The airways of cystic fibrosis (CF) patients are chronically colonized by patient-specific polymicrobial communities. The conditions and nutrients available in CF lungs affect the physiology and composition of the colonizing microbes. Recent work in bioreactors has shown that the fermentation product 2,3-butanediol mediates cross-feeding between some fermenting bacteria and Pseudomonas aeruginosa, and that this mechanism increases bacterial current production. To examine bacterial fermentation in the respiratory tract, breath gas metabolites were measured and several metagenomes were sequenced from CF and non-CF volunteers. 2,3-butanedione was produced in nearly all respiratory tracts. Elevated levels in one patient decreased during antibiotic treatment, and breath concentrations varied between CF patients at the same time point. Some patients had high enough levels of 2,3-butanedione to irreversibly damage lung tissue. Antibiotic therapy likely dictates the activities of 2,3-butanedione-producing microbes, which suggests a need for further study with larger sample size. Sputum microbiomes were dominated by P. aeruginosa, Streptococcus spp. and Rothia mucilaginosa, and revealed the potential for 2,3-butanedione biosynthesis. Genes encoding 2,3-butanedione biosynthesis were disproportionately abundant in Streptococcus spp, whereas genes for consumption of butanedione pathway products were encoded by P. aeruginosa and R. mucilaginosa. We propose a model where low oxygen conditions in CF lung lead to fermentation and a decrease in pH, triggering 2,3-butanedione fermentation to avoid lethal acidification. We hypothesize that this may also increase phenazine production by P. aeruginosa, increasing reactive oxygen species and providing additional electron acceptors to CF microbes.
Cystic fibrosis (CF) is a life-threatening inherited disease most prominent among Caucasians (affecting 1 in 3200 births), and is characterized by destruction of pulmonary structure and function arising from chronic airway polymicrobial infections. Life expectancy for CF patients has risen from infancy to nearly 40 years since the 1960s (Strausbaugh and Davis, 2007). Despite this progress, maintaining lung function remains problematic. The inability to clear abnormal, thick mucus from lung airways promotes chronic infection, and requires time-consuming treatments to physically loosen and remove mucus from the airways. Starting as early as childhood, CF patients develop long-term bacterial infections characterized by the presence of opportunistic pathogens, such as Pseudomonas aeruginosa. Daily symptoms include increased sputum production and cough, punctuated by intermittent periods of more severe symptoms referred to as pulmonary exacerbations (Bilton et al., 2011). A poorly understood combination of changes in microbial infection and inflammation causes exacerbations, which are difficult to define or diagnose (Goss and Burns, 2007). Lung function is usually restored toward pre-exacerbation levels after several days of intravenous antibiotic administration. Each exacerbation is thought to cause irreversible scarring and damage to lung tissue (Sanders et al., 2010, 2011).
Microbes living in the CF lung persist in the nutrient rich mixture of abnormally thick mucus, extracellular DNA, cell debris and toxic immune molecules (Conrad et al., 2012; Lynch and Bruce, 2013). Decreasing oxygen availability toward the center of sputum drives some fraction of the microbial population to fermentation and anaerobic respiration (Worlitzsch et al., 2002; Yoon et al., 2002). The fluid lining the airways in CF has a lower pH relative to healthy tissue, even before microbial colonization (Pezzulo et al., 2012), likely because of impaired bicarbonate transport, and during exacerbation pH has been shown to drop even further in exhaled breath condensate samples (Tate et al., 2002; Ojoo et al., 2005). Oral microbes that can aspirate to the lung are known to produce and tolerate acid in response to fermentation of dietary sugars (McLean et al., 2012). One mechanism employed by microbes to avoid lethal acidification from low pH fermentation products is an alternative fermentation pathway, known as acetoin metabolism, which produces the pH neutral and buttery flavored compounds 2,3-butanedione (also known as diacetyl) and 2,3-butanediol (Figure 1) (Bartowsky and Henschke, 2004).
2,3-butanedione has the potential to harm lung tissue and benefit microbes. The basis of its toxicity in the lung may be its reactivity with guanidinium groups such as those found in arginine side chains (Mathews et al., 2010). Reactivity with guanidinium groups also enables colorimetric detection of 2,3-butanedione with the Voges–Proskauer reaction developed in the 1880s (Voges and Proskauer, 1898). Although at high concentrations (>1 mM), 2,3-butanedione has broad antimicrobial activity (Jay, 1982; Kim et al., 2013), lower doses (nM to μM) may enhance microbial survival. For example, when E. coli was exposed to 2,3-butanedione emitted by B. subtilis, broad changes in gene expression suggesting increased antibiotic resistance and motility were observed (Kim et al., 2013).
If present in the lung, 2,3-butanedione could also impact lung function and the resident microbial community through its effects on the production of toxic redox active molecules known as phenazines. In the presence of oxygen, phenazines generate the deadly oxygen radicals that originally led to their designation as antibiotics. However, at low oxygen tensions found in CF lungs, the phenazines could act as alternative electron acceptors and enable anaerobic respiration for other members of the community, potentially recycling their redox state through contact with occasional oxygen molecules or abundant iron molecules in the CF lung (Wang and Newman, 2008; Wang et al., 2010; Ghio et al., 2012). The last step in the biosynthesis of pyocyanin highlights the relationship between pyocyanin and oxygen, as the conversion of phenazine-1-carboxylic acid to pyocyanin requires oxygen for one of the phenazine-modifying genes (PhzS), a flavin-containing mono-oxygenase. Pyocyanin may serve an important function in low oxygen conditions as an alternative electron acceptor, and yet pyocyanin production depends on the presence of oxygen. This is an interesting puzzle that may relate to the currently under-explored specializations of different phenazines. Each phenazine type has unique properties including redox potential; the ability to transfer electrons to O2 or Fe3+ varies and is dependent on pH (Wang and Newman, 2008).
Although the main CF pathogen and phenazine producer P. aeruginosa is not known to synthesize 2,3-butanedione, it consumes 2,3-butanedione produced by cocultured Staphylococcus aureus (Filipiak et al., 2012b), and responds to 2,3-butanediol produced by cocultured Enterobacter aerogenes by increasing its current production rate and producing more of the phenazine pyocyanin (Venkataraman et al., 2011). Increasing concentrations of pyocyanin along with another phenazine, phenazine-1-carboxylic acid, are associated with disease severity in CF patients (Hunter et al., 2012).
Because these studies have been limited to controlled experimental cultures, we took an ecosystem-level approach that investigated whether the microaerophilic conditions of the CF lung could steer microbial metabolism toward production of 2,3-butanedione. Here we show that 2,3-butanedione is a component of CF and non-CF breath gas, and identify microbial genes for 2,3-butanedione synthesis in CF and non-CF sputum. 2,3-butanedione, likely to be produced by Streptococcus spp., may lead to the increased phenazine production when consumed by P. aeruginosa, a relevant and drastic combination for the health of CF patients. We discuss a model where increased production of phenazines offers an alternative electron acceptor, which may enable phenazines to recycle their redox state through donation of electrons to distant oxygen molecules, nitrate or abundant Fe3+ molecules in the lung.
Materials and methods
All collection was in accordance with the University of California Institutional Review Board (HRPP 081500) and San Diego State University Institutional Review Board (SDSU IRB#2121).
Metagenome collection and analysis
For the longitudinal analysis, breath gases were sampled from one CF patient and one healthy individual at approximately monthly intervals. For the combined cross-sectional analysis of breath gases and metagenomes, induced sputum samples were collected from seven CF patients and one healthy control. Separation of microbial and human cells was achieved through hypotonic lysis of eukaryotic cells, followed by washing and DNA extraction from microbial cells (Lim et al., 2012). Ion Torrent sequencing of these samples yielded 19.8 million sequences. After removing low quality reads with PRINSEQ (Schmieder and Edwards, 2011a) and human sequences using DeconSeq (Schmieder and Edwards, 2011b) with the commands specified in the Supplementary Materials, 13.6 million reads of ∼140 bp were retained for further analysis (Supplementary Table 7). Genes related to butanedione synthesis from the SEED database (Aziz et al., 2012) and phenazine synthesis genes from the Patric database (Snyder et al., 2007) were used in BLASTn searches for related sequences in metagenomic data from CF patients. Metagenomic sequences were selected if they matched butanedione and phenazine synthesis pathway genes with a minimum length of 40 bp, sequence identity of 40% and a BLAST e-value cutoff of 1 × 10−10. Microbial DNA isolated from SF sputum samples as part of a related study (Lim et al., 2012) was also mined for butanedione metabolism related genes. Metatranscriptome data from 454 sequencing of 10 sputum samples from four CF patients (Lim et al., 2012) consisted of 1 549 273 reads with an average length of 280 bp, while 806 009 of the reads come from five time-points taken from patient CF1 (Lim et al., 2012). Bacterial mRNAs were not especially abundant in these data sets, which have been published previously (Lim et al., 2012). However, we were able to examine the transcription of the human ferritin gene, as mentioned in the Discussion and Supplementary Information. BLAST hits that were at least 60 bp long with an e-value cutoff 1 × 10−5 were retained. Several queries were searched against the transcriptome data, including: the heavy and light chain of ferritin (GI:56682958 and GI:56682960) and the two standards (GI:223459775 and GI:183603937) chosen for their transcription rate stability across tissue types (Neville et al., 2011). Raw counts are reported to avoid the potential for false positives demonstrated with the reads per kilobase per million mapped reads measure (Dillies et al., 2012).
Species indicator values were calculated from the metagenome data using the R package LABDSV (http://cran.r-project.org/web/packages/labdsv/index.html) (R: www.R-project.org). An operational taxonomical unit table with the relative abundance of each genus in each sputum sample was used as input for the ‘indval’ function. The ‘Acute’ and ‘Suppressive’ antibiotic groupings were used to cluster genera for the ‘indval’ function.
Breath gas sample collection
At each time point, three breath samples were collected within 5 min from a single CF patient in a 1.9 L custom-built electro-polished stainless-steel canister (Kamboures et al., 2005). At the beginning of the second sample, a simultaneous breath sample from a healthy control occupying the same room was taken. At the same time, a background sample of room air was taken by placing a canister within a few feet of the human breath sample donors. Volunteers were instructed to allow the first third of their breath to escape to the room before turning the valve to collect the sample in the canister to avoid collecting breath gases from the oral cavity. Food and drink in the hours before sampling along with health status were recorded; volunteers were instructed to eat and drink normally until 1 h before sample collection. The analytical system used to analyze the breath samples is similar to the system described in (Colman et al., 2001). Briefly, 235±3 cm3 (at Standard Temperature and Pressure) of an air sample is pre-concentrated in a stainless-steel loop filled with glass beads and submerged in liquid nitrogen. The sample is heated to ∼80 °C and split into six different column/detector combinations housed in three gas chromatographs using UHP helium as the carrier gas: (1) DB-1 column (J&W, Agilent, Santa Clara, CA, USA; 60 m, 0.32 mm I.D., 1 μm film thickness) output to a flame ionization detector and a sulfur chemiluminescence detector; (2) DB-5 column (J&W, 30 m, 0.25 mm I.D., 1 μm film thickness) connected in series to a RESTEK 1701 column (5 m, 0.25 mm I.D., 0.5 μm film thickness) and output to an electron capture detector; (3) RESTEK 1701 column (60 m, 0.25 mm I.D., 0.50 μm film thickness) output to an electron capture detector; (4) PLOT column (J&W GS-Alumina; 30 m, 0.53 mm I.D.) connected in series to a DB-1 column (J&W; 5 m, 0.53 mm I.D., 1.5 μm film thickness) and output to an flame ionization detector; (5) DB-5ms column (J&W; 60 m, 0.25 mm I.D., 0.5 μm film thickness) output to a quadrupole mass selective detector (MSD, HP 5973). The MSD is set to operate in scan mode (SCAN) and selected ion monitoring mode simultaneously. Scan mode was used for identification, whereas selected ion monitoring (one ion chosen to quantify each compound) was used in order to achieve the maximum selectivity and to avoid potential interferences. All gas chromatographs and detectors used in this study were manufactured by Hewlett Packard (Palo Alto, CA, USA).
The first three of the seven longitudinal time-points were analyzed globally without focused identification of a particular compound. After 2,3-butanedione was identified in the first two time-points, pure 2,3-butanedione was diluted to the parts per billion (ppb) level and then used as a qualitative standard, focusing the instrument for detection of 2,3-butanedione in the last four time-points and for all time-points in the cross-sectional study. Quantification of 2,3-butanedione was carried out using both mass spectrometry and one of the flame ionization detectors.
Box-plots, linear regressions, analysis of variance and non-parametric tests were performed in R (v3.0.1) or JMP (v188.8.131.52).
2,3-butanedione occurs in healthy and CF breath samples, and is affected by intravenous antibiotic therapy
Gas chromatography was used to monitor 2,3-butanedione concentrations longitudinally over seven time-points in one patient, and cross-sectionally at the same time-point in seven patients. These samplings always included simultaneous breath gas sampling of healthy volunteers in the same room, and background samples of room air. Volunteers were instructed to collect only the last two-thirds of each breath to avoid the gases produced by oral microbes.
A CF patient produced more 2,3-butanedione than the healthy control, except when receiving intravenous antibiotic therapy
In the longitudinal study one patient and a healthy control were simultaneously sampled approximately monthly. The non-CF and air controls contained between 3 and 2287 parts per trillion (ppt) 2,3-butanedione, whereas the CF samples contained between 1482 and 26 751 ppt (Figure 2 and Supplementary Table 3). In this longitudinal sample, 2,3-butanedione concentrations in CF versus non-CF were significantly different (repeated measures analysis of variance; F=336.7; P=0.0004). Most interestingly, the 2,3-butanedione concentration decreased over 10-fold in this patient during treatment with intravenous antibiotics (azithromycin, trimethoprim/sulfamethoxazole and tobramycin) (Figure 2).
2,3-butanedione production varied significantly between CF and non-CF volunteers
The results from our longitudinal study prompted us to examine 2,3-butanedione in additional CF and non-CF volunteers. CF patients harboring microbial communities dominated by different bacteria as indicated by clinical sputum culture data were chosen. This cross-sectional study sampled six CF patients in addition to the one patient followed longitudinally (Figure 2), four non-CF controls (each of which were sampled at the same time and in the same room as the matched CF patient), and ambient room air (Figure 3 and Supplementary Table 4). Only four non-CF volunteers donated breath samples because one volunteer donated samples (at different times) for multiple CF patients (CF2, CF4, CF5 and CF7 in Figure 3 and Table 1).
Four of the seven CF patients sampled (CF1-4) had elevated 2,3-butanedione concentrations in their breath samples compared with the simultaneous non-CF volunteers and room air samples. They were considered to be in a stable disease state at the time of sampling (Table 1). However, at the time of sampling patients CF6 and CF7 were undergoing antibiotic treatment for exacerbation, and patient CF5 was completing a 4 week course of intravenous tobramycin and aztreonam. These three patients were further classified as undergoing ‘Acute’ antibiotic therapy. Importantly, all of the patients regularly take antibiotics for maintenance, and those patients only undergoing maintenance therapy were classified as ‘Suppressive’ (Table 1).
Antibiotic therapy may affect 2,3-butanedione production in all patients
On the basis of the results from the longitudinal sampling, we examined the effect of antibiotic therapy on 2,3-butanedione production in this cross-sectional sample of CF and non-CF volunteers (Figure 3b). CF patients were classified as either being only on ‘Suppressive’ therapy, which is the maintenance dose of antibiotics all CF patients are prescribed during times of relatively good health, or ‘Acute’ therapy, which is typically intravenous administration of antibiotics during times of exacerbation or relatively poor health. Non-CF volunteers were not taking antibiotics, and were classified as ‘Healthy’.
When all replicate measurements were analyzed as separate data points, patients undergoing ‘Acute’ versus ‘Suppressive’ antibiotic therapy had significantly different levels of 2,3-butanedione present (analysis of variance; F=11.384; P=0.00251). ‘Healthy’ breath gases were intermediate (Figure 3b shows a box-plot of all measurements for each category). However, because replicate measurements were not combined for this analysis, we also performed the same analysis using the median value of replicate measurements. Using a single median value for each patient led to results that were statistically insignificant, though the trend was maintained. A power analysis suggested that the available sample size was insufficient to detect an effect: a sample size of 12 with an α=0.05 had only 0.0961 power (1 is maximum). Obtaining significance at the α=0.5 level would require 93 volunteers, and at the α=0.1 level would require 72 volunteers.
Metagenomes indicate potential for 2,3-butanedione production
To identify microbial candidates that may be responsible for 2,3-butanedione production, we sequenced metagenomes from sputum induced in our cross-sectional CF volunteers, and one non-CF volunteer. Although our conclusions will be limited by this small sample size, complete metagenomes provide an enormous volume of data for generating new, and testing existing, hypotheses.
Genes for butanedione metabolism and phenazine production are present in sputa from CF patients
Microbial DNA was isolated and sequenced as described in the Materials and methods. The overall taxonomic distribution of each sample was determined through identification of sequences known to be unique to sequenced strains of bacteria using Metaphlan (Segata et al., 2012), revealing that polymicrobial infections in sputum samples in these patients are unique to each individual, and dominated by R. mucilaginosa, Streptococcus spp., and P. aeruginosa (Figure 4). Interestingly, the microbes found in the healthy volunteer were remarkably similar to those from the CF patients, being dominated by Rothia, Pseudomonas and Streptococcus. Although R. mucilaginosa was present in both CF and non-CF, the dominant Streptococcus spp. in CF samples were S. parasanguinis and S. salivarius, whereas the non-CF volunteer had S. mitis, S. oralis, S. infantis and S. australis.
The metagenomes were mined for genes related to acetoin biosynthesis, including acetolactate synthase (budB), acetolactate decarboxylase (budA) and butanediol dehydrogenase (budC; the metabolic pathways are summarized in Figure 1). A total of 6278 raw reads matched the known butanedione metabolism genes (BLASTn; e-value cutoff 1 × 10−10, with at least 40 bp query coverage and 40% sequence identity). The taxonomic distribution of these genes was distinct from that of the total community, by having an over-representation of Streptococcus spp. (Figure 5). The 466 reads with high quality hits to acetoin metabolism genes (BLASTn; e-value cutoff 1 × 10−10, with at least 60 bp query coverage and 90% sequence identity) were heavily dominated by Streptococcus spp. (335 of 446 top hits), despite P. aeruginosa and R. mucilaginosa being numerically dominant in most patients. Reanalysis of 18 published metagenomes from six CF patients (Lim et al., 2012) confirmed the over-representation of Streptococcus-associated genes for butanedione metabolism (Supplementary Figure 1 and Supplementary Table 1). Fragment recruitment of metagenomic reads against the butanedione pathway genes from S. parasanguinus, a common species in these samples, is shown in Figure 6.
Streptococcus spp. were the only bacteria in these microbial communities that encoded all of the enzymes in the 2,3-butanedione pathway. budA was not present in P. aeruginosa (in these CF metagenomes from San Diego nor in publically available fully sequenced genomes (Winsor et al., 2011), and budC was not present in the highly abundant R. mucilaginosa. However, R. mucilaginosa and/or P. aeruginosa have the ability to consume 2,3-butanedione, as they encode acoA and acoB, the genes whose products catabolize acetoin for use in central metabolism.
Electrical current production increases when P. aeruginosa is directly fed 2,3-butanediol or when it is cocultured with microbes that produce it (Venkataraman et al., 2011). Under these micro-aerobic conditions, P. aeruginosa increases its production of the redox active phenazine, pyocyanin (Venkataraman et al., 2011), which may act as an alternative electron acceptor (Cox, 1986; Wang and Newman, 2008; Wang et al., 2011). Therefore, to identify whether these microbial communities had the potential for this 2,3-butanediol-induced phenazine production, we mined the metagenome data for genes that encode phenazines. As shown in Figure 5, phenazine biosynthesis genes were present in the CF metagenomes (BLASTn; 4109 hits with e-value 1 × 10−10, 40 bp length and 40% identity), the vast majority of which (95%) were found in P. aeruginosa.
Microbial abundance and 2,3-butanedione production
To identify how varying abundances of each candidate genus could predict the amount of 2,3-butanedione produced, we used linear models to identify how much variation in 2,3-butanedione concentration could be explained by the relative abundances of Streptococcus, Rothia and Pseudomonas in the CF patients. Only variability in Streptococcus could significantly predict differences in 2,3-butanedione concentration (Supplementary Figure 4: r2=0.76; P=0.01), whereas Rothia (r2=0.00; P=0.94) and Pseudomonas (r2=0.00; P=0.97) abundances had no effect. Additional patient information, microbial abundances and a corroborating correlation analysis can be found in Supplementary Tables 8 and 9.
The effects of antibiotic treatment on microbial communities
The potential for ‘Acute’ antibiotic therapies to influence the production of 2,3-butanedione prompted us to examine how these therapies affect the microbial composition and physiology of lung communities. Particularly, we aimed to identify which genera were indicative of antibiotic therapy group membership. Using the LABDSV package in R, we attempted to identify genera that were significantly associated with ‘Acute’ or ‘Suppressive’ therapies. None of the genera in the metagenomic data set were significantly associated with patients undergoing ‘Acute’ or ‘Suppressive’ therapy. Either this analysis suffered from the same lack of power as the analysis of variance mentioned above, or the different antibiotic therapies do not predictably alter the underlying microbial communities. Thus, any effects antibiotic treatment may have on 2,3-butanedione production could be due to altering the physiology of the microbes present, rather than altering the abundances of individual microbes.
The presence of 2,3-butanedione in breath indicates low pH, low oxygen conditions and can serve as a cue to neighboring microbes. Here we have shown that 2,3-butanedione is abundant in CF patients, that its concentration varies with antibiotic therapy, and that it may be produced by Streptococcus species.
2,3-butanedione in the breath gases
Healthy people emit hundreds to thousands of breath gases in the ppb to parts per quadrillion concentration range (Pauling et al., 1971; Cao and Duan, 2006). These products are derived from: (i) exchange of human metabolic products from the blood across the lung epithelia; (ii) inhalation of gases from the environment, which may be altered enzymatically or absorbed in the lung; (iii) microbial metabolites produced in the airways or oral cavity (Kamboures et al., 2005; Scott-Thomas et al., 2010) and (iv) hydrocarbons that may derive from the breakdown of cell membranes by reactive oxygen species and other toxic molecules secreted in the context of inflammation (Robroeks et al., 2010). Breath gases can be used to identify the cause of an infection if the metabolite is unique to a particular species of bacteria, or the physiology of the microbial community if the metabolite is only produced under particular conditions, such as low pH or oxygen (Bos et al., 2013).
Healthy people can have a low background of 2,3-butanedione from intestinal and oral microbial metabolism (de Graaf et al., 2010). This may explain higher levels of 2,3-butanedione in healthy controls compared with the room signal. To mitigate the signal from these oral microbes as much as possible, we included non-CF volunteers, and all sampled individuals were instructed to discard the first few seconds of their breath sample.
In this study, volunteers were requested not to consume anything but water for 1 h before sampling, and reported what they had consumed in the hours leading up to sample collection. One non-CF volunteer who had high concentrations of breath 2,3-butanedione (H4) reported that he or she did not consume anything other than water in the 2 h before sampling, and that he or she did not have any respiratory infections or symptoms in the month preceding the sampling. The origin of 2,3-butanedione in this individual is unknown, and warrants further study of 2,3-butanedione concentrations in breath gases from a larger study population. In general, detection of 2,3-butanedione in the breath may derive from food or from the metabolism of microbes in the airways. It is not found in the blood, and when compared with the room air was found to be at a threefold higher concentration in the breath samples of 28 healthy volunteers who did not fast and remained still for 10 min in the same room where samples were collected (Mochalski et al., 2013). Alcohol metabolism may also lead to detectable levels of 2,3-butanediol in human blood and urine (Otsuka et al., 1999).
During a 6-month longitudinal study, the concentration of 2,3-butanedione was consistently elevated in CF1 with the exception of time-point C (Figure 2). The first two and the last four samples were taken during periods of stability for the CF patient. Time-point C was the only one taken when the patient was in the hospital; breath sampling occurred 5 days after the patient began a course of acute antibiotic treatment. Furthermore, in the cross-sectional study, patients who had recently finished (CF5), or were undergoing (CF6 and CF7), acute treatment also had lower levels of 2,3-butanedione. 2,3-butanedione in breath samples taken after discarding the first third of the breath may indicate that oral microbes such as Streptococcus have moved into the lung. There, these immigrant microbes may influence the physiology of the microbial community, though their activities may be more sensitive to antibiotics than long-time residents of the lung such as P. aeruginosa. Decreases in 2,3-butanedione concentration during acute therapy could be attributed to a reduction in the density of the producing bacteria, a change in the metabolism of the bacterial community, or the consumption of this metabolite. Identifying whether a causative link exists between 2,3-butanedione production, antibiotic therapy and patient health is an important goal for future research with a larger cohort.
Streptococcus spp. likely produced 2,3-butanedione detected in the CF breath gases
The presence of 2,3-butanedione in the breath of these individuals suggests active production of 2,3-butanedione. Our metagenome data combined with the presence of 2,3-butanedione in culture headspace samples (Filipiak et al., 2012a, 2012b) indicate that Streptococcus spp. were most likely producing 2,3-butanedione in these samples. Activity of Streptococcus spp. in one patient, with significant 2,3-butanedione production, was suggested by metatranscriptome data from a previous study; however, sequence read coverage was too low to detect the presence of acetoin biosynthesis genes (Lim et al., 2012). Although the Pseudomonas in the samples described here did encode part of the acetoin biosynthesis pathway, they lacked the essential enzyme BudA (Figure 5). 2,3-butanedione can be produced spontaneously from acetolactate (Figure 1), however, Lactococcus mutants lacking acetolactate decarboxylase (BudA) do not produce nearly as much 2,3-butanedione (Aymes et al., 1999). This is consistent with previous reports showing P. aeruginosa does not produce 2,3-butanedione (Filipiak et al., 2012b).
The interplay between Streptococcus and Pseudomonas is important for a polymicrobial understanding of CF lung communities, because these bacteria usually colonize CF children and adults for the long term (Zemanick et al., 2011; Delhaes et al., 2012; Zhao et al., 2012). Streptococcous spp are considered to be generally dominant in the oral cavity of humans, comprising >20% of the oral microbial communities that were sequenced as part of the human microbiome project (Bik et al., 2010; Grice and Segre, 2012). Likewise, R. mucilaginosa is a common although less dominant oral bacteria (Grice and Segre, 2012). Oral origin of lung infection is well accepted; aspiration of oral material is known to cause about half of Pneumonia in the general population (Bousbia et al., 2012); a similar mechanism may be even more important in CF.
In several recent studies using culture independent approaches, Streptococcus spp. are among the top 5–10 most abundant microbes in the CF sputum samples (Blainey et al., 2012; Filkins et al., 2012; Fodor et al., 2012; Goddard et al., 2012; Lim et al., 2012; Zhao et al., 2012; Supplementary Table 2). The Streptococcus milleri group (S. anginosus, S. constellatus, and S. intermedius) has been associated with exacerbations in a Canadian CF cohort and antibiotic treatment targeting this group resolved respiratory symptoms in the patients (Sibley et al., 2008). S. pneumoniae and its virulent phage Dp-1 were abundant in patient CF1 (Supplementary Figure 2) (Lim et al., 2012), and Streptococcus reads accounted for a relatively high percentage of all sequence reads from CF patients examined herein, further supporting the presence of Streptococcus spp. in CF microbial communities, though most clinical labs discard plates containing Streptococcus spp. and other typical members of the oral cavity as contaminants.
2,3-butanedione and its potential effects on CF lung microbial community physiology
Placing these results in the context of the phenazine literature, we propose a model of cross-feeding between 2,3-butanedione producers such as Streptococcus spp. and phenazine producing P. aeruginosa (Figure 7a). Cross-feeding could occur throughout the CF airways, as a volatile molecule such as 2,3-butanedione could easily travel through the airways, affecting microbes at greater distances. In response to 2,3-butanediol, P. aeruginosa produces phenazines (Venkataraman et al., 2011) that are known to increase in concentration as CF progresses (Hunter et al., 2012). The abundance of phenazines could then offer an alternative electron acceptor in oxygen limited conditions, thereby increasing 2,3-butanedione production and growth or survival of acetoin metabolizing strains (for example, Streptococcus spp.). Phenazine producing mutants of P. aeruginosa have been shown to form biofilms with architecture that increases surface area to increase access to oxygen, supporting the role of phenazines as alternative electron acceptors when access to oxygen is reduced (Dietrich et al., 2013). As shown in Figure 7b, phenazines that accept electrons from NADH that is produced in the course of microbial catabolism may recycle their redox state when they come into contact with O2 or Fe3+, depending on oxygen availability, pH and the redox potential of the phenazine (Wang and Newman, 2008).
Elucidating the relationship between the redox state of phenazines and Fe3+ is important because CF patients are often anemic, and high sputum iron content has been measured in CF patients during stable periods and exacerbations (Stites et al., 1998; Reid et al., 2007; Ghio et al., 2012; Gifford et al., 2012). The amount of iron sequestered in CF sputum is a considerable fraction of the total iron stores in the body, and is consistent with the possibility that iron in sputum originated from ferritin, which stores an average of 20–30% of the iron in a healthy adult (Lieu et al., 2001). Several studies of CF sputum have observed high iron and ferritin concentrations. The ferritin transcription in the San Diego CF patient’s sputa (Supplementary Figure 3) is consistent with antioxidants controlling transcription of ferritin, and demonstrates the co-occurrence of ferritin transcription and high butanedione levels in the breath of the same CF patient. Under low oxygen conditions, nitrate or abundant Fe3+ could act as an alternative electron acceptor, recycling the redox state of the phenazines and maintaining a supply of NAD+ (Figure 7b). Evidence supporting this mechanism can be found in recent studies of iron redox state in CF sputum, where an increasing fraction of iron was observed to be in the Fe2+ rather than the Fe3+ state as disease state progressed (Hunter et al., 2013). Because alternative electron acceptors provide a crucial survival advantage in the CF lung, limiting access to components that may contribute to their production—iron, butanedione or phenazines—could be a tool to control microbial infection and inflammation in the CF lung. For example, Gallium has been used successfully to interfere with P. aeruginosa iron metabolism (Kaneko et al., 2007).
2,3-butanedione as a biomarker for Streptococcus activity and an anoxic lung environment
A colorimetric assay to detect acetoin known as the Voges–Proskauer test was developed in Germany in the 1890s (Voges and Proskauer, 1898). Using this inexpensive assay, it may be possible to develop accessible methods for detecting the active, low pH metabolism of Streptococcus spp. and other butanedione-producing bacteria in respiratory patients. Detection of 2,3-butanedione in breath gases is important to better understand the resident bacterial community, and also has practical importance for lung health (Supplementary Tables 5 and 6). For example, microwave popcorn factory workers developed Bronchiolitis Obliterans after occupational exposure to 2,3-butanedione, leading to passage of the Popcorn Workers Lung Disease Prevention Act (H.R. 2693) in 2007 with recommendations to reduce exposure to inhaled 2,3-butanedione. The concentrations of 2,3-butanedione that were detected in our study are thought to be high enough to cause lung damage, and are above the proposed standard of 1 ppb over an 8 h workday (Egilman et al., 2011).
Both 2,3-butanedione and 2,3-butanediol have been studied in a wide variety of host–microbe interactions (Supplementary Tables 5 and 6). 2,3-butanedione has been shown to reduce the ability of mosquitos to detect CO2, preventing them from finding a host to prey on (Turner et al., 2011). In plant infections, microbial acetoin metabolism triggers the plant immune response, and is carefully timed to occur after cellulose degrading enzymes have already caused the damage needed for a successful infection (Effantin et al., 2011). One Vibrio cholera biotype secretes 2,3-butanediol and inhibits pro-inflammatory signals from epithelial cells (Bari et al., 2011), and 2,3-butanediol has also been shown to inhibit neutrophils in rats (Hsieh et al., 2007). The complexity of these interactions suggests that acetoin producing microbes and hosts have evolved together.
The physicians and spouses of some CF patients report that they can detect an odor associated with exacerbation (Cao and Duan, 2006). CF also leads to changes in the abundance of breath gases that are universally detected in human breath (Montuschi et al., 2012). In the case of infection, distinct gases that are unique to specific microbial metabolism or immune action may be present.
Linking together products unique to microbial metabolism from breath gas measurements with the genes detected by metagenomic sequences of microbial communities in sputum may enable development of biomarkers for early detection of exacerbations. Elucidation of the molecular signaling that occurs in CF microbial communities could also lead to new treatment strategies for altering microbial physiology. The detection of 2,3-butanedione in the breath of CF patients indicates: (i) active metabolism in the airways by 2,3-butanedione-producing bacteria, such as Streptococcus spp; (ii) synergism with other bacteria, where 2,3-butanedione acts as a carbon source and/or signaling molecule and (iii) 2,3-butanedione likely interacts with the host immune system, and causes direct physical damage through destruction of arginine side chains.
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We would like to thank Clarence C Lee and Timothy T Harkins from the Advance Applications Group, and Life Technologies for generously providing sequence data with Ion Torrent technology. Anthony Fodor and Barbara Bailey provided statistics guidance. The clinical sampling coordination was greatly assisted by Doris Kwan. We thank Jeremy Barr for critical readings and discussions of the manuscript. This work was supported by the National Institute of Health through grants R01 GM095384-01 awarded to Forest Rohwer, and R01GM095384–01S1 to Katrine Whiteson.
Sequence data was depositied in the NCBI database under accession numbers SRX151603, SRX151605, SRX151606, 151607-151615, SRX106094, SRX106095, SRX106105, SRX106106, SRX108115, SRX108128-SRX108130 for the 454 data, and Ion Torrent data can be found publically available in MG-RAST with ID# 4541773.3.
KLW, SM, YWL, DRB, DC and FR designed research; KLW, SM and YWL performed research; KLW, SM, YWL, RQ and DC collected samples; KLW, SM, YWL and RS analyzed data and KLW, SM, HM and FR wrote the paper.
The authors declare no conflict of interest.
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Whiteson, K., Meinardi, S., Lim, Y. et al. Breath gas metabolites and bacterial metagenomes from cystic fibrosis airways indicate active pH neutral 2,3-butanedione fermentation. ISME J 8, 1247–1258 (2014). https://doi.org/10.1038/ismej.2013.229
- breath gas
- cystic fibrosis
- polymicrobial infection
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