» Articles » PMID: 34361908

Microbial Diversity of Terrestrial Geothermal Springs in Armenia and Nagorno-Karabakh: A Review

Overview
Journal Microorganisms
Specialty Microbiology
Date 2021 Aug 7
PMID 34361908
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

The microbial diversity of high-altitude geothermal springs has been recently assessed to explore their biotechnological potential. However, little is known regarding the microbiota of similar ecosystems located on the Armenian Highland. This review summarizes the known information on the microbiota of nine high-altitude mineralized geothermal springs (temperature range 25.8-70 °C and pH range 6.0-7.5) in Armenia and Nagorno-Karabakh. All these geothermal springs are at altitudes ranging from 960-2090 m above sea level and are located on the Alpide (Alpine-Himalayan) orogenic belt, a seismically active region. A mixed-cation mixed-anion composition, with total mineralization of 0.5 mg/L, has been identified for these thermal springs. The taxonomic diversity of hot spring microbiomes has been examined using culture-independent approaches, including denaturing gradient gel electrophoresis (DGGE), 16S rRNA gene library construction, 454 pyrosequencing, and Illumina HiSeq. The bacterial phyla Proteobacteria, Bacteroidetes, Cyanobacteria, and Firmicutes are the predominant life forms in the studied springs. Archaea mainly include the phyla Euryarchaeota, Crenarchaeota, and Thaumarchaeota, and comprise less than 1% of the prokaryotic community. Comparison of microbial diversity in springs from Karvachar with that described for other terrestrial hot springs revealed that Proteobacteria, Bacteroidetes, Actinobacteria, and Deinococcus-Thermus are the common bacterial groups in terrestrial hot springs. Contemporaneously, specific bacterial and archaeal taxa were observed in different springs. Evaluation of the carbon, sulfur, and nitrogen metabolism in these hot spring communities has revealed diversity in terms of metabolic activity. Temperature seems to be an important factor in shaping the microbial communities of these springs. Overall, the diversity and richness of the microbiota are negatively affected by increasing temperature. Other abiotic factors, including pH, mineralization, and geological history, also impact the structure and function of the microbial community. More than 130 bacterial and archaeal strains (, , and ) have been reported, some of which may be representative of novel species (sharing 91-97% sequence identity with their closest matches in GenBank) and producers of thermozymes and biomolecules with potential biotechnological applications. Whole-genome shotgun sequencing of K1, as well as of the potentially new sp. J25 and sp. K1, were performed. Most of the phyla identified by 16S rRNA were also identified using metagenomic approaches. Detailed characterization of thermophilic isolates indicate the potential of the studied springs as a source of biotechnologically valuable microbes and biomolecules.

Citing Articles

The Bacterial Genus Ramlibacter: Betaproteobacteria Capable of Surviving in Oligotrophic Environments Thanks to Several Shared Genetic Adaptation Traits.

De Luca G, Barakat M, Vermeglio A, Achouak W, Heulin T Environ Microbiol. 2025; 27(2):e70059.

PMID: 39987915 PMC: 11847603. DOI: 10.1111/1462-2920.70059.


Characterization by 16S Amplicon Sequencing of Bacterial Communities Overall and During the Maturation Process of Peloids in Two Spas of an Italian Thermal Complex.

Paduano S, Marchesi I, Valeriani F, Frezza G, Facchini M, Romano Spica V Microb Ecol. 2024; 87(1):152.

PMID: 39633061 PMC: 11618213. DOI: 10.1007/s00248-024-02469-x.


Characterization of prokaryotic communities from Italian super-heated fumaroles.

Rossi A, Barbagli I, Vannini C Extremophiles. 2024; 29(1):4.

PMID: 39579247 DOI: 10.1007/s00792-024-01371-1.


Comparing microbial populations from diverse hydrothermal features in Yellowstone National Park: hot springs and mud volcanoes.

Rowe L, Dowd S, Davidson K, Kovarik C, VanAken M, Jarabek A Front Microbiol. 2024; 15:1409664.

PMID: 38993494 PMC: 11236564. DOI: 10.3389/fmicb.2024.1409664.


Abridgement of Microbial Esterases and Their Eminent Industrial Endeavors.

Akram F, Fatima T, Shabbir I, Ul Haq I, Ibrar R, Mukhtar H Mol Biotechnol. 2024; 67(3):817-833.

PMID: 38461181 DOI: 10.1007/s12033-024-01108-7.


References
1.
Sahm K, John P, Nacke H, Wemheuer B, Grote R, Daniel R . High abundance of heterotrophic prokaryotes in hydrothermal springs of the Azores as revealed by a network of 16S rRNA gene-based methods. Extremophiles. 2013; 17(4):649-62. DOI: 10.1007/s00792-013-0548-2. View

2.
Wang S, Hou W, Dong H, Jiang H, Huang L, Wu G . Control of temperature on microbial community structure in hot springs of the Tibetan Plateau. PLoS One. 2013; 8(5):e62901. PMC: 3647046. DOI: 10.1371/journal.pone.0062901. View

3.
Urbieta M, Gonzalez-Toril E, Bazan A, Giaveno M, Donati E . Comparison of the microbial communities of hot springs waters and the microbial biofilms in the acidic geothermal area of Copahue (Neuquén, Argentina). Extremophiles. 2015; 19(2):437-50. DOI: 10.1007/s00792-015-0729-2. View

4.
Mehetre G, Paranjpe A, Dastager S, Dharne M . Complete metagenome sequencing based bacterial diversity and functional insights from basaltic hot spring of Unkeshwar, Maharashtra, India. Genom Data. 2016; 7:140-3. PMC: 4778638. DOI: 10.1016/j.gdata.2015.12.031. View

5.
Lopez-Lopez O, Knapik K, Cerdan M, Gonzalez-Siso M . Metagenomics of an Alkaline Hot Spring in Galicia (Spain): Microbial Diversity Analysis and Screening for Novel Lipolytic Enzymes. Front Microbiol. 2015; 6:1291. PMC: 4653306. DOI: 10.3389/fmicb.2015.01291. View