко В.А., Аминин Д.Л. Зурочка А.В., Зурочка В.А., Иванов Ю.Б. Некоторые биологические эффекты иммуномодуляторов естественного и синтетического происхождения in vitro как основа создания новых лекарственных средств для борьбы с эндогенными инфекциями // Бюллетень Оренбургского научного центра УрО РАН. 2012. № 3. С. 1–17.
  5. Гриценко В.А., Иванов Ю.Б. Роль персистентных свойств в патогенезе эндогенных инфекций // Журнал микробиологии, эпидемиологии и иммунобиологии. 2009. № 4. С. 66–71.
  6. Добрынина М.А. Зурочка В.А., Зурочка А.В., Гриценко В.А. Сравнительный анализ влияния синтетического пептида активного центра гранулоцитарно-макрофагального колониестимулирующего фактора — ZP2 на рост музейных культур бактерий родов Staphylococcus и Escherichia in vitro // Бюллетень Оренбургского научного центра УрО РАН. 2015. № 2. С. 1–10.
  7. Добрынина М.А., Зурочка А.В., Тяпаева Я.В., Белозерцева Ю.П., Гриценко В.А. Оценка влияния синтетического пептида активного центра гранулоцитарно-макрофагального колониестимулирующего фактора — ZP2 на рост и биопленкообразование клинических изолятов энтеробактерий in vitro // Бюллетень Оренбургского научного центра УрО РАН. 2018. № 4. С. 1–20.
  8. Добрынина М.А., Зурочка А.В., Тяпаева Я.В., Белозерцева Ю.В., Мругова Т.М., Гриценко В.А. Антибактериальная активность косметического средства «Ацеграм» в отношении грамотрицательных бактерий // Бюллетень Оренбургского научного центра УрО РАН. 2017. № 4. С. 1–13.
  9. Зурочка В.А., Зурочка А.В, Добрынина М.А., Зуева Е.Б., Гриценко В.А., Тяпаева Я.В., Белозерцева Ю.П. Анализ чувствительности клинических изолятов стафилококков к синтетическому пептиду активного центра гранулоцитарно-макрофагального колониестимулирующего фактора (ГМ-КСФ) // Российский иммунологический журнал. 2015. Т. 9 (18), № 3 (1). С. 82–85.
  10. Зурочка А.В., Суховей Ю.Г., Зурочка В.А., Добрынина М.А., Петров С.А., Унгер И.Г., Костоломова Е.Г., Аргунова Е.Г., Субботин А.М., Колобов А.А., Симбирцев А.С. Антибактериальные свойства синтетических пептидов активного центра GM-CSF // Цитокины и воспаление. 2010. Т. 9, № 4. С. 32–34.
  11. Иммунология: структура и функции иммунной системы / Под ред. Р.М. Хаитова. М.: ГЭОТАР-Медиа, 2014. 280 с.
  12. Лакин Г.Ф. Биометрия. М.: Высшая школа, 1990. 352 с.
  13. Медицинские лабораторные технологии: Справочник; в 2 т. / Под ред. А.И. Карпищенко. 2-е изд., перераб. и доп. СПб.: Интермедика, 1999. Т. 2. 653 с.
  14. Ронь Г.И., Еловикова T.M. Инновационные технологии в диагностике и лечении воспалительных заболеваний пародонта. Екатеринбург: УГМА, 2011. 276 с.
  15. Слесарев В.И. Химия: Основы химии живого: учебник для вузов. СПб.: Химиздат, 2017. 784 с.
  16. Трухачева Н.В. Математическая статистика в медико-биологических исследованиях с применением пакета Statistica. М.: ГОЭТАР-Медиа, 2013. 384 с.
  17. Улитовский С.Б. Гигиена полости рта в пародонтологии. Медицинская книга, 2006. 268 с. Ulitovskii S.B.
  18. Янушевич О.О., Максимовский Ю.М., Максимовская Л.Н., Орехова Л.Ю. Терапевтическая стоматология. Учебник для вузов. М.: ГЭОТАР-Медиа, 2016. 760 с.
  19. Christensen G.D., Simpson W.A., Younger J.J., Baddour L.M., Barrett F.F., Melton D.M., Beachey E.H. Adherence of coagulasenegative staphylococci to plastic tissue culture plates: a quantitative model for the adherence of staphylococci to medical devices. J. Clin. Microbiol., 1985, no. 22, pp. 996–1006.
  20. Izano E.A., Izano E.A., Amarante M.A., Kher W.B., Kaplan J.B. Differential roles of poly-N-acetylglucosamine surface polysaccharide and extracellular DNA in Staphylococcus aureus and Staphylococcus epidermidis biofilms. Appl. Environ. Microbiol., 2008, no. 74 (2), pp. 470–476. doi: 10.1128/AEM.02073-07
  21. Mack D., Becker P., Chatterjee I., Dobinsky S., Knobloch J.K., Peters G., Rohde H., Herrmann M. Mechanisms of biofilm formation in Staphylococcus epidermidis and Staphylococcus aureus: functional molecules, regulatory circuits, and adaptive responses. Int. J. Med. Microbiol., 2004, no. 294, pp. 203–212. doi: 10.1016/j.ijmm.2004.06.015
  22. Murphy J.M., Young I.G. IL-3, IL-5, and GM-CSF signaling: crystal structure of the human beta-common receptor. Vitam. Horm., 2006, no. 74, pp. 1–30. doi: 10.1016/S0083-6729(06)74001-8
  23. O’Gara J.P. ica and beyond: biofilm mechanisms and regulation in Staphylococcus epidermidis and Staphylococcus aureus. FEMS Microbiol. Lett., 2007, no. 270 (2), pp. 179–188. doi: 10.1111/j.1574-6968.2007.00688.x
  24. O’Neill E., Pozzi C., Houston P., Smyth D., Humphreys H., Ashley Robinson D., O’Gara J.P. Association between methicillin susceptibility and biofilm regulation in Staphylococcus aureus isolates from device-related. J. Clin. Microbiol., 2007, no. 45 (5), pp. 1379–1388. doi: 10.1128/JCM.02280-06
  25. O’Toole G.A., Kaplan H.B., Kolter R. Biofilm formation as microbial development. Ann. Rev. Microbiol., 2000, no. 54, pp. 49–79. doi: 10.1146/annurev.micro.54.1.49
  26. Stepanović S., Vuković D., Hola V., Di Bonaventura G., Djukić S., Cirković I., Ruzicka F. Quantification of biofilm in microtiter plates: overview of testing conditions and practical recommendations for assessment of biofilm production by staphylococci. APMIS, 2007, no. 115, pp. 891–899.

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2019 Sarkisian N.G., Kataeva N.N., Tuzankina I.A., Melikyan S.G., Zurochka V.A., Zurochka A.V.

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

СМИ зарегистрировано Федеральной службой по надзору в сфере связи, информационных технологий и массовых коммуникаций (Роскомнадзор).
Регистрационный номер и дата принятия решения о регистрации СМИ: серия ПИ № ФС 77 - 64788 от 02.02.2016.


This website uses cookies

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

About Cookies