Photosynthetic microbial mats are complex, stratified ecosystems in which high rates of primary production create a demand for nitrogen, met partially by N2 fixation. Dinitrogenase reductase (nifH) genes and transcripts from Cyanobacteria and heterotrophic bacteria (for example, Deltaproteobacteria) were detected in these mats, yet their contribution to N2 fixation is poorly understood. We used a combined approach of manipulation experiments with inhibitors, nifH sequencing and single-cell isotope analysis to investigate the active diazotrophic community in intertidal microbial mats at Laguna Ojo de Liebre near Guerrero Negro, Mexico. Acetylene reduction assays with specific metabolic inhibitors suggested that both sulfate reducers and members of the Cyanobacteria contributed to N2 fixation, whereas 15N2 tracer experiments at the bulk level only supported a contribution of Cyanobacteria. Cyanobacterial and nifH Cluster III (including deltaproteobacterial sulfate reducers) sequences dominated the nifH gene pool, whereas the nifH transcript pool was dominated by sequences related to Lyngbya spp. Single-cell isotope analysis of 15N2-incubated mat samples via high-resolution secondary ion mass spectrometry (NanoSIMS) revealed that Cyanobacteria were enriched in 15N, with the highest enrichment being detected in Lyngbya spp. filaments (on average 4.4 at% 15N), whereas the Deltaproteobacteria (identified by CARD-FISH) were not significantly enriched. We investigated the potential dilution effect from CARD-FISH on the isotopic composition and concluded that the dilution bias was not substantial enough to influence our conclusions. Our combined data provide evidence that members of the Cyanobacteria, especially Lyngbya spp., actively contributed to N2 fixation in the intertidal mats, whereas support for significant N2 fixation activity of the targeted deltaproteobacterial sulfate reducers could not be found.
In photosynthetic microbial mats high CO2 fixation activity often creates a great demand for nitrogen (N), which is partially met by high rates of N2 fixation (Bebout et al., 1994; Herbert, 1999). It was hypothesized that microbial mat development is dependent on the activity of N2-fixing microorganisms (diazotrophs) (Bergman et al., 1997). Microbial mats inhabiting the intertidal zone from Laguna Ojo de Liebre (Supplementary Figures S1 and S2) close to Guerrero Negro, Baja California Sur, Mexico, experience frequent alternating periods of desiccation (and thereby aeration) and tidal flooding (Omoregie et al., 2004b; Rothrock and Garcia-Pichel, 2005) and are subject to frequent physical disruption. This environment leads to a ‘pioneering stage’ of habitat colonization, where N2 fixation is an important process, providing a source of N for mat growth (Bebout et al., 1994).
Although N2 fixation has previously been investigated in the intertidal mats from Laguna Ojo de Liebre (Bebout et al., 1993; Omoregie et al., 2004a, 2004b), the identity of the active diazotrophs remains elusive. Historically, Cyanobacteria were believed to be responsible for N2 fixation in microbial mats given their visual dominance and cultivation without an exogenous N source (Stal and Krumbein, 1981; Stal and Bergman, 1990; Paerl et al., 1991). This was further supported by biogeochemical assays using an inhibitor of oxygenic photosynthesis (3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU)) (Stal et al., 1984; Bebout et al., 1993). However, molecular methods indicated that additional microorganisms (such as heterotrophic bacteria) present in microbial mats have the genetic potential for N2 fixation and may play an important role in microbial mat N2 fixation (Zehr et al., 1995; Steppe et al., 1996). In particular, sulfate-reducing bacteria (SRB) were hypothesized to contribute to N2 fixation in microbial mats (Steppe and Paerl, 2002). Indeed, earlier studies of the Laguna Ojo de Liebre intertidal mats, combining biogeochemical and molecular assays, were unable to detect nifH genes or transcripts from the visually dominating cyanobacterium Lyngbya spp. (Omoregie et al., 2004a, 2004b), despite the fact that several Lyngbya spp. possess the capability to fix N2 in culture (for example, Paerl et al., 1991; Bebout et al., 1993). Instead, nifH sequences from Cluster III, including SRB that belong to the Deltaproteobacteria, dominated these nifH gene libraries and were also found in the transcript library (Omoregie et al., 2004a, 2004b). In addition to these deltaproteobacterial sulfate-reducing diazotrophs, Cluster III also contains sequences from spirochetes, methanogens, acetogens, green sulfur bacteria and Clostridia (Zehr et al., 2003). Comparative investigation of available nifH sequences indicates that Cluster III contains the greatest diversity of all nifH lineages and that its diversity is still not fully understood (Gaby and Buckley, 2011).
The presence and/or transcription of the nifH gene does not necessarily mean that an organism actively fixes N2 in the environment since the nitrogenase enzyme activity can be regulated on multiple levels ranging from transcription (Chen et al., 1998) to post-translational protein modification (Kim et al., 1999). As such, identification of active diazotrophs requires investigation on the functional level, for example through stable isotope probing (SIP) with 15N2. The incorporation of 15N into biomass can be directly imaged with secondary ion mass spectrometry (SIMS; Cliff et al., 2002; Lechene et al., 2006; Popa et al., 2007), and especially the NanoSIMS 50 has been used recently to investigate diazotrophic communities at the single-cell level across diverse environments (for example, Dekas et al., 2009; Halm et al., 2009; Foster et al., 2011; Ploug et al., 2011; Woebken et al., 2012).
We sought to identify the diazotrophic community in intertidal mats at Laguna Ojo de Liebre, Mexico, and ascertain using a 15N2-SIP single-cell approach the actively N2-fixing populations. We applied a combination of inhibitor amendment experiments, nifH gene and transcript sequencing, and 15N2 incubations followed by single-cell isotope measurements. As in previous studies, inhibitor experiments coupled to acetylene reduction assays (ARAs) suggested that Cyanobacteria and SRB both have a major role in N2 fixation. However, further investigations through inhibitor addition experiments combined with 15N2-incubations, molecular and NanoSIMS analyses provided strong evidence that members of the Cyanobacteria (especially Lyngyba spp.) were the most active diazotrophs in the investigated mats.
Materials and methods
Mats with a phototrophic layer dominated by Lyngbya spp. (in terms of biomass, as assessed by light microscopy) were sampled from the intertidal zone at Laguna Ojo de Liebre, Baja California, Mexico (27.758 N (Lat.) and −113.986 W (Long.)) on 15 September 2010 (Supplementary Figures S1 and S2) during low tide. The N2 fixation activity of two replicate mat pieces of ca. 20 cm × 30 cm was investigated over a diel cycle at a nearby field laboratory (outdoor setup in Guerrero Negro, Baja California, performed in acrylic aquaria as described below) from 15 to 16 September 2010. Other mat pieces were transported to the NASA Ames Research Center, CA, USA, on 16 September 2010 for additional diel cycle studies including inhibition experiments, stable isotope incubations as well as nucleic acid-based investigations. For experiments at NASA Ames, mats were placed in acrylic aquaria transparent to ultraviolet radiation and covered with in situ water for 2 days before the beginning of the diel study (starting at 1200 hours and ending at 1500 hours the next day). To ensure full photosynthetic activity in the mats during the N2 fixation experiments, resumption of photosynthetic activity after rewetting was investigated by pulse amplitude modulation fluorescence. The quantum yield of PSII (ΦPSII) for a light-adapted sample was calculated based on FS (steady-state fluorescence under actinic light) and FM′ (maximum fluorescence under actinic light) measurements using the following equation: ΦPSII=(FM′−FS)/FM′. Rehydrated mats exhibited maximal photosynthetic activity (ΦPSII=0.30–0.40) within 4 h of wetting in congruence with earlier studies (Fleming et al., 2007); thus, diel cycle studies were conducted with fully active mats. Diel cycle studies were carried out under natural solar irradiance, and the water temperature was kept constant at ∼18 °C.
Nitrogenase activity was measured with ARAs and 15N2 incubations as previously described (Bebout et al., 1993; Woebken et al., 2012). For more details see Supplementary Information. Bulk sample 15N/14N isotope ratios were determined by isotope-ratio mass spectrometry (IRMS; ANCA-IRMS, PDZE Europa Limited, Crewe, England) at the University of California, Berkeley, corrected relative to National Institute of Standards and Technology (NIST, Gaithersburg, MD, USA) standards and are expressed as 15N/(14N+15N) isotope fractions, given in at% (means±s.e.).
All inhibition experiments were conducted at the NASA Ames Research Center. For photosynthesis inhibition experiments, DCMU was added to intact mat slabs before sunrise on the first day of the diel cycle study with a final concentration of 20 μM to ensure complete inhibition of photosystem II (PSII) (Oremland and Capone, 1988). For ARAs or 15N2 incubation experiments, mat cores were subsampled from these mat slabs and incubated as described in Supplementary Information, but with in situ water containing DCMU. Mat cores from mat slabs without DCMU treatment served as controls and were incubated in seawater without DCMU. For sulfate reduction inhibition experiments, sodium molybdate (Na2MoO4, a structural analog of sulfate) was added to intact mat slabs submerged in in situ seawater or artificial seawater in the early morning of the first day of the diel cycle study to achieve a final concentration of 30 mM (Oremland and Capone, 1988). Mat slabs incubated in in situ seawater or artificial seawater without molybdate served as controls. Two diel experiments were conducted: (A) mat samples in in situ seawater (control) versus mat samples in molybdate-amended seawater; and (B) mat samples in artificial seawater containing 23 mM sulfate (control) versus mat samples in artificial seawater without sulfate and with added molybdate. Incubations for ARA or 15N2 experiments were conducted as described in Supplementary Information.
All diel cycle experiments were accompanied by mat sampling for molecular analysis. At multiple time points during a diel experiment, four mat cores of 1 cm diameter were flash frozen in liquid nitrogen and stored at −80 °C until further processing. DNA and RNA extractions were conducted as previously described (Woebken et al., 2012) and are further described in Supplementary Information. As N2 fixation was observed only during the night, all sequence data were derived from night-time samples.
454 pyrotag amplicon libraries (V6–V8 region) and clone libraries for Sanger sequencing of 16S rRNA genes/transcripts from two biological replicate mats, as well as clone libraries of the nifH genes/transcripts, were constructed and analyzed as previsously described (Woebken et al., 2012). Detailed information about the construction and analysis of these libraries can also be found in Supplementary Information. 16S rRNA 454 pyrotag sequencing resulted in 20 616 and 15 524 reads from both DNA templates and 20 138 and 22 246 reads from both cDNA templates (Supplementary Table S1). 16S rRNA Sanger sequencing resulted in 520 sequences from DNA samples (D3=256 and D5=264 sequences) and 316 sequences from cDNA samples (C3=150 and C5=166 sequences). Regarding nifH sequences, 313 sequences were retrieved from DNA, 522 sequences from cDNA and 181 from cDNA of the molybdate inhibition experiment. 16S rRNA and 16S rRNA gene sequences obtained in this study are deposited in GenBank under accession numbers KJ997979–KJ998814. Sequences of nifH genes and transcripts are deposited in GenBank under accession numbers KM212180–KM212266.
Single-cell NanoSIMS analyses were performed to identify active diazotrophs. The upper 2 mm of paraformaldehyde-fixed mat samples from 15N2 incubation experiments and negative control mat cores were prepared on 5 mm × 5 mm silicon wafer pieces (Ted Pella, Redding, CA, USA) for NanoSIMS analysis as previously described (Woebken et al., 2012). Filamentous cyanobacteria (Lyngbya spp.-related and small filamentous cyanobacteria) were identified based on their red autofluorescence when illuminated with green light by epifluorescence microscopy (excitation: BP 546/12, beam splitter: FT 560, emission: BP 607/80) and based on their morphology, as imaged by scanning electron microscopy (SEM; FEI Inspect F, FEI, Hillsboro, OR, USA). Deltaproteobacteria were stained by catalyzed reporter deposition-fluorescence in situ hybridization (CARD-FISH) as previously described (Pernthaler et al., 2002; Woebken et al., 2012) using probes DELTA495 a-c (Loy et al., 2002; Lücker et al., 2007). Stained cells were identified and localized by epifluorescence microscopy. All targeted cells were localized and imaged by reflected light microscopy and SEM to ensure that the target cells were free of overlying cells or other material so that 15N/14N ratios could unambiguously be attributed to the target cells. SIMS analysis was performed at the Lawrence Livermore National Laboratory (LLNL) using a NanoSIMS 50 (Cameca, Gennevilliers Cedex, France) as previously described (Woebken et al., 2012). Isotopic compositions are expressed as the abundance of the tracer relative to the total tracer element (aN=15N/(14N+15N)) in at%. Reported data refer to the arithmetic mean of all measurements per cell type ±s.e. Detailed methods are provided in Supplementary Information.
Data retrieved in the ARAs, IRMS data of vertical sections and inhibition experiments as well as NanoSIMS data were analyzed for significant differences using Student’s t-test or analysis of variance (ANOVA) with an alpha error of 0.05 and the Tukey–Kramer honestly significant difference as a multiple means comparison test (JMP Version 7, SAS Institute Inc., Cary, NC, USA). Normal distribution was tested with the Shapiro–Wilk W-test, and in cases where the data did not meet the standard of homogeneity of variance, the Welch ANOVA was used to confirm the initial result. As 15N enrichment levels were very low in Deltaproteobacteria measured by NanoSIMS, the natural abundance values for Deltaproteobacteria were used to test for significant enrichment based on a 95% confidence interval.
Bulk-level N2 fixation analysis
Nitrogenase activities in ARAs were significantly higher during the night than during the day-time (average± s.d. 131±67 vs 5±7 μmol C2H4 m−2 h−1, P<0.0001, Figure 1a) and well within the range of previously reported rates (Bebout et al., 1994; Omoregie et al., 2004b). The potential contribution of oxygenic phototrophs to N2 fixation was investigated by inhibiting photosystem II (PSII) with DCMU. In experiments where DCMU was added before sunrise on the first day of a diel experiment, nitrogenase activities were significantly reduced compared to un-amended control incubations (average±s.d.: 11±3 vs 66±22 C2H4 m−2 h−1, P<0.0001, Figure 1b). The potential contribution of SRB to N2 fixation was investigated by adding the sulfate reduction inhibitor molybdate. Samples exposed to molybdate had lower nitrogenase activities compared to un-amended incubations (average±s.d.: 12±5 vs 63±35 C2H4 m−2 h−1, P<0.0001, Figure 1c).
N2 fixation activity (that is, net 15N incorporation) in the intertidal mats was directly assessed with 15N2 incubation experiments (for 10 h in the dark) and subsequent IRMS analysis of both upper and lower mat layers (0 to 2 mm and 2 to 4 mm, respectively). The upper layer was significantly enriched in 15N relative to the deeper layer (Figure 2; average±s.e.: 0.486±0.023 vs 0.373±0.001 at% 15N, P<0.001). Mat cores incubated in air without 15N2 served as control samples for natural abundance and had values of (average±s.e.) 0.371±0.001 (0 to 2 mm) and 0.373±0.001 (2 to 4 mm) at% 15N. On the basis of these results, we focused all additional analyses on the upper layer. In 15N2 incubation experiments of this upper layer with and without inhibitors, mats incubated with DCMU had significantly lower 15N incorporation relative to control incubations without DCMU (Figure 2; average±s.e.: 0.380±0.007 vs 0.452±0.021 at% 15N, P<0.05). In molybdate addition experiments, incubations where molybdate was added had a slightly lower 15N enrichment than un-amended mats (average±s.e.: 0.429±0.013 vs 0.466±0.015 at% 15N, P=0.063), but the difference was not significant at the P<0.05 level.
Microbial diversity based on 16S rRNA and 16S rRNA gene analysis
Lyngbya spp. and other filamentous cyanobacteria dominated the biomass of the upper phototrophic layer of the microbial mats from Laguna Ojo de Liebre based on light micrographs (Supplementary Figure S3). However, 16S rRNA and 16S rRNA gene sequencing indicated that the microbial community of this layer was diverse and composed of multiple bacterial phyla (Figure 3 and Supplementary Table S2). DNA-derived Sanger sequences were affiliated with nine different phyla based on the RDP classifier (Wang et al., 2007). The majority of DNA sequences were classified as Proteobacteria (30–36%) and Bacteroidetes (17–33%), followed by Chloroflexi (6–12%), Cyanobacteria (5–9.5%) and Verrucomicrobia (1–9.5%). In contrast, the majority of 16S rRNA sequences (cDNA-based) grouped with Cyanobacteria (57–62%), followed by Proteobacteria, Chloroflexi and Bacteroidetes (6–20%). Based on phylogenetic analyses, all 16S rRNA cyanobacterial sequences were related to filamentous cyanobacteria (Supplementary Figure S4), and 24.4% of these cyanobacterial 16S rRNA sequences were related to Lyngbya spp., with up to 98.7% sequence identity to Lyngbya aestuarii PCC 7419 and Lyngbya sp. PCC 8106, or 97.9% identity to Lyngbya majuscula CCAP. 454 pyrotag amplicon sequencing was used to investigate the 16S rRNA and 16S rRNA gene diversity with greater coverage, and revealed reads clustering in 15 phyla (Figure 3 and Supplementary Table S2). However, the trend was the same as in Sanger-based sequences (Figure 3); most of the amplicons recovered from DNA were assigned to Proteobacteria, Chloroflexi, Cyanobacteria and Bacteroidetes, while the majority of reads originating from cDNA clustered with Cyanobacteria. Calculation of the Chao1 estimator and the Shannon index revealed greater diversity in DNA-based reads than in cDNA-based reads (Supplementary Table S1).
Community analysis of potential diazotrophs (nifH gene and transcript analysis)
The diversity of bacteria with the genetic capability to fix N2 was specifically analyzed by sequencing nifH genes and transcripts from the upper 2 mm of the intertidal mats. Deduced amino-acid sequences formed 87 OTUs based on a cutoff of 97% sequence identity. Phylogenetic analysis of the deduced (amino-acid) NifH sequences derived from extracted DNA revealed that the majority (64.2%) grouped with Cluster III (based on Zehr et al., 2003; with uncultured microorganisms and Deltaproteobacteria), and the rest with Cluster I (with Cyanobacteria, Alpha-, Gamma- and Betaproteobacteria) (Figure 4). To focus on the community that was expressing the nifH gene, we also analyzed sequences derived from extracted RNA after reverse transcription into cDNA. The majority of these sequences (80.8%) were related to Cyanobacteria forming three major groups (Lyngbya spp.-cluster, cyanobacterial cluster 1 and 2, Figure 4 and Supplementary Figure S5), with Lyngbya spp.-related sequences being the most abundant. The other two abundant groups of cyanobacterial sequences clustered with sequences of filamentous cyanobacteria such as Phormidium and Leptolyngbya, and sequences from other microbial mats, freshwater, sponge or sediment samples. A minor proportion of the cyanobacterial nifH sequences (0.2%) were related to a cyanobacterium that is a dominant diazotroph in mats of Northern California (ESFC-1; Woebken et al., 2012; Everroad et al., 2013). Of all cDNA-based sequences, 16.9% grouped with Cluster III (1.3% of all sequences with deltaproteobacterial clusters containing known SRB and 15.5% with unclassified Cluster III sequences).
NifH clone libraries (based on cDNA) of samples from the molybdate addition experiments were almost completely comprised of cyanobacterial sequences (97.2%), and only a minor portion of the sequences clustered with Cluster III (1.7%) or Deltaproteobacteria within this cluster (0.6%). Mat samples treated with DCMU during the diel cycle study failed to produce any detectable PCR product from cDNA with nifH-targeting primers (tested in two replicate RNA extractions, see Supplementary Information for details).
Single-cell isotope analysis of potential diazotrophic microbial community members
Based on the results of the inhibitor addition experiments and sequencing of expressed nifH genes, we focused our single-cell isotope analyses on Cyanobacteria and Deltaproteobacteria. The latter group was targeted to test as broadly inclusive as possible the 15N2 fixation activity of SRB within the Deltaproteobacteria. All detected Cyanobacteria were filamentous, and Lyngbya spp. filaments were easily distinguishable from other filamentous cyanobacteria based on their morphology (Supplementary Figure S3). The highest 15N enrichments in these mats were measured in Lyngbya spp. filaments (maximum of 14.54 at%), with an average (±s.e.) 15N tracer content of 4.40±0.57 at% (Figure 5, Supplementary Table S3). The enrichment in Lyngbya spp. filaments was significantly higher than in any other analyzed cells (P<0.0001 compared to small filamentous cyanobacteria; P<0.0001 compared to Deltaproteobacteria; and P=0.01 compared to unidentified single cells). Smaller filamentous cyanobacteria had an average enrichment (±s.e.) of 0.60±0.02 at% 15N with a maximum of 1.32 at%. The 15N enrichment of CARD-FISH-stained deltaproteobacterial cells from 15N2-labeled mats was not significantly different from those in control mat samples (average±s.e.: 0.38±0.00 vs 0.37±0.00 at% 15N, P=0.170). The highest 15N enrichment measured in an individual deltaproteobacterial cell was 0.41 at%.
Members of the Proteobacteria, Bacteroidetes, Chloroflexi and Cyanobacteria dominated the investigated mats based on 16S rRNA gene sequences (Figure 3), yet members of the Cyanobacteria mostly comprised the active microbial community (as inferred by 16S rRNA sequence-based community analysis). This dominance of cyanobacterial sequences in libraries derived from RNA seems to be common for microbial mats containing large filamentous cyanobacteria and was previously described (Burow et al., 2012, 2013; Lee et al., 2014). A similar pattern was observed for the nifH sequence analysis; sequences of Cluster III (including known SRB) dominated the DNA sequence pool, whereas cyanobacterial sequences dominated by far the pool of expressed nifH genes while the proportion of Cluster III sequences was strongly decreased. These data are in disagreement with earlier studies of mats from Laguna Ojo de Liebre in which nifH gene and transcript analyses suggested that both Cyanobacteria and Deltaproteobacteria (including SRB) were the major contributors for N2 fixation (Omoregie et al., 2004a, 2004b; Moisander et al., 2006). Interestingly, our detected nifH sequences in Cluster I and Cluster III, specifically sequences related to Lyngbya spp. were not detected in these previous studies. This lack of congruence could reflect temporal differences in the microbial community at the time studied (2001–2010), as these mats are characterized by a ‘pioneering life style’ (Bebout et al., 1993) and thereby will most likely be dynamic in their microbial community composition. Other explanations for the differences in the detected microbial communities could be the depth of sequencing or a bias in the nucleic acid extraction. Although the same primer set was used in all studies (Zehr and Turner, 2001), in our study we added a pre-homogenization step prior to nucleic acid extraction, which could have increased the lysis efficiency of Lyngbya spp. cells.
The application of inhibitors in diel cycle studies can suggest the contribution of certain functional groups to N2 fixation, an approach that has been used extensively in the past (for example, Stal et al., 1984; Griffiths and Gallon, 1987; Bebout et al., 1993; Pinckney and Paerl, 1997; Steppe and Paerl, 2002). The addition of DCMU, an inhibitor of oxygenic photosynthesis (Oremland and Capone, 1988), during the day-time photoperiod strongly and significantly decreased N2 fixation the subsequent night, based on ARAs (Figure 1b) and 15N2 incubation experiments (Figure 2). This pattern was previously observed in non-heterocystous cyanobacterial mats (Griffiths and Gallon, 1987; Bebout et al., 1993), and also in Lyngbya spp. cultures (Bebout et al., 1993). DCMU interrupts the photosynthetic electron flow by inhibiting the O2-evolving PS II, which depletes the reductant formation required for N2 fixation (Oremland and Capone, 1988). This decrease in reductant will most likely also prevent CO2 fixation (Bebout et al., 1993; Paerl et al., 1996; Pinckney and Paerl, 1997), leading to a shortage of organic storage compounds that can be used for N2 fixation. This combined shortage in reductant can explain the observed decrease in N2 fixation rates upon DCMU addition and suggests that members of the Cyanobacteria contributed to N2 fixation activity.
This observation was supported by the detection of expressed cyanobacterial nifH genes in untreated control mats that showed N2 fixation (Figure 4). NifH transcripts related to Lyngbya spp. dominated the transcript pool, indicating that in these mats Lyngbya spp. were actively expressing nifH and potentially fixing N2. In addition, in DCMU-treated mats, we were unable to PCR amplify nifH transcripts, which is in congruence with a strong inhibition of N2 fixation activity in the DCMU addition experiment as observed in ARAs and 15N2 incubations followed by IRMS. Together, inhibitor experiments and sequence data suggested that Cyanobacteria were actively fixing N2 in the investigated mats, especially members of Lyngbya spp. However, care must be taken to infer N2 fixation activity from detected nifH transcripts or relative sequence abundance. First, nitrogenase enzyme activity can be regulated after transcription until the post-translational level (Kim et al., 1999). Furthermore, the potential for PCR biases (Suzuki and Giovannoni, 1996; Polz and Cavanaugh, 1998) makes it difficult to infer the activity of certain groups based on their nifH transcript abundance. Therefore, direct N2 fixation measurements coupled to the identification of cells are needed to clearly identify active diazotrophs in environmental samples. Incubation experiments with 15N2 and single-cell isotope analysis through NanoSIMS allowed us to investigate the active diazotrophs by measuring the incorporation of 15N into cellular biomass. This analysis revealed 15N enrichment in filamentous cyanobacteria of different morphotypes (Figures 5a–c), which corresponded to multiple detected clusters of cyanobacterial nifH sequences (Supplementary Figure S5). Consistent with the result of the nifH transcript analysis, within the filamentous cyanobacteria, Lyngbya spp. had by far the highest enrichments in 15N, demonstrating that Lyngbya spp. were the most active cyanobacterial diazotrophs in this mat. As previously detected in other diazotrophic populations (Lechene et al., 2007; Woebken et al., 2012), we observed large variations in 15N enrichments of Lyngbya spp. filaments indicating differing N2 fixation activities. A possible explanation could be spatial heterogeneity in the local environment.
In this study, we sought to take a function-based approach to investigate previous reports that SRB were contributing to N2 fixation in this mat type (Omoregie et al., 2004a, 2004b; Moisander et al., 2006). In a parallel study, our group measured significant sulfate reduction (as sulfide production) in these same mat samples (Lee et al., 2014). Therefore we can conclude that the sampled mats contained SRB that were physiologically active and that sulfate reduction was not inhibited on account of sampling and transport to the laboratory. On the intertidal flats at Laguna Ojo de Liebre, the mats experience naturally frequent alternating periods of desiccation (leading to aeration) and tidal flooding (Javor and Castenholz, 1984; Omoregie et al., 2004b; Rothrock and Garcia-Pichel, 2005). It appears that SRB in these mats are tolerant against oxygen exposure and maintain their capacity for sulfate reduction even after long oxic periods. The oxygen tolerance of SRB is a phenomenon previously described in cultured SRB and different mats (Canfield and Des Marais, 1991; Minz et al., 1999; Baumgartner et al., 2006; Fike et al., 2008). Detection of expressed dsrA genes (a key functional gene for sulfate reduction) by Lee et al. (2014) in the mats supports our conclusion that SRB were active, and sequencing revealed that the vast majority of the SRB that expressed dsrA (97%) belonged to previously known clusters within the Deltaproteobacteria (to Desulfobacteraceae and Desulfovibrionales). Sequences assigned to the Desulfobacterales (Desulfobacteraceae) and Desulfovibrionales (Desulfohalobiaceae) were also identified through 16S rRNA sequencing. These data further support our focus on deltaproteobacterial SRB in our single-cell isotope measurements. We are aware of the possibility that non-deltaproteobacterial heterotrophic diazotrophs exist in these mats, for example related to unidentified groups in Cluster III (designated ‘unclassified clusters’; Figure 4). Unfortunately, owing to lack of isolates in these clusters, these bacteria are unidentified at the 16S rRNA level and thus cannot be targeted by a FISH-NanoSIMS approach.
Adding molybdate to the mats resulted in reduced nitrogenase activities in ARAs compared to un-amended samples (Figure 1c). Molybdate serves as a structural analog of sulfate and blocks the sulfate activation, thereby depleting ATP pools in SRB and ultimately causing death (Oremland and Capone, 1988). This effect of molybdate in ARAs was previously observed in an intertidal photosynthetic mat, where molybdate inhibited night-time nitrogenase activity by as much as 64% (Steppe and Paerl, 2002). However, it was previously recognized that reduced N2 fixation rates in response to molybdate additions could result from many direct effects, but also indirect consequences, such as altered environmental conditions due to the inhibition of sulfide production (Steppe and Paerl, 2002). Results based on this ‘specific inhibitor’ should be interpreted with caution, a conclusion further supported by our study. In mats from Laguna Ojo de Liebre, the effect of molybdate on overall N2 fixation rates was only significant in ARAs, whereas 15N2 incubation experiments revealed a much less pronounced (and not significant) effect (Figure 2). This observed difference in the effect based on the applied assays could conceivably be caused by an enhanced consumption of ethylene, the measured product in ARAs, in molybdate-treated mats relative to un-amended controls. Ethylene can be metabolized aerobically (de Bont, 1976), and anaerobically (Koene-Cottaar and Schraa, 1998) by microorganisms, and especially the possibility of methanogens reducing ethylene (Oremland, 1981; Elsgaard, 2013) should be mentioned in experiments where SRB are inhibited. Thus, enhanced ethylene consumption in the molybdate treatments could mistakenly be interpreted as a large contribution of SRB to N2 fixation.
In this study, molybdate addition experiments coupled with 15N2 incubations and IRMS analyses did not indicate a significant contribution of SRB to N2 fixation, whereas earlier studies suggested that Deltaproteobacteria in nifH Cluster III, and more specifically SRB within the Deltaproteobacteria, were potentially important diazotrophs in photosynthetic mats (Steppe and Paerl, 2002; Omoregie et al., 2004a, 2004b). Sequencing of nifH genes and transcripts in our study indicated that sequences of Cluster III (including known SRB) dominated the DNA sequence pool, whereas cyanobacterial sequences dominated vastly the pool of expressed nifH genes, and the proportion of Cluster III sequences was strongly decreased (Figure 4). On account of potential PCR biases, one can only interpret the data semiquantitatively; however, these observations suggest that members of the Cyanobacteria were more actively expressing nifH genes than SRB within Cluster III. This hypothesis is supported by our NanoSIMS analyses, in which Deltaproteobacteria were not significantly enriched in 15N relative to controls (average of 0.38 vs 0.37 at% 15N, P=0.170). These cells were stained by CARD-FISH in contrast to the Cyanobacteria, which could introduce 14N-containing compounds during the procedure leading to a dilution of 15N and thereby to an underestimation of the 15N enrichment. Therefore, we analyzed the effect of CARD-FISH on the 15N (and for completeness also 13C) isotope content in isotopically labeled reference cells (Escherichia coli and Bacillus subtilis) and detected significantly reduced 15N and 13C isotope contents in these cells by NanoSIMS measurements (P<0.001, Supplementary Figures S6–S8, Supplementary Tables S4–S6; experiments are explained in detail in Supplementary Information). Our data indicate that CARD-FISH can result in an apparent dilution of up to 28% for N (and 38% for C). By using these data (28% dilution as a worst-case scenario for N), we tested whether the 15N isotope enrichments measured in microbial mat Deltaproteobacteria were strongly influenced by CARD-FISH (see Supplementary Information for calculations and discussion). On the basis of these calculations, when the CARD-FISH 15N dilution is accounted for, the deltaproteobacterial 15N isotope fraction values increase only slightly, and their corrected values are still not significantly enriched above natural abundance values (average of 0.38 at% 15N, P=0.131). We also considered the individual measured values (as opposed to the population mean), and found that, based on the uncorrected values, 20.4% of the cells are significantly enriched in 15N based on a 95% confidence interval. This number increases to 31.5% if the dilution through CARD-FISH is taken into account. However, the levels of enrichments were very low compared to the values measured in Cyanobacteria. We conclude that even though CARD-FISH has an effect on the 15N isotopic composition, the 15N enrichment values of investigated Deltaproteobacteria in this study changed very little when CARD-FISH dilution was accounted for.
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We thank Angela Detweiler, Jan Dolinsek, Mike Kubo and Christina Ramon for their excellent technical assistance, José Q García-Maldonado for his assistance in the field, Andrew McDowell at UC Berkeley for IRMS analyses, and Stephanie A Eichorst for helpful comments on the manuscript. We are grateful for access to the field site and for the logistical support provided by Exportadora de Sal, S.A. de C.V. This work was performed under Fishery Permit DAPA/2/080310/734 granted by the National Commission of Aquaculture and Fishery of the Ministry of Agriculture, Livestock, Rural Development, Fisheries and Food (Mexico). Work at LLNL was performed under the auspices of the DOE under contract DE-AC52-07NA27344. Work at LBNL was performed under the auspices of the DOE under contract DE-AC02-05CH11231. This material is based upon work supported by the U.S. Department of Energy, Office of Science, Office of Biological and Environmental Research, Genomic Sciences Program, under contract number SCW1039. This work was further financially supported by the German Research Foundation (Deutsche Forschungsgemeinschaft) (to DW) and the Austrian Science Fund (FWF) (P 25700-B20 to DW). FB and MW were supported by the European Research Council (Advanced Grant Nitrification Reloaded (NITRICARE) 294343).
The authors declare no conflict of interest.
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Woebken, D., Burow, L., Behnam, F. et al. Revisiting N2 fixation in Guerrero Negro intertidal microbial mats with a functional single-cell approach. ISME J 9, 485–496 (2015). https://doi.org/10.1038/ismej.2014.144
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