alexa Comparison of Extremely Halophilic Archaea Isolated from Three Salt Lakes in China

ISSN: 2168-9652

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Comparison of Extremely Halophilic Archaea Isolated from Three Salt Lakes in China

Wen H*, Yin X#, Gao B, Su S and Xu X
School of Life Science, JIANGSU NORMAL UNIVERSITY, Jiangsu, People’s Republic of China
#Contributed equally to this work
*Corresponding Author: Wen H, School of Life Science, JIANGSU NORMAL UNIVERSITY, Jiangsu, People’s Republic of China, Tel: +86 13815310346, Email: [email protected]

Received Date: Dec 15, 2017 / Accepted Date: Jan 30, 2018 / Published Date: Feb 07, 2018

Abstract

There’re many kinds of extremely halophilic archaea living in salt lakes all over the world and the ecological environment of lakes can affect their archaeal species. To illustrate the relationships between archaeal species and salt lake environment, we isolated and cultured 25 extremely halophilic archaeal strains from three salt lakes in China (Gou Salt Lake, Huama Salt Lake and Yuncheng Salt Lake). According to the 16S rRNA gene sequence analysis and the construction of Neighbor-Joining phylogenetic trees, the isolates were closely related to each other. The most dominant archaea was genus halorubrum (88.0%), followed by genus haloarcula (8.0%) and a small amount of genus halovivax (4.0%). Yuncheng salt lake (YC) had the most abundant number of species. Through the study of the basic information of the three sampling sites, we considered the species of extremely halophilic archaea were related to their living natural conditions of brine. Warm weather and high mineralization degree are likely to be functional components to enrich the species diversity.

Keywords: Salt lakes; Halophilic archaea; 16S rDNA; PCR; Phylogenetic tree

Introduction

Hypersaline salt lakes represent an extreme type of habitat where halophilic prokaryotes are the dominant forms of life [1]. Salt lakes are important mineral resources which contain a variety of salts (mainly NaCl). The formation of salt lake is closely related with natural conditions. In arid or semi-arid climate, when the evaporation of the lake is more than its resupply, the salts constantly concentrate and various elements in water become saturated or supersaturated [2]. Under strong evaporation, water disappears while salts are piling up, which creates salt lakes.

Extremely halophilic archaea (order Halobacteriales, family Halobacteriaceae, phylum Euryarchaeota, domain archaea) inhabit hypersaline regions [3,4]. They could survive extreme conditions such as high salinity, high temperatures, and neutral to alkaline pH, low water activity, and extreme gamma radiations [5]. People have proven that Na+ can maintain cell membrane, cell wall structure and functions to prevent lysis [6]. Na+ can also support the active transport system of amino acid and sugar [7]. Halophilic archaea mainly grow in salt lakes, salt marshes, Dead Sea, the saltern and other environments. They play an important role in the biogeochemistry of carbon and phosphorus in salt lake environments [8] and some halophiles have been shown to degrade organic compounds [9,10] such as pesticides and crude oil [11] for potential use in bioremediation studies and applications [12]. Moreover, halophiles may also have potential uses as biocontrol agents against certain pathogenic fungi [13,14]. Salt lakes are interesting model systems for studies on microbial diversity and ecosystem functions in extreme environments which are highly desirable due to their potential applications [15].

In this study, the extremely halophilic archaea were cultured from three salt lakes of China that were collected: Gou salt lake (GC), Huama salt lake (HMC) and Yuncheng salt lake (YC) respectively. We used phylogenetic analysis to research their compositions and the dominant halophilic archaea. The aim of this study is to find how the different ecological environment of the salt lakes affects the extremely halophilic archaeal species.

Methods

Sampling sites

The water samples were collected of the top 10 cm layer from three Chinese salt lakes in June 2012: Gou salt lake (GC) and Huama salt lake (HMC) are located in Shanxi province. Yuncheng salt lake (YC) is located in Shanxi province, China. After being sieved through microporous membranes of whose pore size is 0.22 μm. The sample was stored at 4°C before the microbial analysis.

Isolation and purification

In order to select extremely halophilic archaea, we chose high salt medium. The ingredients are: Yeast extract (Oxoid) 10 g, Peptone 7.5 g, Trisodium citrate 3 g, NaCl 200 g, KCl 2 g, MgSO4.7H2O 10 g, H2O 1000 ml, agar powder 20 g (solid medium), pH 7.5, 121°C, sterilized 25 min, for using later.

Saltern samples were diluted with dilution gradients of 10-1, 10-2, 10-3, 10-4, 10-5 and 10-6. Then extracted 100 μl diluted liquid to solid MGM medium plate for a 10 to 15 days spread plate cultivation under the temperature of 37°C. The cultivated archaea were then streak cultivated to get a single colony. Archaea from the single colony were streak cultivated again to obtain purified strains [16,17].

DNA extraction, PCR and phylogenetic tree construction

DNA were extracted according to the instruction of Bacterial genomic DNA Extraction Kit by Shanghai Sangon Biological Engineering Technology & Services Co., Ltd. Sequences of primers were the consensus primer of Halophilic archaea--H21F/H1540R [18]. Forward primer: 5'-ATTCCGGTTGATCCTGCCGG-3' and reverse primer: 5'-AGGAGGTGATCCAGCCGCAG-3' were used for amplifying the archaeal 16S rRNA genes. The template 3 μl, every primer 1 μl, dNTP 1.5 μl, 10x PCR buffer 5 μl, MgCl2 4 μl, Taq enzyme 0.3 μl, steam sterilization water to 50 μl by using the PCR Gene Amp 9700 (Applied Biosystems, Foster City, CA, USA). The PCR thermal cycling conditions were as follows: 95°C predenaturation for 5 min, 95°C denaturation for 1 min, 50°C annealing for 1 min, 72°C extension for 1 min 30 s, 35 cycles at 72°C for 10 min, 4°C for preservation. The PCR product was purified by UNIQ-10 column DNA gel extraction kit (Shanghai Sangon Biological Engineering Technology & Services Co., Ltd.) and sequenced by Shanghai Sangon Biological Engineering Technology & Services Co., Ltd.

The 16S rRNA gene sequences were compared with the other strains from the EzTaxon Server database. ClustalX software was used to determine the matching alignment of multiple sequences. Phylogenetic trees were constructed using the Neighbor-Joining method under MEGA5.0 and appraised by using bootstrap value with 1,000 repeats [19].

Results

Descriptions of sampling sites

The basic information about three salt lakes was obtained from ‘Chinese Salt Lakes’ writen by Zheng [20] and we listed them in Table 1. It illustrated that HMC, GC and YC are located in Chinese inland and their climates were dry. What’s more, HMC was an alkaline lake while YC was acidic lake. HMC and GC had the highest altitude and the lowest temperature.

Sites pH Annual Average Temperature(°) Mineralization degree (g/L) Altitude (m) Coordinates
GC 7.3 7 156.77 1303 107°31′25″E, 37°45′30″N
HMC 8 7 108.5 1310 107°30′15″E, 37°41′20″N
YC 5.5 14 236.4 311.77 107°31′-111°03′E, 34°56′15″-35°02′30″N

Table 1: Basic information for the sampling sites.

Also, we listed the selected general physical and chemical properties of sampling sites according to reference book in Table 2 [20]. The cationic detection method is atomic absorption, and the anion’s is ion chromatography. The three study sites showed obvious differences with regard to the inorganic ions concentrations (Table 2). In general, Na+ was the most abundant cation among the four samples followed by Mg2+. The most abundant anion of the samples was Cl- except YC. It’s worth noting that the concentration of SO4 2- was the highest anion in YC.

Sites Na+ (mg/L) K+ (mg/L) Mg2+ (mg/L) Ca2+ (mg/L) Cl- (mg/L) SO42- (mg/L)
GC 55025 189 3731 434 96309 20
HMC 28740 157 8710 248 69998 13
YC 32671 835 28284 218 53220 119364

Table 2: General physical and chemical properties for the sampling sites.

Diversity of halophilic archaea

We isolated and enriched 25 extremely halophilic archaeal strains from three samples, 4 of GC, 2 of HMC and 19 of YC respectively. After amplifying of PCR, there’re 1400 bp-1500 bp lengths of each sample’s 16S rDNA for phylogenetic analyses. Three phylogenetic trees were constructed (Figures 1-3) and Methanosarcina lacustera was chosen as the out-group.

biochemistry-physiology-Phylogenetic-tree

Figure 1: Phylogenetic tree showing the position of GC halophilic archaeal strains among selected clones or strains belonging to division Halobacteriaceae. The tree, which was rooted using Methanosarcina lacustera as the out-group, was generated by the neighbour-joining method. The number at each branch of phylogenetic tree represents the bootstrap value (1000 replicates).

biochemistry-physiology-position-halophilic

Figure 2: Phylogenetic tree showing the position of HMC halophilic archaeal strains among selected clones or strains belonging to division Halobacteriaceae. The tree, which was rooted using Methanosarcina lacustera as the out-group, was generated by the neighbour-joining method. The number at each branch of phylogenetic tree represents the bootstrap value (1000 replicates).

biochemistry-physiology-out-group

Figure 3: Phylogenetic tree showing the position of YC halophilic archaeal strains among selected clones or strains belonging to division Halobacteriaceae. The tree, which was rooted using Methanosarcina lacustera as the out-group, was generated by the neighbour-joining method. The number at each branch of phylogenetic tree represents the bootstrap value (1000 replicates).

There is another phylogenetic tree that compared the species of three samples (Figure 4). Comparison of the sample sequences with other halobacterial sequences in the database indicated that they were most closely related to the other species of the genus Halorubrum.

biochemistry-physiology-halophilic-archaeal

Figure 4: Phylogenetic tree showing the position of all halophilic archaeal strains among three samples. The tree was generated by the neighbour-joining method. The number at each branch of phylogenetic tree represents the bootstrap value (1000 replicates).

GC-6 was highly homologous to GC-8which belonged to genus Halorubrum and clustered into one branch. There were two different strains in HMC but they belonged to different genus. HMC-1 was one species of genus Halorubrum while HMC-3 was confirmed to Haloarcula marismortui . YC had the most abundant diversity of strains, which harbored representatives of all the three genera. Much of them belonged to genus Halorubrum and they’re scattered throughout the phylogenetic tree, representing different species. In addition, YC-14 was same with Halovivax ruber and YC-16 was a species of genus Haloarcula.

When comparing the three samples together, most of them are homologous with each other, except for the following four: HMC-3, YC-14, YC-16 and YC-X1. YC-14 was more homologous to YC-16 by contrast.

From the perspective of all 25 samples, there were 22 of them belonged to genus Halorubrum (88.0%), suggesting that it may be the dominant genus in salt lakes. Moreover, genus Haloarcula (8.0%) and Halovivax (4.0%) also appeared in our study, but only a few, so they did not account for the advantage in salt lakes. This study didn’t found any unknown or novel archaea, but the species diversity in the salt lake is great and needed to be further investigated and studied.

Discussion

YC had the most abundant strains among the three. Previous studies have shown that pH correlated with prokaryotic distributions in highly saline environments [21]. We found that Yuncheng salt lake was an acidic lake, but alkaline environments were more suitable for the survival of halophilic bacteria [22]. The high archaeal diversity in YC could be due to the fact that some kinds of halorubrum can tolerate the relative low pH and there have been researches reported that some halorubrum species can live in pH 5.5-9.5 [23]. The contrary discovery indicated that there could be no direct correlation between pH and halophilic archaeal diversity and there were a lot of factors that could affect the results.

What’s more, mineralization degree, which means the amount of salts in water, can also have impact on species. It had been proved that high level of mineralization degree was necessary for the survival of halobacteria [24]. As the amount of salt increases, the diversity enriches too. Among the three sample sites, the mineralization degree of YC was much higher than the others, which may result in their abundant species.

The locations of Huama salt lake and Gou salt lake are very close. They have the same climate and natural environment. In this study, we only collected and cultured 4 strains in GC and 2 in HMC. These four strains in GC were clustered into one branch, which meant they had very close genetic relationships. However, the two strains in HMC belonged to different genus. We didn’t culture many clones in our media due to the high salt concentration (NaCl 20%). Some studies considered that optimal salinity for moderately halophilic bacteria growth was 3%-15% NaCl [25,26]. Also, their diversity was affected by temperature. The temperature of the two samples was relatively low, which is not conducive to the growth of microorganisms.

The extreme halophilic archaea of the three salt lakes have been shown to be phylogenetically distinct, a result which is consistent with both the natural environmental conditions and the brine physicochemical properties. It’s clear that the warm weather and high mineralization degree are likely to be functional components to enrich the species diversity. In addition, halorubrum was the dominant genus in salt lakes. Although the temperatures were low at these three sample sites, archaea grew at 37°C, they are mostly resistant to high temperatures due to the properties of halophilic archaea and some extreme halophilic archaea are lightly thermophilic, so we don’t think this temperature could eliminate some archival species in isolated samples and that couldn’t reduce diversity of species in samples. However, other factors that can affect the diversity of halophilic archaea as well, and the specific mechanism of these factors are needed to be further investigated and studied.

Conclusion

There are many kinds of extremely halophilic archaea living in salt lakes all over the world and the ecological environment of lakes can affect their archaeal species. Through the study of the basic information of the three sampling sites, we considered the species of extremely halophilic archaea were related to their living natural conditions of brine. Warm weather and high mineralization degree are likely to be functional components to enrich the species diversity. In addition, Halorubrum was the dominant genus in salt lakes.

Acknowledgement

The authors gratefully acknowledge the financial support given by Priority Academic Program Development (PAPD). The authors are also grateful to Shanghai Sangon Biological Engineering Technology & Services Co., Ltd. (Shanghai, China) for their help in sample sequencing.

References

Citation: Wen H, Yin X, Gao B, Su S, Xu X (2018) Comparison of Extremely Halophilic Archaea Isolated from Three Salt Lakes in China. Biochem Physiol 7: 227 DOI: 10.4172/2168-9652.1000227

Copyright: ©2018 Wen H, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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