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Biodiversity of colon microbiota in residents of Arkhangelsk

https://doi.org/10.31631/2073-3046-2025-24-2-51-58

Abstract

Relevance. The colon microbiota represents the richest human biotope in its biodiversity. The region of residence, particularly the Arctic zone, takes part in its formation. Currently, there are few studies examining the nature of the intestinal microbiota in individuals exposed to severe climatic conditions in northern regions.
Aim. To study the biodiversity of the colon microbiota in permanent and temporary residents of one of the Arctic regions (the city of Arkhangelsk).
Materials and methods. A cross-sectional study was conducted on 90 participants. A PCR study tested feces from 45 permanent and 45 temporary residents, with the reasearch of 33 indicators of microbial composition. The sample included young people from 18 to 45 years old, BMI within normal limits, without acute and chronic inflammatory diseases. Data presented in the form of quantitative data (lg CFU/g) and categorical (not detected, normal, less and more than normal). Statistical analysis included the use of Pearson and Mann-Whitney chi-square tests.
Results. Study showed common features among all residents of this region – a deficiency of obligate representatives of microflora: lactobacilli, enterococci, a reduced number of bifidobacteria, and functional Escherichia coli. Also, temporary residents had a higher number of B. thethaiotaomicron (p=0.005), Ruminococcus spp. (p = 0.01), F. nucleatum (p = 0.039), F.prausnitzii (p = 0.029), A.rectalis (p=0.042), Bacteroides spp. (p = 0.048), below A.municiphila (p = 0.057), Enterococcus spp. were more often detected (p = 0.008). Moreover, the results are comparable with data from residents of Irkutsk, St. Petersburg and Canadian Inuit, which indicates a tendency towards a decrease in obligate representatives of the microbiota among residents of the northern regions and an increase in opportunistic flora.
Conclusions. The results of the study demonstrate differences in the microbial composition of the colon in permanent and temporary residents of the city of Arkhangelsk, which belongs to the Arctic zone of the Russian Federation. Additional study of the diet of the subjects will allow us to analyze the hypothesis about the geographical features of this region and the impact of factors on the number of obligate representatives of microflora: lactobacilli, bifidobacteria, E. coli, enterococci.

Keywords


About the Authors

N. N. Kukalevskaya
Northern State Medical University
Russian Federation

Natalya N. Kukalevskaya – assistant at the Department of Clinical Biochemistry, Microbiology and Laboratory Diagnostics

51, Troitsky Ave., Arkhangelsk region, Arkhangelsk, 163069

+7 (911) 874-73-10



T. A. Bazhukova
Northern State Medical University
Russian Federation

Tatyana A. Bazhukova – Dr. Sci. (Med.), Professor, Head of the Department of Clinical Biochemistry, Microbiology and Laboratory Diagnostics

Arkhangelsk

+7 (960) 001-60-61



A. M. Grjibovski
Northern State Medical University; Northern (Arctic) Federal University named after M.V. Lomonosov; North-Eastern Federal University named after M.K. Ammosov
Russian Federation

Andrej M. Grjibovski – Phd, Head of the Directorate for Research and Innovations

Arkhangelsk

+7 (921) 495-10-62



N. V. Davidovich
Northern State Medical University
Russian Federation

Natalia V. Davidovich – Cand. Sci. (Med.), Associate Professor, Associate Professor of the Department of Clinical Biochemistry, Microbiology and Laboratory Diagnostics

Arkhangelsk

+7 (902) 190-49-29



S. N. Pisareva
Northern State Medical University
Russian Federation

Svetlana N. Pisareva – senior lecturer at the Department of Clinical Biochemistry, Microbiology and Laboratory Diagnostics

Arkhangelsk

+7 (996) 503-96-09



M. A. Sabanaev
Northern State Medical University
Russian Federation

Mikhail A. Sabanaev – assistant at the Department of Clinical Biochemistry, Microbiology and Laboratory Diagnostics

Arkhangelsk

+7 (904) 866-72-33



References

1. Lloyd-Price J, Abu-Ali G, Huttenhower C. The healthy human microbiome. Genome Med. 2016;8(1):51. doi:10.1186/s13073-016-0307-y.

2. Gupta VK, Paul S, Dutta C. Geography, Ethnicity or Subsistence-Specific Variations in Human Microbiome Composition and Diversity. Front Microbiol. 2017;8:1162. doi:10.3389/fmicb.2017.01162

3. Goodrich JK, Davenport ER, Beaumont M, et al. Genetic Determinants of the Gut Microbiome in UK Twins. Cell Host Microbe. 2016;19(5):731–743. doi:10.1016/j. chom.2016.04.017

4. Li J, Quinque D, Horz HP, et al. Comparative analysis of the human saliva microbiome from different climate zones: Alaska, Germany, and Africa. BMC Microbiol. 2014;14(1):316. doi:10.1186/s12866-014-0316-1

5. Solonin Yu.G., Boyko E.R. Medical and physiological problems in the Arctic. News of the Komi Scientific Center of the Ural Branch of the Russian Academy of Sciences. 2017. No. 4 (32). P. 33–40 (In Russ).

6. Chashchin V, Kovshov AA, Thomassen Y, et al. Health Risk Modifiers of Exposure to Persistent Pollutants among Indigenous Peoples of Chukotka. Int J Environ Res Public Health. 2019;17(1):128. doi:10.3390/ijerph17010128

7. Tyakht AV, Kostryukova ES, Popenko AS, et al. Human gut microbiota community structures in urban and rural populations in Russia. Nat Commun. 2013;4(1):2469. doi:10.1038/ncomms3469

8. Popova AYu, Kaftyreva LA, Suzhaeva LV, et al. Comparative characteristics of intestine microbiome of republic of guinea and russian federation residents. J Infect Immun. 2018;7(4):375–382. doi:10.15789/2220-7619-2017-4-375-382 (In Russ)

9. Egorova SA, Makarova MA, Kaftyreva LA, et al. Antimicrobial susceptibility of enterobacteriacaeisolated from intestinal microbiota of residents of the Republic of Guinea and Russia (Saint Petersburg). Russ J Infect Immun. 2018;8(3):349–354 (In Russ). doi:10.15789/2220-7619-2018-3-349-354

10. Nekrasova A.I. et al. Characteristics of the Gut Microbiota Composition of the Arctic Zone Residents in the Far Eastern Region // Biomedicines. 2024. Vol. 12, № 11. P. 2472.

11. Leshuk S.I., Popkova S.M., Budnikova Z.I., et al. Features of intestinal microbiocenosis among the population of an industrial city. Hygiene i sanitariya. 2011. No. 2. P.33– 37 (In Russ).

12. Girard C., Tromas N., Amyot M., et al. Gut Microbiome of the Canadian Arctic Inuit // mSphere. 2017. N 2(1):e00297-16. doi:10.1128/mSphere.00297-16

13. Khan S, Waliullah S, Godfrey V, et al. D ietary simple sugars alter microbial ecology in the gut and promote colitis in mice.Sci Transl Med. 2020;12(567):eaay6218. doi:10.1126/scitranslmed.aay6218

14. Afroz KF, Reyes N, Young K, et al. Altered gut microbiome and autism like behavior are associated with parental high salt diet in male mice [published correction appears in Sci Rep. 2022 Apr 5;12(1):5686]. Sci Rep. 2021;11(1):8364. Published 2021 Apr 16. doi:10.1038/s41598-021-87678-x

15. Meng Y, Chen L, Lin W, et al. Exercise Reverses the Alterations in Gut Microbiota Upon Cold Exposure and Promotes Cold-Induced Weight Loss. Front Physiol. 2020;11:311. Published 2020 May 4. doi:10.3389/fphys.2020.00311

16. Myers B, Vidhatha R, Nicholas B, et al. Sleep and the gut microbiome in psoriasis: clinical implications for disease progression and the development of cardiometabolic comorbidities. J Psoriasis Psoriatic Arthritis. 2021;6(1):27–37. doi:10.1177/2475530320964781

17. Lu Y, Li Z, Peng X. Regulatory effects of oral microbe on intestinal microbiota and the illness. Front Cell Infect Microbiol. 2023;13:1093967. Published 2023 Feb 1. doi:10.3389/fcimb.2023.1093967


Review

For citations:


Kukalevskaya N.N., Bazhukova T.A., Grjibovski A.M., Davidovich N.V., Pisareva S.N., Sabanaev M.A. Biodiversity of colon microbiota in residents of Arkhangelsk. Epidemiology and Vaccinal Prevention. 2025;24(2):51-58. (In Russ.) https://doi.org/10.31631/2073-3046-2025-24-2-51-58

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ISSN 2073-3046 (Print)
ISSN 2619-0494 (Online)