The impact of systemic homeostatic regulator — associates of peroxide anion radicals on the activity of microorganisms
- Authors: Iksanova T.I.1, Stekhin A.A.2, Yakovleva G.V.2, Kamenetskaya D.B.1, Mikhailova R.I.1, Zagainova A.V.1
-
Affiliations:
- Center for Strategic Planning and Management of Biomedical Health Risk of Federal Medical Biological Agency
- National Medical Research Center for Rehabilitation and Balneology of the Ministry of Health of the Russian Federation
- Issue: Vol 101, No 4 (2022)
- Pages: 368-374
- Section: ENVIRONMENTAL HYGIENE
- Published: 06.05.2022
- URL: https://rjsocmed.com/0016-9900/article/view/639321
- DOI: https://doi.org/10.47470/0016-9900-2022-101-4-368-374
- ID: 639321
Cite item
Full Text
Abstract
Introduction. This work is devoted to the study of the effect of peroxide anion radicals in submicromol concentrations and the structural organization of the associated water phase in drinking waters, activated by physical methods on the viability of a number of microorganisms in the human gastrointestinal tract.
Materials and methods. Studies were carried out using standard methods of microbiological analysis of drinking water on microorganisms of Escherichia coli 1257, Pseudomonas aeruginosa, Salmonella enteritidis 5765, Enterococcus faecalis ATCC 29212, Klebsiela pneumoniae subsp. pneumoniae ATCC 700603, Citrobacter freundii 101/57. Evaluation of changes in the physical parameters of water before and after treatment with the studied technologies was carried out using electrophysical and physical-chemical parameters (hydrogen index, redox potential, content of peroxide anion radical); structural and energy indicators (by the share of the associated water phase and the density of its distribution by energy levels).
Results. The data obtained indicate the strongest stabilizing effect on the viability of microorganisms implementing ATP-phase energy metabolism to be exerted by associates of peroxide anion radicals controlling metabolic processes and providing an extra-substrate channel for maintaining the energy function of microorganisms. We assume that catalytically active waters have a systemic regulatory effect, ensuring the maintenance of homeostasis of microorganisms. Similar regulation is also possible in the intestinal microbiota of the body to maintain or suppress the activity of competing microorganisms when a person uses biocatalytically active (in the range of concentrations of peroxide anion radicals in drinking water from 0.1 to 40 drinking water µg/L) drinking water. We assume that this will solve a number of issues related to the etiology and pathophysiology of a number of gastroenterological diseases caused by changes in the electrophysical state of the internal environment of the gastrointestinal tract, promoting the emergence and development of a competing, adapted to an environment with low electron-donor capacity, bacterial microbiota.
Limitations. The data obtained as a result of the experiment on biota similar to the human intestinal microbiota are of scientific interest and research involving warm-blooded animals is necessary to continue work in this direction.
Conclusion. Physically treated waters affect the growth or inhibition of intestinal biota colonies, which may be associated with the controlling role of peroxide anion radicals on intracellular metabolic processes in microorganisms.
Contribution:
Iksanova T.I. — concept and design of the study, collection and processing of the material;
Kamenetskaya D.B., Zagainova A.V. — concept and design of the study, collection and processing of the material;
Stekhin A.A.,Yakovleva G.V. — writing text;
Mikhailova R.I. — editing.
All authors are responsible for the integrity of all parts of the manuscript and approval of the manuscript final version.
Conflict of interest. The authors declare no conflict of interest.
Acknowledgement. The article was prepared within the framework of State Assignment No. АААА-А18-118020590087-5 of the Federal Medical and Biological Agency.
Received: February 2, 2022 / Accepted: April 12, 2022 / Published: April 30, 2022
About the authors
Tatiana I. Iksanova
Center for Strategic Planning and Management of Biomedical Health Risk of Federal Medical Biological Agency
Author for correspondence.
Email: tiksanova@cspmz.ru
ORCID iD: 0000-0002-3153-8706
Leading biologist, Environmental Health department of the Centre for Strategic Planning and Management of Biomedical Health Risks of the FMBA of Russia (Centre for Strategic Planning, Moscow, 119121, Russian Federation.
e-mail: TIksanova@cspmz.ru
Russian FederationAnatoly A. Stekhin
National Medical Research Center for Rehabilitation and Balneology of the Ministry of Health of the Russian Federation
Email: noemail@neicon.ru
ORCID iD: 0000-0002-8750-0686
Russian Federation
Galina V. Yakovleva
National Medical Research Center for Rehabilitation and Balneology of the Ministry of Health of the Russian Federation
Email: noemail@neicon.ru
ORCID iD: 0000-0002-8766-2773
Russian Federation
Darya B. Kamenetskaya
Center for Strategic Planning and Management of Biomedical Health Risk of Federal Medical Biological Agency
Email: noemail@neicon.ru
ORCID iD: 0000-0002-9050-3757
Russian Federation
Rufina I. Mikhailova
Center for Strategic Planning and Management of Biomedical Health Risk of Federal Medical Biological Agency
Email: noemail@neicon.ru
ORCID iD: 0000-0001-7194-9131
Russian Federation
Angelika V. Zagainova
Center for Strategic Planning and Management of Biomedical Health Risk of Federal Medical Biological Agency
Email: noemail@neicon.ru
ORCID iD: 0000-0003-4772-9686
Russian Federation
References
- Kurmangulov A.A., Dorodneva E.F., Isakova D.N. Functional activity of intestinal microbiota with metabolic syndrome. Ozhirenie i metabolizm. 2016; 13(1): 16–9. https://doi.org/10.14341/omet2016116-19. (in Russian)
- Lyte M. Microbial endocrinology in the microbiome-gut-brain axis: how bacterial production and utilization of neurochemicals influence behavior. PLoS Pathog. 2013; 9(11): e1003726. https://doi.org/10.1371/journal.ppat.1003726
- Stekhin A.A., Yakovleva G.V., Iksanova T.I., Pronko K.N., Zemskov V.M. Evoluation of the effect of structural-physical changes in water on biological activity. Clin. Pract. 2018; 15(5): 861–71. https://doi.org/10.4172/clinical-practice.1000419
- Rakhmanin Yu.A., Stekhin A.A., Yakovleva G.V. Water Biophysics: Quantum Nonlocality in Water Treatment Technologies; Regulatory Role of Associated Water in Cellular Metabolism; Regulation of Bioenergetic Activity of Drinking Water [Biofizika vody: Kvantovaya nelokal’nost’ v tekhnologiyakh vodopodgotovki; regulyatornaya rol’ assotsiirovannoy vody v kletochnom metabolizme; normirovanie bioenergeticheskoy aktivnosti pit’evoy vody]. Moscow: LENAND; 2016. (in Russian)
- Kulagin M.V., Yakovleva G.V., Stekhin A.A., Gukasov V.M., Shovkoplyas Yu.A. Parameterization of the associated water phase using high performance liquid chromatography. Meditsina i vysokie tekhnologii. 2018; (4): 33–43. (in Russian)
- Methodical instructions MUK 4.2.1018-01. Sanitary-microbiological analysis of drinking water (Change No. 1). Moscow; 2001. (in Russian)
- Methodical instructions 2.1.4.1184-03. Guidelines for the implementation and application of sanitary and epidemiological rules and regulations SanPiN 2.1.4.1116-02 “Drinking water. Hygienic requirements for the quality of water packaged in a container. Quality control” (with Change No. 1). Moscow; 2003. (in Russian)
- Trindade I.B., Invernici M., Cantini F., Louro R.O., Piccioli M. 1H, 13C and 15N assignment of the paramagnetic high potential iron-sulfur protein (HiPIP) PioC from Rhodopseudomonas palustris TIE-1. Biomol. NMR Assign. 2020; 14(2): 211–5. https://doi.org/10.1007/s12104-020-09947-6
- Read A.D., Bentley R.E., Archer S.L., Dunham-Snary K.J. Mitochondrial iron-sulfur clusters: Structure, function, and an emerging role in vascular biology. Redox Biol. 2021; 47: 102164. https://doi.org/10.1016/j.redox.2021.102164
- Brzoza P., Godlewska U., Borek A., Morytko A., Zegar A., Kwiecinska P., et al. Redox active antimicrobial peptides in controlling growth of microorganisms at body barriers. Antioxidants (Basel). 2021; 10(3): 446. https://doi.org/10.3390/antiox10030446
- Hopkins E.G.D., Frankel G. Overview of the effect of Citrobacter rodentium infection on host metabolism and the microbiota. In: Schüller S., Bielaszewska M., eds. Shiga Toxin-Producing E. coli. Methods in Molecular Biology. New York: Humana; 2021: 2291. https://doi.org/10.1007/978-1-0716-1339-9_20
- Amulya K., Mohana S.V. Augmenting succinic acid production by bioelectrochemical synthesis: Influence of applied potential and CO2 availability. Chem. Eng. J. 2021; 411: 128377. https://doi.org/10.1016/j.cej.2020.128377
- Tkach S.M., Puchkov K.S., Sizenko A.K., Kuzenko Yu.G. Intestinal microbiota and functional bowel diseases. Sovremennaya gastroenterologiya. 2014; (1): 118–29. (in Russian)
- Ohman L., Simren M. Pathogenesis of IBS: role of inflammation, immunity and neuroimmune interactions. Nat. Rev. Gastroenterol. Hepatol. 2010; 7(3): 163–73. https://doi.org/10.1038/nrgastro.2010.4
- Parkes G.C., Brostoff J., Whelan K., Sanderson J.D. Gastrointestinal microbiota in irritable bowel syndrome: their role in its pathogenesis and treatment. Am. J. Gastroenterol. 2008; 103(6): 1557–67. https://doi.org/10.1111/j.1572-0241.2008.01869.x
- Tomasova L., Grman M., Ondrias K., Ufnal M. The impact of gut microbiota metabolites on cellular bioenergetics and cardiometabolic health. Nutr. Metab. (Lond). 2021; 18(1): 72. https://doi.org/10.1186/s12986-021-00598-5
Supplementary files
