DETECTION OF POTENTIALLY PATHOGENIC BACTERIA IN THE BRACKISH RIVERS FLOWING INTO THE ELTON LAKE BY HIGH-THROUGHPUT SEQUENCING

Cover Page


Cite item

Full Text

Abstract

Aim. To indicate potentially pathogenic bacteria in plankton of the brackish rivers flowing into the Elton Lake by high-throughput sequencing of 16S ssuRNA gene. Materials and methods. The water samples from brackish rivers Lantsug and Chernavka, flowing into the Elton Lake, were taken up in a volume of 50 ml, filtered through membrane filters (pore diameter - 0.22 pm). Total DNAwas obtained by phenol-chloroform extraction with preliminary homogenization and enzymatic lysis. DNA libraries for sequencing were created by protocol Illumina with primers to a variable V3-V4 region of 16S ssuRNA gene. Sequencing was performed on a platform MiSeq («Illumina», США). Results.There were found the phylotypes of potentially pathogenic bacteria of Proteobacteria phylum from the families Enterobacteriaceae, Pseudomonadaceae, Campylobacteraceae, Vibrionaceae, Aeromonadaceae, Moraxellaceae, Legionellaceae, Alcaligenaceae, Campylobacteraceae, and also of Firmicutes, Bacteroidetes, Actinobacteria phyla in the plankton samples of the brackish rivers. Probable source of bacterial contamination is large and small cattle. Conclusion. These data demonstrate that the continental brackish waters, along with freshwater and marine habitats perform a reservoir function to potentially pathogenic microorganisms. High-throughput sequencing can be used to screen the presence of pathogens in water.

About the authors

E. A. Selivanova

Institute of Сellular and Intracellular Symbiosis

Author for correspondence.
Email: noemail@neicon.ru
Russian Federation

Yu. A. Khlopko

Institute of Сellular and Intracellular Symbiosis

Email: noemail@neicon.ru
Russian Federation

N. E. Gogoleva

Kazan Institute of Biochemistry and Biophysics; Kazan Federal University

Email: noemail@neicon.ru
Russian Federation

A. O. Plotnikov

Institute of Сellular and Intracellular Symbiosis

Email: noemail@neicon.ru
Russian Federation

References

  1. Davies C.M., Long J.A.H., Donald M., Ashbolt N.J. Survival of Fecal Microorganisms in Marine and Freshwater Sediments. Appl. Env. Microbiology. 1995, 61 (5):1888-1896.
  2. Edgar R.C. Search and clustering orders of magnitude faster than BLAST. Bioinformatics. 2010, 26 (19): 2460-2461. doi: 10.1093/bioinformatics/btq461.
  3. Figueras M. J., Latif-Eugenнn F., Ballester F. et al. Aeromonas intestinalis and Aeromonas enterica isolated from human faeces, Aeromonas crassostreae from oyster and Aeromonas aquatilis isolated from lake water represent novel species. New Microbe and New Infect. 2017, 15: 74-76.
  4. Gast R.J., Moran D.M., Dennett M.R. et al. Amoebae and Legionella pneumophila in saline environments. J. Water Health. 2011, 9(1): 37-52.
  5. Girones R., Ferrus M.A., Alonso J.L. et al. Molecular detection of pathogens in water. The pros and cons of molecular techniques. Water Research. 2010, 44: 4325-4339.
  6. Han X.Y, Ihegword A., Evans S.E. et al. Microbiological and Clinical Studies of Legionellosis in 33 Patients with Cancer. J. Clin. Microbiol. 2015, 53 (7): 2180-2187.
  7. Lastovica A.J., On S.L.W., Zhang L. The Family Campylobacteraceae. In: Rosenberg E. et al. (Ed.). The Prokaryotes. Springer, Berlin, Heidelberg, 2014.
  8. Levin-Edens E., Bonilla N., Meschke J. Scott et al. Survival of environmental and clinical strains of methicillin-resistant Staphylococcus aureus (MRSA) in marine and fresh waters. Water Research. 2011, 45: 5681-5686.
  9. Micana-Galbis D., Farfоn M., Gaspar Loren J. Proposal to assign Aeromonas diversa sp. nov. as a novel species designation for Aeromonas group 501. Systematic Applied Microbiology. 2010, 33: 15-19.
  10. Ng C., Goh S.G., Saeidi N. et al. Occurrence of Vibrio species, beta-lactam resistant Vibrio species, and indicator bacteria in ballast and port waters of a tropical harbor. Science of the Total Environment. 2018, 610-611: 651-656.
  11. Novakova D., Sedlacek I., Pantucek R. Staphylococcus equorum and Staphylococcus succinus isolated from human clinical specimens. J. Medical Microbiology. 2006, 55: 523-528.
  12. Rajilic -Stojanovic M.,deVosWM.The first 1000 cultured speciesofthe human gastrointestinal microbiota. FEMS Microbiol. Rev. 2014, 38 (5): 996-1047.
  13. RamKrez-Castillo F.Y, Loera-Muro A., Jacques M. et al. Waterborne Pathogens: Detection Methods and Challenges. Pathogens. 2015, 4: 307-334.
  14. Robins P.E., Skov M.W., Lewis Matt J. et al. Impact of climate change on UK estuaries: A review of past trends and potential projections. Estuarine Coastal Shelf Science. 2016, 169: 119-135.
  15. Rose J.B., Epstein P.R., Lipp E.K. et al. Climate Variability and Change in the United States: Potential Impacts on Waterand Foodborne Diseases Caused by Microbiologic Agents Environmental Health Perspectives. 2001, 109 (suppl. 2): 211-221.

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2018 Selivanova E.A., Khlopko Y.A., Gogoleva N.E., Plotnikov A.O.

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: ПИ № ФС77-75442 от 01.04.2019 г.


This website uses cookies

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

About Cookies