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At the Shores of a Vanishing Sea: Microbial Communities of Aral and Southern Aral Sea Region

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Abstract

Since the early 1960s, agricultural development in the irrigated areas of Uzbekistan resulted in a 90% decrease of the Aral Sea area, while the water salinity increased from 1 to 20%. The goal of the present work was to investigate the diversity of microbial communities of the water and sediments of the Western Aral Sea, as well as of the adjacent soils and basins, using high-throughput sequencing of the V4 variable region of the 16S rRNA genes. It was found that Aral Sea water with a salinity of 22% was inhabited by uncultured Archaea of the family Haloferacaceae (22‒43%), as well as by bacteria of the genera Spiribacter and Psychroflexus. In the Aral Sea sediments, the share of archaea was much lower (2‒17%), and among them uncultured Woesearchaeales predominated. Predominant bacteria of Aral sediments were sulfate reducers of the phylum Desulfobacterota, as well as members of the genera Fusibacter, Halanaerobium, Guyparkeria, Marinobacter, Idiomarina, and Thiomicrospira. In soil samples of the former Aral Sea bed with salinity of 8.2%, a variety of archaea of the phylum Halobacterota were present, as well as uncultured bacteria of the family Nitrosococcaceae. However, in the rhizosphere of Ewresmann’s teresken plant (Kraschennininikovia ewresmanniana) growing there, archaea accounted for only 4% and mainly belonged to the family Nitrososphearaceae. In the rhizosphere microbiome, 33% of all prokaryotes were uncultured members of the phylum Actinomycetota. The microbial community of the teresken rhizosphere turned out to be similar to the soil microbial communities of the Ustyurt plateau located 3 km from the Aral Sea shore. The fresh water flowing along the former Aral Sea bed from an artificially drilled well also caused significant changes in the microbial communities: cyanobacterial mats and associated organotrophic bacteria developed along the stream bed with the increasing salinity (0.25‒2%). Finally, the greatest prokaryotic diversity was found in the microbial community of the Lake Sudochye sediment with salinity of 1%, which is probably a modern analog of the Aral Sea microbiome before its shallowing.

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REFERENCES

  1. Alexyuk, M., Bogoyavlensky, A., Alexyuk, P., Molakhanov, Y., Berezin, V., and Diegel, I., Epipelagic microbiome of the Small Aral Sea: metagenomic structure and ecological diversity, Microbiol. Open, 2021, vol. 10, no. 1, pp. 1–10.

    Article  Google Scholar 

  2. Aripov, T.F., Kukanova, S.I., Zaynatdinova, L.I., and Tashpulatov, J.J., Microorganisms of the extreme zones of the Southern Aral Sea region, Biotechnology: An Indian Journal, 2016, vol. 12, pp. 1–7

    Google Scholar 

  3. Bowman, J.P., McCammon, S.A., Lewis, T., Skerratt, J.H., Brown, J.L., Nichols, D.S., and McMeekin, T.A., Psychroflexus torquis gen. nov., sp. nov., a psychrophilic species from Antarctic sea ice, and reclassification of Flavobacterium gondwanense (Dobson et al. 1993) as Psychroflexus gondwanense gen. nov., comb. nov., Microbiology (SGM), 1998, vol. 144, no. 6, pp. 1601–1609.

    Article  CAS  PubMed  Google Scholar 

  4. Callahan, B.J., McMurdie, P.J., Rosen, M.J., Han, A.W., Johnson, A.J., and Holmes, S.P., Dada2: high-resolution sample inference from Illumina amplicon data, Nat. Methods, 2016, vol. 13, pp. 581–587.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Callahan, B., McMurdie, P., and Holmes, S., Exact sequence variants should replace operational taxonomic units in marker-gene data analysis, ISME J., 2017, no. 11, pp. 2639–2643.

  6. Caruso, V., Song, X., Asquith, M., and Karstens, L., Performance of microbiome sequence inference methods in environments with varying biomass, mSystems, 2019, vol. 4, no. 1, pp. 163–18.

    Article  Google Scholar 

  7. Donachie, S.P., Bowman, J.P., and Alam, M., Psychroflexus tropicus sp. nov., an obligately halophilic Cytophaga-Flavobacterium-Bacteroides group bacterium from an Hawaiian hypersaline lake, Int. J. Syst. Evol. Microbiol., 2004, vol. 54, no. 3, pp. 935–940.

    Article  CAS  PubMed  Google Scholar 

  8. Fadrosh, D.W., Ma, B., Gajer, P., Sengamalay, N., Ott, S., Brotman, R.M., and Ravel, J., An improved dual-indexing approach for multiplexed 16S rRNA gene sequencing on the Illumina MiSeq platform, Microbiome, 2014, vol. 2, pp. 1–7.

    Article  Google Scholar 

  9. Jiang, H., Huang, J., Li, L., Huang, L., Manzoor, M., Yang, J., Wu, G., Sun, X., Wang, B., Egamberdieva, D., Panosyan, H., Birkeland, N.K., Zhu, Z., and Li, W., Onshore soil microbes and endophytes respond differently to geochemical and mineralogical changes in the Aral Sea, Sci. Total. Environ., 2021, vol. 765, no. 15, pp. 142675–142679.

    Article  CAS  PubMed  Google Scholar 

  10. Lagkouvardos, I., Fischer, S., Kumar, N., and Clavel, T., Rhea: a transparent and modular R pipeline for microbial profiling based on 16S rRNA gene amplicons, PeerJ., 2017, vol. 5, pp. 2836–2840.

    Article  Google Scholar 

  11. León, M.J., Fernández, A.B., Ghai, R., Sánchez-Porro, C., Rodriguez-Valera, F., and Ventosa, A., From metagenomics to pure culture: isolation and characterization of the moderately halophilic bacterium Spiribacter salinus gen. nov., sp. nov., Appl Environ Microbiol., 2014, vol. 80, no. 13, pp. 3850–3857.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Merkel, A.Y., Tarnovetskii, I.Y., Podosokorskaya, O.A., and Toshchakov, S.V., Analysis of 16S rRNA primer systems for profiling of thermophilic microbial communities, Microbiology (Moscow), 2019, vol. 88, no. 6, pp. 671–680.

    Article  CAS  Google Scholar 

  13. Perez-Molphe-Montoya, E., Küsel, K., and Overholt, W.A., Redefining the phylogenetic and metabolic diversity of phylum Omnitrophota, Environ. Microbiol., 2022, vol. 24, no.11, pp. 5437–5449.

    Article  CAS  PubMed  Google Scholar 

  14. Quast, C., Pruesse, E., Yilmaz, P., Gerken, J., Schweer, T., Yarza, P., Peplies, J., and Glöckner, F.O., The SILVA ribosomal RNA gene database project: improved data processing and web-based tools, Nucleic Acids Res., 2013, vol. 41, pp. 590–596.

    Article  Google Scholar 

  15. Shurigin, V., Hakobyan, A., Panosyan, H., Egamberdieva, D., Davranov, K., and Birkeland, N.K., A glimpse of the prokaryotic diversity of the Large Aral Sea reveals novel extremophilic bacterial and archaeal groups, Microbiology Open, 2019, vol. 8, no. 9, pp. 850–865.

    Article  Google Scholar 

  16. Stulina, G., Verkhovtseva, N., and Gorbacheva, M., Composition of the microorganism community found in the soil cover of the dry seabed of the Aral Sea, J. Geosci. Environ. Prot., 2019, no. 7, pp. 1–23.

  17. Zhao, D., Zhang, S., Kumar, S., Zhou, H., Xue, Q., Sun, W., Zhou, J., and Xiang, H., Comparative genomic insights into the evolution of Halobacteria-associated “Candidatus Nanohaloarchaeota”, mSystems, 2022, vol. 7, no. 6, pp. 669–691.

    Article  Google Scholar 

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ACKNOWLEDGMENTS

The authors are grateful to S.S. Buriev and A.I. Kulonov for their help in organizing the expedition and in sample collection, to N.Yu. Beshko for the identification of halophyte plants, and to A.R. Stroeva for the help in DNA isolation.

Funding

The main work was supported by the project A-FA-2021-428 “Microbial Communities of the Modern Aral Sea and the Aral Region: Diversity, Properties, and Biotechnological Potential.” The work on analysis of sequencing results was supported by the RF Ministry of Science and Higher Education.

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Correspondence to N. A. Chernyh.

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ETHICS APPROVAL AND CONSENT TO PARTICIPATE

This article does not contain any studies involving animals or human participants performed by any of the authors.

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The authors of this work declare that they have no conflicts of interest.

AUTHORS’ CONTRIBUTION

Sampling: NAC, AYM, AIS, and JEA; physicochemical characterization: KVK; metagenomic DNA isolation: NAC and AYM; barcoding and pooling the 16S rRNA gene libraries: AYM; profiling of the microbial community based on sequencing results: AYM; data analysis and manuscript preparation: NAC, AYM, AIS, KDD, and EAB-O; project management: KDD and EAB-O. All authors participated in discussion of the results.

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Translated by P. Sigalevich

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Chernyh, N.A., Merkel, A.Y., Kondrasheva, K.V. et al. At the Shores of a Vanishing Sea: Microbial Communities of Aral and Southern Aral Sea Region. Microbiology 93, 1–13 (2024). https://doi.org/10.1134/S0026261723602944

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