Skip to main content
Log in

Cultivation of Diverse Microorganisms from Hypersaline Lake and Impact of Delay in Sample Processing on Cell Viability

  • Published:
Current Microbiology Aims and scope Submit manuscript

Abstract

The Sambhar Salt Lake is a halite rich athalassohaline basin, provides a unique opportunity for microbial ecologists to study halophiles. The lake has a high proportion of Na+ and Cl ions making it a hypersaline ecosystem. In the current study, archaea and bacteria from Sambhar Lake were isolated using two cultivation approaches. A total of 449 isolates were obtained, out of which 13 represent archaeal while 12 represent bacterial genera. Natronococcus and Alkalibacillus were found predominant groups among archaea and bacteria, respectively. Apart from the common genera in both the approaches Alteribacillus, Halobacillus, Halorubrum, Lentibacillus, Natronorubrum, Piscibacillus and Thalassobacillus were found only in the samples processed onsite however only three genera Aliidiomarina, Natrinema and Natronolimnobius were isolated when samples were processed in the laboratory after transportation using the same growth conditions. Other than the isolation of diverse group of organisms 13 putative novel taxa with similarity less than 98% were identified using 16S rRNA gene sequencing.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  1. Amoozegar MA, Siroosi M, Atashgahi S, Smidt H, Ventosa A (2017) Systematics of haloarchaea and biotechnological potential of their hydrolytic enzymes. Microbiology 163:623–645

    Article  CAS  Google Scholar 

  2. Amoozegar MA, Safarpour A, Noghabi KA, Bakhtiary T, Ventosa A (2019) Halophiles and their vast potential in biofuel production. Front Microbiol 10:1895

    Article  Google Scholar 

  3. Antony CP, Kumaresan D, Hunger S, Drake HL, Murrell JC, Shouche YS (2013) Microbiology of Lonar Lake and other soda lakes. ISME J 7(3):468–476

    Article  Google Scholar 

  4. APHA (1998) Standard methods for the examination of water and wastewater, 20th edn. WEF, Washington, DC

    Google Scholar 

  5. Baricz A, Cristea A, Muntean V, Teodosiu G, Andrei AS, Molnar I (2015) Culturable diversity of aerobic Halophilic archaea (Fam. Halobacteriaceae) from hypersaline, meromictic Transylvanian lakes. Extremophiles 19(2):525–537

    Article  CAS  Google Scholar 

  6. Bilen M, Dufour JC, Lagier JC, Cadoret F, Daoud Z, Dubourg G, Raoult D (2018) The contribution of culturomics to the repertoire of isolated human bacterial and archaeal species. Microbiome 6(1):94

    Article  Google Scholar 

  7. DeMarco AL, Rabe LK, Austin MN, Stoner KA, Avolia HA, Meyn LA (2017) Survival of vaginal microorganisms in three commercially available transport systems. Anaerobe 45:44–49

    Article  CAS  Google Scholar 

  8. Deocampo DM, Jones BF (2013) Geochemistry of saline lakes. In: Drever J (ed) Treaties on geochemistry, 2nd edn. Elsevier, San Diego, pp 437–469

    Google Scholar 

  9. Elvi R, Assa P, Birbir M, Ogan A, Oren A (2004) Characterization of extremely halophilic archaea isolated from Ayvalik salterns, Turkey. World J Microbiol Biotechnol 20:563–566

    Article  Google Scholar 

  10. Esteves AI, Amer N, Nguyen M, Thomas T (2016) Sample processing impacts the viability and cultivability of the sponge microbiome. Front Microbiol 7:499

    Article  Google Scholar 

  11. Gunde-Cimerman N, Plemenitas A, Oren A (2018) Strategies of adaptation of microorganisms of the three domains of life to high salt concentrations. FEMS Microbiol Rev 42(3):353–375

    Article  CAS  Google Scholar 

  12. Kumbhare SV, Dhotre DP, Dhar SK, Jani K, Apte DA, Shouche YS, Sharma A (2015) Insights into diversity and imputed metabolic potential of bacterial communities in the continental shelf of Agatti Island. PLoS ONE 10(6):e0129864

    Article  Google Scholar 

  13. Lane DJ (1991) 16S/23S rRNA sequencing. In: Stackebrandt E, Goodfellow M (eds) Nucleic acids techniques in bacterial systematics. Wiley, Chichester, pp 115–147

    Google Scholar 

  14. Ling LL, Schneider T, Peoples AJ, Spoering AL, Engels I et al (2015) A new antibiotic kills pathogens without detectable resistance. Nature 517:455–459

    Article  CAS  Google Scholar 

  15. Reuter JA, Spacek DV, Snyder MP (2015) High-throughput sequencing technologies. Mol Cell 58(4):586–597

    Article  CAS  Google Scholar 

  16. Reysenbach AL, Longnecker K, Kirshtein L (2000) Novel bacterial and archaeal lineages from an in situ growth chamber deployed at a Mid-Atlantic Ridge hydrothermal vent. Environ Microbiol 66:3798–3806

    Article  CAS  Google Scholar 

  17. Rodriguez-Valera F, Ruiz-Berraquero F, Ramos-Cormenzana A (1980) Isolation of extremely halophilic bacteria able to grow in defined inorganic media with single carbon sources. J Gen Microbiol 119:535–538

    Google Scholar 

  18. Singh BP, Singh N, Singh SP (2013) Modern salt (halite) deposits of the Sambhar Lake, Rajasthan and their formative conditions. Curr Sci 104(11):1482–1484

    Google Scholar 

  19. Sharma A, Shouche Y (2014) Microbial Culture Collection (MCC) and International Depositary Authority (IDA) at National Centre for Cell Science, Pune. Indian J Microbiol 54(2):129–133

    Article  Google Scholar 

  20. Sharma A, Jani K, Shouche YS, Pandey A (2015) Microbial diversity of the Soldhar Hot Spring, India, assessed by analyzing 16S rRNA and protein-coding genes. Ann Microbiol 65:1323

    Article  CAS  Google Scholar 

  21. Sharma A, Paul D, Dhotre D, Jani K, Pandey A, Shouche YS (2017) Deep sequencing analysis of bacterial community structure of Soldhar Hot Spring, India. Microbiology 86:136

    Article  CAS  Google Scholar 

  22. Sharma A, Jani K, Feng GD, Karodi P, Vemuluri VR et al (2018) Subsaxibacter sediminis sp. nov., isolated from Arctic glacial sediment and emended description of the genus Subsaxibacter. Int J Syst Evol Microbiol 68(5):1678–1682

    Article  CAS  Google Scholar 

  23. Sharma A, Jani K, Thite V, Dhar S, Shouche YS (2018) Geochemistry shapes bacterial communities and their metabolic potentials in tertiary coalbed. Geomicrobiol J 36(2):179–187

    Article  Google Scholar 

Download references

Acknowledgements

We are grateful to Mr. Kunal Jani for helping us during sampling.

Funding

This work was supported by the Department of Biotechnology (DBT), Government of India (Grant No. BT/Coord.II/01/03/2016) under the Project ‘Establishment of National Centre for Microbial Resource’.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Avinash Sharma.

Ethics declarations

Conflicts of interest

The authors declare that there are no conflicts of interest.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

The GenBank accession number for the 16S rRNA gene sequences of representative strains are MK862575–MK862680.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary file1 (DOCX 46 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Kajale, S., Deshpande, N., Shouche, Y. et al. Cultivation of Diverse Microorganisms from Hypersaline Lake and Impact of Delay in Sample Processing on Cell Viability. Curr Microbiol 77, 716–721 (2020). https://doi.org/10.1007/s00284-019-01857-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00284-019-01857-8

Navigation