Impact Factor 4.019

The world's most-cited Microbiology journal

Original Research ARTICLE

Front. Microbiol., 24 February 2016 | https://doi.org/10.3389/fmicb.2016.00215

Changes in the Relative Abundance of Two Saccharomyces Species from Oak Forests to Wine Fermentations

Sofia Dashko1,2, Ping Liu3, Helena Volk1, Lorena Butinar1, Jure Piškur1,2 and Justin C. Fay3*
  • 1Wine Research Center, University of Nova Gorica, Vipava, Slovenia
  • 2Department of Biology, Lund University, Lund, Sweden
  • 3Department of Genetics and Center for Genome Sciences and System Biology, Washington University, St. Louis, MO, USA

Saccharomyces cerevisiae and its sibling species Saccharomyces paradoxus are known to inhabit temperate arboreal habitats across the globe. Despite their sympatric distribution in the wild, S. cerevisiae is predominantly associated with human fermentations. The apparent ecological differentiation of these species is particularly striking in Europe where S. paradoxus is abundant in forests and S. cerevisiae is abundant in vineyards. However, ecological differences may be confounded with geographic differences in species abundance. To compare the distribution and abundance of these two species we isolated Saccharomyces strains from over 1200 samples taken from vineyard and forest habitats in Slovenia. We isolated numerous strains of S. cerevisiae and S. paradoxus, as well as a small number of Saccharomyces kudriavzevii strains, from both vineyard and forest environments. We find S. cerevisiae less abundant than S. paradoxus on oak trees both within and outside the vineyard, but more abundant on grapevines and associated substrates. Analysis of the uncultured microbiome shows, that both S. cerevisiae and S. paradoxus are rare species in soil and bark samples, but can be much more common in grape must. In contrast to S. paradoxus, European strains of S. cerevisiae have acquired multiple traits thought to be important for life in the vineyard and dominance of wine fermentations. We conclude, that S. cerevisiae and S. paradoxus currently share both vineyard and non-vineyard habitats in Slovenia and we discuss factors relevant to their global distribution and relative abundance.

Introduction

The ability to ferment sugar in the presence of oxygen originated around the time of a whole genome duplication and is shared by many yeast species (Hagman et al., 2013). Among these yeasts, Saccharomyces species are distinguished in being present and intentionally used by humans for the production of alcoholic beverages. While strains of Saccharomyces cerevisiae are the most widely used, other Saccharomyces species and their hybrids are involved in various types of fermentations. S. cerevisiae × S. eubayanus hybrids are used for lager production (Nakao et al., 2009; Libkind et al., 2011), S. cerevisiae × S. kudriavzevii and S. cerevisiae × S. uvarum hybrids are used for low temperature wine production (Bradbury et al., 2006; Oliva et al., 2006; Le Jeune et al., 2007; Lopandic et al., 2007; Belloch et al., 2009; Borneman et al., 2012; Erny et al., 2012), and S. uvarum is used to ferment apple cider and wine at low temperatures (Rainieri et al., 1999; Naumov et al., 2000, 2001). One of the clearest differences among these species and one taken advantage of for certain types of fermentations is their thermal growth profile; S. cerevisiae and S. paradoxus are thermophilic and S. kudriavzevii and S. uvarum are cryophilic (Gonçalves et al., 2011; Salvadó et al., 2011). However, other aspects of the ecology and evolution of these species might also be relevant to the origin of industrial yeast strains and the predominant use of S. cerevisiae.

Outside human ferments, the Saccharomyces species have primarily been isolated from arboreal habitats. Originally noted to be associated with sap seeping from slim fluxes (Naumov et al., 1998), these yeast species have now been consistently isolated from bark, leaves, and surrounding soil of Quercus (Oak) and other tree species. Both S. cerevisiae and S. paradoxus are widely distributed and have been isolated from temperate forests in North America (Sniegowski et al., 2002; Hyma and Fay, 2013; Charron et al., 2014; Sylvester et al., 2015), Europe (Johnson et al., 2004; Koufopanou et al., 2006; Sampaio and Gonçalves, 2008; Naumov, 2013; Bozdag and Greig, 2014; Almeida et al., 2015), Asia (Naumov et al., 1997; Wang et al., 2012; Almeida et al., 2015), and Oceania (Zhang et al., 2010), often sympatrically. S. uvarum and S. eubayanus have also been found to be widely distributed (Almeida et al., 2014). However, S. kudriavzevii, S. arboricola, and S. mikatae have thus far only been found in restricted geographic regions (Naumov et al., 2013). Currently, it is unknown whether arboreal habitats are a primary habitat or just one of many environments able to sustain populations of these species (Goddard and Greig, 2015).

Vineyards are likely an important interface between wild yeast populations and those used for wine fermentations (Hyma and Fay, 2013). Grapes periodically provide an abundant source of sugar, attract a high density of potential insect vectors, and generate exceptionally high concentrations of yeast by the end of fermentation. Furthermore, wine must is not sterilized prior to fermentations and the skins, stems and microbial sediments from fermentation are typically discarded back into the vineyard. Thus, before the now common practice of inoculating wine must, there was ample opportunity for both inter- and intra-specific competition within vineyard environments. Indeed, commercial wine yeast is found dispersed throughout vineyards in France (Valero et al., 2005), and European “wine” strains and North American “wild” strains of S. cerevisiae are both present on grapes and oak trees in vineyards in North America, while only North American “wild” strains are found in arboreal habitats outside of vineyards (Hyma and Fay, 2013). Mixing of various S. cerevisiae populations also occurs in Italy, facilitated by wasps (Stefanini et al., 2012). Finally, the above mentioned hybrids of Saccharomyces species have thus far only been isolated from vineyard and brewing environments.

The historical acquisition of S. cerevisiae but not S. paradoxus into human-associated fermentative environments is particularly perplexing given they are both strong fermenters and widely distributed. For example, S. paradoxus has only been reported as a significant contributor to wine fermentations in Croatia (Redzepovic et al., 2002). Furthermore, many of the growth characteristics, that give S. cerevisiae a competitive advantage during wine fermentations are shared with S. paradoxus and the two species are equally competitive in high sugar environments such as grape juice (Williams et al., 2015). Consistent with these observations, both S. cerevisiae and S. paradoxus have been isolated from vineyards in North America (Hyma and Fay, 2013).

In Europe, however, there appears to be ecological differentiation between wine strains of S. cerevisiae and wild populations of S. paradoxus. Historically, S. paradoxus was isolated from arboreal habitats while S. cerevisiae was isolated from vineyards (Naumov, 2013), which lead to the reasonable proposition that S. cerevisiae is a domesticated species (Martini, 1993; Mortimer, 2000). While absent from northern European arboreal habitats (Johnson et al., 2004; Koufopanou et al., 2006; Sampaio and Gonçalves, 2008), S. cerevisiae has now been isolated from multiple Mediterranean oak trees (Sampaio and Gonçalves, 2008; Almeida et al., 2015) and may constitute a wild stock from which European wine strains were derived. In contrast, S. paradoxus has been isolated from arboreal habitats throughout Europe (Naumov et al., 1992; Naumov, 1996, 2013; Glushakova et al., 2007; Sampaio and Gonçalves, 2008; Boynton and Greig, 2014). One caveat, however, is that concurrent sampling of vineyard and arboreal habitats within the same region is needed to tease apart geographic and habitat effects on the abundance and distribution of these species.

In this study, we examine the abundance of S. cerevisiae and S. paradoxus across sympatric ecological environments and fine-scale geographic locations in Slovenia. Our sampling strategy was arboreal sources, including bark, and soil from oak trees, within and outside of vineyards compared to wine must, soil and berries from grapevines within vineyards. Using enrichments we find both species present within and outside the vineyard, and analyze their abundance in arboreal- and grape-associated habitats. We also quantify species abundance using enrichment free microbial profiling of bark, soil, and wine must before and during fermentation. By quantifying phenotypes relevant to life in the vineyard we provide an explanation for why S. paradoxus is rare or absent in autochthonous wine fermentations despite its presence in the vineyard.

Materials and Methods

Sample Collection and Strain Isolation

Samples were obtained from seven vineyards and four forest sites in Slovenia (Table S1 in Data Sheet S5, Figure S1, Data Sheet S1). The majority of samples were soil, bark, and berries from grapevines and soil and bark from oak trees (Quercus robur, Q. petrea, Q. ilex, Q. pubescens, and Q. cerris). A small number of samples were from insects, fruits, cellar swabs, and wine must. Oak samples were obtained by prying off bark at the base of the tree and sampling soil at the base of the tree. Samples were obtained between July of 2013 and April of 2014. Samples within vineyards targeted vines spanning the entire property of the vineyard and oak trees bordering the grapevines. Three of the forest locations were from trails starting in Vipava Valley and leading up into the surrounding mountains and these forested areas began immediately adjacent to vineyards. One forest location was on a hill above the town of Vipava surrounding an abandoned castle.

For each sample, approximately 5–25 cm3 of substrate was placed into a sterile falcon tube using ethanol sterilized forceps or scalpels. Twenty-five millilitre of enrichment medium (1% yeast extract, 2% peptone, 10% glucose, and 5% of ethanol, pH 5.3) was added to each sample (Mortimer and Polsinelli, 1999; Hyma and Fay, 2013). After 4 to 10 days of fermentation at room temperature, approximately 20–25°C, 2 μl of well mixed enrichment medium was spread on Petri dishes and incubated for 2–4 days. Bacteria-like colonies were excluded by testing for growth on chloramphenicol (100 mg/L). A single yeast colony was isolated from each enrichment and place into 3 ml of liquid YPD and incubated with 200 rpm shaking overnight. For 13 enrichments we isolated two colonies from the same enrichment corresponding to different morphology. Only one of the two isolates was used in the analysis.

A subset of 518 samples collected in October were enriched at both room temperature and 37°C. These samples were derived by thoroughly mixing each sample with enrichment media, then pouring off 10 ml of the enrichment into a sterile, 15 ml tube and incubated at high temperature. The high temperature enrichments were subsequently treated the same as those at room temperature and single colonies were obtained from both.

Species Identification

Isolates were screened for Saccharomyces species by PCR and restriction digests as in Hyma and Fay (2013). Briefly, total DNA was extracted from yeast using lyticase and glass beads. A multiplex PCR assay was used to distinguish Saccharomyces and non-Saccharomyces species (Nardi et al., 2006). Saccharomyces isolates were further distinguished using restriction digests of the ITS PCR products (McCullough et al., 1998). Identification failed for 56 (6%) isolates, either because of PCR failure or digests with unexpected band sizes.

Sampling Analyses

For each species, the frequency of isolation from all oak- and grapevine-associated samples was fit to a logistic model with terms for source (oak, grapevine), location type (vineyard, non-vineyard), location (11 sampling sites), and month of isolation (July, September, October, April). Significant terms were identified by dropping single terms and comparing models using a likelihood ratio test.

Microbiome Analysis

Microbiome samples were collected after harvest from vineyards and wine must. From five vineyards, we obtained 20 samples from oak bark and soil and grapevine soil and 20 must samples from uninoculated fermentations. Nine of the must samples were from pressed grapes or pomace within a day of harvest, the remainder were from within the first week of fermentation. Temporal samples were taken from fermenting must from two vineyards, Carga, and Burja (previously part of the Sutor estate). From Burja, samples were taken from Malvazija pomace at harvest (20.2°Brix, pH 3.37, total titratable acidity 7.1 g/L, supplemented with ammonium bisulfite at 0.1 g/L) and at seven subsequent points over 18 days of fermentation in the cellar. The same must was also brought to the lab and 800 ml of must was fermented in flasks in triplicate during which we obtained 8 samples over 14 days. On the eleventh day of fermentation, must in the lab and in the cellar was pressed to remove the skins and seeds and the remaining juice continued to ferment. From Carga, juice from pressed Tokaj grapes (17.9°Brix, pH 3.21, total titratable acidity 8.1 g/L, supplemented with potassium metabisulfite at 0.1 g/kg) was brought to the lab and 800 ml of must was fermented in flasks in triplicate during which we obtained 10 samples over 17 days.

For soil samples, DNA was extracted from 150 mg of soil using ZR Soil Microbe DNA extraction kit (Zymo Research, CA, USA). For bark, berry and juice/pomace samples, samples were immersed and shaken in water, solid material removed, and DNA was extracted from the pellet after centrifugation using either the ZR Soil Microbe kit (bark) or a Qiagen Plant DNA kit (Hilden, Germany). ITS1 was amplified using BITS1 and B58S3 primers (Bokulich and Mills, 2013). For the BITS1 primer we included an 8 bp barcode followed by a linker (CT) at the 5′ end (Table S2 in Data Sheet S5) in order to multiplex the samples. Illumina sequencing adaptors were added via a second round of PCR and these included a 9 bp index for further multiplexing. Amplicons were purified, quantified, and pooled then sequenced using an Illumina MiSeq with single-end 250 bp reads.

Barcodes and index were identified and removed using custom perl scripts allowing 1 mismatch in each. Adaptors and low quality sequences were trimmed using ea-utils (v1.04.676 https://code.google.com/archive/p/ea-utils/) using a window size of 3 and a quality threshold of 20. Sequences less than 100 bp were removed. Sequences were aligned by blastall [v2.2.26 (Camacho et al., 2009)] using a cutoff of 1e-20 to 287,101 sequences in the UNITE + INSD database [4/7/2014 (Kõljalg et al., 2013)] after removing sequences from uncultured fungi. For classification into taxonomic groups all top hits were used. For species classification, the top hit for each sequence was retained when greater than 97% identity, resulting in the retention of 75% of all sequences. To eliminate rare and potentially spurious hits, species representatives were only kept if two or more samples had more than 10 hits each to that representative. This eliminated 3091 out of 3935 species representatives. After these filters, the median number of hits per sample was 46,619 with a range of 1086 to 822,149 (Data Sheet S2).

Species' richness was estimated from each sample using the rarefied number of species and species' diversity was estimated by Simpson's diversity index using the vegan package in R (Oksanen et al., 2015). Species' richness and diversity were tested for association with sample substrate (bark, soil, must) using an ANOVA and pairwise differences were assessed using Tukey's method. For the fermentation time-course, species diversity, and richness did not change linearly over time and so we fit a linear model to the ranked order of richness and diversity from each fermentation. Nonmetric multidimensional scaling was implemented using the metaMDS function in the vegan package of R with 20 starting points based on Bray-Curtis dissimilarity among samples.

Wine Phenotypes

Strains were grown in 200 μl of complete medium (2% glucose, 2% yeast nitrogen base with ammonium sulfate) overnight in 96-well plates. Strains were then resuspended 1:20 in complete medium with sulfite, copper, ethanol, tartaric acid, or unaltered and grown for 48 h without shaking at 30°C in 96-well plates. Sulfite medium was 0.7 and 1.5 mM Na2SO3 buffered to a pH of 3.5 with tartaric acid. Low pH was 5 mg/mL of tartaric acid which reduced the pH from 4.4 to 2.9, copper medium was 0.5 mM and 1.0 mM copper sulfate, ethanol medium was 6 and 10% (v/v) ethanol. These concentrations were selected based on preliminary assays to distinguish North American and commercial wine strains and to ensure some level of growth inhibition. Cell density (OD600) was measured (iEMS plate reader, Thermo Lab Systems, Helsinki, Finland) at 0, 19, 24, 36, and 48 h after treatment. Data for certain time-points, 1.4% of all the data, was interpolated due to plate reader malfunction: two of the plates for sulfite treatment at 19 h, one plate for tartaric acid at 24 h, and one plate at 48 h for the no stress control. Data were interpolated by taking the average of the prior and subsequent time-points. The phenotype of each strain was measured by the area under the growth curve (AUC) and we used the average AUC when growth was measured under two different stress concentrations (Data Sheet S3). Commercial strains were obtained from yeast distributors. North American oak tree strains were those from Hyma and Fay (2013) from which we excluded S. cerevisiae and S. paradoxus strains closely related to European strains.

Reanalysis of North American Samples

From the raw data of Hyma (2010) we analyzed 187 S. cerevisiae and 240 S. paradoxus isolates from 977 oak- and 492 grape-associated samples for which the same enrichment medium was used (Data Sheet S4). The frequency of each species was fit to a logistic model with terms for state (MO, OR), location type (vineyard, non-vineyard), source (oak, grapes), and year of isolation (2008, 2009). Significant terms were identified by dropping single terms and comparing models using a likelihood ratio test.

Results

Isolation of Saccharomyces Yeasts

To characterize the distribution and abundance of Saccharomyces species we sampled 1233 substrates from 7 vineyards and 4 non-vineyard locations in Slovenia between July of 2013 and April of 2014. Substrates were primarily from oak trees (66%) and grapevines (24%). The remaining samples were from wine cellars, must, fruit, insects, and other plant material (Table S3 in Data Sheet S5). Following enrichment of the samples, we isolated 869 strains and distinguished Saccharomyces species from one another and from non-Saccharomyces species (Materials and Methods). Our sample yield was highest for non-Saccharomyces species (28%), followed by S. paradoxus (23%), S. cerevisiae (12%), and S. kudriavzevii (2.1%; Table S3 in Data Sheet S5).

To test whether enrichment at higher temperature increased our recovery of S. cerevisiae, we split 518 of the samples into enrichments at room temperature and 37°C. High temperature enrichments yielded a higher ratio of S. cerevisiae relative to S. paradoxus strains (29:1 compared to 81:123, Fisher's Exact Test P < 0.01). However, substantially fewer high temperature enrichments yielded yeast (11%) compared to those at room temperature (80%) due to proliferation of bacteria (Fisher's Exact Test P < 0.01). The higher ratio of S. cerevisiae to S. paradoxus strains from high temperature enrichments was not a primary consequence of temperature since most of the corresponding low temperature enrichments from the same sample yielded the same species and in only four cases was S. paradoxus isolated at the low temperature when S. cerevisiae was isolated at the high temperature. To avoid potentially redundant samples, we removed the 55 high temperature isolates from the remainder of the analysis.

Species Abundance Differs by Source, Geographic Location, and Time of Year

As a proxy for species abundance, we compared rates of isolation from 1055 samples associated with oak trees within the vineyard (467), oak trees outside the vineyard (316), and grapevines (272). While we found no differences between vineyard and non-vineyard locations, S. cerevisiae and non-Saccharomyces yeasts were more prevalent on grapevine- compared to oak-associated substrates and S. paradoxus was depleted (Figure 1, Table S4 in Data Sheet S5). We also found variation across sampling locations for both S. cerevisiae and S. paradoxus, but not for non-Saccharomyces yeast as a group (Tables S4, S5 in Data Sheet S5). One apparent outlier was an abandoned castle on a hill overlooking the town of Vipava; it was the only non-vineyard location with more S. cerevisiae than S. paradoxus isolates. However, removing this location still yielded equivalent ratios of S. cerevisiae to S. paradoxus from vineyard oaks and non-vineyard oaks (odds ratio [95% confidence interval] = 0.23 [0.16, 0.32] and 0.13 [0.052, 0.26], respectively, P = 0.172).

FIGURE 1
www.frontiersin.org

Figure 1. Rates of isolation depend on sample source. The sampling frequency of each species is shown for oak-associated samples within and outside of vineyards, and for grapevine-associated samples.

Time of year influenced the sampling rate of all species except for S. cerevisiae (Table S3 in Data Sheet S5). In September during harvest time we found the lowest rates of S. paradoxus and the highest rates of non-Saccharomyces yeast (Table S4 in Data Sheet S5). Except for one isolate from April, all S. kudriavzevii strains were obtained in October, mostly from non-vineyard oak samples.

Saccharomyces Abundance within the Oak- and Grape-Associated Microbiomes

To quantify the relative abundance of Saccharomyces and other yeast species without enrichment, we performed ITS1 sequencing on 20 vineyard samples of oak bark and soil and 20 samples from uninoculated wine must. Bark and soil samples contained more species than must samples (Tukey P < 0.001), but there was no difference in Simpson's diversity index, which measures the skew toward one or a small number of abundant species (Tukey P > 0.05, Table S6 in Data Sheet S5). However, species' relative abundance differed across sample substrates. At a broad taxonomic level, five out of six classes with overall abundance above 5% differed in frequency among must, bark, and soil samples (Figure 2, ANOVA P < 0.01), with the one exception being Dothideomycetes which were abundant in all samples. Must samples were enriched for Saccharomycetes and Leotiomycetes, with the most common species being S. cerevisiae, and the grape pathogen Botryotinia fuckeliana, respectively. Bark samples were enriched for Lecanoromycetes, with the most common species being the lichen Physciella chlorantha, and soil samples were enriched for Agaricomycetes, with the most common being the mushroom Russula fragilis. Multidimensional scaling of species' abundance also distinguished must from bark and soil samples, the latter two of which were more similar to one another (Figure S2).

FIGURE 2
www.frontiersin.org

Figure 2. Frequency of abundant taxonomic classes differs across samples. Boxplots are shown for six abundant classes (>5%) grouped by substrate from which they were obtained.

The frequency of Saccharomyces species was highly variable across samples (Figure 3). Both S. cerevisiae and S. paradoxus were rare in soil and bark samples, averaging 6.9 × 10−4 for S. cerevisiae and 6.6 × 10−5 for S. paradoxus. The two species were more variable in must samples, with S. paradoxus constituting up to 82% and S. cerevisiae up to 87% of identified species (Table S6 in Data Sheet S5). Although S. cerevisiae tended to have a higher frequency than S. paradoxus across all samples (Mann-Whitney test, P = 6.7 × 10−5), there was no significant difference among substrates in the relative abundance of S. cerevisiae to S. paradoxus (Kruskal-Wallis test, P = 0.085). Another Saccharomyces species found, S. kudriavzevii, was only present in a single sample (SM56) at a frequency of 4.8 × 10−5.

FIGURE 3
www.frontiersin.org

Figure 3. Frequency of S. cerevisiae and S. paradoxus in soil, bark and must samples. Points shown on the x-axis had no S. paradoxus counts.

S. cerevisiae Increases in Abundance during Wine Fermentations

To capture changes in temporal dynamics that occur during fermentation we obtained juice from the Carga estate and grape pomace from the Burja estate (previously a part of Sutor), and carried out triplicate fermentations in the lab, taking 8–10 samples over 14–17 days of fermentation. In parallel, we sampled the same pomace from the Burja estate that was being fermented in the Burja winery cellar.

Species' richness and Simpson's diversity index decreased over time for both the Burja (P = 0.02 and P = 3.3 × 10−5, respectively) and Carga (2.9 × 10−6 and 4.1 × 10−9, respectively) experimental fermentations but not for the Burja cellar fermentation (P > 0.05, see Methods). Initial richness and diversity of the experimental fermentations was within the range of the 20 must samples (Table S7 in Data Sheet S5) and primarily consisted of Saccharomycetes (Figure 4). By the end of fermentation, only three species were above 5%: S. cerevisiae, Starmerella bacillaris, and B. fuckeliana. Interestingly, S. paradoxus did not reach our threshold of 10 counts for any of the Carga fermentation samples, and was only present at an initial frequency of 3.8 × 10−4 in the Burja fermentation and did not increase in frequency (linear regression, P > 0.05). In comparison, S. cerevisiae was at an initial frequency of 8.7 × 10−3 and 8.2 × 10−2 in the Carga and Burja fermentations, respectively, and increased in frequency during the fermentations (linear regression, P = 1.5 × 10−6 and P = 0.009, respectively, Figure S3).

FIGURE 4
www.frontiersin.org

Figure 4. Changes in species abundance during fermentation. Twelve species with at least 5% abundance at one time-point are shown for Burja and Carga fermentations at the start (cellar) and end (lab, 3 replicates) of each time-course. Also shown is a Burja cellar sample at the start and end of fermentation. Counts of Saccharomyces boulardii were included in those of S. cerevisiae.

European Strains of S. cerevisiae have Acquired Resistance to Stresses Applied during Wine Making

The presence of both S. cerevisiae and S. paradoxus within vineyard and wine must suggests S. paradoxus should often make it into wine fermentations. However, the Carga and Burja fermentations along with previous work (Gayevskiy and Goddard, 2012; Setati et al., 2012; Bokulich et al., 2014; David et al., 2014; Pinto et al., 2014, 2015; Taylor et al., 2014; Wang et al., 2015) indicate, that it may not often be a major contributor to fermenting wine must. One potential cause for a shift in the relative abundance of these two species going from the vineyard into the winery is the addition of copper and sulfites to the grape must. Indeed, sulfites were added to both the Carga and Burja musts before being brought to the lab. Previous studies have shown wine strains are particularly resistant to copper and sulfites (Liti et al., 2009; Warringer et al., 2011). To characterize sensitivity to the wine making environment among our isolates we measured the growth profiles of 168 S. cerevisiae and 263 S. paradoxus from Slovenia in comparison to a set of 35 reference commercial wine strains, 29 North American strains, and 34 North American S. paradoxus strains (Hyma and Fay, 2013). As a control we measured growth in the absence of stress and in the presence of ethanol, which has not been reported to differ between the two species.

As expected, North American S. cerevisiae strains are more sensitive than commercial wine strains to sulfites, copper and low pH, but not high ethanol (FDR < 0.01, Figure 5, Figure S4, Table S8 in Data Sheet S5). Slovenian S. cerevisiae strains are resistant to sulfites, copper and low pH; more so than North American S. cerevisiae or S. paradoxus (FDR < 0.01 Table S8 in Data Sheet S5). This high level of resistance of Slovenian S. cerevisiae strains is indistinguishable from that of commercial wine strains (FDR > 0.01). In contrast to differences between species and continents, there were no differences in resistance to sulfites, copper, pH, or ethanol between vineyard and forest strains or between oak and vine strains (Figure S5). The only exception was slightly higher sulfite resistance of vineyard compared to forest strains (ANOVA, uncorrected P = 0.004).

FIGURE 5
www.frontiersin.org

Figure 5. Slovenian S. cerevisiae strains are resistant to sulfite, copper and tartaric acid. Growth rates (area under the growth curve) in the presence of sulfite (A), copper (B), and tartaric acid (C) relative to the absence of stress for S. cerevisiae (Scer), S. paradoxus (Spar) and commercial wine strains. Black circles and bars represent the mean and its 95% confidence interval.

Discussion

Strains of S. cerevisiae have been widely used for the production of beer, bread, wine, and other human-associated fermentations (Sicard and Legras, 2011). Its sibling species, S. paradoxus, is rarely associated with human fermentations (Boynton and Greig, 2014) but is a strong fermenter and is competitive with S. cerevisiae in grape juice (Williams et al., 2015). The distinction between these two species is particularly well defined in Europe, where S. cerevisiae is most often isolated from vineyards whereas S. paradoxus is most often isolated outside of vineyards.

In this study, we used intensive sampling and microbial profiling to show that there is not a clear cut difference in the abundance and distribution of these two species within Slovenian vineyards and forests. Similar to North American vineyards and forests (Hyma and Fay, 2013), the two species can occur sympatrically in Europe and we find they only differ in their relative abundance: S. paradoxus is more abundant on oak tree-associated substrates and S. cerevisiae is more abundant on grapevine-associated substrates. Although there are likely many factors, discussed below, that contribute to variation in the relative abundance of these two species, our results support the idea that current wine making practices greatly enrich S. cerevisiae within the vineyard via the acquisition of multiple traits by European wine strains.

Is S. paradoxus Rare within Vineyard Environments?

Our results based on both enrichment and microbiome analysis indicate, that S. paradoxus is not excluded from vineyard environments, including wine must, and can be as abundant as S. cerevisiae. While our findings differ from those of prior studies, multiple factors influence the relative abundance of these two species and may explain these differences.

Distinguishing Saccharomyces Species

Because the Saccharomyces species were not clearly delineated until the 1990s (Naumov et al., 1992; Naumov, 1996), early work on yeasts present within vineyard and wine fermentation may not have distinguished between S. cerevisiae and S. paradoxus. Even so, S. cerevisiae remains the predominant yeast isolated from European vineyards, e.g. in Spain (Cordero-Bueso et al., 2011), Portugal (Schuller et al., 2005), Italy (Di Maio et al., 2012; Stefanini et al., 2012), and France (Valero et al., 2007). With the exception of Mediterranean regions where S. cerevisiae is found to co-occur with S. paradoxus on trees (Sampaio and Gonçalves, 2008; Almeida et al., 2015), S. paradoxus is the predominant Saccharomyces species isolated from forest environments (Johnson et al., 2004; Koufopanou et al., 2006; Glushakova et al., 2007; Bozdag and Greig, 2014; Kowallik et al., 2015), reinforcing the notion that S. paradoxus is a wild yeast and absent from vineyards (Boynton and Greig, 2014).

More recently, the diversity of yeasts present within fermenting wine have been examined by direct sequencing of the wine microbiome (Gayevskiy and Goddard, 2012; Setati et al., 2012; Bokulich et al., 2014; David et al., 2014; Pinto et al., 2014, 2015; Taylor et al., 2014; Wang et al., 2015). While these microbiome studies have not reported S. paradoxus within the wine must, certain methods of analysis do not distinguish it from S. cerevisiae. One common practice is the representation of closely related sequences at the level of 97–99% identity by operational taxonomic unites (OTUs). In the UNITE database (Kõljalg et al., 2013), these groups are termed species hypothesis (SH) and do not distinguish S. cerevisiae from S. paradoxus even though they are readily distinguishable by their ITS1 sequence (McCullough et al., 1998). Thus, the absence of reports of S. paradoxus within vineyards and wine must may be partly attributed to not specifically distinguishing it from S. cerevisiae.

Variation Across Ecological Niches

In our samples, we found the relative abundance of S. cerevisiae to S. paradoxus is related to habitat, grapevines, or oak trees, but not whether the oak trees occur within or outside of vineyards. As such, it is not surprising, that we also isolated S. paradoxus from grapevine-associated substrates and, that the habit surrounding vineyards is relevant to the microbial community colonizing grapevines and being incorporated into wine must (Setati et al., 2012; Bokulich et al., 2014; Knight et al., 2015).

In contrast to our enrichment samples, our microbial profiling experiments detected no significant differences in the relative abundance of S. cerevisiae to S. paradoxus among must, bark, or soil samples; S. cerevisiae was found to be uniformly more abundant. The higher abundance of S. cerevisiae is not likely caused by amplification bias since we previously validated the use of ITS to quantify the relative abundance of S. cerevisiae to S. paradoxus (Williams et al., 2015). However, the frequency of both species was close to the detection limit for many of the bark and soil samples, 10−4 to 10−5 determined by the number of sequence reads per sample, and we did not quantify the accuracy of the method for low abundance species in complex samples. Finally, we cannot exclude the possibility, that our enrichment process generated a biased representation of species abundance. The presence of other microbes in a sample can influence yeast growth (Kowallik et al., 2015) and so it is possible, that differences in sample abundance occurred because S. cerevisiae and S. paradoxus differ in their ability to compete with microbes that are not evenly distributed across oak and grapevine habitats.

Local Geographic and Temporal Variation

By design we sampled multiple vineyards to help ensure our results were reflective of Slovenian vineyards and the Vipava valley. By necessity we sampled multiple times during the year, with the majority of samples being collected before (July) and after (October) harvest. Both location and time of year are associated with the relative abundance of S. cerevisiae to S. paradoxus. The most interesting deviation within our sampling locations was an abandoned castle on a hill in Vipava. While the castle itself is old (13th Century) the oak forest surrounding it consist of young oak trees, ~10–20 cM in diameter at the base of the tree. While not optimal for characterizing species abundance in European forests, this location highlights the importance of fine-scale variation and historical context in sampling locations. Another important consideration is that the Vipava valley is full of vineyards and so all of our forest locations were within a few kilometers of a vineyard. The close proximity of these sites makes it reasonable to suppose that many of the S. cerevisiae strains isolated from forests originated from nearby vineyards.

While our finding of sympatric S. cerevisiae and S. paradoxus within and outside of vineyards in Slovenia may be a regional finding, it is consistent with certain studies. S. paradoxus was found in a vineyard in a region of Croatia ~150 km East of Vipava (Redzepovic et al., 2002), and wild populations of S. cerevisiae associated with Mediterranean oaks have been isolate from Southern Europe (Almeida et al., 2015).

Global Geographic Variation

Our work establishes S. paradoxus as part of the vineyard environment, at least in Slovenia. While this raises the possibility, that it may also occur in vineyards outside of the Balkans, S. paradoxus has thus far only been isolated from North American vineyards (Hyma and Fay, 2013). Because, Hyma and Fay (2013) did not report rates of isolation, we analyzed the raw data for comparison with our results from Slovenia.

Similar to Slovenia, numerous isolates (130) of S. paradoxus were obtained from vineyards (Table S9 in Data Sheet S5). Highlighting the importance of geographic variation, S. paradoxus was almost exclusively isolated from both vineyard and forest locations in Oregon. Yet even accounting for geographic variation, S. paradoxus was less abundant in vineyards (OR = 0.55, P = 0.03) and not significantly different from S. cerevisiae when comparing oak versus grapevine samples (OR = 0.83, P = 0.73, Table S10 in Data Sheet S5). Thus, while both the Slovenian and United States samples show evidence of geographic variation, the United States samples differ by sample location (vineyard vs. forest) rather than sample source (grapevine versus oak). However, it should be noted that in the US only 22 isolates were obtained from grapes and 16 of these were S. cerevisiae.

Transition into the Winery and Competition during Fermentation

Similar to other studies of microbial diversity (Combina et al., 2005; Mercado et al., 2007; Pinto et al., 2015), we found a diverse fungal community from harvested and/or pressed grapes before or at the initial stages of fermentation followed by a rapid decline in diversity as S. cerevisiae became the dominant species. While the grape must community was distinct from oak bark and soil communities, the community was also quite variable at the species level. This variability could be related to any number of differences in location, method, and time of harvest or contact with winery equipment. Along with overall variation in the grape must microbiome, the relative abundance of S. cerevisiae and S. paradoxus also varied, with one sample of must from pressed grapes containing 82% S. paradoxus and only 14% S. cerevisiae.

One limitation of our grape/must samples is, that we did not control for sulfite or other treatments of the grapes or must before sampling. Although, we sampled from wineries that carry out autochthonous fermentations, the vineyards also spray copper sulfate as a fungicide and use sulfites to inhibit the growth of bacteria and other microorganisms. Indeed, sulfites were added by the wineries prior to deriving wine fermentations in the lab. Such treatments very likely alter initial microbial diversity or their dynamics during fermentation to wine (Bokulich et al., 2015). Our observation that S. paradoxus is initially rare or absent from the fermentations, 19- (Carga) and 21-fold (Burja) less abundant than S. cerevisiae (Table S7 in Data Sheet S5), raises the possibility that it's abundance relative to S. cerevisiae differs at harvest or changes during processing of the grapes, for example due to sulfite treatment.

Even after being brought into the lab we observed substantial variation in species abundance during fermentation to wine. The most notable difference was the maintenance of much higher levels of diversity in the Burja wine fermented at large volume in the cellar and in one of our laboratory replicates as compared to the other two replicates carried out in the lab. The cellar fermentation could be different due to a slower rate of fermentation, larger volume, or lower temperature, but could also be due to our mixing the lab fermentation prior to every sample taken.

Resistance to Copper, Sulfites, and Tartaric Acid Distinguishes Slovenian Strains of S. cerevisiae and S. paradoxus

Prior work has shown, that both resistance to copper and sulfites are common in wine strains compared to oak strains of S. cerevisiae and S. paradoxus (Pérez-Ortín et al., 2002; Fay et al., 2004; Yuasa et al., 2004; Liti et al., 2009; Warringer et al., 2011; Strope et al., 2015), as might be expected given their frequent use in vineyards and wineries. Our phenotypic analysis of Slovenian yeast adds resistance to low pH to these two previously characterized “domestication” phenotypes and shows, that these phenotypes differentiate vineyard isolates of S. paradoxus from European but not North American S. cerevisiae. Thus, we can conclude that the sensitivity of S. paradoxus to copper, sulfite and low pH is not because S. paradoxus is absent from vineyards and hasn't had the opportunity of facing selective pressures, that are common in the vineyard environment.

The acquisition of copper and sulfite resistance in wine strains has been extensively studied and is known to be primarily caused by changes at CUP1 (Fogel and Welch, 1982; Adamo et al., 2012; Chang et al., 2013; Zhao et al., 2014; Strope et al., 2015) and SSU1 (Goto-Yamamoto et al., 1998, 1; Yuasa et al., 2004, 1; Nardi et al., 2010; Zimmer et al., 2014), respectively. However, the relationship between resistance to sulfite and tartaric acid is less clear. Sensitivity to sulfite was measured at a pH of 3.5 since there is little of the active agent sulfur dioxide at higher pH (Casalone et al., 1992). Sensitivity to low pH was measured by adding tartaric acid, since it is abundant in grapes (Kliewer et al., 1967). While resistance between the two is correlated (r2 = 0.44), resistance to tartaric acid only explains 3% of variation in sulfite resistance once differences among major groups (64% of variation, Figure 5) are accounted for.

Conclusions

The history and origins of wine strains has begun to emerge with detailed studies of S. cerevisiae in comparison to its closest known relative S. paradoxus (Boynton and Greig, 2014). While certain aspects of these two species are notably different, they are sympatric in North American forests (Sniegowski et al., 2002; Hyma and Fay, 2013) and our present results demonstrate, that they can inhabit the same vineyard environments. Thus, S. paradoxus may be similar to S. cerevisiae in its opportunistic colonization of certain environments (Goddard and Greig, 2015). However, one of the fundamental differences between these two species is the higher diversity and stronger geographic structure of S. paradoxus compared to S. cerevisiae (Liti et al., 2009). Not only is the spread of European wine strains relevant to S. cerevisiae population structure (Fay and Benavides, 2005), but there is now also evidence for the spread of wild oak populations of S. cerevisiae based on the clonal relatedness of isolates from North America and Japan (Hyma and Fay, 2013; Almeida et al., 2015). Thus, the current sympatric relationship between S. cerevisiae and S. paradoxus in Slovenian vineyards, and perhaps North American forests, may be a relatively recent development.

Further, elucidation of the history and relationship between these two species will have to meet the challenge of geographic and temporal heterogeneity while accounting for the historic use or vegetation of the habitats sampled. With sufficient fortitude or luck we may be able to better define the vectors and environmental reservoirs, humans-associated or otherwise, pertinent to these closely related but differentially exploited species.

Author Contributions

Conceived and designed the experiments: SD, LB, JP, and JF. Collected and analyzed data: SD, PL, HV, LB, JP, and JF. Wrote the paper: SD and JF.

Funding

This work was supported by RS-MIZS and European Regional Development Fund Research (the Creative Core program “AHA-MOMENT,” contract no. 3330-13-500031), by the Slovenian Research Agency (ARRS J4-4300 and BI-US/13-14-028) and the National Institutes of Health (GM080669).

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

We thank Janez Kokošar, Mojca Brložnik and Uroš Petrovič for assistance in collecting and handling samples and we are particularly grateful to the owners and staff of the Carga, Guerilla, Sveti Martin, Sutor, Burja, University of Nova Gorica, Rencelj and Tilia estates and wineries for allowing us to sample their vineyards, wine cellars and wine.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/article/10.3389/fmicb.2016.00215 and microbiome raw reads and metadata at NCBI SRA under SRP070142 and BioProject PRJNA311212

Figure S1. Sampling locations in Slovenia. Forest (green) and vineyard (red) locations are plotted using GPS coordinates of either the start or end of collecting samples.

Figure S2. Multidimensional scaling of microbiome samples. First and second coordinates are from non-metric multidimensional scaling using Bray-Curtis dissimilarity.

Figure S3. The relative frequency of common species during fermentation. Species with a frequency of 5% or more are shown as a percent of total abundance for Sutor (A, C, E, G) and Burja (B, D, F) fermentations in days. Ferments are Sutor cellar (A), Sutor lab replicates 1-3 (C, E, G) and Burja lab replicates 1-3 (B, D, F).

Figure S4. Slovenian and North American strains' resistance to ethanol. Growth rates (AUC) in the presence of ethanol relative to its absence. Black circles and bars represent the mean and its 95% confidence interval.

Figure S5. Slovenian strains' resistance to sulfites (A), copper (B), tartaric acid (C) and ethanol (D) in relation to location (forest vs vineyard) and source (vine vs oak).

Data Sheet S1. Samples used for enrichment and species identified.

Data Sheet S2. Species counts across microbiome samples.

Data Sheet S3. Phenotype data.

Data Sheet S4. Samples analyzed from North America.

Data Sheet S5. Supporting Tables S110.

References

Adamo, G. M., Lotti, M., Tamás, M. J., and Brocca, S. (2012). Amplification of the CUP1 gene is associated with evolution of copper tolerance in Saccharomyces cerevisiae. Microbiol. Read. Engl. 158, 2325–2335. doi: 10.1099/mic.0.058024-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Almeida, P., Barbosa, R., Zalar, P., Imanishi, Y., Shimizu, K., Turchetti, B., et al. (2015). A population genomics insight into the Mediterranean origins of wine yeast domestication. Mol. Ecol. 24, 5412–5427. doi: 10.1111/mec.13341

PubMed Abstract | CrossRef Full Text | Google Scholar

Almeida, P., Gonçalves, C., Teixeira, S., Libkind, D., Bontrager, M., Masneuf-Pomarède, I., et al. (2014). A Gondwanan imprint on global diversity and domestication of wine and cider yeast Saccharomyces uvarum. Nat. Commun. 5, 4044. doi: 10.1038/ncomms5044

PubMed Abstract | CrossRef Full Text | Google Scholar

Belloch, C., Pérez-Torrado, R., González, S. S., Pérez-Ortín, J. E., García-Martínez, J., Querol, A., et al. (2009). Chimeric genomes of natural hybrids of Saccharomyces cerevisiae and Saccharomyces kudriavzevii. Appl. Environ. Microbiol. 75, 2534–2544. doi: 10.1128/AEM.02282-08

PubMed Abstract | CrossRef Full Text | Google Scholar

Bokulich, N. A., and Mills, D. A. (2013). Improved selection of internal transcribed spacer-specific primers enables quantitative, ultra-high-throughput profiling of fungal communities. Appl. Environ. Microbiol. 79, 2519–2526. doi: 10.1128/AEM.03870-12

PubMed Abstract | CrossRef Full Text | Google Scholar

Bokulich, N. A., Swadener, M., Sakamoto, K., Mills, D. A., and Bisson, L. F. (2015). Sulfur dioxide treatment alters wine microbial diversity and fermentation progression in a dose-dependent fashion. Am. J. Enol. Vitic. 66, 73–79. doi: 10.5344/ajev.2014.14096

CrossRef Full Text | Google Scholar

Bokulich, N. A., Thorngate, J. H., Richardson, P. M., and Mills, D. A. (2014). Microbial biogeography of wine grapes is conditioned by cultivar, vintage, and climate. Proc. Natl. Acad. Sci. U.S.A. 111, E139–E148. doi: 10.1073/pnas.1317377110

PubMed Abstract | CrossRef Full Text | Google Scholar

Borneman, A. R., Desany, B. A., Riches, D., Affourtit, J. P., Forgan, A. H., Pretorius, I. S., et al. (2012). The genome sequence of the wine yeast VIN7 reveals an allotriploid hybrid genome with Saccharomyces cerevisiae and Saccharomyces kudriavzevii origins. FEMS Yeast Res. 12, 88–96. doi: 10.1111/j.1567-1364.2011.00773.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Boynton, P. J., and Greig, D. (2014). The ecology and evolution of non-domesticated Saccharomyces species. Yeast Chichester Engl. 31, 449–462. doi: 10.1002/yea.3040

PubMed Abstract | CrossRef Full Text | Google Scholar

Bozdag, G. O., and Greig, D. (2014). The genetics of a putative social trait in natural populations of yeast. Mol. Ecol. 23, 5061–5071. doi: 10.1111/mec.12904

PubMed Abstract | CrossRef Full Text | Google Scholar

Bradbury, J. E., Richards, K. D., Niederer, H. A., Lee, S. A., Rod Dunbar, P., and Gardner, R. C. (2006). A homozygous diploid subset of commercial wine yeast strains. Antonie Van Leeuwenhoek 89, 27–37. doi: 10.1007/s10482-005-9006-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Camacho, C., Coulouris, G., Avagyan, V., Ma, N., Papadopoulos, J., Bealer, K., et al. (2009). BLAST+: architecture and applications. BMC Bioinform. 10:421. doi: 10.1186/1471-2105-10-421

PubMed Abstract | CrossRef Full Text

Casalone, E., Colella, C. M., Daly, S., Gallori, E., Moriani, L., and Polsinelli, M. (1992). Mechanism of resistance to sulphite in Saccharomyces cerevisiae. Curr. Genet. 22, 435–440. doi: 10.1007/BF00326407

PubMed Abstract | CrossRef Full Text | Google Scholar

Chang, S.-L., Lai, H.-Y., Tung, S.-Y., and Leu, J.-Y. (2013). Dynamic large-scale chromosomal rearrangements fuel rapid adaptation in yeast populations. PLoS Genet. 9:e1003232. doi: 10.1371/journal.pgen.1003232

PubMed Abstract | CrossRef Full Text | Google Scholar

Charron, G., Leducq, J.-B., Bertin, C., Dubé, A. K., and Landry, C. R. (2014). Exploring the northern limit of the distribution of Saccharomyces cerevisiae and Saccharomyces paradoxus in North America. FEMS Yeast Res. 14, 281–288. doi: 10.1111/1567-1364.12100

PubMed Abstract | CrossRef Full Text | Google Scholar

Combina, M., Elía, A., Mercado, L., Catania, C., Ganga, A., and Martinez, C. (2005). Dynamics of indigenous yeast populations during spontaneous fermentation of wines from Mendoza, Argentina. Int. J. Food Microbiol. 99, 237–243. doi: 10.1016/j.ijfoodmicro.2004.08.017

PubMed Abstract | CrossRef Full Text | Google Scholar

Cordero-Bueso, G., Arroyo, T., Serrano, A., and Valero, E. (2011). Remanence and survival of commercial yeast in different ecological niches of the vineyard. FEMS Microbiol. Ecol. 77, 429–437. doi: 10.1111/j.1574-6941.2011.01124.x

PubMed Abstract | CrossRef Full Text | Google Scholar

David, V., Terrat, S., Herzine, K., Claisse, O., Rousseaux, S., Tourdot-Maréchal, R., et al. (2014). High-throughput sequencing of amplicons for monitoring yeast biodiversity in must and during alcoholic fermentation. J. Ind. Microbiol. Biotechnol. 41, 811–821. doi: 10.1007/s10295-014-1427-2

CrossRef Full Text | Google Scholar

Di Maio, S., Polizzotto, G., Di Gangi, E., Foresta, G., Genna, G., Verzera, A., et al. (2012). Biodiversity of indigenous Saccharomyces populations from old wineries of south-eastern Sicily (Italy): preservation and economic potential. PLoS ONE 7:e30428. doi: 10.1371/journal.pone.0030428

PubMed Abstract | CrossRef Full Text | Google Scholar

Erny, C., Raoult, P., Alais, A., Butterlin, G., Delobel, P., Matei-Radoi, F., et al. (2012). Ecological success of a group of Saccharomyces cerevisiae/Saccharomyces kudriavzevii hybrids in the northern european wine-making environment. Appl. Environ. Microbiol. 78, 3256–3265. doi: 10.1128/AEM.06752-11

PubMed Abstract | CrossRef Full Text | Google Scholar

Fay, J. C., and Benavides, J. A. (2005). Evidence for domesticated and wild populations of Saccharomyces cerevisiae. PLoS Genet. 1:e5. doi: 10.1371/journal.pgen.0010005

PubMed Abstract | CrossRef Full Text | Google Scholar

Fay, J. C., McCullough, H. L., Sniegowski, P. D., and Eisen, M. B. (2004). Population genetic variation in gene expression is associated with phenotypic variation in Saccharomyces cerevisiae. Genome Biol. 5:R26. doi: 10.1186/gb-2004-5-4-r26

PubMed Abstract | CrossRef Full Text | Google Scholar

Fogel, S., and Welch, J. W. (1982). Tandem gene amplification mediates copper resistance in yeast. Proc. Natl. Acad. Sci. U.S.A. 79, 5342–5346. doi: 10.1073/pnas.79.17.5342

PubMed Abstract | CrossRef Full Text | Google Scholar

Gayevskiy, V., and Goddard, M. R. (2012). Geographic delineations of yeast communities and populations associated with vines and wines in New Zealand. ISME J. 6, 1281–1290. doi: 10.1038/ismej.2011.195

PubMed Abstract | CrossRef Full Text | Google Scholar

Glushakova, A. M., Ivannikova, I. V., Naumova, E. S., Chernov, I. I., and Naumov, G. I. (2007). Massive isolation and identification of Saccharomyces paradoxus yeasts from plant phyllosphere. Mikrobiologiia 76, 236–242. doi: 10.1134/s0026261707020129

PubMed Abstract | CrossRef Full Text | Google Scholar

Goddard, M. R., and Greig, D. (2015). Saccharomyces cerevisiae: a nomadic yeast with no niche? FEMS Yeast Res. 15:fov009. doi: 10.1093/femsyr/fov009

PubMed Abstract | CrossRef Full Text | Google Scholar

Gonçalves, P., Valério, E., Correia, C., de Almeida, J. M. G. C. F., and Sampaio, J. P. (2011). Evidence for divergent evolution of growth temperature preference in sympatric Saccharomyces species. PLoS ONE 6:e20739. doi: 10.1371/journal.pone.0020739

PubMed Abstract | CrossRef Full Text | Google Scholar

Goto-Yamamoto, N., Kitano, k, Shiki, K., Yoshida, Y., Suzuki, T., Iwata, T., et al. (1998). SSU1-R, a sulfite resistance gene of wine yeast, is an allele of SSU1 with a different upstream sequence. J. Ferment. Bioeng. 86, 427–433. doi: 10.1016/S0922-338X(98)80146-3

CrossRef Full Text | Google Scholar

Hagman, A., Säll, T., Compagno, C., and Piskur, J. (2013). Yeast “make-accumulate-consume” life strategy evolved as a multi-step process that predates the whole genome duplication. PLoS ONE 8:e68734. doi: 10.1371/journal.pone.0068734

PubMed Abstract | CrossRef Full Text | Google Scholar

Hyma, K. (2010). Genetic and Phenotypic Differentiation between Winemaking and Wild Strains of Saccharomyces Cerevisiae. PhD dissertation, Washington University. doi: 10.7936/K7XD0ZP9

CrossRef Full Text | Google Scholar

Hyma, K. E., and Fay, J. C. (2013). Mixing of vineyard and oak-tree ecotypes of Saccharomyces cerevisiae in North American vineyards. Mol. Ecol. 22, 2917–2930. doi: 10.1111/mec.12155

PubMed Abstract | CrossRef Full Text | Google Scholar

Johnson, L., Koufopanou, V., Goddard, M., Hetherington, R., Schäfer, S., and Burt, A. (2004). Population genetics of the wild yeast Saccharomyces paradoxus. Genetics 166, 43–52. doi: 10.1534/genetics.166.1.43

PubMed Abstract | CrossRef Full Text | Google Scholar

Kliewer, W. M., Howarth, L., and Omori, M. (1967). Concentrations of tartaric acid and malic acids and their salts in Vitis vinifera grapes. Am. J. Enol. Vitic. 18, 42–54.

Google Scholar

Knight, S., Klaere, S., Fedrizzi, B., and Goddard, M. R. (2015). Regional microbial signatures positively correlate with differential wine phenotypes: evidence for a microbial aspect to terroir. Sci. Rep. 5:14233. doi: 10.1038/srep14233

PubMed Abstract | CrossRef Full Text | Google Scholar

Kõljalg, U., Nilsson, R. H., Abarenkov, K., Tedersoo, L., Taylor, A. F. S., Bahram, M., et al. (2013). Towards a unified paradigm for sequence-based identification of fungi. Mol. Ecol. 22, 5271–5277. doi: 10.1111/mec.12481

PubMed Abstract | CrossRef Full Text | Google Scholar

Koufopanou, V., Hughes, J., Bell, G., and Burt, A. (2006). The spatial scale of genetic differentiation in a model organism: the wild yeast Saccharomyces paradoxus. Philos. Trans. R. Soc. Lond. B Biol. Sci. 361, 1941–1946. doi: 10.1098/rstb.2006.1922

PubMed Abstract | CrossRef Full Text | Google Scholar

Kowallik, V., Miller, E., and Greig, D. (2015). The interaction of Saccharomyces paradoxus with its natural competitors on oak bark. Mol. Ecol. 24, 1596–1610. doi: 10.1111/mec.13120

PubMed Abstract | CrossRef Full Text | Google Scholar

Le Jeune, C., Lollier, M., Demuyter, C., Erny, C., Legras, J.-L., Aigle, M., et al. (2007). Characterization of natural hybrids of Saccharomyces cerevisiae and Saccharomyces bayanus var. uvarum. FEMS Yeast Res. 7, 540–549. doi: 10.1111/j.1567-1364.2007.00207.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Libkind, D., Hittinger, C. T., Valério, E., Gonçalves, C., Dover, J., Johnston, M., et al. (2011). Microbe domestication and the identification of the wild genetic stock of lager-brewing yeast. Proc. Natl. Acad. Sci. U.S.A. 108, 14539–14544. doi: 10.1073/pnas.1105430108

PubMed Abstract | CrossRef Full Text | Google Scholar

Liti, G., Carter, D. M., Moses, A. M., Warringer, J., Parts, L., James, S. A., et al. (2009). Population genomics of domestic and wild yeasts. Nature 458, 337–341. doi: 10.1038/nature07743

PubMed Abstract | CrossRef Full Text | Google Scholar

Lopandic, K., Gangl, H., Wallner, E., Tscheik, G., Leitner, G., Querol, A., et al. (2007). Genetically different wine yeasts isolated from Austrian vine-growing regions influence wine aroma differently and contain putative hybrids between Saccharomyces cerevisiae and Saccharomyces kudriavzevii. FEMS Yeast Res. 7, 953–965. doi: 10.1111/j.1567-1364.2007.00240.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Martini, A. (1993). Origin and domestication of the wine yeast Saccharomyces cerevisiae. J. Wine Res. 4, 165–176. doi: 10.1080/09571269308717966

CrossRef Full Text | Google Scholar

McCullough, M. J., Clemons, K. V., McCusker, J. H., and Stevens, D. A. (1998). Intergenic transcribed spacer PCR ribotyping for differentiation of Saccharomyces species and interspecific hybrids. J. Clin. Microbiol. 36, 1035–1038.

PubMed Abstract | Google Scholar

Mercado, L., Dalcero, A., Masuelli, R., and Combina, M. (2007). Diversity of Saccharomyces strains on grapes and winery surfaces: analysis of their contribution to fermentative flora of Malbec wine from Mendoza (Argentina) during two consecutive years. Food Microbiol. 24, 403–412. doi: 10.1016/j.fm.2006.06.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Mortimer, R. K. (2000). Evolution and variation of the yeast (Saccharomyces) genome. Genome Res. 10, 403–409. doi: 10.1101/gr.10.4.403

PubMed Abstract | CrossRef Full Text | Google Scholar

Mortimer, R., and Polsinelli, M. (1999). On the origins of wine yeast. Res. Microbiol. 150, 199–204. doi: 10.1016/S0923-2508(99)80036-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Nakao, Y., Kanamori, T., Itoh, T., Kodama, Y., Rainieri, S., Nakamura, N., et al. (2009). Genome sequence of the lager brewing yeast, an interspecies hybrid. DNA Res. 16, 115–129. doi: 10.1093/dnares/dsp003

PubMed Abstract | CrossRef Full Text | Google Scholar

Nardi, T., Carlot, M., De Bortoli, E., Corich, V., and Giacomini, A. (2006). A rapid method for differentiating Saccharomyces sensu stricto strains from other yeast species in an enological environment. FEMS Microbiol. Lett. 264, 168–173. doi: 10.1111/j.1574-6968.2006.00450.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Nardi, T., Corich, V., Giacomini, A., and Blondin, B. (2010). A sulphite-inducible form of the sulphite efflux gene SSU1 in a Saccharomyces cerevisiae wine yeast. Microbiol. Read. Engl. 156, 1686–1696. doi: 10.1099/mic.0.036723-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Naumov, G. (1996). Genetic identification of biological species in the Saccharomyces sensu stricto complex. J. Ind. Appl. Microbiol. 17, 295–302.

Google Scholar

Naumov, G. I. (2013). Ecological and biogeographical features of Saccharomyces paradoxus Batschinskaya yeast and related species: I. The early studies. Microbiology 82, 397–403. doi: 10.1134/s0026261713040073

CrossRef Full Text | Google Scholar

Naumov, G. I., Lee, C.-F., and Naumova, E. S. (2013). Molecular genetic diversity of the Saccharomyces yeasts in Taiwan: Saccharomyces arboricola, Saccharomyces cerevisiae and Saccharomyces kudriavzevii. Antonie Van Leeuwenhoek 103, 217–228. doi: 10.1007/s10482-012-9803-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Naumov, G. I., Masneuf, I., Naumova, E. S., Aigle, M., and Dubourdieu, D. (2000). Association of Saccharomyces bayanus var. uvarum with some French wines: genetic analysis of yeast populations. Res. Microbiol. 151, 683–691. doi: 10.1016/S0923-2508(00)90131-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Naumov, G. I., Naumova, E. S., and Sniegowski, P. D. (1997). Differentiation of European and far East Asian populations of Saccharomyces paradoxus by allozyme analysis. Int. J. Syst. Bacteriol. 47, 341–344. doi: 10.1099/00207713-47-2-341

PubMed Abstract | CrossRef Full Text | Google Scholar

Naumov, G. I., Nguyen, H. V., Naumova, E. S., Michel, A., Aigle, M., and Gaillardin, C. (2001). Genetic identification of Saccharomyces bayanus var. uvarum, a cider-fermenting yeast. Int. J. Food Microbiol. 65, 163–171. doi: 10.1016/S0168-1605(00)00515-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Naumov, G., Naumova, E., and Korhola, M. (1992). Genetic identification of natural Saccharomyces sensu stricto yeasts from Finland, Holland and Slovakia. Antonie Van Leeuwenhoek 61, 237–243. doi: 10.1007/BF00584230

PubMed Abstract | CrossRef Full Text | Google Scholar

Naumov, G., Naumova, E., and Sniegowski, P. (1998). Saccharomyces paradoxus and Saccharomyces cerevisiae are associated with exudates of North American oaks. Can. J. Microbiol. 44, 1045–1050. doi: 10.1139/cjm-44-11-1045

PubMed Abstract | CrossRef Full Text | Google Scholar

Oksanen, J., Blanchet, F. G., Kindt, R., Legendre, P., Minchin, P. R., O'Hara, R. B., et al. (2015). vegan: Community Ecology Package. Available online at: http://CRAN.R-project.org/package=vegan.

Oliva, J. M., Negro, M. J., Saez, F., Ballesteros, I., Manzanares, P., Gonzalez, A., et al. (2006). Effects of acetic acid, furfural and catechol combinations on ethanol fermentation of Kluyveromyces marxianus. Process Biochem. 41, 1223–1228. doi: 10.1016/j.procbio.2005.12.003

CrossRef Full Text | Google Scholar

Pérez-Ortín, J. E., Querol, A., Puig, S., and Barrio, E. (2002). Molecular characterization of a chromosomal rearrangement involved in the adaptive evolution of yeast strains. Genome Res. 12, 1533–1539. doi: 10.1101/gr.436602

PubMed Abstract | CrossRef Full Text | Google Scholar

Pinto, C., Pinho, D., Cardoso, R., Custódio, V., Fernandes, J., Sousa, S., et al. (2015). Wine fermentation microbiome: a landscape from different Portuguese wine appellations. Front. Microbiol. 6:905. doi: 10.3389/fmicb.2015.00905

PubMed Abstract | CrossRef Full Text | Google Scholar

Pinto, C., Pinho, D., Sousa, S., Pinheiro, M., Egas, C., and Gomes, A. C. (2014). Unravelling the diversity of grapevine microbiome. PLoS ONE 9:e85622. doi: 10.1371/journal.pone.0085622

PubMed Abstract | CrossRef Full Text | Google Scholar

Rainieri, S., Zambonelli, C., Hallsworth, J. E., Pulvirenti, A., and Giudici, P. (1999). Saccharomyces uvarum, a distinct group within Saccharomyces sensu stricto. FEMS Microbiol. Lett. 177, 177–185. doi: 10.1111/j.1574-6968.1999.tb13729.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Redzepovic, S., Orlic, S., Sikora, S., Majdak, A., and Pretorius, I. S. (2002). Identification and characterization of Saccharomyces cerevisiae and Saccharomyces paradoxus strains isolated from Croatian vineyards. Lett. Appl. Microbiol. 35, 305–310. doi: 10.1046/j.1472-765X.2002.01181.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Salvadó, Z., Arroyo-López, F. N., Guillamón, J. M., Salazar, G., Querol, A., and Barrio, E. (2011). Temperature adaptation markedly determines evolution within the genus Saccharomyces. Appl. Environ. Microbiol. 77, 2292–2302. doi: 10.1128/AEM.01861-10

PubMed Abstract | CrossRef Full Text | Google Scholar

Sampaio, J. P., and Gonçalves, P. (2008). Natural populations of Saccharomyces kudriavzevii in Portugal are associated with oak bark and are sympatric with S. cerevisiae and S. paradoxus. Appl. Environ. Microbiol. 74, 2144–2152. doi: 10.1128/AEM.02396-07

PubMed Abstract | CrossRef Full Text | Google Scholar

Schuller, D., Alves, H., Dequin, S., and Casal, M. (2005). Ecological survey of Saccharomyces cerevisiae strains from vineyards in the Vinho Verde Region of Portugal. FEMS Microbiol. Ecol. 51, 167–177. doi: 10.1016/j.femsec.2004.08.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Setati, M. E., Jacobson, D., Andong, U.-C., Bauer, F. F., and Bauer, F. (2012). The vineyard yeast microbiome, a mixed model microbial map. PLoS ONE 7:e52609. doi: 10.1371/journal.pone.0052609

PubMed Abstract | CrossRef Full Text | Google Scholar

Sicard, D., and Legras, J.-L. (2011). Bread, beer and wine: yeast domestication in the Saccharomyces sensu stricto complex. C. R. Biol. 334, 229–236. doi: 10.1016/j.crvi.2010.12.016

PubMed Abstract | CrossRef Full Text | Google Scholar

Sniegowski, P. D., Dombrowski, P. G., and Fingerman, E. (2002). Saccharomyces cerevisiae and Saccharomyces paradoxus coexist in a natural woodland site in North America and display different levels of reproductive isolation from European conspecifics. FEM Yeast Res. 1, 299–306. doi: 10.1016/S1567-1356(01)00043-5

PubMed Abstract | CrossRef Full Text | Google Scholar

Stefanini, I., Dapporto, L., Legras, J.-L., Calabretta, A., Di Paola, M., De Filippo, C., et al. (2012). Role of social wasps in Saccharomyces cerevisiae ecology and evolution. Proc. Natl. Acad. Sci. U.S.A. 109, 13398–13403. doi: 10.1073/pnas.1208362109

PubMed Abstract | CrossRef Full Text | Google Scholar

Strope, P. K., Skelly, D. A., Kozmin, S. G., Mahadevan, G., Stone, E. A., Magwene, P. M., et al. (2015). The 100-genomes strains, an S. cerevisiae resource that illuminates its natural phenotypic and genotypic variation and emergence as an opportunistic pathogen. Genome Res. 25, 762–774. doi: 10.1101/gr.185538.114

PubMed Abstract | CrossRef Full Text | Google Scholar

Sylvester, K., Wang, Q.-M., James, B., Mendez, R., Hulfachor, A. B., and Hittinger, C. T. (2015). Temperature and host preferences drive the diversification of Saccharomyces and other yeasts: a survey and the discovery of eight new yeast species. FEMS Yeast Res. 15:fov002. doi: 10.1093/femsyr/fov002

PubMed Abstract | CrossRef Full Text | Google Scholar

Taylor, M. W., Tsai, P., Anfang, N., Ross, H. A., and Goddard, M. R. (2014). Pyrosequencing reveals regional differences in fruit-associated fungal communities. Environ. Microbiol. 16, 2848–2858. doi: 10.1111/1462-2920.12456

PubMed Abstract | CrossRef Full Text | Google Scholar

Valero, E., Cambon, B., Schuller, D., Casal, M., and Dequin, S. (2007). Biodiversity of Saccharomyces yeast strains from grape berries of wine-producing areas using starter commercial yeasts. FEMS Yeast Res. 7, 317–329. doi: 10.1111/j.1567-1364.2006.00161.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Valero, E., Schuller, D., Cambon, B., Casal, M., and Dequin, S. (2005). Dissemination and survival of commercial wine yeast in the vineyard: a large-scale, three-years study. FEMS Yeast Res. 5, 959–969. doi: 10.1016/j.femsyr.2005.04.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, C., García-Fernández, D., Mas, A., and Esteve-Zarzoso, B. (2015). Fungal diversity in grape must and wine fermentation assessed by massive sequencing, quantitative PCR and DGGE. Front. Microbiol. 6:1156. doi: 10.3389/fmicb.2015.01156

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, Q.-M., Liu, W.-Q., Liti, G., Wang, S.-A., and Bai, F.-Y. (2012). Surprisingly diverged populations of Saccharomyces cerevisiae in natural environments remote from human activity. Mol. Ecol. 21, 5404–5417. doi: 10.1111/j.1365-294X.2012.05732.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Warringer, J., Zörgö, E., Cubillos, F. A., Zia, A., Gjuvsland, A., Simpson, J. T., et al. (2011). Trait variation in yeast is defined by population history. PLoS Genet. 7:e1002111. doi: 10.1371/journal.pgen.1002111

PubMed Abstract | CrossRef Full Text | Google Scholar

Williams, K. M., Liu, P., and Fay, J. C. (2015). Evolution of ecological dominance of yeast species in high-sugar environments. Evol. Int. J. Org. Evol. 69, 2079–2093. doi: 10.1111/evo.12707

PubMed Abstract | CrossRef Full Text | Google Scholar

Yuasa, N., Nakagawa, Y., Hayakawa, M., and Iimura, Y. (2004). Distribution of the sulfite resistance gene SSU1-R and the variation in its promoter region in wine yeasts. J. Biosci. Bioeng. 98, 394–397. doi: 10.1016/S1389-1723(04)00303-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, H., Skelton, A., Gardner, R. C., and Goddard, M. R. (2010). Saccharomyces paradoxus and Saccharomyces cerevisiae reside on oak trees in New Zealand: evidence for migration from Europe and interspecies hybrids. FEMS Yeast Res. 10, 941–947. doi: 10.1111/j.1567-1364.2010.00681.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhao, Y., Strope, P. K., Kozmin, S. G., McCusker, J. H., Dietrich, F. S., Kokoska, R. J., et al. (2014). Structures of naturally evolved cup1 tandem arrays in yeast indicate that these arrays are generated by unequal nonhomologous recombination. G3 (Bethesda) 4, 2259–2269. doi: 10.1534/g3.114.012922

PubMed Abstract | CrossRef Full Text | Google Scholar

Zimmer, A., Durand, C., Loira, N., Durrens, P., Sherman, D. J., and Marullo, P. (2014). QTL dissection of lag phase in wine fermentation reveals a new translocation responsible for Saccharomyces cerevisiae adaptation to sulfite. PLoS ONE 9:e86298. doi: 10.1371/journal.pone.0086298

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: wine, microbiome, yeast, ecology, fermentation

Citation: Dashko S, Liu P, Volk H, Butinar L, Piškur J and Fay JC (2016) Changes in the Relative Abundance of Two Saccharomyces Species from Oak Forests to Wine Fermentations. Front. Microbiol. 7:215. doi: 10.3389/fmicb.2016.00215

Received: 10 December 2015; Accepted: 09 February 2016;
Published: 24 February 2016.

Edited by:

Kate Howell, University of Melbourne, Australia

Reviewed by:

Christian R. Landry, Université Laval, Canada
Jean-luc Legras, Institut National De La Recherche Agronomique Montpellier, France

Copyright © 2016 Dashko, Liu, Volk, Butinar, Piškur and Fay. 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) or licensor 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: Justin C. Fay, jfay@genetics.wustl.edu