Halophiles are relatively unexplored as potential sources of novel species. However, little is known about the culturable bacterial diversity thrive in hypersaline lakes. In this work, a total of 343 bacteria from sediment samples of Aiding Lake, China, were isolated using nine different media supplemented with 5% or 15% (w/v) NaCl. The number of species and genera of bacteria recovered from the different media varied, indicating the need to optimize the isolation conditions. The results showed an unexpected level of bacterial diversity, with four phyla (Actinobacteria, Firmicutes, Proteobacteria, and Rhodothermaeota), fourteen orders (Actinopolysporales, Alteromonadales, Bacillales, Balneolales, Chromatiales, Glycomycetales, Jiangellales, Micrococcales, Micromonosporales, Oceanospirillales, Pseudonocardiales, Rhizobiales, Streptomycetales, and Streptosporangiales), including 17 families, 43 genera (including two novel genera), and 71 species (including four novel species). The predominant phyla included Actinobacteria and Firmicutes and the predominant genera included Actinopolyspora, Gracilibacillus, Halomonas, Nocardiopsis, and Streptomyces. To our knowledge, this is the first time that members of phylum Rhodothermaeota were identified in sediment samples from a salt lake.
Citation: Guan T-W, Lin Y-J, Ou M-Y, Chen K-B (2020) Isolation and diversity of sediment bacteria in the hypersaline aiding lake, China. PLoS ONE 15(7): e0236006. https://doi.org/10.1371/journal.pone.0236006
Editor: Paula V. Morais, Universidade de Coimbra, PORTUGAL
Received: July 24, 2019; Accepted: June 26, 2020; Published: July 10, 2020
Copyright: © 2020 Guan 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.
Data Availability: All relevant data are within the paper. The sequences of the bacterial isolates reported in this study have been deposited to GenBank (Accession no. MK818765- MK818834, MK296404).
Funding: The National Natural Science Foundation of China (Project No. 30660005) and Office of education in Sichuan Province, China (Project Nos. 13205688, 13ZB0024) supported this study. Chunhui Project for Ministry of Education of China (Project No. 191649).
Competing interests: The authors have declared that no competing interests exist.
Halophiles thrive in hypersaline niches and have potential applications in biotechnology [1, 2]. Microbial diversity in most hypersaline environments is often studied using culture-dependent and -independent methods [3–7]. Previous studies have shown that the taxonomic diversity of microbial populations in terrestrial saline and hypersaline environments is relatively low [8, 9]. Halophilic microbial communities vary with season , and in general, microbial diversity decreases with increased salinity [11, 12]. Hypersaline lakes are considered extreme environments for microbial life. A variety of salt lakes have been surveyed for bacterial diversity such as Chaka Lake in China, Chott El Jerid Lake in Tunisia, Meyghan Lake in Iran, Keke Lake in China, and Great Salt Lake in the United States [5, 13–16]. In addition, groups of novel halophilic or halotolerant bacteria in salt lakes have been described using culture-dependent methods: Actinopolyspora lacussalsi sp. nov., Amycolatopsis halophila sp. nov., Brevibacterium salitolerans sp. nov., Halomonas xiaochaidanensis sp. nov., Paracoccus halotolerans sp. nov., and Salibacterium nitratireducens sp. nov. of phyla Actinobacteria, Firmicutes, or Proteobacteria [17–22]. Despite these previous studies, our understanding of bacterial diversity in hypersaline lakes remains limited, particularly in athalassohaline lakes at low elevations. Aiding Lake represents an ideal site for studying halophilic or halotolerant bacteria in a hypersaline lake. The salt lake is located on the Turpan Basin and surround by the Gobi desert in Xinjiang province, China. In fact, our current understanding of the bacterial diversity in the Aiding Lake using a culture-dependent method is limited. To our knowledge, this is the first attempt to comprehensively characterize the bacterial diversity in dry salt lake sediments. The aim of the study was to investigate the bacterial diversity and to mine novel bacterial species from Aiding Lake.
2 Materials and methods
2.1 Site description and sample collection
Aiding Lake is a dry salt lake located on the Turpan Basin in Xinjiang Province, China (S1 Fig), with an elevation of 154 m–293 m below sea level. Aiding Lake covers an area of about 60 km2 and is a closed ecosystem, without the influx of perennial rivers. Three soil samples, namely, S1 (89°21′98″E, 42°40′42″N), S2 (89°16'6″E, 42°38'55″N), and S3 (89°20'26″E, 42°41'53″N) were collected from the lake sediments, respectively. Soil samples temperature are 23.6°C-25.1°C. Three sediment samples at different sites were collected from a same depth of 1 to 30 cm in mid-July of 2012. The distance between two sample points was greater than 5 km. Samples were stored at 4°C in the field and immediately transported to the laboratory. The pH was measured with portable meters after the sediments were resuspended in distilled water. The concentrations of major cations and trace elements in the dissolved sediments were measured according to Yakimov et al. (2002) .
2.2 Isolation of microorganisms
Three sediment samples were selected for cultivation of bacteria. To isolate halophilic and/or halotolerant bacteria, the sediments (10 g wet weight) were dispersed into 90 mL of sterilized NaCl brine (5% or 15%, w/v) and incubated at 37°C for 60 min with shaking at 200 rpm. The resulting slurry was then serially diluted with sterilized NaCl brine (5% or 15%, w/v). Aliquots (0.1 mL) of each dilution were spread onto Petri dishes using nine media (Table 1) for the isolation of bacteria. The no. of colonies on each kind of medium plate was calculated by three repeats. All agar plates were supplemented with 5% or 15% (w/v) NaCl. To suppress the growth of nonbacterial fungi, the solidified media were supplemented with nystatin (50 mg·L-1). The Petri dishes were incubated at 37°C for one to six weeks. Based on size and color, colonies were picked and further purified on inorganic salts-starch agar  or TSA supplemented with 5% or 15% (w/v) NaCl, and as glycerol suspension (20%, v/v) at -20°C or as lyophilized cells for long-term storage at -4°C.
2.3 Identification of bacteria
Isolated strains were subjected to 16S rRNA gene sequence analysis for precise genus and species identification. Genomic DNA was extracted from each isolate, and the 16S rRNA gene sequence was amplified as described by Li et al. (2007)  with primers PA (5'-CAGAGTTTGATCCTGGCT-3') and PB (5'-AGG AGGTGATCCAGCCGC A-3'), or the primers 27F (5'-AGAGTTTGATCMTGGCTCAG-3') and 1492R (5'-GGTTACCTTGTT ACGACTT-3'). PCR products were purified using a PCR purification kit (Sangon, Shanghai, China). The almost-complete 16S rRNA gene sequence (about 1450bp) of isolated strains was obtained. Multiple alignments with sequences of the most closely related recognized species and calculations of levels of sequence similarity were conducted using EzBioCloud server . Phylogenetic analysis was performed using the software package MEGA version 6.0 . Phylogenetic trees were constructed according to the neighbor-joining method . Evolutionary distance matrices were generated as described by Kimura (1980) . The topology of the phylogenetic tree was evaluated using the bootstrap resampling method of Felsenstein (1985)  with 1000 replicates. DNA-DNA relatedness values were determined using the fluorometric microwell method . The identities of these organisms were determined based on nearly full-length 16S rRNA gene sequence analysis. The sequences of 100% identity were clustered into one species.
2.4 Spearman correlation analysis
Pearson’s test was performed to reveal the correlations between physicochemical properties and bacterial genera using SPSS Statistics19.0.
3.1 Sediment geochemistry
Physicochemical parameters were distinct among the three sediment samples (Table 2). In the S1, S2, and S3 samples, Na+ concentrations ranged from 26.37 g/Kg to 83.93 g/Kg and Cl- concentrations ranged from 33.28 g/Kg to 389.11 g/Kg, which are typical of chloride-type environments. The pH of the sediment samples ranged from 7.6 to 8.3, indicating a slightly alkaline environment. In sample S3, ionic composition (e.g., Mg2+, Na+, K+, Mn2+, and Cl-) was significantly lower than the other samples. The other physicochemical properties of the samples are presented in Table 2.
3.2 Diversity of sediment bacteria
According to the analysis of sequencing results, many of isolated strains had exactly the same 16S rRNA sequence. 343 isolated strains belong to 71 different bacterial species after merging the duplicated strains (Table 3). The percentages of 16S rRNA gene sequence similarities (91.14% to 100%) of these isolates to the closest type strains are presented in Table 3. As the results indicated, most of the strains exhibited > 97% similarity to other published type species. While the similarity of three strains (ADL013, ADL014, and ADL023) were less than 97%, which represented three different novel species (Table 3). It is generally accepted that organisms displaying 16S rRNA gene sequence similarity values of 97% or less belong to different species . For example, strain ADL014 shared 96.51% similarity with Anaerobacillus alkalidiazotrophicus F01CH1-61-65, and DNA-DNA hybridization experiments from the two strains revealed that levels of DNA-DNA relatedness were 36.8± 4.3%. Sequence analysis indicated that strain ADL014 formed a distinct lineage within the genus Anaerobacillus and always had the closest phylogenetic affinity to members of the genus Anaerobacillus (Fig 1). Phylogenetic reconstruction also indicated that strain ADL014 could represent a novel species.
Bar, 0.01 nucleotide substitutions per site.
These halophilic or halotolerant bacteria were compared to those deposited in the public database (EzBioCloud, https://www.ezbiocloud.net/identify). The bacteria isolated in this study displayed considerable diversity. The predominant phyla were Firmicutes (149 strains, 43.4%) and Actinobacteria (121 strains, 35.3%). The other bacterial isolates belonged to phyla Rhodothermaeota (5 strains, 1.5%) and Proteobacteria (68 strains, 19.8%). The isolates were distributed among 14 orders, namely, Actinopolysporales (26 strains), Alteromonadales (8 strains), Bacillaceae (149 strains), Balneolales (5 strains), Chromatiales (12 strains), Glycomycetales (2 strains), Jiangellales (3 strains), Micrococcales (8 strains), Micromonosporineae (5 strains), Oceanospirillales (45 strains), Pseudonocardiales (11 strains), Rhizobiales (3 strains), Streptomycetales (27 strains), and Streptosporangiales (26 strains), including 41 known genera (Tables 3 and 4). Other organisms (ADL013 and ADL023) could not be accurately identified to the genus level because of the lower homology (Table 3). Strain ADL013 exhibited 94.71% similarity to the 16S rRNA gene sequence of Alteribacillus persepolensis HS136, and the hybridization values of 11.3±2.1% to each other; and strain ADL023 exhibited 91.14% similarity to the 16S rRNA gene sequence of Caldalkalibacillus uzonensis JW/WZ-YB58, and the hybridization values of 8.3±1.7% to each other. Phylogenetic analysis also showed that strain ADL013 and ADL023 can be distinguished from representatives of genera in the family Bacillaceae, and two strains formed a distinct lineage within family Bacillaceae, respectively (Fig 2). Meanwhile, two strains had such low degrees of sequence similarity, suggesting that these may represent two novel genera of Bacillaceae. In the study, Halomonas (42 strains, 12.2%), Gracilibacillus (33 strains, 9.6%), Streptomyces (27 strains, 7.9%), Actinopolyspora (26 strains, 7.6%), Nocardiopsis (17 strains, 5.0%), Bacillus (12 strains, 4.4%), Aquisalimonas (12 strains, 3.5%), Marinococcus (11 strains, 3.2%), Virgibacillus (11 strains, 3.2%), and Sediminibacillus (11 strains, 3.2%) were some dominant group in sediment samples of Aiding Lake. The number of microorganisms in each of the other genus is relatively small (Table 3; Fig 3). For example, Anaerobacillus, Prauserella, and Ornithinibacillus include only one strain, respectively. To isolate halophilic or halotolerant bacteria in the sediments of Aiding Lake, the agar plates were supplemented with 5% or 15% (w/v) NaCl. Approximately 141 strains isolated from these media with 5% NaCl belonged to 25 different genera, and 202 strains isolated from the media using 15% NaCl belonged to 23 different genera (Table 3).
Numbers at nodes indicate levels of bootstrap support (%) based on neighbor-joining analysis of 1000 resampled datasets; only values above 50% are shown. Bar, 0.01 nucleotide substitutions per site.
3.3 Bacterial isolates from different media
To obtain additional bacterial groups, the sediment samples from Aiding Lake were isolated using nine different media (Table 1). Five class of bacteria, namely, Actinobacteria, Bacilli, Alphaproteobacteria, Gammaproteobacteria, and Balneolia, including 14 orders, 17 families, and 43 genera (including 2 novel genera) were obtained (Table 4). Most of the bacterial groups were isolated using microcrystalline cellulose-sorbitol agar (G), and 13 bacterial genera (Aquibacillus, Aquisalimonas, Bacillus, Filobacillus, Gracilibacillus, Halomonas, Kocuria, Nocardiopsis, Ornithinibacillus, Phytoactinopolyspora, Piscibacillus, Virgibacillus, and Zhihengliuella) were isolated. At the same time, microcrystalline cellulose-proline agar (C), stachyose tetrahydrate-alanine agar (F), casein hydrolysate acid-starch agar (B), and glycerin-asparagine agar (D) resulted in relatively efficient isolations for 11 genera (Actinopolyspora, Anaerobacillus, Glycomyces, Haloactinospora, Jeotgalibacillus, Kocuria, Myceligenerans, Nesterenkonia, Pontibacillus, Saccharomonospora, and Salinifilum), 8 genera (Aquibacillus, Halobacillus, Haloechinothrix, Halomonas, Marinactinospora, Marinobacter, Nocardiopsis, and Streptomyces), 7 genera (Actinopolyspora, Halobacillus, Marinobacter, Micromonospora, Planococcus, Saccharopolyspora, and Streptomyces), and 6 genera (Actinopolyspora, Longimycelium, Marinococcus, Nocardiopsis, Saccharomonospora, and Streptomyces), respectively. Only two known genera (Gracilibacillus and Sinobaca) and one novel genus (ADL013) were isolated using yeast extract-glycerin agar (I). The results of isolation using the other media are shown in Table 4. From the number of isolated strains, 95, 57, and 57 strains were isolated using media G, F, and C, respectively, and the number of strains isolated from media A, B, D, E, H and I was relatively small (Tables 3 and 4). In addition, the bacterial diversity recovered using different media also varied considerably. Medium G had the best recoverability, with 14 of the total bacterial genera recovered. Media I and E showed the lowest recoverability at the genus level (Table 4). In short, to obtain more bacterial resources, it is also necessary to develop different types of media.
3.4 Bacterial isolates from different sediments and Pearson correlation
The number of isolates of bacteria recovered from three sediments (S1, S2, and S3) are different.164, 88 and 91 strains were isolated from sediment samples S1, S2, and S3, respectively (S1 Table). In sediment sample S1, 28 bacterial genera were isolated, while another 27, and 24 bacterial genera were isolated from samples S2 and S3, respectively (S1 Table). Although there was a small difference in the number of genera per sample, there was a large difference in the type of genera per sample (S1 Table). For example, Haloactinospora, Nesterenkonia, Phytoactinopolyspora, Saccharomonospora, Saccharopolyspora, ADL013, and ADL023 were isolated only from sample S1; Glycomyces, Haloechinothrix, Myceligenerans, Ornithinibacillus, and Prauserella were isolated only from sample S2; meanwhile, Anaerobacillus, Kocuria, Salinifilum, and Zhihengliuella were also isolated only from sample S3 (S1 Table). In addition, Actinopolyspora, Aquibacillus, Aquisalimonas, Bacillus, Gracilibacillus, Halomonas, Marinococcus, Nocardiopsis, Salinicoccus, Streptomyces, and Virgibacillus were distributed in all three samples (S1 Table). The results showed that the number and diversity of bacteria were different even in different sites from the same salt lake.
Pearson’s correlation analysis revealed that Na+, K+, Cl- and HCO3- were mainly positively correlated with the relative abundances of Actinopolyspora, Gracilibacillus, Pontibacillus, Aidingimonas, Aquisalimonas, Halobacillus, Bacillus, Haloactinospora, Nesterenkonia, Phytoactinopolyspora, Saccharomonospora, Saccharopolyspora, ADL013, ADL023, Alteribacillus, and Nocardiopsis, respectively (Table 5). Mn2+ was mainly positively correlated with the relative abundances of Aquibacillus, Filobacillus, and Marinococcus but negatively correlated with Micromonospora. Fe2+ was mainly positively correlated with the relative abundances of Marinactinospora. SO42- was mainly positively correlated with the relative abundances of Salinicoccus but negatively correlated with Piscibacillus (Table 5).
Bacterial diversity in Aiding Lake was based on the 16S rRNA gene sequences, which was relatively higher than other salt lakes at the genus level. For example, sequencing of 16S rRNA genes indicated the presence of members of bacterial genera Bacillus, Halomonas, Pseudomonas, Exiguobacterium, Vibrio, Paenibacillus, and Planococcus in the salt lake La Sal del Rey, in extreme South Texas (USA) . Previous studies also have shown that bacterial diversity in other saline lake ecosystems were mainly composed of the bacteria (including 16 genera: Bacillus, Chromohalobacter, Gracilibacillus, Halobacillus, Halolactibacillus, Halomonas, Halovibrio, Idiomarina, Oceanobacillus, Piscibacillus, Salicola, Salimicrobium, Salinicoccus, Staphylococcus, Thalassobacillus, and Virgibacillus) [34, 35]. Notably, some rare genera from the sediments of Aiding Lake such as Aidingimonas, Aliifodinibius, Filobacillus, Haloechinothrix, Jeotgalibacillus, Longimycelium, Myceligenerans, Ornithinibacillus, Phytoactinopolyspora, and Piscibacillus were discovered in the present study. In addition, phylum Rhodothermaeota was detected for the first time in sediment samples from a salt lake.
The richness and diversity of actinobacteria isolated from Aiding Lake in the present study were relatively high, consisting of eight orders (Actinopolysporales, Glycomycetales, Jiangellales, Micrococcales, Micromonosporales, Pseudonocardiales, Streptomycetales and Streptosporangiales). Wu et al. (2008) have found six actinobacterial orders using pure culture in salt lake, hypersaline spring, and salt mine of China, and these orders were Actinopolysporales, Glycomycetales, Micrococcales, Pseudonocardiales, Streptomycetales, and Streptosporangiales . Our results suggested that the diversity of actinobacterial 16S rRNA gene sequences of strains from Aiding Lake were more diverse at the genus level than those reported in saline environment. For examples, twelve genera, namely Actinomadura, Actinomycetospora, Microbispora, Micromonospora, Mycobaterium, Nocardia, Nocardiopsis, Pseudonocardia, Saccharopolyspora, Sphaerosporangium, Streptomyces, and Streptosporangium were isolated from marine sponges in Florida, USA , and ten genera, including Actinotalea, Arthrobacter, Brachybacterium, Brevibacterium, Kocuria, Kytococcus, Microbacterium, Micrococcus, Mycobacterium, and Pseudonocardia from Arctic marine sediments were obtained by culture-dependent approaches . Atika et al. isolated fifty-two halophilic actinomycetes belonging to the Actinopolyspora, Nocardiopsis, Saccharomonospora, Saccharopolyspora, and Streptomonospora genera from Saharan saline soils of Algeria . Ronoh et al. identified four genera (Dietzia, Microbacterium, Nocardia, and Rhodococcus) of actinobacteria from Lake Magadi, Kenya . However, 18 genera, namely Actinopolyspora, Glycomyces, Haloactinospora, Haloechinothrix, Kocuria, Longimycelium, Marinactinospora, Micromonospora, Myceligenerans, Nesterenkonia, Nocardiopsis, Phytoactinopolyspora, Prauserella, Saccharomonospora, Saccharopolyspora, Salinifilum, Streptomyces, and Zhihengliuella were isolated in this study. Therefore, bacterial diversity may differ between different sample collection regions and different saline samples. Of course, it is also possible that the diversity of isolated bacteria may vary due to different media or isolated technology.
In addition to strains ADL013, ADL014, and ADL023 are novel species because of low similarity, the 16S rRNA gene sequences of strain XHU5135 showed 97.52% identities to the nearest neighbors, Aidingimonas halophila YIM 90637 . Although it showed higher 16S rRNA gene similarities (97.52%) to the closest recognized strains, DNA-DNA hybridization experiments revealed that levels of DNA-DNA relatedness between strain XHU 5135 and Aidingimonas halophila YIM 90637 were 23.3± 2.8%. This values is below the 70% cut-off point recommended for recognition of genomic species . Thus, strain XHU 5135 represents a novel species of the genus Aidingimonas. The neighbour-joining phylogenetic tree based on 16S rRNA gene sequences of strain XHU 5135 and other related species is shown in Fig 4 with high levels of bootstrap support. At present, we isolated and cultured 71 species (including 4 novel genera) of 43 bacterial genera (including 2 novel genera). To our knowledge, this is the first study to recover such a high diversity of culturable bacteria from salt lake sediments. In addition, Aidingimonas halophila YIM 90637 , Streptomyces aidingensis TRM46012 , Longimycelium tulufanense TRM 46004 , Salinifilum aidingensis TRM 46074 , and Gracilibacillus aidingensis YIM 98001  were also isolated from Aiding Lake, and above strains have been characterized as some novel species. These results indicate that there are potentially unique, novel sources of bacteria in Aiding Lake.
Numbers at nodes are bootstrap percentages based on 1000 replicates. Bar, 0.01 nucleotide substitutions per site.
The dry lake has a high NaCl content. However, a large number of bacteria are isolated using the media employed a lower content of NaCl (5%). Possible reasons for such inconsistency could be twofold: (1) bacteria may tolerate a large range of salinity. For example, Halomonas xinjiangensis TRM 0175 could grow at 0–20% NaCl ; (2) surface layer of the soil samples have a high salinity, while the other parts have a low salinity.
Generally, bacterial diversity in extreme environments is relatively low. Therefore, according to the differences in the utilization of carbon and nitrogen sources by microorganisms, as well as the high repetition rate of microorganisms isolated from conventional media, we designed some media containing rare carbon and nitrogen source (microcrystalline cellulose, glycerin, stachyose tetrahydrate, sorbitol, Beta-Cyclodextrin, casein hydrolysate acid, proline, arginine, asparagine, or alanine) in the hope of mining more novel species and presenting better bacterial diversity. To our satisfaction, an unexpectedly high bacterial diversity was observed from sediment samples from Aiding Lake. Forty-three bacterial genera were identified. The results indicate that it is feasible to use rare carbon and nitrogen source media to mine more species, and some strains might represent a valuable source of new species, thereby providing a new reference for further understanding bacterial diversity in hypersaline environments. This study also suggested that the diversity of bacteria isolated from Aiding Lake is largely dependent on the isolation media. Obviously, the number and diversity of bacteria isolated from different media are different in this study. Although media I and E showed the lowest recoverability at the genus level, the microorganism of Sinobaca genus was only isolated using medium I, and a novel strain ADL013 was found using the medium too. At the same time, the microorganism of phylum Rhodothermaeota was detected only using medium E. Of all the media, the most actinobacterial genera (7) were isolated from medium C. This result suggests that medium C is suitable for the isolation of actinomycetes in sediments of salt lake. In addition, the most abundant bacterial genera were obtained from medium G (Microcrystalline cellulose-sorbitol agar), this may indicate that these bacteria have a special utilization for microcrystalline cellulose, or sorbitol, or Beta-Cyclodextrin, but at present the mechanism of why medium G is suitable for the isolation of bacteria from Aiding lake is unclear. No universal medium or uniform isolation technology has been established for microbial resources around the world. Therefore, there is a need to develop novel isolation media or isolation techniques to better mine non-culturable bacterial resources.
- 1. Oren A. Industrial and environmental applications of halophilic microorganisms. Environ Technol 2010; 31: 825–834. pmid:20662374
- 2. Oren A. Halophilic microbial communities and their environments. Curr Opin Biotech 2015; 33: 119–124. pmid:25727188
- 3. Oren A. Molecular ecology of extremely halophilic Archaea and Bacteria. FEMS Microbiol Ecol 2003; 39(1): 1–7. https://doi.org/10.1111/j.1574-6941.2002.tb00900.x
- 4. Antonio V, Rafael RLH, Cristina SP, Thane PR. Microbial diversity of hypersaline environments: a metagenomic approach. Curr Opin Microbiol 2015; 25: 80–87. pmid:26056770
- 5. Ali N, Giti E, Mohammad AA, Mariana SC, Lucas JS, Zahra E, et al. Microbial diversity in the hypersaline lake meyghan, Iran. Scientific Reports 2017; 7: 11522. pmid:28912589
- 6. Manel BA, Fatma K, Najwa K, Fabrice A, Najla M, Marianne Q, et al. Abundance and diversity of prokaryotes in ephemeral hypersaline lake Chott El Jerid using Illumina Miseq sequencing, DGGE and qPCR assays. Extremophiles 2018; 22(5): 811–823. pmid:30014241
- 7. Nahid O, David JC, Inmaculada L, Victoria B, Fernando MC. Study of bacterial community composition and correlation of environmental variables in Rambla Salada, a hypersaline environment in south-eastern Spain. Front Microbiol 2018; 9: 1377–1383. pmid:29977233
- 8. DasSsrma S, Arora P. 2001. Halophiles, p. 458–466. In Battista J. R. et al. (ed.), Encyclopedia of life sciences, vol. 8. Nature Publishing Group, London, Untied Kingdom.
- 9. Oren A. The bioenergetics basis for the decrease in metabolic diversity ecosystems. Hydrobiologia 2001; 466: 61–72.
- 10. Meglio LD, Santos F, Gomariz M, Almansa C, Lopez C, Anton J, et al. Seasonal dynamics of extremely halophilic microbial communities in three argentinian salterns. FEMS Microbiol Ecol 2016; 92(12): 184. https://doi.org/10.1093/femsec/fiw184
- 11. Oren A. Diversiyt of halophilic microorganisms: environments, phylogeny, physiology, and applications. J Ind Microbiol Biotechnol 2002; 28(1): 56–63. pmid:11938472
- 12. Addis S, Anders L, Amare G, Lise O. Prokaryotic community diversity along an increasing salt gradient in a soda Ash concentration Pond. Microbiol Ecology 2016; 71(2): 326–338. https://doi.org/10.1007/s00248-015-0675-7
- 13. Jiang HC, Dong HL, Zhang GX, Yu BS, Leah RC, Matthew WF. Microbial diversity in water and sediment of lake Chaka, an athalassohaline lake in northwestern China. Appl Environ Microbiol 2006; 72(6): 3832–3845. pmid:16751487
- 14. Loubna T, Donald PB, Alan RH, Keith AC. Life in extreme environments: microbial diversity in Great Salt Lake, Utah. Extremophiles 2014; 18(3): 525–535. pmid:24682608
- 15. Han R, Zhang X, Liu J, Long QF, Chen LS, Liu DL, et al. Microbial community structure and diversity within hypersaline Keke salt lake environments. Can J Microbiol 2017; 63(11): 895–908. pmid:28850799
- 16. Baxter BK. Great Salt Lake microbiology: a historical perspective. Int Mcrobiology 2018; 21(3): 79–95. https://doi.org/10.1007/s10123-018-0008-z
- 17. Guan TW, Wei B, Zhang Y, Xia ZF, Che ZM, Chen XG, et al. Actinopolyspora lacussalsi sp. nov., Actinopolyspora lacussalsi sp. nov., an exteremely halophilic actinomycete isolated from a salt lake. Int J Syst Evol Microbiol 2013; 63: 3009–3013. pmid:23396724
- 18. Guan TW, Zhao K, Xiao J, Liu Y, Xia ZF, Zhang XP, et al. Brevibacterium salitolerans sp. nov., an actinobacterium isolated from a salt lake in Xinjiang, China. Int J Syst Evol Microbiol 2010; 60: 2991–2995. pmid:20118289
- 19. Tang SK, Wang Y, Guan TW, Lee JC, Kim CJ, Li WJ. Amycolatopsis halophila sp. nov., a novel halophilic actinomycete isolated from a salt lake in China. Int J Syst Evol Microbiol 2010; 60(5): 1073–1078. https://doi.org/10.1099/ijs.0.012427-0
- 20. Duangmal K, Suksaard P, Pathom-aree W, Mingma R, Matsumoto A, Takahashi Y, et al. Actinopolyspora salinaria sp. nov., a halophilic actinomycete isolated from solar saltern soil. Int J Syst Evol Microbiol 2016; 68(4): 3506–3511. https://doi.org/10.1099/ijsem.0.000926
- 21. Meng XL, Ming H, Huang JR, Zhang LY, Cheng LJ, Zhao ZL, et al. Paracoccus halotolerans sp. nov., isolated from a salt lake. Int J Syst Evol Microbiol 2019: 69: 523–528. pmid:30570476
- 22. Harjodh S, Manpreet K, Shweta S, Sunita M, Shekhar K, Venkata RV, et al. Salibacterium nitratireducens sp nov., a haloalkalitolerant bacterium isolated from a water sample from Sambhar salt lake, India. Int J Syst Evol Microbiol 2018; 68: 3506–3511. pmid:30226463
- 23. Yakimov M, Giuliano L, Crisafi E, Chernikova T, Timmis K, Golyshin P. Microbial community of a saline mud volcano at San Biagio-Belpasso, Mt. Etna (Italy). Environ Microbiol 2002; 4(5): 249–256. pmid:12030850
- 24. Shirling EB, Gottlieb D. Methods for characterization of Streptomyces species. Int J Syst Bacteriol 1966; 16: 313–340. https://doi.org/10.1099/00207713-16-3-313
- 25. Li WJ, Xu P, Schumann P, Zhang YQ, Pukall R, Xu LH, et al. Georgenia ruanii sp. nov., a novel actinobacterium isolated from forest soil in Yunnan (China), and emended description of the genus Georgenia. Int J Syst Evol Microbiol 2007; 57: 1424–1428. pmid:17625169
- 26. Yoon SH, Ha SM, Kwon S, Lim J, Kim Y, Seo H, et al. Introducing EzBioCloud: A taxonomically united database of 16S rRNA and whole genome assemblies. Int. J. Syst. Evol. Microbiol 2017; 67: 1613–1617. pmid:28005526
- 27. Tamura K, Stecher G, Peterson D, Filipski A, Kumar S. MEGA6: Molecular Evolutionary enetics Analysis Version 6.0. Mol Biol Evol 2013; 30(12): 2725–2729. pmid:24132122
- 28. Saitou N, Nei M. The neighbor-joining method: a new method for reconstructing phylogenetic tree. Mol Biol Evol 1987; 4(4): 406–425. pmid:3447015
- 29. Kimura M. A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequence. J Mol Evol 1980; 16(2): 111–120. pmid:7463489
- 30. Felsenstein J. Confidence limits on phylogenies: an approach using the bootstrap. Evolution 1985; 39: 783–789. pmid:28561359
- 31. Ezaki T, Hashimoto Y, Yabuuchi E. Fluorometric deoxyribonucleic acid-deoxyribonucleic acid hybridization in microdilution wells as an alternative to membrane filter hybridization in which radioisotopes are used to determine genetic relatedness among bacterial strains. Int J Syst Bacteriol 1989; 39: 224–229.
- 32. Stackebrandt E, Goebel BM. Taxonomic note: a place for DNA-DNA reassociation and 16S rRNA sequence analysis in the present species definition in bacteriology. Int J Syst Bacteriol 1994; 44: 846–849. https://doi.org/10.1099/00207713-44-4-846
- 33. Phillips K, Frederic 3rd Z, Elizondo OR, Lowe KL. Phenotypic characterization and 16S rDNA identification of culturable non-obligate halophilic bacterial communities from a hypersaline lake, La Sal del Rey, in extreme South Texas (USA). Aquatic. Biosystems 2012; 8(1): 5–15. pmid:22480362
- 34. Li X, Yu YH. Biodiversity and screening of halophilic bacteria with hydrolytic and antimicrobial activities from yuncheng salt lake, China. Biologia 2015; 70(2): 151–156. https://doi.org/10.1515/biolog-2015-0033
- 35. Rohban R, Amoozegar MA, Ventosa A. Screening and isolation of halophilic bacteria producing extracellular hydrolyses from Howz Soltan Lake, Iran. J Ind Microbiol Biot 2009; 36(3): 333–340. https://doi.org/10.1007/s10295-008-0500-0
- 36. Wu JY, Guan TW, Jiang HC, Zhi XY, Tang SK, Dong HL, et al. Diversity of actinobacterial community in saline sediments from Yunnan and Xinjiang, China. Extremophiles 2009; 13(4): 623–632. pmid:19504229
- 37. Ellis GA, Thomas CS, Chanana S, Adnani N, Szachowicz E, Braun DR, et al. Brackish habitat dictates cultivable actinobacterial diversity from marine sponges. Plos One 2017; 12(7): e0176968. pmid:28692665
- 38. Zhang GY, Cao TF, Ying JX, Yang YL, Ma LQ. Diversity and novelty of actinobacteria in Arctic marine sediments. Antonie. Van. Leeuwenhoek 2014; 105(4): 743–754. pmid:24519808
- 39. Atika M, Nasserdine S, Abdelghani Z, Florence M, Ahmed L. Isolation, taxonomy, and antagonistic properties of halophilic actinomycetes in Saharan soils of Algeria. Appl Environ Microbiol 2011; 77(18): 6710–6714. pmid:21764956
- 40. Ronoh RC, Budambula NLM, Mwirichia RK, Boga HI. Isolation and characterization of actinobacteria from lake Magadi, Kenya. Afr J Microbiol Res 2013; 7: 4200–4206. https://doi.org/10.5897/AJMR2012.2296
- 41. Wang Y, Tang SK, Lou K, Lee JC, Jeon CO, Xu LH, et al. Aidingimonas halophila gen. nov., sp. nov., a moderately halophilic bacterium isolated from a salt lake. Int J Syst Evol Microbiol 2009; 59(12): 3088–3094. https://doi.org/10.1099/ijs.0.010264-0
- 42. Wayne LG, Brenner DJ, Colwell RR, et al. International Committee on Systematic Bacteriology. Report of the ad hoc committee on reconciliation of approaches to bacterial systematics. Int J Syst Bacteriol 1987; 37: 463–464.
- 43. Xia ZF, Ruan JS, Huang Y, Zhang LL. Streptomyces aidingensis sp. nov., an actinomycete isolated from lake sediment. Int J Syst Evol Microbiol 2013; 63(9): 3204–3208. https://doi.org/10.1099/ijs.0.049205-0
- 44. Xia ZF, Guan TW, Ruan JS, Huang Y, Zhang LL. Longimycelium tulufanense gen. nov., sp. nov., a filamentous actinomycete of the family Pseudonocardiaceae. Int J Syst Evol Microbiol 2013; 63(8): 2813–2818. https://doi.org/2813-2818.10.1099/ijs.0.044222-0
- 45. Nikou MM, Ramezani M, Harirchi S, Makzoom S, Amoozegar MA, Shahzadeh FSA, et al. Salinifilum gen. nov., with description of Salinifilum proteinilyticum sp nov., an extremely halophilic actinomycete isolated from Meighan wetland, Iran, and reclassification of Saccharopolyspora aidingensis as Salinifilum aidingensis comb. nov and Saccharopolyspora ghardaiensis as Salinifilum ghardaiensis comb. Nov Int J Syst Evol Microbiol 2017; 67(10): 4221–4227. pmid:28920832
- 46. Guan TW, Tian L, Li EY, Tang SK, Zhang XP. Gracilibacillus aidingensis sp. nov., a novel moderately halophilic bacterium isolated from Aiding salt lake. Arch Microbiol 2017; 199(9): 1277–1281. pmid:28624973
- 47. Guan TW, Xiao J, Zhao K, Luo XX, Zhang XP, Zhang LL. Halomonas xinjiangensis sp. nov., a halotolerant bacterium isolated from a salt lake. Int J Syst Evol Microbiol 2010; 60(2): 349–352. https://doi.org/10.1099/ijs.0.011593-0