

Elemental composition of sputum, immune status, and features of pharyngeal microbiota in workers of the anode department of a copper smelter
https://doi.org/10.31089/1026-9428-2024-64-12-820-826
EDN: kmfzdm
Abstract
The development of bronchial and pulmonary pathology depends on characteristics of the aerosols and individual resistance of the body, largely determined by the immune system, to their exposure. Mucous membranes of a healthy person are colonized by saprophytic bacteria or normal microbiota. Yet, changes in the composition and properties of the microbial landscape induced by adverse environmental factors increase the risk of inflammation and contribute to changes in the reactivity of the immune system.
The study aims to establish the immune status, microbiota of the pharyngeal mucosa, and the elemental composition of sputum, given its cellular composition, in workers of the anode department of a copper smelter.
We tested sputum culture and elemental composition, established clinical and immunological status, and analyzed pharyngeal microbiota in 28 workers of the anode department of a copper smelter. Based on the results of testing, the subjects were divided into two groups with (1) and without (2) leukocytosis (>10 cells in the field of view) detected in sputum.
We found no acute or chronic diseases of the bronchi and lungs in the examined workers. In group 1, we observed shifts in the immune response manifested by a decrease in the number of immunocompetent cells, activation of neutrophil phagocytosis, formation of reactive oxygen species in neutrophils, and displacement of normal microbiota of the oropharyngeal mucosa by opportunistic microorganisms (in 100% versus 35%, p<0.05). The elemental composition of sputum was noted for a higher frequency of iron and lead detection and increased concentrations of barium, lead, iron, arsenic, molybdenum, antimony, vanadium, and cadmium. We established a significant effect of metals contained in sputum on cellular, humoral, and local immunity.
The inflammatory bronchopulmonary response to toxic aerosol exposure is accompanied by changes in the cellular and phagocytic links of immunity, as well as in the microbial landscape on the mucous membrane of the upper respiratory tract characterized by displacement of normal biota by opportunistic microorganisms.
Limitations. This study has certain limitations associated with the small sample size and the lack of opportunity to compare metal concentrations found in sputum with reference levels.
Ethics. The study was approved by the Local Ethics Committee of the Yekaterinburg Medical Research Center for Prophylaxis and Health Protection in Industrial Workers (extract from the minutes of the meeting No. 8 dated 12/26/2016).
Contributions:
Karpova E.P. — study conception and design, draft manuscript preparation;
Bushueva T.V. — study conception and design, draft manuscript preparation;
Roslaya N.A. — study conception and design, draft manuscript preparation;
Shtin T.N. — physicochemical analysis of sputum;
Fedoruk A.A. — description of working conditions of the subjects;
Gurvich V.B. — study conception;
Labzova A.K. — clinical tests;
Gribova Yu.V. — clinical tests;
Gazimova V.G. — sample enumeration;
Khlystov I.A. — data analysis.
Funding. This research received no external funding.
Conflict of interest. The authors have no conflicts of interest to declare.
Received: 08.11.2024 / Accepted: 02.12.2024 / Published: 10.12.2024
About the Authors
Elizaveta P. KarpovaRussian Federation
Junior Researcher, Research and Production Department Laboratory and Diagnostic Technologies, Yekaterinburg Medical Research Center for Prophylaxis and Health Protection in Industrial Workers
e-mail: karpovaep@ymrc.ru
Tatiana V. Bushueva
Russian Federation
Head of the Research and Production Department Laboratory and Diagnostic Technologies, Yekaterinburg Medical Research Center for Prophylaxis and Health Protection in Industrial Workers, Cand. Sci. (Med.)
e-mail: bushueva@ymrc.ru
Natalia A. Roslaya
Russian Federation
Leading researcher, Research and Production Department "Laboratory and Diagnostic Technologies", Yekaterinburg Medical Research Center for Prophylaxis and Health Protection in Industrial Workers; Associate Professor, Department of Public Health and Healthcare, Ural State Medical University, Dr. Sci. (Med.)
e-mail: naroslaya@gmail.com
Tatiana N. Shtin
Russian Federation
Head of the Department of Physical and Chemical Research Methods, Yekaterinburg Medical Research Center for Prophylaxis and Health Protection in Industrial Workers, Cand. Sci. (Chem.)
e-mail: shtintn@ymrc.ru
Anna A. Fedoruk
Russian Federation
Head of the Department of Occupational Medicine, Yekaterinburg Medical Research Center for Prophylaxis and Health Protection in Industrial Workers, Cand. Sci. (Med.)
e-mail: annaf@ymrc.ru
Vladimir B. Gurvich
Russian Federation
Scientific Director, Yekaterinburg Medical Research Center for Prophylaxis and Health Protection in Industrial Workers, Dr. Sci. (Med.)
e-mail: gurvich@ymrc.ru
Alla K. Labzova
Russian Federation
Researcher, Research and Production Department Laboratory and Diagnostic Technologies, Yekaterinburg Medical Research Center for Prophylaxis and Health Protection in Industrial Workers
e-mail: labzovaak@ymrc.ru
Yulia V. Gribova
Russian Federation
Doctor of clinical laboratory diagnostics, Research and Production Department "Laboratory and Diagnostic Technologies", Yekaterinburg Medical Research Center for Prophylaxis and Health Protection in Industrial Workers
e-mail: gribova@ymrc.ru
Venera G. Gazimova
Russian Federation
Head of the Department of Occupational Medicine Organization, Yekaterinburg Medical Research Center for Prophylaxis and Health Protection in Industrial Workers, Cand. Sci. (Med.)
e-mail: venera@ymrc.ru
Ivan A. Khlystov
Russian Federation
Head of the Laboratory of Environmental Hygiene and Human Ecology, Yekaterinburg Medical Research Center for Prophylaxis and Health Protection in Industrial Workers, Cand. Sci. (Biol.)
e-mail: hlistovia@ymrc.ru
References
1. Semenov S.A., Khasanova G.R. Risk factors for development of Streptococcus pneumoniae resistance to antibiotics. Prakticheskaya Meditsina. 2020; 18(6): 113–118 (in Russian). https://doi.org/10.32000/2072-1757-2020-6-113-118
2. Forte G., Bocca B., Pisano A., Collu C., Farace C., Sabalic A., et al. The levels of trace elements in sputum as biomarkers for idiopathic pulmonary fibrosis. Chemosphere. 2021; 271: 129514. https://doi.org/10.1016/j.chemosphere.2020.129514
3. Prozorova G.G., Burlachuk V.T., Tribuntseva L.V., Olysheva I.A., Nikonorova M.V. The cellular composition of induced sputum in patients with asthma as a prognostic criterion for efficiency of the disease’s treatment. Zhurnal anatomii i gistopatologii. 2016; 5(1): 52–57 (in Russian). https://doi.org/10.18499/2225-7357-2016-5-1-52-57
4. Cao C., Li W., Hua W., Yan F., Zhang H., Huang H. et al. Proteomic analysis of sputum reveals novel biomarkers for various presentations of asthma. J. Transl. Med. 2017; 15(1): 171. https://doi.org/10.1186/s12967-017-1264-y
5. Suzuki T., Hidaka T., Kumagai Y., Yamamoto M. Environmental pollutants and the immune response. Nat. Immunol. 2020; 21(12): 1486–95. https://doi.org/10.1038/s41590-020-0802-6
6. Menshikov V.V., ed. Methods of Clinical Laboratory Testing: A Handbook. Мoscow: Meditsina Publ.; 1987 (in Russian).
7. Walsh D., Bevan J., Harrison F. How does airway surface liquid composition vary in different pulmonary diseases, and how can we use this knowledge to model microbial infections? Microorganisms. 2024; 12(4): 732. https://doi.org/10.3390/microorganisms12040732
8. Monsé C., Westphal G., Raulf M., Jettkant B., van Kampen V., Kendzia B. et al. No inflammatory effects after acute inhalation of barium sulfate particles in human volunteers. BMC Pulm. Med. 2022; 22(1): 233. https://doi.org/10.1186/s12890-022-02021-y
9. Skalny A.V., Lima T.R.R., Ke T., Zhou J.C., Bornhorst J., Alekseenko S.I., et al. Toxic metal exposure as a possible risk factor for COVID-19 and other respiratory infectious diseases. Food Chem. Toxicol. 2020; 146: 111809. https://doi.org/10.1016/j.fct.2020.111809
10. Ray P., Haideri N., Haque I., Mohammed O., Chakraborty S., Banerjee S., et al. The impact of nanoparticles on the immune system: A gray zone of nanomedicine. J. Immunol. Sci. 2021; 5(1): 19–33. https://doi.org/10.29245/2578-3009/2021/1.1206
11. Kumah E.A., Fopa R.D., Harati S., Boadu P., Zohoori F.V., Pak T. Human and environmental impacts of nanoparticles: A scoping review of the current literature. BMC Public Health. 2023; 23(1): 1059. https://doi.org/10.1186/s12889-023-15958-4
12. Katsnelson B.A., Privalova L.I., Degtyareva T.D., Kuzmin S.V., Sutunkova M.P., Minigalieva I.A., etc. Comparative characterization of the biological gressivity of particles having different dimensions in nano- and micrometric ranges. Zdorov’e naseleniya i sreda obitaniya. 2011; (5(218)): 32–36 (in Russian).
13. Wang Z., Sun Y., Yao W., Ba Q., Wang H. Effects of cadmium exposure on the immune system and immunoregulation. Front. Immunol. 2021; 12: 695484. https://doi.org/10.3389/fimmu.2021.695484
14. Mirkov I., Popov Aleksandrov A., Ninkov M., Tucovic D., Kulas J., Zeljkovic M. et al. Immunotoxicology of cadmium: Cells of the immune system as targets and effectors of cadmium toxicity. Food Chem. Toxicol. 2021; 149: 112026. https://doi.org/10.1016/j.fct.2021.112026
15. Dai L., Xu W., Li H., Frank J.A., He C., Zhang Z., et al. Effects of hexavalent chromium on mouse splenic T lymphocytes. Toxicol. In Vitro. 2017; 45(1): 166–171. https://doi.org/10.1016/j.tiv.2017.09.006
16. Genchi G., Carocci A., Lauria G., Sinicropi M.S., Catalano A. Nickel: Human health and environmental toxicology. Int. J. Environ. Res. Public Health. 2020; 17(3): 679. https://doi.org/10.3390/ijerph17030679
17. Wu Q., Mu Q., Xia Z., Min J., Wang F. Manganese homeostasis at the host–pathogen interface and in the host immune system. Semin. Cell Dev. Biol. 2021; 115: 45–53. https://doi.org/10.1016/j.semcdb.2020.12.006
18. Vieceli T., Tejada S., Martinez-Reviejo R., Pumarola T., Schrenzel J., Waterer G.W., et al. Impact of air pollution on respiratory microbiome: A narrative review. Intensive Crit. Care Nurs. 2023; 74: 103336. https://doi.org/10.1016/j.iccn.2022.103336
19. Wang Y., Tang M. PM2.5 induces autophagy and apoptosis through endoplasmic reticulum stress in human endothelial cells. Sci. Total Environ. 2020; 710: 136397. https://doi.org/10.1016/j.scitotenv.2019.136397
Review
For citations:
Karpova E.P., Bushueva T.V., Roslaya N.A., Shtin T.N., Fedoruk A.A., Gurvich V.B., Labzova A.K., Gribova Yu.V., Gazimova V.G., Khlystov I.A. Elemental composition of sputum, immune status, and features of pharyngeal microbiota in workers of the anode department of a copper smelter. Russian Journal of Occupational Health and Industrial Ecology. 2024;64(12):820-826. (In Russ.) https://doi.org/10.31089/1026-9428-2024-64-12-820-826. EDN: kmfzdm