We developed Growth Rate InDex (GRiD) for estimating in situ growth rates of ultra-low coverage (>0.2×) and de novo-assembled metagenomes. Applying GRiD to human and environmental metagenomic datasets to demonstrate its versatility, we uncovered new associations with previously uncharacterized bacteria whose growth rates were associated with several disease characteristics or environmental interactions. In addition, with GRiD-MG (metagenomic), a high-throughput implementation of GRiD, we estimated growth dynamics of 1756 bacteria species from a healthy skin metagenomic dataset and identified a new Staphylococcus-Corynebacterium antagonism likely mediated by antimicrobial production in the skin. GRiD-MG significantly increases the ability to extract growth rate inferences from complex metagenomic data with minimal input from the user.
Metagenomic shotgun sequencing has emerged as a powerful tool to interrogate the composition and function of complex microbial communities1,2. Yet such characterizations do not reflect the dynamic nature of a complex microbial community in which microbial growth rate can change under different environmental conditions or during disease. Bacterial growth rate measurements can reveal the contributions of viable populations to overall microbial abundance, providing insight into microbes that may be the active contributors to the community phenotype. Moreover, new insights into antagonistic interspecies interactions can be identified by estimating ratios of rapidly growing vs. dead/stationary cells.
Korem and colleagues3 first developed an estimation of bacterial growth rate from metagenomic shotgun data using peak-to-trough ratio (PTR). This is based on the principle that most bacteria harbor a single circular chromosome that is replicated bi-directionally commencing from the origin of replication (ori) to the terminus (ter) region4. Therefore, rapidly dividing cells will have higher read coverage and thus, higher PTR at ori vs. ter (Supplementary Fig. 1A). However, this method relies on a closed circular reference genome and is therefore inadequate for the vast majority of microbial genomes.
A similar approach, iRep5, was recently developed to estimate growth rate using draft genomes. iRep maps metagenomic reads to a draft genome to calculate coverage, then orders the contigs from highest to lowest coverage to approximate a PTR-like distribution in the absence of a complete genome. Very high and very low coverage regions are excluded to reduce noise from strain variation or highly conserved regions. A linear regression model is then used to deduce if a population is replicating. iRep’s key limitation is a requirement for >5× coverage, which on average, represents fewer than 5% of genomes in human microbial communities, such as the skin (Supplementary Fig. 1B).
Finally, both methods rely on identification and mapping of reads to a genome of interest on per-species basis. Given that many microbial communities contain hundreds of species, both PTR and iRep can be burdensome to scale. Moreover, if species of interest are selected based on relative abundance within a community, growth analyses of some biologically relevant microbes may be excluded, no/poor correlation has been observed between relative abundance and growth rate3.
Because of these restrictions, both methods have limited potential for real world metagenomes. Microbial communities vary in biomass, microbial complexity (the diversity of genomes present in an ecosystem), and population composition, with varying numbers of low-abundance bacteria. These factors significantly affect metagenomic assembly and analysis. This is important because improvements in metagenomic binning has made it possible to identify previously uncharacterized microbes from complex microbial communities. However, most of these reconstructed genomes are fragmented and only partially cover the genome. Moreover, complex metagenomes often contain closely related species and strains. Neither approach provide robust error estimates to account for noise or ambiguous read mapping. Being able to accurately and systematically estimate growth dynamics of microbes in a complex community would provide new insights into microbial interactions and disease associations.
Here, we developed Growth Rate Index (GRiD) for the measurement of microbial growth rate from complete/draft genomes and metagenomic bins at ultra-low sequencing coverage (0.2×, which is roughly equivalent to 0.05% relative abundance of a 2.5 Mbp genome from a metagenomic sample of 100 bp x 10 million reads). GRiD can be applied to a specific genome of interest, or can be utilized in a high-throughput mode for which prior knowledge of microbial composition and coverage is not required.
Results and Discussion
Overview of GRiD
GRiD calculates the coverage of all contigs of a reference genome or metagenomic bin in a given sample and sorts them from high to low coverage. The sorted contigs are then reordered to two groups, with the goal of placing an ori-containing contig at or near an arbitrary genome “start” and a ter-containing contig near the mid-region of a genome (Fig. 1a). This approach approximates a synthetic circular genome. Next, like both iRep and PTR, GRiD calculates coverage drops across a sliding 10 Kb window.
GRiD then calculates a “refined” growth value with additional statistical filters to reduce noise. After removing an initial set of outliers, a smoothing curve is fitted by a re-descending M estimator with Tukey’s biweight function6. This enables a local fit that is resistant to noise arising from species heterogeneity. Then, like PTR, GRiD values represent the coverage ratio of the peak and trough of the curve, with higher ratios representing faster growth rates. But because genomes with very low coverage can be prone to noise (which we define as peak and trough means with large residual errors), GRiD refines growth values. Here, GRiD chooses for the peak coverage value the lowest point of expected variation of the mean, while the upper point of variance of the mean is selected for the trough coverage value (Supplementary Fig. 1C). This refinement step markedly increases the reproducibility (i.e., reduced delta values) of growth estimates at ultra-low coverage levels (Supplementary Fig. 1D).
In contrast to both iRep and PTR, GRiD provides as standard output multiple confidence estimates, including confidence intervals by bootstrapping, estimates of error contributed by closely related species and strains in the community, and guidelines for growth rate correction. First, the GRiD algorithm accounts for uncertainty in contig ordering by subsampling mapped reads and re-calculating growth rate to derive a 95% confidence interval of growth estimates. Additionally, because metagenomic bins can be contaminated with contigs from other genomes, which may impact growth predictions in samples with high coverage of the contaminant, we introduced a quality control step using the position of the universal chromosome initiator replication gene (dnaA), and deletion-induced filamentation (dif) sequences (a conserved 28 bp sequence) across the genome, when available. In most bacterial genomes, dnaA is located in close proximity to the ori7 (Supplementary Fig. 1E), while replication typically terminates at/near dif sequences8,9. Therefore, accurate GRiD predictions in rapidly dividing cells should have dnaA and dif coverage similar to those of ori and ter, respectively (Fig. 1a). Finally, GRiD outputs a metric, called “species heterogeneity” which is an estimate of the degree to which closely related species contributes to variance in growth predictions, which would result from reads that are incorrectly assigned to the genome of interest.
GRiD is accurate for draft genomes at ultra-low coverage
We tested our method using pure cultures of Staphylococcus epidermidis (NIHLM023) and Corynebacterium simulans (Wattiau) harvested at different time points during exponential growth (Supplementary Fig. 1F). To calculate GRiD and iRep, we utilized draft sequences of strains of the aforementioned species (S. epidermidis NIHLM023; C. simulans strain 1B08) and asked if initial estimates by both methods can be accurately reproduced when subsampled to ultra-low coverage levels. GRiD was highly reproducible compared to iRep’s low reproducibility (Fig. 1b).
To demonstrate real-world applications enabled by GRiD, we examined S. epidermidis growth rate in a longitudinal skin metagenomic dataset of 698 samples of varying depth and microbial diversity10. We chose S. epidermidis because of its ubiquity yet large relative abundance range in the skin. Moreover, it would provide a difficult scenario for growth rate prediction due to prevalent genetic strain variation11, which would increase noise. First, we benchmarked PTR using a closed reference genome, and then the same genome fragmented into 100kb fragments and reshuffled to mimic a draft genome for GRiD and iRep measurements. Reads mapping to S. epidermidis were subsampled to 0.4× and 0.2× coverage and subsequently used for GRiD and iRep estimates. iRep performed similarly to the PTR benchmark, but GRiD had a much lower percentage of error in comparison to iRep at both 0.4× and 0.2× coverage (Fig. 1c). To highlight the importance of accounting for ambiguous reads during growth estimation, reads mapping to S. epidermidis were re-mapped to S. capitis, S. aureus, and Propionibacterium acnes genomes to determine the proportion of multiple-mapping reads. Samples with increasing numbers of multi-mapped, ambiguous reads were significantly correlated with our metric of increasing species heterogeneity (Fig. 1d), which can increase uncertainty in growth rate estimation. For quality control, we found that a combination of dnaA coverage, dif coverage, and species heterogeneity can be used to ascertain the accuracy of growth predictions. Our findings suggest that growth rates are most accurate when dnaA/ori and ter/dif coverage ratios approach one, and species heterogeneity is low (<0.3, Supplementary Fig. 2A). Finally, we demonstrated that GRiD is effective even with highly fragmented genome/metagenomic bins – at 0.2× coverage, we found that GRiD requires ≤90 fragments/Mbp. At 1× coverage, GRiD is accurate even with >200 fragments/Mbp and 50% genome completeness (Supplementary Fig. 2B and C).
To demonstrate its versatility, we also benchmarked GRiD using uncultivated Candidate Phyla Radiation (CPR) genomes recovered from an environmental groundwater dataset5. CPR is a major subdivision within the domain Bacteria, and is characterized by small cells and genomes suggested to be symbionts5. Growth estimates using GRiD and iRep indicated these genomes are generally slow-growing (i.e., ori/ter < 1.5, Fig. 1e). GRiD and iRep values were uncorrelated. However, when we subsampled mapped reads to mimic ultra-low coverage, GRiD values were reproducible whereas iRep was not (Fig. 1e), underscoring iRep’s decreased performance as a function of coverage.
GRiD uncovers new biology from metagenomic datasets
We next investigated GRiD’s ability to provide new biological insights from metagenomic data by calculating growth dynamics of rare uncharacterized skin microbes reconstructed de novo from a large metagenomic dataset. We assembled reads, grouping contigs into “bins” approximating genomes based on co-abundance clustering and nucleotide composition12 (Supplementary Fig. 4). Using high quality bins (see Methods for criteria), we defined a genome bin as rare if it was present in fewer than 3% of samples. Three bins that could not be annotated to the species level met this threshold (bin.443, bin.481, and bin.257; Fig. 2a). These putative microbes were only present in a few individuals and had relatively stable growth rates over time despite fluctuations in relative abundance. Surprisingly, bin.257 appeared to stably colonize the toenail of one individual as indicated by increasing relative abundance over time while maintaining a constant growth rate (Fig. 2a). We noted that despite the low coverage (1.68×) and high fragmentation (415 contigs, median size = 5.5 Kb) of bin.443, GRiD contig reordering accurately positioned dnaA and dif sequences near the peak and trough regions respectively (Fig. 2a).
We further applied GRiD to a skin metagenomic dataset of individuals with psoriasis13, a long-lasting autoimmune disease characterized by patches of abnormal skin14, to see if GRiD could identify rapidly growing microbes or antagonistic interactions that could be associated with the disease state. Using draft genomes, the growth rate of three microbes differed between disease and unaffected sites (Fig. 2b). Strikingly, we found previously unidentified associations between microbial growth rate and patient characteristics (Fig. 2c and Supplementary Fig. 3A). For instance, Corynebacterium pseudogenitalium had higher average growth rates in male patients compared to females (Fig. 2c), in agreement with previous reports suggesting gender-specificity of some Corynebacterium species15. Inter-individual comparisons indicated that some microbes grew more rapidly in individuals with increased disease severity—Psoriasis Area Severity Index (PASI) and Body Surface Area (BSA)—were correlated with Staphylococcus auricularis growth, and longer disease duration with Acinetobacter ursingii (Fig. 2c and Supplementary Fig. 3A). These represent significant new biological insights that underscore the importance of the GRiD approach, as no associations were previously observed between microbial relative abundance and patient characteristics13.
Finally, we measured growth dynamics of uncharacterized Bdellovibrio species reconstructed from different environmental samples16. Bdellovibrio species are predators of Gram-negative bacteria and grow within the periplasmic space of their host17 (Fig. 2d). Although, we identified Bdellovibrio as generally slow-growing (consistent for endosymbionts, Supplementary Fig. 3B), certain microbes with very high GRiD values were identified in some samples (Fig. 2d). Such high GRiD values would be expected for fast growing microbes employing multi-fork replication. Notably, this is the first observation of a potential multi-fork replication in an endosymbiont. GRiD also corroborated known biology, identifying a negative correlation between Bdellovibrio growth and relative abundance of Gram-negative bacteria (Fig. 2d). Interestingly, Bdellovibrio growth was not correlated with abundance of Gram-positive bacteria, suggesting that microbial competition in non-human environmental communities is mainly restricted to Gram-negatives and Fungi (Fig. 2d).
High-throughput estimation of bacterial growth
Having benchmarked our algorithm with diverse human and environmental datasets, we noted the significant value that could be derived from a systematic investigation of growth rate within a microbial community. Thus, we expanded GRiD’s utility as a high-throughput and systematic metagenomic (MG) analysis tool (GRiD-MG). In this case, growth rate can be estimated for most identified bacteria in a given sample passing coverage thresholds, without a requirement for prior knowledge of microbial composition or abundance. GRiD-MG maps samples from a dataset to a GRiD-MG database comprising of 32,819 representative bacterial species (Fig. 3a). The GRiD-MG database can be readily updated using metagenomic bins or custom genome sequences. Depending on user preferences, reads mapping to multiple genomes are re-assigned using Pathoscope 2.018 and genomes with coverage values below the user-defined threshold are discarded (Fig. 3a). To ensure that growth estimates using GRiD-MG were concordant with results obtained using individual reference genomes, we synthesized mock reads for five genomes with varying coverage to mimic growing bacteria and calculated growth rate. Growth estimates were highly concordant in both cases (Fig. 3b).
We next applied GRiD-MG to our 698-sample metagenomic skin dataset and sought to identify potential antagonistic associations within the community. These samples were obtained from several body sites broadly classified based on skin site morphology as either dry, moist, oily, or foot sites10. Interestingly, growth antagonism was observed among several microbes that were site specific (Fig. 3c, Supplementary Fig. 3C – E). Notably, in foot sites, growth rates of Staphylococcus capitis and Staphylococcus pasteuri were antagonistic to several Corynebacterium species, and the observed antagonism was a likely scenario of competitive exclusion (Fig. 3c).
While S. capitis has previously been identified as a producer of antimicrobials capable of inhibiting numerous Gram-positive bacteria19, there is little information on S. pasteuri. We therefore hypothesized that S. pasteuri may produce antimicrobials to provide a competitive growth advantage within the skin community. We first screened all publicly available sequences of S. pasteuri strains for the presence of antimicrobial biosynthetic gene clusters (BGC) and identified two strains harboring a lantipeptide BGC (Fig. 3d). We then analyzed the presence of this BGC across all foot sites and found that its abundance was positively correlated with S. pasteuri growth, suggesting that its viability in foot sites is strongly dependent on antimicrobial production (Fig. 3e). Similarly, the occurrence of the lantipeptide BGC was also consistent with a putative inhibition of Corynebacterium (Fig. 3e). These data underscore the ability of GRiD-MG to uncover new associations and hypotheses based on large-scale analyses of growth rate dynamics within a microbial community.
In summary, GRiD and GRiD-MG provide a significant advance in their ability to systematically estimate bacterial growth rate using metagenomic data. GRiD is highly effective even at ultra-low sequencing coverage, making it particularly applicable to complex metagenomic datasets with draft quality and de novo assembled, uncultivated bacteria. However, it is important to note that the performance of many algorithms for metagenomic analyses can vary based on different input parameters. For example, using different assemblers or reference genomes with varying degrees of fragmentation with GRiD, iRep, or PTR can affect growth rate inferences. Therefore, best practice remains to broadly survey different predictions to avoid misrepresentations of the underlying biology. Here, we particularly recommend, where possible, to utilize a reference strain with the least fragmentation. Correspondingly, we constructed our default GRiD-MG database using the most complete set of representative strains as possible. This also supports GRiD’s particular attention to robustness and accuracy, as it provides multiple statistical estimates to minimize erroneous estimations due to noise that may arise from misassemblies in reconstructed genome bins or significant genetic strain variation that may be present in a sample. Finally, by examining growth rates in high-throughput, new associations between bacterial growth dynamics can be inferred, either in interspecies interactions or in new associations with, for example, host characteristics.
GRiD measures the growth rate of uncharacterized bacteria or bacteria with draft quality genomes from metegenomic samples. GRiD is designed for use with a specific reference genome, or in a high-throughput manner for multiplex analysis of identified bacterial population present within a sample.
The GRiD algorithm is based on the principle that most bacteria harbor a circular chromosome that is replicated bi-directionally from the origin of replication (ori) to the terminus (ter) region4. Therefore, a rapidly dividing bacterium at any given time will have more copies of DNA close to the ori in comparison to the ter.
Reads from a metagenomic sample are first mapped to a given genome (including metagenomic bins or draft genome) and the mean coverage of each contig is calculated and contigs are sorted from high-to-low coverage. The sorted coverage information is then sequentially distributed alternatively between two temporary files, with one of the files re-sorted from low-to-high coverage (Fig. 1a). Both temporary files are then merged to produce a coverage pattern with high coverage contigs at both extremes, while low coverage contigs located mid-region. Using this sorted reordering, contigs are concatenated and coverage across each nucleotide is derived. GRiD then calculates coverage drops across a 10 Kb window and outlier points (i.e. values below Q1 – (1.5 × IQR) and above Q3 + (1.5 ×IQR); where Q1 and Q3 are the first and third quartiles, respectively, while IQR is the interquartile range) are excluded. A smoothing curve is then fitted by a re-descending M estimator with Tukey’s biweight function6. This enables the fit to be resistant to noise arising from species heterogeneity and low coverage. GRiD values represent the coverage ratio of the peak and trough of the curve, in which case, GRiD values are directly proportional to growth rate.
Generally, coverage information derived from a sample containing multiple diverse strains can be prone to noise, which will invariably have an impact on accurate growth estimates. In other words, core regions of genomes will have unusually high coverage compared to accessory regions. Similarly, microbes present at ultra-low coverage can be prone to noise due to a wider coverage distribution resulting from contigs with an average coverage of zero. To circumvent these limitations, GRiD incorporates a refinement step. Here, for the peak coverage value, the lowest point of expected variation of the mean value is chosen. Likewise, the upper point of variance of the trough mean is selected for the trough value (Supplementary Fig. 1C). The resulting growth value is called “GRiD_refined”. This refinement step markedly improves the reproducibility of GRiD predictions (Supplementary Fig. 1D). Additionally, to account for uncertainty arising from contig reordering, GRiD performs a subsampling step twice by randomly extracting 85% of reads that mapped to a genome. GRiD then calculates and outputs a 95% confidence interval from all three growth values (i.e., including GRiD_refined). Finally, ambiguous reads (i.e., reads mapping to multiple genomes) can result in erroneous estimates. GRiD outputs a metric called “species heterogeneity” which measures the contribution of ambiguous reads to growth estimate. Here, species heterogeneity = (1 – r/u), where r = GRiD_refined, and u = GRiD_unrefined (i.e., growth rate calculated directly from the means of the peak and trough).
Additionally, since metagenomic bins can be contaminated with contigs from other genomes, which may impact growth predictions especially in samples where contaminating contigs contain high coverage, GRiD estimates can be quality-checked, whenever possible, using the coverage information of chromosome initiator replication gene (dnaA) and deletion-induced filamentation (dif) sequences across the genome. dnaA is usually located close to the ori (Supplementary Fig. 1E), whereas replication terminates at or near dif sequences7,8,9. Therefore, in rapidly dividing cells, the coverage values for the peak and dnaA should be similar. Likewise, the coverage values for dif and ter should be identical. GRiD output includes both dnaA/ori and ter/dif ratios. Growth rate estimates are most likely accurate when dnaA/ori and ter/dif coverage ratios approach one, and species heterogeneity is low (<0.3) (Supplementary Fig. 2A). Altogether, GRiD outputs seven values for every sample; (i) GRiD refined, (ii) 95% confidence interval, (iii) GRiD unrefined, (iv) species heterogeneity, (v) coverage, (vi) dnaA/ori ratio, and (vii) ter/dif ratio.
For multiplex screening of the identified bacterial population in a given sample, GRiD-MG maps metagenomics reads to a custom GRiD-MG database consisting of 32,819 bacterial genomes (Fig. 3a). This database contains one representative genome per specie. In additional, the GRiD-MG database can be easily updated using metagenomic bins or newly sequenced genomes. Depending on user preferences, reads mapping to multiple genomes are reassigned using Pathoscope 2.018 and the extent to which reads are reassigned is defined using the “theta-prior” option. In addition, a user can specify a coverage cutoff greater than 0.2× in which case, genomes with coverage below the cutoff are discarded. For coverage cutoff <1×, only genomes with 90 fragments/Mbp or less are included in the analysis since increased fragmentation results in inaccurate results at ultra-low coverage (Supplementary Figure 2B). We included additional stringency to the algorithm to reduce the likelihood of outputting false growth estimates. First, upon coverage calculation using a 10kb window as described above, genomes with coverage medians <0.15 are considered as non-replicating. Second, GRiD values greater than 10 are discarded as this may be due to a high coverage of a contaminant contig present in a metagenomic bin or genome in a given sample. Third, GRiD values greater than 3 for genomes with sizes less than 4 Mb are discarded. This is because GRiD values greater than 2 indicate the presence of multi-fork replication machinery which has mostly been identified in genomes with sizes >4Mb20,21,22. Two output files are generated per sample; a text file of genomes and their respective GRiD scores, and a pdf file displaying heatmap of growth values with hierarchical clustering (Fig. 3a). Text output for all samples can be merged into a single matrix file.
dnaA and dif database
To determine the coverage of dnaA and dif sequences, we built a database comprising of 217 bacterial dnaA sequences that were obtained from NCBI, and 714 dif sequences retrieved from the Database of Bacterial Replication Terminus (http://www.g-language.org/data/repter/db.html). We then searched for homologs within a bin or genome using BLAST23 (-evalue 0.05) and the topmost hit was selected.
GRiD and iRep growth calculation from in vitro S. epidermidis and C. simulans
S. epidermidis (NIHLM023) and C. simulans (Wattiau) were grown in Tryptic Soy Broth at 37 °C. During cultivation, samples were harvested at five different time points between early and mid-exponential growth phase for DNA extraction and whole genome sequencing. We calculated GRiD and iRep using draft genomes of S. epidermidis (NIHLM023; 87 contigs) and C. simulans (strain 1B08; 66 contigs).
GRiD and iRep growth calculation for CPR genomes
We retrieved previously reported iRep data calculated from 12 samples using 99 CPR genomes5. However, we restricted GRiD analysis to bacteria with draft genomes.
Metagenomic binning of skin dataset
We retrieved 698 metagenomic shotgun skin samples from our previous work10. Some samples (n = 594) in this dataset were derived from longitudinal sampling of 12 individuals at three different time points with sampling intervals of 10–30 months between time points 1 and 2 (T1 vs T2), and 5–10 weeks between time points 2 and 3 (T2 vs T3). We began by concatenating all samples and assembling sequence reads into contigs and scaffolds using MEGAHIT24. We initially chose MEGAHIT due to its capability for handling large data, low memory requirements, and short run time. We discarded contigs shorter than 1 kb, mapped each individual sample back to the contigs catalogue using bowtie225, and extracted unmapped reads (Supplementary Fig. 4). Next, we concatenated unmapped reads and re-assembled using SPAdes (--meta)26. We chose SPAdes due to its ability to produce scaffolds from contigs. The newly extracted contigs/scaffolds were merged with the previous catalogue. We grouped our contigs/scaffolds into genome bins using MetaBAT (--sensitive, -m 1500)12, which resulted in 556 bins, and subsequently utilized MEGAN27 for taxonomic identification of contigs/scaffolds present within each bin. We excluded 22 bins that were of non-microbial origin and further evaluated the quality of each bin and marker lineage using CheckM28. For stringent annotation, we required that ≥65% of contigs/scaffolds present in a bin are assigned to the lowest level taxonomy; the sole exception being the kingdom-level taxonomy where our requirement was 40%.
Determining the effect of genome fragmentation and completeness on GRiD
We selected 12 bacteria bins (≥95% completeness and ≤5% contamination) with varying degree of fragmentation ranging from 55 to 202 fragments/Mbp to determine the role of fragmentation on GRiD scores. For each bin, we used the sample producing the highest bin coverage. Reads mapping to each bin was subsampled to 0.2×, 0.4×, and 1× coverage for GRiD analysis. We concluded that bins with 90 or more fragments/Mbp are unsuitable for GRiD analysis at coverage levels below 1× (Supplementary Fig. 2B).
We used a bin having 89 fragments/Mbp, which was at the boundary for our accuracy cutoff at ultra-low coverage, to evaluate the impact of genome completeness on GRiD output. We subsampled contigs within each bin to attain the desired level of completeness prior to GRiD analysis. This subsampling step was repeated 10 times.
GRiD estimate of rare bacteria
We chose only high-quality bins (i.e., ≥75% completeness and ≤5% contamination based on single copy marker genes) for analysis. We defined a bin as rare if it was present in fewer than 3% of samples. Three bins (bins 257, 443, 481) met this threshold and were considered uncharacterized since they were unable to be annotated to the species level using either our 65% cutoff as mentioned above, or single copy marker gene lineage using CheckM28. Since these bins had >90 fragments/Mbp, we calculated GRiD in samples having bin coverage ≥1×.
GRiD calculations from psoriasis skin dataset
We retrieved 73 metagenomic samples from Tett et al.13, which was a collection of skin samples from individuals with psoriasis. We obtained the species composition using Pathoscope 2.018 and selected only species that were present in at least five samples (n = 35).
GRiD estimate of Bdellovibrio species
From a previous genome construction effort using >1500 samples16, we retrieved samples where species of Bdellovibrio were reconstructed (n = 22). Of these, 15 samples were from marine environments, 3 from sludge, 2 from freshwater, and 1 each from groundwater and hydrocarbon environment. We calculated a total of 134 replication rates from these environments. We used Pathoscope 2.018 to determine the relative abundance of microbes.
Generation of mock reads for GRiD-MG
We generated mock read for Lactobacillus gasseri, Parabacteroides distasonis, Staphylococcus aureus, Staphylococcus epidermidis, and Campylobacter upsaliensis using wgsim package implemented in samtools29. Each genome was split into 100kb fragments and varying amount of reads was generated for each fragment in order to achieve differential coverage across the genome, and thus, mimic a replicating genome.
Growth antagonism of skin bacteria
We applied GRiD-MG to 698 metagenomic skin dataset collected from different skin sites. These samples were earlier classified into four groups based on their site characteristics as either dry, moist, oily, or foot sites10. We subsampled 1 million reads for samples containing over a million reads. We used a coverage cutoff of 0.2× thereby discarding growth rate for genomes having <90 fragments/Mbp. We also did not utilize the Pathoscope reads reassignment option. This resulted in growth estimates for 1,756 bacterial species. For each site, correlation analyses were conducted for genomes present in >40% of samples. We identified biosynthetic gene clusters in Staphylococcus pasteuri strains using antiSMASH30
The GRiD algorithm is available at https://github.com/ohlab/GRiD.
Sequence reads generated for S. epidermidis and C. simulans in vitro growth analyses have been deposited in SRA with accession/identification number SRP151711. The accession numbers are available from NCBI for longitudinal skin dataset (BioProject PRJNA46333), groundwater filtrates (BioProject PRJNA268031), and psoriasis patients (BioProject PRJNA281366). For Bdellovibrio (BioProject PRJNA348753) analysis, the following Sequence Reads Archive accessions were used; SRR948155, SRR948284, SRR2043728, SRR636581, ERR599000, ERR594331, ERR594318, ERR599136, ERR599142, ERR594299, ERR594326, ERR594335, ERR599038, ERR599044, ERR594348, ERR594349, ERR594311, ERR594294, ERR594308, SRR1506988, SRR1506983, SRR1506986. CPR genomes (BioProject PRJNA273161) are available from NCBI GenBank. A reporting summary for this Article is available as a Supplementary Information file. The source data underlying Fig. 1–3, and Supplementary Figs 1–3 are provided as a Source Data file. All relevant data are available upon request.
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Nielsen, H. B. et al. Identification and assembly of genomes and genetic elements in complex metagenomic samples without using reference genomes. Nat. Biotechnol. 32, 822–828 (2014).
Tsai, Y. C. et al. Resolving the complexity of human skin metagenomes using single-molecule sequencing. mBio 7, e01948–01915 (2016).
Korem, T. et al. Growth dynamics of gut microbiota in health and disease inferred from single metagenomic samples. Science 349, 1101–1106 (2015).
Wang, J. D. & Levin, P. A. Metabolism, cell growth and the bacterial cell cycle. Nat. Rev. Microbiol. 7, 822–827 (2009).
Brown, C. T., M. Olm, M. R., Thomas, B. C. & Banfield, J. F. Measurement of bacterial replication rates in microbial communities. Nat. Biotechnol. 34, 1256–1263 (2016).
Kafadar, K. The efficiency of the biweight as a robust estimator of location. J. Res Natl. Bur. Stand. 88, 105–116 (1983).
Mackiewicz, P., Zakrzewska-Czerwińska, J., Zawilak, A., Dudek, M. R. & Cebrat, S. Where does bacterial replication start? Rules for predicting the oriC region. Nucleic Acids Res. 32, 3781–3791 (2004).
Hendrickson, H. & Lawrence, J. G. Mutational bias suggests that replication termination occurs near the dif site, not at Ter sites. Mol. Microbiol. 64, 42–56 (2007).
Kono, N., Arakawa, K. & Tomita, M. Comprehensive prediction of chromosome dimer resolution sites in bacterial genomes. BMC Genom. 12, 19 (2011).
Oh, J. et al. Temporal stability of the human skin microbiome. Cell 165, 854–866 (2016).
Conlan, S. et al. Staphylococcus epidermidis pan-genome sequence analysis reveals diversity of skin commensal and hospital infection-associated isolates. Genome Biol. 13, R64 (2012).
Kang, D. D., Froula, J., Egan, R. & Wang, Z. MetaBAT, an efficient tool for accurately reconstructing single genomes from complex microbial communities. PeerJ 3, e1165 (2015).
Tett, A. et al. Unexplored diversity and strain-level structure of the skin microbiome associated with psoriasis. NPJ Biofilms Micro. 3, 14 (2017).
Parisi, R., Symmons, D. P., Griffiths, C. E. & Ashcroft, D. M. Global epidemiology of psoriasis: a systematic review of incidence and prevalence. J. Invest. Dermatol. 133, 377–385 (2013).
Belmares, J., Detterline, S., Pak, J. B. & Parada, J. P. Corynebacterium endocarditis species-specific risk factors and outcomes. BMC Infect. Dis. 7, 4 (2007).
Parks, D. H. et al. Recovery of nearly 8,000 metagenome-assembled genomes substantially expands the tree of life. Nat. Microbiol. 2, 1533 (2017).
Harini, K., Ajila, V. & Hegde, S. Bdellovibrio bacteriovorus: a future antimicrobial agent? J. Indian Soc. Periodontol. 17, 823 (2013).
Hong, C. et al. PathoScope 2.0: a complete computational framework for strain identification in environmental or clinical sequencing samples. Microbiome 2, 33 (2014).
Kumar, R., Jangir, P. K., Das, J., Taneja, B. & Sharma, R. Genome analysis of Staphylococcus capitis TE8 reveals repertoire of antimicrobial peptides and adaptation strategies for growth on human skin. Sci. Rep. 7, 10447 (2017).
Youngren, B., Nielsen, H. J., Jun, S. & Austin, S. The multifork Escherichia coli chromosome is a self-duplicating and self-segregating thermodynamic ring polymer. Genes & Dev. 28, 71–84 (2014).
Soler-Bistué, A., Timmermans, M. & Mazel, D. The proximity of ribosomal protein genes to oriC enhances Vibrio cholerae fitness in the absence of multifork replication. mBio 8, e00097–17 (2017).
Trojanowski, D., Hołówka, J., Ginda, K., Jakimowicz, D. & Zakrzewska-Czerwińska, J. Multifork chromosome replication in slow-growing bacteria. Sci. Rep. 7, 43836 (2017).
Camacho, C. et al. BLAST+: architecture and applications. BMC Bioinforma. 10, 421 (2009).
Li, D., Liu, C. M., Luo, R., Sadakane, K. & Lam, T. W. MEGAHIT: an ultra-fast single-node solution for large and complex metagenomics assembly via succinct de Bruijn graph. Bioinformatics 31, 1674–1676 (2015).
Langmead, B. & Salzberg, S. L. Fast gapped-read alignment with Bowtie 2. Nat. Methods 9, 357–359 (2012).
Bankevich, A. et al. SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing. J. Comput. Biol. 19, 455–477 (2012).
Huson, D. H., Auch, A. F., Qi, J. & Schuster, S. C. MEGAN analysis of metagenomic data. Genome Res. 17, 377–386 (2007).
Parks, D. H., Imelfort, M., Skennerton, C. T., Hugenholtz, P. & Tyson, G. W. CheckM: assessing the quality of microbial genomes recovered from isolates, single cells, and metagenomes. Genome Res. 25, 1043–1055 (2015).
Li, H. et al. The sequence alignment/map format and SAMtools. Bioinformatics 25, 2078–2079 (2009).
Weber, T. et al. antiSMASH 3.0-a comprehensive resource for the genome mining of biosynthetic gene clusters. Nucleic Acids Res. 43, W237–W243 (2015).
We thank the Maximilian E. and Marion O. Hoffman Foundation for postdoctoral fellowship to A.E., and funding from the National Institutes of Health (1 DP2 GM126893-01 and K22 AI119231-01) for J.O. We also thank Asaf Peer for making GRiD installation possible through Bioconda, Wei Zhou for providing the genomes used in creating the GRiD database, and Elizabeth Fleming for sequence library preparation. We thank the Oh lab for critical commentary and algorithm testing.
About this article