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Original Research ARTICLE

Front. Microbiol., 16 April 2018 | https://doi.org/10.3389/fmicb.2018.00739

Building a Geochemical View of Microbial Salt Tolerance: Halophilic Adaptation of Marinococcus in a Natural Magnesium Sulfate Brine

  • 1UK Centre for Astrobiology, School of Physics and Astronomy, The University of Edinburgh, Edinburgh, United Kingdom
  • 2School of Earth and Environmental Sciences, University of St Andrews, St Andrews, United Kingdom

Current knowledge of life in hypersaline habitats is mostly limited to sodium and chloride-dominated environments. This narrow compositional window does not reflect the diversity of brine environments that exist naturally on Earth and other planetary bodies. Understanding the limits of the microbial biosphere and predicting extraterrestrial habitability demands a systematic effort to characterize ionic specificities of organisms from a representative range of saline habitats. Here, we investigated a strain of Marinococcus isolated from the magnesium and sulfate-dominated Basque Lakes (British Columbia, Canada). This organism was the sole isolate obtained after exposure to exceptionally high levels of Mg2+ and SO42- ions (2.369 and 2.840 M, respectively), and grew at extremes of ionic strength not normally encountered in Na+/Cl- brines (12.141 mol liter-1). Its association at the 16S rDNA level with bacterial halophiles suggests that ancestral halophily has allowed it to adapt to a different saline habitat. Growth was demonstrated in media dominated by NaCl, Na2SO4, MgCl2, and MgSO4, yet despite this plasticity the strain was still restricted; requiring either Na+ or Cl- to maintain short doubling times. Water activity could not explain growth rate differences between media, demonstrating the importance of ionic composition for dictating microbial growth windows. A new framework for understanding growth in brines is required, that accounts for the geochemical history of brines as well as the various stresses that ions impose on microbes. Studies such as this are required to gain a truly universal understanding of the limits of biological ion tolerance.

Introduction

Hypersaline brines occur naturally on every continent on Earth, as well as on the ocean floor (Wallmann et al., 2002), in the subsurface (Hanor, 1994), and on other planetary bodies (Kargel, 2000; Tosca et al., 2008). Understanding the factors that limit and control microbial growth in brines is therefore crucial to charting the extent of the terrestrial biosphere, as well as predicting likely habitable environments off the Earth.

Knowledge of microbial life in saline systems is largely based on observations of sodium and chloride-dominated environments, which form the majority of hypersaline water bodies on Earth(Hardie, 1985). These are commonly populated by ‘halophilic’ (salt-requiring) or ‘halotolerant’ (salt-tolerant) microbes, and thanks to a focused body of work, we have gained a detailed understanding of the strategies employed by these organisms for coping with molar levels of Na+ and Cl- ions (Oren, 2011; Mcgenity and Oren, 2012). High concentrations of salt ions reduce the thermodynamic availability of water (water activity) (Grant, 2004), and because hydration is a fundamental requirement for biomolecular function, reduced water activity is widely recognized as the most significant challenge to life in hypersaline environments (Stevenson et al., 2015).

Yet due to complex ion-specific interactions both with the solvent and directly with biomolecules, there is a strong rationale to expect that brines of different compositions will exert different stresses on microorganisms. Indeed, many studies of both halophiles and their biomolecules have shown that changing the ionic composition of the milieu can influence every aspect of biological function, including protein conformation, enzymatic activity, cellular morphology, growth rate and culture density (e.g., Flannery, 1956; Abram and Gibbons, 1961; Boring et al., 1963; Houchstein and Dalton, 1968; Lanyi, 1974; Madern et al., 2000). Many of these historical studies, whilst they suggest important ion-specific effects, do not account for variations in water activity across different salt solutions, thus making discrimination between ion-specific and hydration-related effects difficult.

More recently, observations of deep-sea hypersaline anoxic basins that contain magnesium chloride brines have shown that chaotropicity (macromolecule-disordering effects), not water activity, defines microbial colonization in the brine: seawater interface (Hallsworth et al., 2007; Yakimov et al., 2015). Chaotropicity is a property of ion combinations, such as Mg2+/Cl-, that is not exhibited by Na+/Cl- brines and which powerfully limits microbial growth (Hallsworth et al., 2003; Ball and Hallsworth, 2015). Furthermore, a previous study has shown that high ionic strength brines rich in divalent ions can limit microbial growth even when water activity is sufficiently permissive (Fox-Powell et al., 2016). Observations such as these raise the questions: how much of what has been learnt about microbial salt adaptation from studying Na+/Cl- environments can we apply generally to all brine environments? And how much is ion-specific?

It is currently unclear whether a tendency for generic salt tolerance exists. There is even uncertainty surrounding the words ‘halophilic’ and ‘halotolerant,’ as often no distinction is made between generic salt tolerance and specific adaptation to Na+ and Cl-. Here, we use the prefix ‘halo’ when discussing specific Na+ and Cl- adaptation. Some authors have used similar terms to describe specific tolerance of other salts (e.g., ‘epsophily’ for life in high Mg2+/SO42- environments; Crisler et al., 2012, or ‘natronophily’ for life in high Na+/HCO3- environments; Banciu and Sorokin, 2013), but such terms are not employed here. The significance of these distinctions (including the widely used ‘halophile’) will remain unclear until it is understood how the effects of different ions manifest themselves on an organismal scale, particularly as most brine environments are characterized by dynamic assemblages of salt ions.

A necessary first step in this effort is to systematically study organisms from a diverse range of hypersaline environments, to understand their ion specificities both as a function of and independent from water activity. If halophilic tendencies equip organisms to inhabit non-Na+/Cl- brines, then it can be expected that inhabitants of such environments will themselves be halophiles or descendants of halophiles. Alternatively, if halophilic adaptation does not permit growth in other saline environments, it should be expected that brine inhabitants are descended from a variety of clades, regardless of ancestral halophily. Molecular surveys of environments such as the Dead Sea, which contains high concentrations of Mg2+ alongside Na+ and Cl-, have revealed dynamic populations of halophiles whose structures fluctuate in response to changes in ionic composition (Bodaker et al., 2010), whilst the Mg2+/SO42- rich Spotted Lake (British Columbia, Canada), and Hot Lake (Washington, Unites States) notably lack the halophilic archaea, which are ubiquitous inhabitants of Na+/Cl- brines (Lindemann et al., 2013; Pontefract et al., 2017). Laboratory-produced sulfate brines have also been shown to select for communities lacking typical halophiles, even when such organisms were present in the inoculum (Fox-Powell et al., 2016). Developing a truly universal understanding of the limits of biological ion tolerance requires marrying such community-level studies with in-depth investigations of the physiological limitations and requirements of specific microorganisms.

Here, we used the Basque Lakes, British Columbia, Canada as a natural laboratory to explore biological adaptation to non-Na+/Cl- brines. Like neighboring Spotted Lake and Hot Lake, these are a series of Mg2+/SO42- dominated hypersaline lakes that in the summer are concentrated to beyond epsomite (MgSO4.7H2O) saturation (Eugster and Hardie, 1978). They bear one of the highest reported divalent: monovalent ion ratios in natural brines and as such are an important analog for divalent ion-rich brines on Mars and elsewhere in the solar system (Foster et al., 2010; Fox-Powell et al., 2016). We report the isolation of a strain of Marinococcus, which was capable of growth in extremely high concentrations of Mg2+ and SO42-. The clustering of this genus with other typical halophiles suggests that the ancestral halophily of Marinococcus strain IS5B2c has allowed it to adapt to grow under high magnesium sulfate conditions.

Materials and Methods

Field Sampling and Geochemical Analyses

The Basque Lakes are a series of magnesium and sulfate brine lakes, pools and playas in the semi-arid interior of British Columbia, Canada (Figure 1). The lakes experience ion concentrations beyond epsomite saturation in the dry summer months (Eugster and Hardie, 1978). Basque Lakes no. 1 (N 50° 36.01 W 121° 21.31) and 2 (N 50° 35.35 W 121° 20.54) were sampled in February 2015. The lakes consisted of numerous smaller ice-covered pools (Figure 1). Brine-inundated sediments were sampled from three pools (one from Lake no. 1 and two from Lake no. 2) using sterile 50 ml tubes and spatulas sterilized in 70% ethanol. Tubes were filled to the top to minimize gas phase, sealed with parafilm and kept at 4° C until shipment back to the laboratory. Oxidation/reduction potential, pH and temperature were measured in situ using a Myron L Company Ultrameter II and a Fisher Scientific Pt-100 platinum sensor digital thermometer. Lake waters for geochemical analyses were filtered (0.22 μm) and stored in 15 ml tubes for shipment back to the laboratory. Samples intended for cation analysis were acidified with HNO3 to a final concentration of 1%.

FIGURE 1
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FIGURE 1. The Basque Lakes sampling locations. (A) Lakes within the regional setting of British Columbia, Canada; (B) an aerial view of Basque Lakes nos. 1 and 2; (C) Basque Lake no. 2 in February 2015; (D) individual ice-covered pool within the Basque Lake no. 2 site.

Major cations were analyzed by Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES) at The University of Edinburgh, United Kingdom, using a Perkin Elmer Optima 5300 DV ICP-OES instrument according to manufacturer’s instructions. Major anions were analyzed by Ion Chromatography (IC) at The University of Edinburgh, United Kingdom, using a Dionex DX-120 system according to manufacturer’s instructions.

Enrichment, Isolation, and Cultivation of a Pure Strain

In order to select for organisms adapted for life in the most extreme concentrations of divalent ions, Basque Lake no. 2 samples were screened using a high ionic strength culture medium (designated IS5) designed to maximize ionic strength whilst keeping water activity relatively high (“Control-5” in Fox-Powell et al., 2016). This medium contained (per liter) 67.7 g/0.333 M MgCl2⋅6H2O, 431.33g/1.75 M MgSO4⋅7H2O, 213.060 g/1.5 M Na2SO4, 0.746g/0.010 M KCl, 4g yeast extract (Oxoid), was adjusted to pH 7.0 with a 1 M solution of Tris–HCl and sterilized by autoclaving at 121°C for 15 min. Due to a small amount of precipitate, the medium was sampled and analyzed by ICP-OES and IC as described above. Ionic strength of the completed medium was 12.141 mol liter-1.

Fifty milliliter aliquots of IS5 medium were inoculated in triplicate with approximately 5 g brine/sediment from each Basque Lake no. 2 sample and shaken at 70 rpm at 30°C for 60 days. Following primary incubation, enrichments were stained with 1× SYBR gold and observed under fluorescence microscopy. Only one sample produced a successful enrichment, which was subsequently transferred (1% v/v) to fresh sterile IS5 medium.

A single pure strain (designated IS5B2c) was isolated in IS5 medium by three rounds of serial dilution-to-extinction. Briefly, a 10-fold dilution series of cells was established, spanning a range of dilutions that encompassed and exceeded the cell density (enumerated by direct counts under fluorescence microscopy). These dilutions were incubated as before and monitored for growth. The highest dilution to exhibit growth, which was founded by a population of approximately 1 cell ml-1, was then used to initiate a second round of dilutions. This process was repeated a total of three times. The highest dilution to exhibit growth from the third round was selected for future experiments. Cells were harvested by filtration (0.22 μm) and frozen for DNA extraction and confirmation of strain purity.

Due to extremely slow growth in IS5 medium, strain IS5B2c was routinely cultured in a medium simulating the relative ionic abundances of Basque Lake no. 2 (hereafter referred to as BL medium). BL medium was less concentrated, possessing a lower ionic strength than IS5 medium (∼8.7 mol liter-1), and preliminary experiments showed dramatic increases in growth rates compared to IS5 medium. BL medium contained (per liter): 4.11 g/0.041 M KHCO3, 1.521 g/0.020 M KCl, 11.379 g/0.056 M MgCl2⋅6H2O, 8.983 g/0.154 M NaCl, 509.775 g /2.068 M MgSO4⋅7H2O, 4 g yeast extract (Oxoid), 3 g casamino acids (Difco), was adjusted to pH 7.0 with a 1 M solution of Tris–HCl and sterilized by autoclaving at 121°C for 15 min.

DNA Extraction, Sequencing, and Phylogenetic Analysis

Strain IS5B2c was grown to stationary phase in BL medium, harvested by filtration onto sterile 0.22 μm-pore 25 mm diameter polycarbonate filters (Merck Millipore) and DNA was extracted using a modified phenol:chloroform:isoamyl alcohol protocol as described in Urakawa et al. (2010). DNA was interrogated by polymerase chain reaction (PCR) using the primers 27F (5′-AGAGTTTGATCMTGGCTCAG-3′) and 1389R (5′-ACGGGCGGTGTGTACAAG-3′) which target bacterial 16S ribosomal RNA (Cameron et al., 2012). Each individual 25 μl PCR reaction contained 1 μl template, 0.4 μM of the relevant forward and reverse primer, 200 μM dNTPs, 1.5 mM MgCl2, 1× PCR buffer and 1 unit Taq polymerase (Invitrogen). Reactions were treated at 95°C for 5 min and then subject to 25 cycles of: melting at 95°C for 60 s, annealing at 55°C for 60 s and extension at 72°C for 90 s, and finished with a final extension step at 72°C for 10 min. Bacterial PCR products were purified using the Qiagen Amplicon Purification Kit according to manufacturer’s instructions, and sequenced on the Sanger ABI 3730 XL platform at Edinburgh Genomics, The University of Edinburgh, in both forward and reverse directions.

Sequence processing, trimming and contig assembly was performed using the DNA Baser software. First, primer sequences were removed from both complementary sequences. Next, the sequences were aligned for contig assembly and low-quality ends and ambiguous bases were removed. The final consensus sequence was exported for phylogenetic analysis and aligned with the NCBI database using the BLASTn tool. Phylogenetic analysis was performed using the CLUSTAL_W program in the MEGA v. 7 software suite. A phylogenetic tree was constructed using the neighbor joining approach (Saitou and Nei, 1987), with Alicyclobacillus acidocaldarius used as the outgroup (Wang et al., 2009). The topology of the tree was evaluated by the bootstrap resampling method based on 1000 replicates.

Growth Response Quantification

Growth of strain IS5B2c was quantified by measuring increase in optical density at 600 nm (OD600) in 96 well plates in a Biotek Synergy 2 microplate reader. Doubling times were calculated from the exponential growth portion of OD600 curves. The pH-defined growth range of strain IS5B2c was investigated by recording OD600 increase in a series of BL media buffered in 0.5 pH unit increments between pH 3.0 and pH 9.0. Levels of pH above 7.5 were achieved by the addition of Tris; levels below pH 6.5 were adjusted with HCl. Temperature ranges were established by recording OD600 increase in BL medium (pH 7.0) at increments of increasing temperature from 4 to 45°C. The NaCl requirement (halophily) of strain IS5B2c was established in a series of NaCl media, in which the most concentrated contained (per liter) 292.2 g/5.0 M NaCl and concentration was decreased in either 0.5 or 0.25 M increments. NaCl media also contained (per liter): 0.746 g/0.010 M KCl, 4 g yeast extract (Oxoid) and 3 g casamino acids (Difco).

The ionic requirements of strain IS5B2c were tested by systematically comparing growth rates between media that contained 2 M of each of four ions (Mg2+, Na+, SO42-, and Cl-) in all possible cation-anion pairings. Apart from the main dissolved salt, the media contained (per liter) 0.746 g/0.010 M KCl, 4 g yeast extract (Oxoid) and 3 g casamino acids (Difco).

Water Activity Measurement

Water activity was quantified at 30°C using a Rotronic HP23-AW water activity meter in AWE mode, calibrated to five points (0.325, 0.595, 0.755, 0.845, and 0.935) using saturated salt solution standards (MgCl2, NH4NO3, NaCl, KCl, and KH2PO4, respectively) prepared as described by Winston and Bates (1960).

Results

The Basque Lakes

At time of sampling, the waters of both Basque Lake no. 1 and Basque Lake no. 2 were in a relatively dilute phase likely due to increased rain and snowmelt input and lower evaporation rates in winter. The three sampled pools (distributed between Lakes nos. 1 and 2) possessed ionic strengths between 0.498 and 1.038 mol liter-1, magnesium/sodium ratios between 1.50 and 3.56 and sulfate/chloride ratios between 28.31 and 86.92 (Table 1).

TABLE 1
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TABLE 1. Ionic composition and physicochemical parameters of the Basque Lakes sample sites.

Marinococcus Strain IS5B2c

A single isolate, originating from Basque Lake no. 2 and designated strain IS5B2c, was obtained by serial dilution-to-extinction. Growth in the high ionic strength (12.141 mol liter-1) enrichment medium was slow; taking around 14 days for cell numbers to increase from inoculum values in microscopic observations. Cells of strain IS5B2c were 1–2 μm diameter coccoids (Figure 2), which when grown to high density in the routine BL medium exhibited a noticeably visible orange-yellow pigmentation.

FIGURE 2
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FIGURE 2. Cells of strain IS5B2c stained with SYBR gold, mounted on polycarbonate 0.22 μm filter and imaged under epifluorescence microscopy.

A partial 16S rDNA sequence was obtained, covering 1,117 base pairs. At the 16S rDNA level, strain IS5B2c clustered most closely with the moderately halophilic, aerobic Gram-positive bacterial genus Marinococcus, sharing >99% identity with all other described species in the genus (Figure 3). BLAST analysis revealed the closest database match at 16S rDNA level to be from a bacterial culture originating from Sehline Sebkha salt lake, Tunisia, which also clustered in the Marinococcus genus (Hedi et al., 2014).

FIGURE 3
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FIGURE 3. Phylogenetic association of strain IS5B2c with the Marinococcus genus and other related taxa, based on partial 16S rDNA sequence. Numbers on branch nodes are percentage bootstrap values from 1000 resampling efforts. The root was the 16S rDNA sequence from Alicyclobacillus acidocaldarius DSM 446. Scale bar represents number of base substitutions per site.

Similar to previously described Marinococcus strains, strain IS5B2c grew optimally at pH 7.0, with short doubling times also recorded at pH 6.5 and 7.5. No growth was observed below pH 6.0 or above pH 7.5 (Figure 4). Strain IS5B2c grew optimally at a similar temperature to other Marinococcus isolates, which have temperature optima around 30°C (Novitsky and Kushner, 1976; Van Hao et al., 1984; Li et al., 2005; Wang et al., 2009) and was capable of slow growth at 15° C (growth rate not quantified), but not at 4°C, or at 45°C (Figure 4).

FIGURE 4
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FIGURE 4. Doubling time of strain IS5B2c under ranges of pH (A) and temperature (B). Dashed red lines represent maximum and minimum growth limits. Bars represent ± 1 standard error of triplicate experiments.

Growth of Strain IS5B2c in Varied Ionic Regimes

NaCl requirements for strain IS5B2c were similar to other members of the genus; growth was demonstrated over a NaCl concentration range of 0.5–4.0 M (approximately 3–24%), with the fastest growth rate around 1.75–2 M (Figure 5). No growth was observed at 5 M or at 0.25 M NaCl. The doubling time of Marinococcus strain IS5B2c was approximately the same in BL medium (dominated by Mg2+ and SO42) as in the optimum concentration of pure NaCl.

FIGURE 5
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FIGURE 5. Growth response of strain IS5B2c to different pure salt media. (A) Growth rate (doubling time) as a function of varied NaCl concentration; (B) growth rate in media comprising 2 M of either each anion (Left) or cation (Right), paired with both corresponding counterions. Error bars represent ± 1 standard error of triplicate experiments.

Strain IS5B2c showed remarkable plasticity with its ionic requirements, growing in media where the main salts were NaCl, Na2SO4, MgCl2, or MgSO4 (Figure 5). Growth rates across the different media compositions varied considerably. The most rapid growth was measured in 2 M Na+/Cl-, and the slowest in 2 M Mg2+/SO42-⋅ 2 M SO42- (paired with Na+) supported a comparable growth rate to 2 M Cl- (paired with Mg2+). Doubling times in 2 M Na+ when paired with SO42- were slightly longer (Figure 5).

To attempt to explain the different growth rates, we measured water activity in all growth media. We found that when grown in NaCl, strain IS5B2c had a water activity optimum of approximately 0.940 aw, with similar growth rates obtained between 0.950 aw and 0.920 aw (Figure 6). Higher and lower water activities produced progressively longer doubling times. Synthetic Basque Lakes medium (BL medium), at 0.925 aw, supported rapid doubling times in agreement with the optimum water activity range in NaCl. Water activity varied considerably across the other salt media, despite sharing absolute concentrations of specific ions. Most ion pairings produced doubling times that fell on or near the NaCl water activity growth response curve, with the notable exception of 2 M Mg2+ paired with Cl- (which prohibited all growth) and 2 M Mg2+/SO42-, which had a water activity near the optimum value yet a growth rate close to the slowest recorded here (Figure 6).

FIGURE 6
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FIGURE 6. Growth response of strain IS5B2c to varied ionic regimes, as a function of water activity. Pure salt media (including all possible cation-anion pairings) are the same as those reported in Figure 5. Green shaded area represents the water activity response curve (±1 standard error) of the strain when grown in pure NaCl media. Square symbols indicate sulfate salts, triangles indicate chloride salts. Filled symbols indicate media containing either 2 M of the anion or 2 M of both anion and cation (in the case of salts with a 1: 1 stoichiometry). Empty symbols indicate media containing 2 M of the cation only. BL = BL medium, plotted for reference. Note that 2 M Mg2+ paired with chloride inhibited all growth (inverted red triangle). Error bars represent ± 1 standard error of triplicate experiments.

Discussion

The Basque Lakes

The Basque Lakes, British Columbia are part of a series of hypersaline playas in western North America that exhibit unusual chemistries (Renaut, 1990). The Basque Lakes are particularly unique for not simply containing Mg2+ and SO42- as major ions, but for being dominated by them, reflected in high Mg2+: Na+ ratios and even higher SO42-: Cl- ratios (Table 1). This water chemistry is similar to that found in nearby Spotted Lake (Pontefract et al., 2017). Such environments provide valuable natural laboratories for understanding microbial salt tolerance, and due to their high divalent : monovalent ion ratios make compelling analogs for sulfate brines on ancient Mars, which likely possessed divalent ion content highly atypical of terrestrial chloride brines (Vaniman et al., 2004; Tosca et al., 2011). Indeed, sulfates (Mg, Fe, and Ca) make up the majority of martian salt minerals both in evaporite outcrops (Bibring et al., 2006; Hynek et al., 2015), and in the globally distributed dust (Yen et al., 2005), recording the widespread presence of sulfate-rich brines during a key transitionary phase of martian surface evolution. It follows that properly understanding how martian habitability has changed through time requires knowledge of how life adapts to cope with highly saline sulfate-rich environments. Thus, isolates from environments such as the Basque Lakes can help inform what establishes boundaries to biologically permissive environments on other planetary bodies, whether that be indigenous life or less speculatively, microorganisms transferred into these environments by robotic or human missions.

Marinococcus Strain IS5B2c: A Magnesium and Sulfate-Loving Halophile

A strain of Marinococcus, designated IS5B2c, was isolated from the Basque Lakes using a high ionic strength growth medium. The successful cultivation of strain IS5B2c at an ionic strength of 12.141 mol liter-1 in IS5 medium, with a Mg2+ concentration of 2.369 M and a SO42- concentration of 2.840 M represents both the highest documented ionic strength and the highest co-occurring concentrations of Mg2+ and SO42- directly demonstrated to be tolerated by a microorganism. Growth at these levels is remarkable, particularly considering that high ionic strength (>10 mol liter-1) can interact with other stressors to powerfully limit microbial growth, precluding halophiles that tolerate more extreme levels of low water activity (Fox-Powell et al., 2016).

Similar growth rates recorded in BL medium (dominated by Mg2+ and SO42- with Na+ and Cl- approximately an order of magnitude lower in concentration) and in the optimum concentration of pure NaCl (Figure 5) is a likely sign of adaptation to its source environment. The replacement of Na+/Cl- with Mg2+/SO42- as the dominant ions with no negative effect on growth hints at a set of evolutionary adaptations in the Basque Lakes which could supply a host of valuable information on the ion specificity of salt stress.

The Marinococcus genus is classified at the high end of moderate halophily; members typically grow optimally over the range 10–15% dissolved NaCl (approximately 1.8–2.6 M), but some can tolerate higher concentrations (up to 25%) (Li et al., 2005; Rice et al., 2009). The placing of strain IS5B2c within the Marinococcus genus, and this genus’s close phylogenetic association with other halophilic genera (including Pontibacillus, Halobacillus, and Salimicrobium) is a clear demonstration that halophilic (NaCl-loving) organisms are not precluded from hypersaline environments of fundamentally different compositions. It is likely that physicochemical stressors common to all hypersaline environments, such as low water activity, ensure that halophilic organisms already equipped to deal with them have a competitive advantage over those that are not.

However, other strains of Marinococcus are associated with brine compositions that suggest deviations from traditional halophily. The closest database match for strain IS5B2c was an isolate from Sehline Sebkha salt lake, Tunisia, which is dominated by Na+ and Cl- but with significant concentrations of Mg2+ and SO42- as secondary ions (Hedi et al., 2014). Marinococcus halotolerans, isolated from hypersaline soils in China, was initially enriched in a medium containing 250 gL-1 MgCl2.6H2O (1.23 M MgCl2), with relatively low concentrations of NaCl (2 g L-1; 33 mM) (Li et al., 2005). The variety of saline conditions tolerated by this organism are remarkable; the authors report similar growth responses across wide concentration ranges of NaCl, KCl, and MgCl2, which is rare for halophilic or halotolerant organisms which usually require NaCl to some degree (Boring et al., 1963; Javor, 1984; Ventosa et al., 1998; Crisler et al., 2012). This plasticity is also reflected in strain IS5B2c, as discussed below. Enrichments done in high levels of Mg2+ by Li et al. (2005) and in the current study both resulted in the culture of a strain of Marinococcus, despite the large degree of geographical separation between the source environments. Due to their ability to tolerate a seeming wide variety of ionic compositions, including those of extreme ionic strength, species within the Marinococcus genus make compelling model organisms for understanding the capacity for life in hypersaline environments that differ significantly from typical Na+/Cl- brines.

Beyond Water Activity: Ion Specificities of Marinococcus Strain IS5B2c

Developing a universal understanding of microbial ion tolerance requires systematic assessments of the ionic requirements of organisms from a range of hypersaline environments. It is only with an appreciation of how ionic composition defines growth in the context of an organism’s phylogenetic associations that we can begin to discriminate between generic salt adaptation tendencies and ion-specific effects. Historical efforts to investigate the ionic dependencies of halophiles produced results that frustrated attempts to generalize; organism-specific idiosyncrasies seemed to be the rule (e.g., Javor, 1984; Ventosa et al., 1998). Consistencies that did emerge were that all halophiles require Na+ to some degree, and that the requirement for Na+ and Cl- ions could be lowered somewhat through substitution with other solutes (including organic solutes such as glucose or glycerol) (Adams et al., 1987). However, these studies lacked systematic consideration of other powerful growth-mediating physicochemical parameters, such as water activity, which can vary significantly across different brines.

Water activity is a measure of the thermodynamic availability of water, expressed relative to pure water at the same temperature and pressure. The degree to which water activity is depressed in an aqueous system varies with the solute. For example, 2 M solutions of NaCl and MgSO4 have respective water activities of approximately 0.93 aw and 0.96 aw, which is greater than the difference between freshwater and seawater. Given that water activity is a powerful mediator of microbial growth (Stevenson et al., 2015), any assessment of the effects of ionic composition on microbial growth requires consideration of this parameter.

Strain IS5B2c was therefore subjected to suite of growth trials in which the main dissolved salt was varied systematically (by concentration), and water activity was measured across all media. When strain IS5B2c was grown in different pure salt media, growth response varied considerably, despite the media sharing absolute concentrations of ions; as has been observed in many strains (Abram and Gibbons, 1961; Boring et al., 1963; Javor, 1984; Ventosa et al., 1998). It is tempting to interpret this as preferences for certain ions; for example in both 2 M Cl- and 2 M SO42-, doubling times were shorter if the cation was Na+ than Mg2+ (Figure 6), inviting the conclusion that strain IS5B2c has a preference for Na+ over Mg2+.

However, considering water activity alongside ionic composition explained some of strain IS5B2c’s apparent ionic preferences. An apparent preference for Na+ over Mg2+ when paired with 2 M Cl- was satisfactorily explained by a higher water activity in the Mg2+/Cl- media (which had a concentration of 1 M); meaning that it lay just outside the organism’s optimum range (Figure 6). When the 2 M Cl- (with Mg2+) growth rates were compared with NaCl media at approximately the same water activity, doubling times were in excellent agreement despite differences in absolute Cl- concentration (Figure 6). This is a clear demonstration that if ionic preferences are to be understood, physicochemical factors such as water activity must be accounted for.

Water activity alone cannot be used to predict doubling time, however, otherwise all doubling times would have fallen somewhere on the optimum curve, which was not the case. Clearly, ion-specific effects were important. 2 M Mg2+ paired with Cl- inhibited all growth, despite possessing a water activity that was demonstrably permissive in NaCl. This is likely due to the highly chaotropic activity of MgCl2 at these concentrations (2 M) (Cray et al., 2013). It has previously been shown that chaotropic solutes such as MgCl2 can impose stresses on microorganisms even when water activity is at permissive levels (Hallsworth et al., 2003), and currently biological activity of any kind above 2.3 M MgCl2 has not been documented (Hallsworth et al., 2007; Yakimov et al., 2015). Both Na2SO4 media produced doubling times slightly faster than that predicted from water activity alone, suggesting a preference for sulfate under more dilute conditions.

Perhaps most striking are the notably long doubling times recorded in 2 M MgSO4, indicating a much slower growth rate than that predicted by the water activity curve in NaCl (Figure 6). This is despite being isolated from an environment characterized by high levels of these ions. Again, this cannot be explained by high ionic strength or some toxic effect of either Mg2+ or SO42-, as the strain grew readily in BL medium (dominated by Mg2+ and SO42- with an ionic strength ∼0.5 mol liter-1 higher than the pure MgSO4 medium), at the shortest doubling time achieved for the strain. It is important to note, however, that BL medium also contained Na+ and Cl- as secondary ions.

When both Na+ and Cl- were omitted from the growth media, growth was dramatically retarded. Surprisingly, it was not a requirement for Na+ and Cl- in combination that defined this limitation, as the organism would grow well in media where one of either Cl- or Na+ had been removed (for instance, in 1 M MgCl2 or 1 and 2 M Na2SO4). Rather, if either of these ions were present in appreciable quantities, it was sufficient to stimulate growth. This is remarkable, as cations and anions are handled by wholly different cellular pathways and thus it is highly implausible that there could be some active cellular process that could readily substitute Na+ for Cl-. It could instead be due to some affinity for specific ions in the structure of the organism’s biomolecules, as is observed in the halophilic archaea, and also in the membrane proteins of some bacterial halophiles (Oren et al., 2005).

The Haloarchaea have evolved to accept molar quantities of K+ (in place of Na+) and Cl- into the cell, and their intracellular machinery must be structurally modified to function in the presence of these ions (Soppa, 2006). The observed changes mostly decrease hydrophobicity and increase protein affinity for water molecules, both of which seem to be approaches to mitigate low water activity stress (Tadeo et al., 2009). However, enzymes from these organisms are shown to have ion specificities beyond a simple need for hydration, and function optimally only if K+ and Cl- are provided (Ortega et al., 2011; Karan et al., 2012). A narrow window of ion-specificity in the Haloarchaea might explain their absence from Mg2+/SO42- environments like Spotted Lake, British Columbia (Pontefract et al., 2017), and sulfate brine enrichments (Fox-Powell et al., 2016), as well as the loss of Haloarchaeal dominance in the Dead Sea following evaporative concentration of Mg2+ (Bodaker et al., 2010).

Due to an ostensible lack of these proteome modifications in halophiles that maintain low cytoplasmic ion concentrations, such as most halophilic bacteria (including the Marinococcus genus; Louis and Galinski, 1997), it could be predicted that such organisms are more plastic with their ionic requirements, responding predominately to changes in water activity. However, studies have shown that even bacterial halophiles still bear some of the signatures of ‘salt-in’ Haloarchaeal proteomes, particularly in their membrane bound proteins which are exposed to the full salinity of the external milieu (Oren et al., 2005). Some specificity should therefore be expected, even in halophiles whose cytoplasmic salt ion content never rises beyond that of non-halophiles. Our data support this prediction, as growth appeared to be controlled predominately by hydration (water activity) effects as long as either Na+ or Cl- were available; when both of these ions were removed, growth was dramatically slowed (Figure 6).

Future work should focus on determining the mechanisms employed by strain IS5B2c for coping with extremely high Mg2+ and SO42- concentrations. In particular, changes in metabolic pathways and substrate utilization in strain IS5B2c under different saline conditions is important follow-on work. As Mg2+ concentrations in the Dead Sea became elevated, archaeal CorA magnesium channels became enriched 11-fold (Bodaker et al., 2010). It was assumed this was a resistance mechanism in the halophilic archaea to cope with the changing composition, and if so implies that the typically ‘salt-in’ Haloarchaea were actively excluding the divalent cation. If this energy-demanding process is the only approach available to organisms in high Mg2+ environments then that may well be a determining factor for brine habitability.

Toward a Geochemical View of Salt Ion Tolerance: Lessons Learned From a Model Strain

Most knowledge of how microorganisms grow in hypersaline environments is drawn from studies of sodium and chloride-rich brines. Whilst this approach has served us well in understanding the distribution and activity of halophiles in the most dominant brine type on Earth, it has limited our ability to predict the extent of microbial habitat into other brine types, including those that exist in evaporites in the deep subsurface (e.g., Payler et al., unpublished) or on other planetary bodies (Fox-Powell et al., 2016).

A future goal of mapping the limits of life in high salt is to be able to analyze the composition of any brine and make informed, accurate predictions about habitability. Trade-offs almost certainly exist, as coping with high levels of salts is energetically expensive, meaning that certain ionic compositions might preclude low-energy metabolisms (Oren, 2011). Additionally, if protein structural changes always bear ion specificity, adaptations required to cope with one major ion might always decrease tolerance of another. These questions and others can be answered with systematic efforts to characterize further organisms from diverse brine types. It is notable that even in a brine fundamentally different from typical Na+/Cl- environments, halophiles such as Marinococcus can thrive, demonstrating that halophily does bestow aspects of a generic salt tolerance. The predictive power of water activity for growth rate was demonstrated across some pure salts, suggesting a limited ionic plasticity of this form of halophily. However, ionic specificity remained; in the absence of Na+ and Cl-, water activity no longer satisfactorily predicted growth rate.

This finding raises many questions about what might be required on a molecular level to develop true independence from sodium and/or chloride, and whether this has occurred on Earth. It is an open question whether organisms from hypersaline environments can be fully composition-independent and respond only to water activity, or if some ion-specificity will always occur. If this requirement for either Na+ or Cl- is indeed a residual trait from strain IS5B2c’s halophilic ancestors, would inhabitants of Mg2+/SO42- brines that don’t share this evolutionary history exhibit a different set of requirements? Such organisms, should they exist, should be the target of future cultivation efforts.

Author Contributions

CC and MF-P obtained the samples and contributed equally to experimental design and interpretation of results. MF-P conducted laboratory work and wrote the manuscript. CC contributed text, reviewed and edited the manuscript.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

This study was conducted with support from the Science and Technology Facilities Council (STFC), grant no. ST/ M001261/1.

References

Abram, D., and Gibbons, N. E. (1961). The effect of chlorides of monovalent cations, urea, detergents, and heat on morphology and the turbidity of suspensions of red halophilic bacteria. Can. J. Microbiol. 7, 741–750. doi: 10.1139/m61-088

PubMed Abstract | CrossRef Full Text | Google Scholar

Adams, R., Bygraves, J., Kogut, M., and Russell, D. N. J. (1987). The role of osmotic effects in haloadaptation of Vibrio costicola. J. Gen. Microbiol. 133, 1861–1861. doi: 10.1099/00221287-133-7-1861

PubMed Abstract | CrossRef Full Text | Google Scholar

Ball, P., and Hallsworth, J. (2015). Water structure and chaotropicity: their uses, abuses and implications for biology. Phys. Chem. Chem. Phys. 17, 8297–8305. doi: 10.1039/C4CP04564E

PubMed Abstract | CrossRef Full Text | Google Scholar

Banciu, H. L., and Sorokin, D. Y. (2013). “Adaptation in haloalkaliphiles and natronophilic bacteria,” in Polyextremophiles: Life Under Multiple Forms of Stress, eds J. Seckbach, A. Oren, and H. Stan-lotter (Dordrecht: Springer), 121–178. doi: 10.1007/978-94-007-6488-0_5

CrossRef Full Text | Google Scholar

Bibring, J.-P., Langevin, Y., Mustard, J. F., Poulet, F., Arvidson, R., Gendrin, A., et al. (2006). Global mineralogical and aqueous mars history derived from omega/mars express data. Science 312, 400–404. doi: 10.1126/science.1122659

PubMed Abstract | CrossRef Full Text | Google Scholar

Bodaker, I., Sharon, I., Suzuki, M. T., Feingersch, R., Shmoish, M., Andreishcheva, E., et al. (2010). Comparative community genomics in the Dead Sea: an increasingly extreme environment. ISME J. 4, 399–407. doi: 10.1038/ismej.2009.141

PubMed Abstract | CrossRef Full Text | Google Scholar

Boring, J., Kushner, D. J., and Gibbons, N. E. (1963). Specificity of the salt requirement of Halobacterium cutirubrum. Can. J. Microbiol. 9, 143–154. doi: 10.1139/m63-020

CrossRef Full Text | Google Scholar

Cameron, K. A., Hodson, A. J., and Osborn, A. M. (2012). Structure and diversity of bacterial, eukaryotic and archaeal communities in glacial cryoconite holes from the Arctic and the Antarctic. FEMS Microbiol. Ecol. 82, 254–267. doi: 10.1111/j.1574-6941.2011.01277.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Cray, J. A., Russell, J. T., Timson, D. J., Singhal, R. S., and Hallsworth, J. E. (2013). A universal measure of chaotropicity and kosmotropicity. Environ. Microbiol. 15, 287–296. doi: 10.1111/1462-2920.12018

PubMed Abstract | CrossRef Full Text | Google Scholar

Crisler, J. D., Newville, T. M., Chen, F., Clark, B. C., and Schneegurt, M. A. (2012). Bacterial growth at the high concentrations of magnesium sulfate found in Martian soils. Astrobiology 12, 98–106. doi: 10.1089/ast.2011.0720

PubMed Abstract | CrossRef Full Text | Google Scholar

Eugster, H. P., and Hardie, L. A. (1978). “Saline lakes,” in Lakes: Chemistry, Geology, Physics, ed. A. Lerman (New York, NY: Springer), 237–293. doi: 10.1007/978-1-4757-1152-3_8

CrossRef Full Text | Google Scholar

Flannery, W. L. (1956). Current status of knowledge of halophilic bacteria. Bacteriol. Rev. 20, 49–66.

PubMed Abstract | Google Scholar

Foster, I. S., King, P. L., Hyde, B. C., and Southam, G. (2010). Characterization of halophiles in natural MgSO4 salts and laboratory enrichment samples: astrobiological implications for Mars. Planet. Space Sci. 58, 599–615. doi: 10.1016/j.pss.2009.08.009

CrossRef Full Text | Google Scholar

Fox-Powell, M. G., Hallsworth, J. E., Cousins, C. R., and Cockell, C. S. (2016). Ionic strength is a barrier to the habitability of Mars. Astrobiology 16, 427–442. doi: 10.1089/ast.2015.1432

PubMed Abstract | CrossRef Full Text | Google Scholar

Grant, W. D. (2004). Life at low water activity. Philos. Trans. R. Soc. B Biol. Sci. 359, 1249–1267. doi: 10.1098/rstb.2004.1502

PubMed Abstract | CrossRef Full Text | Google Scholar

Hallsworth, J. E., Heim, S., and Timmis, K. N. (2003). Chaotropic solutes cause water stress in Pseudomonas putida. Environ. Microbiol. 5, 1270–1280. doi: 10.1111/j.1462-2920.2003.00478.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Hallsworth, J. E., Yakimov, M. M., Golyshin, P. N., Gillion, J. L. M., D’Auria, G., De Lima Alves, F., et al. (2007). Limits of life in MgCl2-containing environments: chaotropicity defines the window. Environ. Microbiol. 9, 801–813. doi: 10.1111/j.1462-2920.2006.01212.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Hanor, J. S. (1994). Origin of saline fluids in sedimentary basins. Geol. Soc. London Spec. Publ. 78, 151–174. doi: 10.1144/GSL.SP.1994.078.01.13

CrossRef Full Text | Google Scholar

Hardie, L. A. (1985). Evaporites: marine or non-marine? Am. J. Sci. 285, 667–672. doi: 10.2475/ajs.285.7.661

CrossRef Full Text | Google Scholar

Hedi, A., Essghaier, B., Cayol, J.-L., Fardeau, M.-L., and Sadfi, N. (2014). Prokaryotic biodiversity of halophilic microorganisms isolated from Sehline Sebkha Salt Lake (Tunisia). Afr. J. Microbiol. Res. 8, 355–367. doi: 10.5897/AJMR12.1087

CrossRef Full Text | Google Scholar

Houchstein, L. I., and Dalton, B. P. (1968). Factors affecting the cation requirement of a halophilic NADH dehydrogenase. Biochim. Biophys. Acta Enzymol. 167, 638–640. doi: 10.1016/0005-2744(68)90062-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Hynek, B. M., Osterloo, M. K., and Kierein-Young, K. S. (2015). Late-stage formation of Martian chloride salts through ponding and evaporation. Geology 43, 787–790. doi: 10.1130/G36895.1

CrossRef Full Text | Google Scholar

Javor, B. J. (1984). Growth potential of halophilic bacteria isolated from solar salt environments: carbon sources and salt requirements. Appl. Environ. Microbiol. 48, 352–360.

PubMed Abstract | Google Scholar

Karan, R., Capes, M. D., and Dassarma, S. (2012). Function and biotechnology of extremophilic enzymes in low water activity. Aquat. Biosyst. 8:4. doi: 10.1186/2046-9063-8-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Kargel, J. (2000). Europa’s crust and ocean: origin, composition, and the prospects for life. Icarus 148, 226–265. doi: 10.1006/icar.2000.6471

CrossRef Full Text | Google Scholar

Lanyi, J. K. (1974). Salt-dependent properties of proteins from extremely halophilic bacteria. Bacteriol. Rev. 38, 272–290.

PubMed Abstract | Google Scholar

Li, W. J., Schumann, P., Zhang, Y. Q., Chen, G. Z., Tian, X. P., Xu, L. H., et al. (2005). Marinococcus halotolerans sp. nov., isolated from Qinghai, north-west China. Int. J. Syst. Evol. Microbiol. 55, 1801–1804. doi: 10.1099/ijs.0.63596-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Lindemann, S. R., Moran, J. J., Stegen, J. C., Renslow, R. S., Hutchison, J. R., Cole, J. K., et al. (2013). The epsomitic phototrophic microbial mat of Hot Lake, Washington: community structural responses to seasonal cycling. Front. Microbiol. 4:323. doi: 10.3389/fmicb.2013.00323

PubMed Abstract | CrossRef Full Text | Google Scholar

Louis, P., and Galinski, E. A. (1997). Characterization of genes for the biosynthesis of the compatible solute ectoine from Marinococcus halophilus and osmoreg u lated expression in Escherichia coli. Microbiology 143, 1141–1141. doi: 10.1099/00221287-143-4-1141

PubMed Abstract | CrossRef Full Text | Google Scholar

Madern, D., Ebel, C., and Zaccai, G. (2000). Halophilic adaptation of enzymes. Extremophiles 4, 91–98. doi: 10.1007/s007920050142

CrossRef Full Text | Google Scholar

Mcgenity, T. J., and Oren, A. (2012). “Hypersaline environments and halophiles,” in Life at Extremes: Environments, Organisms and Strategies for Survival, ed. E. M. Bell (Wallingford: CAB International), 402–437. doi: 10.1079/9781845938147.0402

CrossRef Full Text

Novitsky, T. J., and Kushner, D. J. (1976). Planococcus halophilus sp. nov., a facultatively halophilic coccus. Int. J. Syst. Bacteriol. 26, 53–57. doi: 10.1099/00207713-26-1-53

CrossRef Full Text | Google Scholar

Oren, A. (2011). Thermodynamic limits to microbial life at high salt concentrations. Environ. Microbiol. 13, 1908–1923. doi: 10.1111/j.1462-2920.2010.02365.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Oren, A., Larimer, F., Richardson, P., Lapidus, A., and Csonka, L. N. (2005). How to be moderately halophilic with broad salt tolerance: clues from the genome of Chromohalobacter salexigens. Extremophiles 9, 275–279. doi: 10.1007/s00792-005-0442-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Ortega, G., Laín, A., Tadeo, X., López-Méndez, B., Castaño, D., and Millet, O. (2011). Halophilic enzyme activation induced by salts. Sci. Rep. 1:6. doi: 10.1038/srep00006

PubMed Abstract | CrossRef Full Text | Google Scholar

Pontefract, A., Zhu, T. F., Walker, V. K., Hepburn, H., Lui, C., Zuber, M. T., et al. (2017). Microbial diversity in a hypersaline sulfate lake: a terrestrial analog of ancient Mars. Front. Microbiol. 8:1819. doi: 10.3389/fmicb.2017.01819

PubMed Abstract | CrossRef Full Text | Google Scholar

Renaut, R. W. (1990). “Recent carbonate sedimentation and brine evolution in the saline lake basins of the Cariboo Plateau, British Columbia, Canada,” in Saline Lakes. Developments in Hydrobiology, Vol. 59, eds F. A. Comín and T. G. Northcote (Dordrecht: Springer), 67–81. doi: 10.1007/978-94-009-0603-7_6

CrossRef Full Text | Google Scholar

Rice, M. S., Bell, J. F. III, Cloutis, E. A., Wang, A., Ruff, S. W., Craig, M. A., et al. (2009). Silica-rich deposits and hydrated minerals at Gusev Crater, Mars: Vis-NIR spectral characterization and regional mapping. Icarus 205, 375–395. doi: 10.1016/j.icarus.2009.03.035

CrossRef Full Text | Google Scholar

Saitou, N., and Nei, M. (1987). The neighbor-joining method: a new method for reconstructing phylogenetic trees’. Mol. Biol. Evol. 4, 406–425.

Google Scholar

Soppa, J. (2006). From genomes to function: haloarchaea as model organisms. Microbiology 152, 585–590. doi: 10.1099/mic.0.28504-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Stevenson, A., Burkhardt, J., Cockell, C. S., Cray, J. A., Dijksterhuis, J., Fox-Powell, M., et al. (2015). Multiplication of microbes below 0.690 water activity: Implications for terrestrial and extraterrestrial life. Environ. Microbiol. 17, 257–277. doi: 10.1111/1462-2920.12598

PubMed Abstract | CrossRef Full Text | Google Scholar

Tadeo, X., López-Méndez, B., Trigueros, T., Laín, A., Castaño, D., and Millet, O. (2009). Structural basis for the aminoacid composition of proteins from halophilic archea. PLoS Biol. 7:e1000257. doi: 10.1371/journal.pbio.1000257

PubMed Abstract | CrossRef Full Text | Google Scholar

Tosca, N. J., Knoll, A. H., and McLennan, S. M. (2008). Water activity and the challenge for life on early Mars. Science 320, 1204–1207. doi: 10.1126/science.1155432

PubMed Abstract | CrossRef Full Text | Google Scholar

Tosca, N. J., McLennan, S. M., Lamb, M. P., and Grotzinger, J. P. (2011). Physicochemical properties of concentrated Martian surface waters. J. Geophys. Res. 116, 1–16. doi: 10.1029/2010JE003700

CrossRef Full Text | Google Scholar

Urakawa, H., Martens-Habbena, W., and Stahl, D. A. (2010). High abundance of ammonia-oxidizing archaea in coastal waters, determined using a modified DNA extraction method. Appl. Environ. Microbiol. 76, 2129–2135. doi: 10.1128/AEM.02692-09

PubMed Abstract | CrossRef Full Text | Google Scholar

Van Hao, M., Kocur, M., Komagata, K., and Komagata, K. (1984). Marinococcus gen. nov., A new genus for motile cocci with meso-diaminopimelic acid in the cell wall; and Marinococcus albus sp. nov. and Marinococcus halophilus (Novitsky and Kushner) comb. nov. J. Gen. Appl. Microbiol. 30, 449–459. doi: 10.2323/jgam.30.449

CrossRef Full Text | Google Scholar

Vaniman, D. T., Bish, D. L., Chipera, S. J., Fialips, C. I., Carey, J. W., and Feldman, W. C. (2004). Magnesium sulphate salts and the history of water on Mars. Nature 431, 663–665. doi: 10.1038/nature02973

PubMed Abstract | CrossRef Full Text | Google Scholar

Ventosa, A., Nieto, J. J., and Oren, A. (1998). Biology of moderately halophilic aerobic bacteria. Microbiol. Mol. Biol. Rev. 62, 504–544.

Google Scholar

Wallmann, K., Aghib, F., Castradori, D., Cita, M., Suess, E., Greinert, J., et al. (2002). Sedimentation and formation of secondary minerals in the hypersaline Discovery Basin, eastern Mediterranean. Mar. Geol. 186, 9–28. doi: 10.1016/S0025-3227(02)00170-6

CrossRef Full Text | Google Scholar

Wang, Y., Cao, L. L., Tang, S. K., Lou, K., Mao, P. H., Jin, X., et al. (2009). Marinococcus luteus sp. nov., a halotolerant bacterium isolated from a salt lake, and emended description of the genus Marinococcus. Int. J. Syst. Evol. Microbiol. 59, 2875–2879. doi: 10.1099/ijs.0.009670-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Winston, P. W., and Bates, D. H. (1960). Saturated solutions for the control of humidity in biological research. Ecology 41, 232–237. doi: 10.2307/1931961

CrossRef Full Text | Google Scholar

Yakimov, M. M., La Cono, V., Spada, G. L., Bortoluzzi, G., Messina, E., Smedile, F., et al. (2015). Microbial community of the deep-sea brine Lake Kryos seawater-brine interface is active below the chaotropicity limit of life as revealed by recovery of mRNA. Environ. Microbiol. 17, 364–382. doi: 10.1111/1462-2920.12587

PubMed Abstract | CrossRef Full Text | Google Scholar

Yen, A. S., Gellert, R., Schröder, C., Morris, R. V., Bell, J. F. III, Knudson, A. T., et al. (2005). An integrated view of the chemistry and mineralogy of Martian soils. Nature 436, 49–54. doi: 10.1038/nature03637

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: brine, habitability, Marinococcus, halophile, magnesium sulfate

Citation: Fox-Powell MG and Cockell CS (2018) Building a Geochemical View of Microbial Salt Tolerance: Halophilic Adaptation of Marinococcus in a Natural Magnesium Sulfate Brine. Front. Microbiol. 9:739. doi: 10.3389/fmicb.2018.00739

Received: 19 December 2017; Accepted: 29 March 2018;
Published: 16 April 2018.

Edited by:

Masahiro Ito, Toyo University, Japan

Reviewed by:

Valeria Souza, Universidad Nacional Autónoma de México, Mexico
Richard Allen White III, RAW Molecular Systems (RMS) LLC, United States

Copyright © 2018 Fox-Powell and Cockell. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Mark G. Fox-Powell, mgfp@st-andrews.ac.uk