Amplicon sequencing for the quantification of spoilage microbiota in complex foods including bacterial spores
- Paulo de Boer†1, 2,
- Martien Caspers†1, 2,
- Jan-Willem Sanders3,
- Robèr Kemperman3,
- Janneke Wijman4,
- Gijs Lommerse4,
- Guus Roeselers1, 2,
- Roy Montijn1,
- Tjakko Abee1, 5 and
- Remco Kort1, 2, 6Email author
© de Boer et al. 2015
Received: 22 January 2015
Accepted: 14 July 2015
Published: 27 July 2015
Spoilage of food products is frequently caused by bacterial spores and lactic acid bacteria. Identification of these organisms by classic cultivation methods is limited by their ability to form colonies on nutrient agar plates. In this study, we adapted and optimized 16S rRNA amplicon sequencing for quantification of bacterial spores in a canned food matrix and for monitoring the outgrowth of spoilage microbiota in a ready-to-eat food matrix.
The detection limit of bar-coded 16S rRNA amplicon sequencing was determined for the number of bacterial spores in a canned food matrix. Analysis of samples from a canned food matrix spiked with a mixture of equinumerous spores from the thermophiles, Geobacillus stearothermophilus and Geobacillus thermoglucosidans, and the mesophiles, Bacillus sporothermodurans, Bacillus cereus, and Bacillus subtilis, led to the detection of these spores with an average limit of 2 × 102 spores ml−1. The data were normalized by setting the number of sequences resulting from DNA of an inactivated bacterial species, present in the matrix at the same concentration in all samples, to a fixed value for quantitative sample-to-sample comparisons. The 16S rRNA amplicon sequencing method was also employed to monitor population dynamics in a ready-to-eat rice meal, incubated over a period of 12 days at 7 °C. The most predominant outgrowth was observed by the genera Leuconostoc, Bacillus, and Paenibacillus. Analysis of meals pre-treated with weak acids showed inhibition of outgrowth of these three genera. The specificity of the amplicon synthesis was improved by the design of oligonucleotides that minimize the amplification of 16S rRNA genes from chloroplasts originating from plant-based material present in the food.
This study shows that the composition of complex spoilage populations, including bacterial spores, can be monitored in complex food matrices by bar-coded amplicon sequencing in a quantitative manner. In order to allow sample-to-sample comparisons, normalizations based on background DNA are described. This method offers a solution for the identification and quantification of spoilage microbiota, which cannot be cultivated under standard laboratory conditions. The study indicates variable detection limits among species of bacterial spores resulting from differences in DNA extraction efficiencies.
KeywordsSpoilage microbiota Lactic acid bacteria Bacterial spores Amplicon sequencing DNA extraction Quantification
Microbial food spoilage results from metabolic processes that lead to the production of off-smelling flavors or textural changes and renders food unacceptable for human consumption. It is by far the most common cause for food losses. It has been estimated that 25 % of all foods produced globally is lost due to microbial spoilage, see [1, 2] and references herein. In this study, we applied the 16S rRNA amplicon pyrosequencing method for the evaluation of microbial spoilage in complex foods, including a ready-to-eat (RTE) meal as well as processed canned food. These are very different in nature with regard to the spoilage process. In the first case, outgrowth of spoilage microorganisms is limited by refrigeration and preservatives, and in the second case, heat processing during manufacturing limits the spoilage problem to outgrowth of bacterial spores that are able to survive the heat regimes applied.
Characterization and enumeration of microbial species on nutrient agar plates is still the standard method to evaluate the cause of microbial spoilage and to find clues for the design of preservation strategies. However, typing and enumeration of strains or communities of species by classic cultivation methods is laborious, time-consuming, and biased by selective germination and outgrowth conditions on nutrient agar plates [3, 4]. Microbial spoilage can be regarded as a complex ecological process, which can involve the presence of multiple species with specific niches and metabolic dependencies; this may be easily overlooked in case of cultivation on nutrient agar plates with a relatively rich and homogenous environment, where a single or a small number of microbial species easily dominate .
A number of cultivation-independent methods have been developed that identify the most abundant microbial species in the spoilage population at the time of sampling by isolation and characterization of their DNA molecules. However, these methods are not suited for the quantification of the species in a population. Until recently, most of these cultivation-independent studies on typing of bacterial populations were based on PCR-DGGE  and microarray technology [6–8]. With the arrival of next-generation sequencing methods, such as pyrosequencing of bar-coded 16S rRNA amplicons [9, 10], it is now feasible to analyze microbial populations in multiple samples in parallel up to the genus and even the species level. This methodology has been applied in a number of cases to characterize spoilage microbiota [11, 12], as reviewed recently by Danilo Ercolini . With the further decrease of DNA sequencing costs, this appears a promising method for future microbiota analyses in complex foods.
The aims linked to the bar-coded 16S rRNA amplicon sequencing for evaluation of spoilage microbiota included methodology development for (i) reproducible and efficient extraction methodology DNA from complex food matrices and (ii) sample-to-sample comparisons of microbial compositions by means of normalization based on background or spiked DNA. In addition, we aim to monitor and interpret differences of amplicon read counts and colony-forming unit (CFU) counts by application of both analyses to the same samples.
In this study, we addressed these challenges associated with bar-coded 16S rRNA amplicon sequencing applied to two types of food matrices. The first part of the study was aimed at establishing the limit of bar-coded amplicon sequencing for detection of bacterial spores and their quantification in a processed canned food matrix. The population composition after incubation at moderate and high temperatures was investigated, in order to observe specific outgrowth of spores from selected mesophilic Bacillus and thermophilic Geobacillus species. In the second part of the study, bacterial outgrowth of the spoilage microbiota was analyzed in a ready-to-eat meal stored at 7 °C in the absence and presence of weak organic acids, which are commonly used food preservatives (reviewed in ). Limitations of this cultivation-independent methodology and differences in the outcome of CFU enumeration have been evaluated by application of both methods to the same samples. This study shows that bar-coded amplicon sequencing can be applied in a quantitative manner at low detection limit in food matrices.
Detection of spores in a canned food matrix by colony enumeration
Filtering of sequence reads and normalization
After DNA extraction from 180 samples, 16S rRNA amplicons were obtained and sequenced by bar-coded amplicon sequencing using the Roche 454 platform, leading to an average of 6171 ± 3367 (SD) raw sequences per sample. A total of 15 samples gave insufficient reads (<1000) and were discarded in further analysis. Processing with the Mothur pipeline yielded 6203 ± 2980 (SD) reads for the canned food or spike samples and 4091 ± 1364 (SD) reads for the RTE rice meal samples. After assigning operational taxonomic units (OTUs), the varying total sequences of the ready-to-eat meal were normalized by setting the total number of sequences for each sample to 10,000 reads. More details regarding the processing of the sequence data have been provided in Additional file 1.
Detection of bacterial spores in a canned food matrix by amplicon sequencing
Sequence analysis of the creamy mushroom soup without inoculum shows the total absence of sequences belonging to four of the five species of the spike (Fig. 2a). The majority of the sequences detected in the canned food did however belong to OTU 1, which was also observed for B. subtilis A163. Since no detectable CFUs were observed for the canned food, this indicated the presence of inactivated spores or cells of B. subtilis A163—or a closely related strain—in the canned food without inoculum. Note that also other bacterial species were observed, which did not correspond to the spike species, in the canned food, but in much lower numbers than OTU 1 (Additional file 2). One example is Aeromonas encheleia (Fig. 2a), which was used in later analysis for normalization purposes.
Amplicon sequence analysis of the inoculated canned food samples that were incubated overnight at 37 or 55 °C confirmed the results of the CFU counts of these samples (cf. Figs. 1 and 2a). After incubation at 37 °C, the read population was dominated by OTU 2 belonging to one of the three initially spiked mesophilic species, the mesophilic spoiler B. cereus, whereas after o/n incubation at 55 °C, OTUs of both thermophilic species (G. stearothermophilus and G. thermoglucosidans) present in the spike, dominated the detected reads (Fig. 2a).
Detection limit for sequence-based evaluation of bacterial spores
In order to determine the detection limit of bar-coded amplicon sequencing in a model food matrix, the serial dilutions of the spike added to canned food used for determining the CFU counts (Fig. 1) were analyzed by 16S rRNA amplicon sequencing. Normalization of the number of sequence reads was done according to a species present in low amounts in the canned food, in this instance A. encheleia (Fig. 2a).
Correlation and detection limit of mass seq read counts with spore counts
Spore spike strain
y = ax + b
Regression coefficient (R 2)
Det. limit x = (y−b)/a (10log(sp/sample) at y = 1 read
G. stearothermophilus ATCC7953
y = 0.644x − 0.5384
G. thermoglucosidans TNO-09.020
y = 0.7464x − 0.3915
G. thermoglucosidans TNO-09.020
y = 0.7222x − 0.5543
B. sporothermodurans IC4
y = 0.9669x − 1.9271
B. cereus TNO-02.0143
y = 0.9239x − 2.5864
B. subtilis A163
y = 1.095x − 2.9748
B. subtilis A163 (canned food and spike)
y = 0.011x + 3.8187
Canned food without an inoculum is dominated by sequence reads belonging to OTU 1. When the spore spike is added (a total of 5 × 106 spores), the number of OTU 1 reads is lower (Fig. 2a) indicating a lower relative abundance of the background flora in the spiked canned food in comparison to the non-spiked canned food. The inoculated canned food samples that have been incubated o/n at 37 or 55 °C also show strongly reduced numbers of sequence reads for OTU 1. Due to a similar dilution effect, the number of reads for OTU 8 (A. encheleia) is below detectable levels in the samples that have been incubated o/n at 37 or 55 °C.
Bacterial outgrowth in a ready-to-eat food matrix by amplicon sequencing
In the untreated samples, a shift in the read numbers was observed indicating bacterial activity over the 12-day incubation period at 7 °C. The first genus showing an increase in relative abundance (from t06 until t08) was Leuconostoc (Fig. 4a). From t08 on, sequences of the genera Bacillus and in particular Paenibacillus increased in relative abundance, while Leuconostoc read numbers decreased at t10 and partly at t12 (Fig. 4a, t10 and t12). With the relative increase of the abundance of the sequences of the genera Paenibacillus, Bacillus, and Leuconostoc, a general decline in relative abundance of the Streptophyta and Pseudomonas sequences is observed (Fig. 4a, t10 and t12). In one sample at t12, however, the number of Pseudomonas reads was high, suggesting that in this particular sample, Pseudomonas actually did grow.
In contrast to the population dynamics observed in the untreated samples, in the sorbate-treated samples, only one genus clearly increased in relative abundance over time: Leuconostoc (Fig. 4b). Numbers of reads belonging to the genera Bacillus and Paenibacillus did not increase during the incubation, indicating sensitivity of these genera to sorbate, in line with previous observations (see e.g., ). In contrast to the untreated and sorbate-treated samples, the propionate-, lactate-, or acetate-treated samples did not show a clear shift in OTU distribution (Fig. 4c), corresponding to the observed lack of outgrowth in these samples (Additional file 4). A minor increase in read numbers was observed for the genus Streptococcus in the lactate-treated samples and to an even lesser extent also in the acetate-treated samples.
Optimization of amplicon sequencing for food matrices with vegetables (chloroplasts)
In order to minimize the influence of chloroplast sequences from vegetables in complex food matrices, a new reverse oligo was designed. The 16S rRNA sequences of common food spoilage bacteria were aligned against a set of various 16S rRNA sequences from chloroplasts from Streptophyta (Arabidopsis, Cucumis, Gossypium, Hordeum, Oryza, Solanum, Spinacia, Triticum, Zea mays). Subsequently, a new reverse oligo was designed (o5958, Additional file 6A), which contained a maximum number of mismatches to the chloroplast sequences, while keeping the highest possible match to common food spoilage bacteria, including members of the phylum Firmicutes (based on RDP Probe Match software (http://rdp.cme.msu.edu/). However, the percentage of identity with most of the other phyla was significantly reduced (Additional file 6B). The forward 16S rRNA amplicon PCR primers used in this study were not modified; they included the forward bar-coded primer(s) o4147-o4382 (Additional file 6A). A clear decrease in the number of Streptophyta sequences was observed in our study with the ready-to-eat food matrix, although a complete exclusion of Streptophyta sequences was not achieved (Additional file 6C).
The aim of this study was to optimize the use of amplicon sequencing as a method for determining spoilage organisms in complex food matrices. Canned food and a RTE meal were chosen as model food matrices as they represent two different relevant food matrices and were suitable for studying different aspects important in food spoilage: the detection limit of amplicon sequencing as detection method for bacterial spore formers in a complex food matrix as well as the possible use of a spikes in order to quantify the detection method (canned food) or the use of amplicon sequencing in following the dynamics of food spoilage at low temperatures caused by spoilage organisms collected during the production process in the presence and absence of commonly used preservatives (RTE rice meal). The results showed that bar-coded amplicon sequencing using the Roche 454 platform is a sensitive and reliable method for detection and simultaneous identification of spoilage organisms, suitable for following population dynamics in time. Moreover, we have described a sensitive normalization procedure utilizing endogenous low-abundant sequences present in the food matrix.
Normalization of sequence read numbers
An important aspect in quantitative analysis is normalization of the data. In the described RTE rice meal experiment, where relative levels of microbiota members are described, normalization is less important than in the canned food experiment where absolute quantification of microbiota members was desired. In the canned food experiment, we used an OTU sequence found in canned food without inoculum for normalizing all other sequence results. This 16S rRNA sequence belonged to A. encheleia, a common water contaminant, which was not detected as CFUs on tryptic soy agar (TSA) and had therefore been inactivated during the canned food production process. This normalization step allowed us to calculate the detection limits for the different spiked bacterial spore species, in terms of the minimum number of spores required to identify a spore contamination. Obviously, a further reduction of the detection limit may be achieved by increasing the sequencing depth (number of amplicon reads per sample).
The normalization procedure and the identified correlation between sequence read numbers and CFUs from the same samples allows for quantification of spores on the basis of amplicon read numbers. A prerequisite for this is a significant number of reads of the OTU used for normalization in all samples. The use of an endogenous OTU can be challenging in heavily contaminated samples as high levels of the contaminant dilute the relative abundance of the OTU used for normalization (as observed in this study for spiked soup samples incubated at 37 and 5 °C). Instead of utilizing an intrinsically present sequence for normalization, it is also possible to spike the samples with a defined amount of unique spores or cells or DNA as an internal control. When such a spike is added, it is important to spike the samples before the DNA extraction step as the DNA extraction step is one of the steps which can introduce sample-to-sample differences which are leveled by normalization. The amount of spike should be adjusted to the expected level of contamination, to allow quantification by amplicon sequencing. The spike is preferably of bacterial origin (to be detectable with the same primers) and unrelated to the expected contamination.
Comparison between viable count determination and amplicon sequencing results
Comparisons between sequence abundance and colony-forming units should be taken with great care. Differences between the two methods can result from variable DNA extraction efficiencies among bacterial species and spores, the presence of dead cells, and selective outgrowth of species on nutrient agar plates. However, detailed comparison between the two methods yields interesting information about the importance of these factors. A comparison could be made with respect to the influence of the food matrix present in the can. The CFU count of the spiked spores is affected by the canned food matrix by approximately 1 log factor compared to direct culturing of the spore spike (Fig. 1). The DNA extraction efficiency, however, is not influenced by the canned food matrix (Additional file 7A). After normalization of the sequence data, there are hardly any differences between the number of sequence reads from the spike in the presence or absence of canned food (Additional file 7B).
One explanation for the negative effect of the canned food matrix on the CFU count is that spores bind to food particles and are lost in the purification steps, resulting in an underestimation of the CFU count in the canned food matrix. This explanation is however unlikely since the same samples have been used for the CFU determination and the DNA extractions. Another explanation could be that the canned food matrix is preventing efficient germination of the spiked spores. Since the spores were taken out of the canned food matrix and are left to germinate on the TSA plates, this is also an unlikely explanation. The most likely explanation is that multiple spores attached to a food particle are counted as one CFU, resulting in an underestimation of the CFU count in the canned food matrix.
In the RTE rice meal study, there also appeared a correlation between the increase of CFUs in time (Additional file 4) and the rise in the relative number of sequence reads (Fig. 4a), especially for the well-known spoilage species Leuconostoc, Bacillus, and Paenibacillus. For confirmation, eight morphologically distinct colonies were typed by ribosomal 16S rRNA sequencing, and all identified species were also found in the mass sequencing data (Additional file 8). Quantitative comparisons cannot be made, however, as calibration curves based on absolute CFU numbers (on TSA and de Man, Rogosa and Sharpe Agar (MRSA)) and OTU read numbers are not available for each genus.
Factors influencing the detection limit of 16S rRNA sequencing
The linear correlation between added spores and detected sequence reads after normalization in the canned food experiment (Figs. 2b, 3, and 4b) allowed the calculation of the detection limits for each added species (Fig. 3). The variation in detection limit in the presence of canned food (Figs. 2b and 3) is directly associated with the differences in detection of the species in the absence of canned food (Fig. 2a). Since equal number of spores of the five species were added (determined via spore counting in a Bürker-Türk counting chamber), this reflects differences in the efficiency of detection by sequencing. Such differences can be attributed to differences in DNA extraction efficiency, to variation in rRNA gene copy numbers, or to differences in DNA amplification or to a combination thereof.
In order to distinguish between these possibilities, individual DNA extractions of the five bacterial spore batches were performed, starting with equal numbers of spores (as determined by using a Bürker-Türk counting chamber). The amount of extracted DNA as determined by a universal quantitative PCR  indicated large differences in the DNA extraction efficiency with G. thermoglucosidans being isolated with more than 3 log units (more than 1000-fold) higher efficiency than B. cereus (Additional file 9A).
Amplicon sequence analysis of a mixture of the individually isolated DNAs indicated that the differences in DNA extraction efficiency are also reflected in the number of sequence reads (Additional file 9B). The only exception is B. subtilis which is now detected in numbers similar to B. sporothermodurans and G. stearothermophilus (Additional file 9B), whereas the DNA extraction appeared ~2 log units less efficient (Additional file 9A).
Amplicon sequencing of a mixture from the individually isolated DNAs, in which the amount of DNA for each species was equalized based on the quantitative PCR (qPCR) results (Additional file 9A) indicated that on the basis of quantitative PCR, it is possible to normalize the number of sequence reads for each species (Additional file 7). Only B. cereus appears still slightly underrepresented, but the ~2.5 log differences between G. thermoglucosidans and B. cereus had been reduced to maximally 1 log. Together, these data indicate that differences in DNA extraction efficiency are the most important cause for the different representation of the used bacterial species when mixed in equal numbers. Although spores have been counted under the microscope prior to the experiment, it is possible that B. cereus spores are recovered less efficient due to their relatively high hydrophobicity. In addition, variations in the spore maturation, spore core water content, and the number and nature of DNA-binding proteins may result in differences in DNA extraction efficiency. Therefore, it will be very difficult to develop a suitable DNA extraction with a comparable efficiency for all bacterial spores. In order to explain the remaining bias in reads in the samples corrected for the amount of extracted DNA (right panel, Additional file 10), we checked the number of copies of 16S rRNA genes per genome. Based on the available complete genomes of bacilli and geobacilli, the average number of 16S rRNA gene copies varies from 8–14 (Additional file 11). Specific information for B. sporothermodurans and G. stearothermophilus is unavailable, but information on the genus level indicates that Bacillus and Geobacillus have a comparable number of 16S rRNA gene copies (Additional file 11). It remains therefore unclear why DNA isolated from B. cereus is not only extracted inefficiently but also leads to a relatively inefficient synthesis of amplicons.
Applicability of 16S rRNA sequencing as method for detection and identification of spoilage organisms
The observed detection limit of 16S rRNA bar-coded amplicon sequencing holds well against other culture-independent (molecular) detection methods such as qPCR  with the advantage that in contrast to qPCR, the method has no specific targets but detects all present spoilage bacteria. The current sensitivity of the method is suitable for early detection of spoilage organisms as well as following population dynamics. However, for detection of extremely low-abundant organisms, e.g., pathogens, the method is less suited, as are all (non-specific) detection methods which do not include specific enrichment for the target species.
In order to improve 16S rRNA sequence-based detection of spoilage bacteria, several options are available. The first is to further minimize the influence of chloroplast sequences by optimizing oligo combinations. Another way for improving the sensitivity of 16S rRNA sequence-based detection method is to increase the number of analyzed sequences. By increasing the sequence read numbers, also lower abundant sequences can be detected. The Illumina technology is capable of producing much higher number of sequences than the method used in this study (pyrosequencing) and could therefore be applied to improve the sensitivity [18, 19]. However, a drawback of the Illumina platform is the reduced read length compared to pyrosequencing (the current study yields ~450-bp amplicons, spanning the V5–V7 region, whereas the most commonly used Illumina amplicon spans the shorter V4 region, ~200 bp .
Evidence for multiple OTUs in one bacterial strain
The finding of the seven OTUs from the spore spike containing spores of all five bacterial species indicated a contamination or the presence of multiple 16S rRNA sequences within at least one species. Alignment of the unique sequences represented by the OTUs indicated that two OTUs were matching with B. subtilis A163 and two OTUs with G. thermoglucosidans TNO-09.020. Evidence for the existence of these two different 16S rRNA sequences was found in the available genome sequences of TNO-09.020  and A163 (Jos Boekhorst, personal communication). Alignment of OTU 1 and OTU 7 with contigs of the genomic sequence of B. subtilis A163 revealed identity of the OTUs with one genomic sequence and a sequence obtained from 16 rRNA sequence typing, respectively (Additional file 12A). Similarly, alignment of OTU 5 and OTU 3 with the genome sequence of G. thermoglucosidans TNO 09.020 revealed at least two different genomic sequences that corresponded to the sequences of the identified OTUs (Additional file 12B). Consequently, a contamination in the spore spike is very unlikely.
The current study assessed the deployment of bar-coded amplicon sequencing for the detection of bacterial spoilage organisms within complex food matrices. In this work, methods were developed and optimized for DNA extraction, amplicon synthesis, and data normalization. Clear evidence for the usefulness of bar-coded amplicon sequencing was obtained, based on the detailed typing of members of the spoilage microbiota and low detection limit of the method (on average 2 × 102 ml−1). Normalization methods allowing sample-to-sample comparisons were applied on the basis of background DNA from an inactivated bacterial water contaminant. A limitation of the method for accurate quantitative determinations is variation in DNA extraction of spores.
Complex food matrices and spoilage conditions
The canned food matrix
Canned creamy mushroom soup (canned food product, purchased in The Netherlands) was used as food matrix for the assessment of bar-coded amplicon sequencing as a feasible method for detection and quantification of bacterial spores. In order to validate the method, a spike of defined bacterial spores was used. Spore crops were purchased for G. stearothermophilus ATCC 7953 (Mesa Laboratories, Denver, CO) or produced according to methods described by Zhao et al.  for B. subtilis A163 , B. sporothermodurans IC4 , B. cereus TNO 02.0143 (TNO food product isolate), and G. thermoglucosidans TNO-09.020 . Spore suspensions were mixed in equivalent amounts based on spore counts, as determined by a hemocytometer according to methods described by Kort et al. . In summary, six randomly selected squares were counted, with a surface area of 0.0025 mm2 and a depth of 0.01 mm each. Spore suspensions containing all five species were added to aliquots of 20 g of creamy mushroom soup in stomacher filter bags (BagFilter S/25, Interscience, France), in tenfold dilutions to final concentrations ranging from 1 × 106 to 1 × 101 spores of each species per ml canned food. After mixing the spores with the canned food, a Pulsifier treatment was performed (1 min in a Pulsifier, LED Techno, Den Bosch, The Netherlands) in order to release the spores or bacteria from the canned food matrix. After passing through the filter of the stomacher bag, the samples were used for determination of CFU counts on TSA plates incubated at 37 or 55 °C, and three samples of each mixture (850 μl, corresponding to 8.5 × 105 to 8.5 × 100 spores each) were taken for total DNA extraction. The outgrowth of added bacterial spores was studied at 37 or 55 °C. Four aliquots (20 g each) of creamy mushroom soup were spiked with the spore mixture until a final concentration of 1 × 106 spores per ml. Two spiked aliquots were incubated o/n at 37 °C and the other two spiked aliquots were incubated o/n at 55 °C (Additional file 13), a starting number of 8.5 × 105 spores of each bacterium) for total DNA extraction.
The ready-to-eat food matrix
The bacterial outgrowth was studied in a ready-to-eat (RTE) meal consisting of fried rice, vegetables, and meat. This meal was purchased in a local supermarket and was packaged in a disposable plastic container, sealed airtight with a plastic cover. The meal consisted of rice (rice, water, 62 %), leek (12 %), pork meat (7 %), ham (pork meat, salt, potato starch, soy protein, aroma, 7 %), egg (7 %), vegetable oil, yeast extracts, salt, and sugar. Several packages of the ready-to-eat rice meal of the same batch were mixed and divided over five portions, with one serving as a control, and the others treated with different organic acids, including 0.3 % propionic acid >99 % (Acros Organics, Belgium), 0.1 % potassium sorbate (Acros Organics, Belgium), 2.5 % acetic acid glacial >99 % (Fisher Scientific, United Kingdom), or 2.5 % Purac FCC 80 (lactic acid; Corbion, The Netherlands). The pH of all five batches was adjusted to 5.5 with HCl, and the batches were then distributed into samples of 15–20 g for each sampling point (see Additional file 14). Each sample was placed into a plastic stomacher filter bag (BagFilter S/25, Interscience, France). The plastic stomacher bags were sealed with a clip and stored at 7 °C until sampling. Every 2 days, two samples were taken from the 7 °C incubator, and three volumes of peptone-physiological salt solution (0.85 % (w/v) NaCl, 0.1 % peptone in demineralized water) were added to each portion, followed by treatment with a stomacher (IUL Masticator, LA-Biosystems, Waalwijk, The Netherlands) for 60 s onto TSA (Oxoid CM0131, 2 days, 37 °C for isolation of all aerobic bacteria) and MRSA (Oxoid CM0361, 2 days, 37 °C under microaerophilic conditions for isolation of lactic acid bacteria) plates.
Based on the observed CFU counts, samples were selected for 16S rRNA gene sequence analysis in order to review the microbial population at that stage. All samples of the untreated and sorbate-treated samples were selected for sequence analysis in duplicate (i.e., from samples 1–2, 3–4, 13–14, 23–24, 33–34, 43–44, 53–54 and 7–8, 17–18,27-28, 37–38, 47–48, 57–58, indicated in bold in Additional file 14, two 300 μl aliquots were analyzed individually). From the propionate-, acetate-, and lactate-treated samples, only time points t = 2 (samples 5–6, 9–10, 11–12) and t = 12 (samples 55–56, 59–60, 61–61) were analyzed in duplicate.
Sample pre-treatment and DNA extraction
Prior to the total DNA extraction, spores were isolated from the canned food samples by adding 150 μl of α-amylase (Sigma Aldrich A7595-250ML 240 l) to each 850-μl sample and subsequent incubation for 6 min at 65 °C, followed by addition of 20 μl proteinase K (15 mg/ml, Sigma P2308). After 2 min of centrifugation in an Eppendorf microcentrifuge, the supernatant was discarded and the pellets were frozen at −20 °C for subsequent DNA extractions. DNA extractions were performed using phenol bead beating in combination with the Agowa Mag mini DNA extraction kit (catalogue 40401, LGC genomics, Berlin, Germany).
To the frozen canned food pellets containing the bacterial spores, a volume of 500 μl phenol, 600 μl zirconium beads, and 500 μl Agowa lysis buffer was added. To each 300-μl RTE meal sample, 600 μl zirconium beads (diameter 0.1 mm, catalogue 11079101z, Biospec Products, Bartlesville, OK), 400 μl lysis buffer (Agowa Mag mini DNA extraction kit), and 300 μl phenol, pH 8.0 (Phenol solution BioUltra, catalogue P4557, Sigma Aldrich, St Louis, MO), were added.
Mechanical disruption of bacterial cells or spores was done by bead beating for 2 min in a mini-beadbeater-8 cell disruptor (Merlin Bio-products, Breda, The Netherlands) at setting fast (homogenize). After bead beating, the samples were cooled on ice prior to a 10 min 10,000 RPM (9300 RCF) centrifugation step. After another phenol extraction step of the aqueous phase, 500 μl of the aqueous phase (corresponding to 0.7 or 1 original volume of the ready-to-eat and canned food samples, respectively) was transferred to a new centrifugation tube prefilled with 1000 μl binding buffer (Agowa) and 20 μl magnetic beads (Agowa). After mixture, the suspension was left for 10 min to allow binding of the chromosomal DNA to the magnetic beads. After washing the beads according to the Agowa Mag mini DNA extraction protocol, the DNA was extracted from the beads with 63 μl elution buffer (Agowa) according to the manufacturer’s instructions. For the canned food samples, this corresponds to DNA from 8.5 × 105 spores.
Bar-coded 16S amplicon sequencing
Quantitative 16S-PCR was performed to determine the relative amount of bacterial template in the isolated DNA samples . Based on this quantification, a maximum of 5 μl of template was used for the generation of a 16S rRNA gene amplicon library spanning variable regions V5–V7 . Sequence analysis of the amplicon library was performed on a 454 GS-FLX-Titanium Sequencer (Life Sciences (Roche), Branford, CT).
Sequence processing and analysis
FASTA-formatted sequences and corresponding quality scores were extracted from the .sff data file generated by the GS-FLX Titanium sequencer using the GS Amplicon software package (Roche, Branford, CT) and processed using modules implemented in the Mothur v. 1.22.2 software platform . Samples yielding insufficient reads (<1000) were excluded in further analysis. The sequences were de-noised using a pseudo-single linkage algorithm with the goal of removing sequences that are likely due to pyrosequencing errors (“pre.cluster” command) . Potentially chimeric sequences were detected and removed using the “chimera.uchime” command . High-quality aligned sequences were classified using the RDP-II naive Bayesian classifier . Aligned 16S rRNA gene sequences were clustered into operational taxonomic units (OTUs) using the average linkage clustering method.
For the study on the ready-to-eat meal, OTUs were defined by 97 % identity (“3 % OTU’s”), and each OTU was classified at tax level 6, resulting in sequence read frequencies for 422 different genera. For the study on the canned food, OTUs were defined by 100 % identity (facilitating comparison of unique sequence reads with the known 16S sequences of the five applied spore isolates), resulting in read frequencies for 2037 OTUs. For both studies the total number of sequence reads per sample was normalized to 10,000 resulting in normalized read frequencies per genus (ready-to-eat meal study) or per OTU (canned food study).
For determination of the detection limit in the canned food experiment, the normalization was performed by using the average number of A. encheleia sequences in the unspiked canned food samples as reference and adjusting all other frequencies of A. encheleia in the spiked samples to this average (assuming a constant distribution of inactivated A. encheleia cells in the single can of canned food that was used, calculations in Additional file 3).
Calculation of detection limits amplicon sequencing in a canned food matrix
Using the above described normalized data for (non-)spiked canned food data (normalized reads/OTU/sample with total reads/sample = 10,000, followed by a second normalization based on A. encheleia reads in (non-)spiked samples), we plotted 10log(reads/OTU/sample) against 10log(spores/sample) for each of the five pairs of OTU/spore-crop and calculated the detection limit (spores/sample) at one read/OTU using linear regression. Samples yielding no reads (at higher spore dilutions) were excluded from the linear regression (Additional file 3). Note that detection limits linearly increase at higher read/OTU levels (e.g., tenfold higher at ten instead of one read/OTU).
Availability of supporting data
The sequence data are available in the European Nucleotide Archive (ENA) under accession number PRJEB7698 (http://www.ebi.ac.uk/ena/data/view/PRJEB7698).
de Man, Rogosa and Sharpe Agar
operational taxonomic unit
ribosomal database project
tryptic soy agar
The authors would like to thank Jordy Coolen (TNO) for the data processing. We would like to acknowledge André van Zuijlen (Unilever) for the advice on food matrices and Erwin Berendsen (TIFN) and Volmar Hatt (TNO) for providing the bacterial spore batches used in this study. The authors thank Michiel Kleerebezem for the skilful management of the TIFN Food Safety and Preservation theme.
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