Sponges (phylum Porifera) are early-diverging metazoa renowned for establishing complex microbial symbioses. Here we present a global Porifera microbiome survey, set out to establish the ecological and evolutionary drivers of these host–microbe interactions. We show that sponges are a reservoir of exceptional microbial diversity and major contributors to the total microbial diversity of the world’s oceans. Little commonality in species composition or structure is evident across the phylum, although symbiont communities are characterized by specialists and generalists rather than opportunists. Core sponge microbiomes are stable and characterized by generalist symbionts exhibiting amensal and/or commensal interactions. Symbionts that are phylogenetically unique to sponges do not disproportionally contribute to the core microbiome, and host phylogeny impacts complexity rather than composition of the symbiont community. Our findings support a model of independent assembly and evolution in symbiont communities across the entire host phylum, with convergent forces resulting in analogous community organization and interactions.
Microbial symbionts are essential for the function and survival of multicellular eukaryotes, ranging from humans to invertebrates to plants1,2,3,4. Most symbioses involve complex communities of microorganisms, often comprising a large phylogenetic breadth of microbial diversity associated with a single host organism. Many factors, including host-derived nutrients, chemico-physical characteristics (for example, pH) and host properties (for example, immune response), determine the composition and structure of symbiont communities over time and space. However, the evolutionary and ecological drivers of symbiont composition in animals and plants remain largely unknown5.
Sponges are among the most ancient living Metazoa and generally form symbiotic relationships with complex communities of microorganisms6,7,8. Sponges can maintain highly diverse, yet specific symbiont communities, despite the constant influx of seawater microorganisms resulting from their filter-feeding activities9. These symbioses are known to be at least partially underpinned by metabolic exchange between symbiont and host, including nitrogen cycling, CO2 fixation, secondary metabolite production, and uptake and conversion of dissolved organic matter10,11,12. In this respect, sponge symbionts perform analogous functions to the symbionts found in mammalian guts and plants5. Therefore sponge-microbe symbioses represent an ecologically relevant example of host–microbe interactions in an early-diverging metazoan clade.
While the diversity of sponge symbionts has been extensively addressed using molecular tools, comparative work has been hindered due to methodological differences in sampling, sample processing and data analyses12,13,14. Large-scale efforts, such as the Human Microbiome Project15 and the Earth Microbiome Project16, have standardized these technical aspects to reliably and consistently describe patterns of microbial diversity and composition. These efforts have generated a large knowledge base for host-associated microbiomes of vertebrates, and especially humans, but equivalent data sets for invertebrates are missing. To gain critical insights into the evolution and complexity of symbiotic interactions, we require a greater understanding of the properties and origins of microbial symbioses in early-divergent Metazoa. Furthermore, microbiome research has primarily focused on within-species comparisons, in particular humans, or the comparative analysis of microbiomes of very disparate host organisms (for example, plants versus mammalian guts)5. However, to define important aspects for the evolution of microbial symbiosis, a deeper understanding of symbiont communities in closely related host species within defined phylogenetic clades (for example, a single phylum) is required.
Here we provide a comprehensive analysis of microbial symbiont communities associated with 81 species from the phylum Porifera. Through a community effort, a total of 804 sponge samples were collected from the waters of 20 countries bordering the Atlantic, Pacific and Indian Oceans as well as the Mediterranean and Red Seas, primarily from shallow water habitats. For environmental comparison, we simultaneously collected 133 seawater and 36 sediment samples as potential sources or sinks of microorganisms associated with sponges9. Microbial community composition for each sample was determined using standardized DNA extraction and 16S rRNA gene-sequencing protocols established by the Earth Microbiome Project16. With this extensive data set, we aimed to define the diversity, variability, specificity and similarity of symbiont communities across the phylum Porifera and determine the interaction patterns and evolutionary forces that shape their complexity and composition.
Symbiont complexity varies greatly across the Porifera
Richness of microbial symbiont communities varies widely across different host species within the phylum Porifera (Fig. 1; Supplementary Data 1). Complexity (as assessed by number of OTUs) ranges from 50 to 3,820 genetically distinct symbionts per host. Seawater operational taxonomic units (OTUs) were removed from sponge samples as they were considered likely to represent ‘environmental contaminants’ obtained during filter feeding and sampling (see Methods for details). The large richness estimates are unlikely to be inflated by sequencing errors as approximately one-third of samples reached complete saturation (Fig. 1). Variation of richness across the sponge samples contrasted with the more consistent richness estimates found within seawater and sediment samples (Fig. 1, Supplementary Data 1). The most diverse sponge samples approach the microbial richness found in seawater or sediment, however, most sponge species appear to have somewhat less complex communities than the other two habitats.
For symbiont communities of the phylum Porifera we observed a continuum of intraspecific dissimilarities across all species investigated (Fig. 2). Variability of symbiont communities between individuals of the same host species is indicative of the nature and strength of host–symbiont interactions, ranging from obligate to facultative17,18. Thus low variability would indicate that only specific symbionts can interact with the host (high specificity), while a relaxed pressure on the interaction would result in higher variability of symbionts among specimens of the same sponge species. Compared with planktonic communities, most sponges maintain low variability within communities (Fig. 2). Variability was also found to be independent of symbiont diversity or richness (Supplementary Fig. 1). This indicates a generally restrictive or selective habitat or interactions at the host species level, for both diverse and more depauperate symbiont communities.
The human microbiome is dominated by four phyla (Firmicutes, Bacteroidetes, Actinobacteria and Proteobacteria) and this phylum-level trend has also been observed in other mammals19. In contrast, only the phylum Proteobacteria (especially classes Alpha- and Gammaproteobacteria) was dominant in most sponges species analysed here, with Chloroflexi, Cyanobacteria and Crenarchaeota occasionally reaching high relative abundances (∼10%). Nevertheless, sponges host a high diversity of phyla (albeit at low relative abundances), with over 32 phyla and candidate phyla regularly reported to associate with sponges20 and a further 6 phyla and 14 candidate phyla recently reported as part of the rare community using a deep Illumina sequencing approach21. In the current study, we detected 41 phyla (including candidate phyla) with all sponges hosting members of at least 13 different phyla (Fig. 3).
Sponges harbour an exceptional microbial diversity
High sample replication (n>20) employed in this study facilitated estimation of total microbial richness for specific sponge species and seawater. Analysis of the 133 surface seawater samples (collected here from disparate geographic areas, including Spain, Florida, Puerto Rico, Sweden, Mexico, Bahamas and Australia) showed that the combined planktonic richness in these regions approaches 15,000 OTUs (at 97% sequence identity) (Fig. 4). This estimate lies between the ∼20,000 and ∼9,000 predicted OTUs (at 97% sequence identity) found in surface waters of the coastal and open ocean, respectively, as part of the International Census of Marine Microbes (ICoMM)22, which was based on pyrosequencing analysis of the V6 region of the 16S rRNA gene. However, the estimated planktonic richness in this and our study is lower than the 29,457 OTUs (at 97% sequence identity) recently reported using Illumina amplicon sequencing of seawater21 or the 37,470 OTUs estimated from metagenomic sequencing of the global Tara Oceans samples23, with the higher richness in the latter two studies likely explained by the inclusion of deep-water samples. Remarkably though, richness estimates show that a single sponge species can harbour as many different OTUs as might be expected from the surrounding seawater. For example, Carteriospongia foliascens and Ircinia variabilis (n≥50 individuals across their sampled biogeographic distribution) contain more than 12,000 OTUs (Fig. 4). Similar richness projections were observed for the species Cliona delitrix, Ircinia strobilina, Ircinia oros, Mycale laxissima, Plakortis halichondrioides, Sarcotragus fasciculatus, Xestospongia sp. and Xestospongia muta, which were each sampled between 20 and 50 times (Fig. 4).
Limited overlap in microbiome structure was observed between different sponge species or between sponges and the seawater and sediment samples (Fig. 5). Thus, considering all OTUs discovered across the 804 sponge samples that included 81 different species, richness estimates approach a value of 40,000 OTUs (Fig. 4b). The 81 sponge species analysed here represent only a tiny fraction of the 8,553 described sponge species (and likely a higher number when considering undescribed species)24 suggesting that sponge-associated (and likely other host-associated) communities are a significant global source of unique microbial diversity.
Symbiont communities consist of generalists and specialists
To better understand the distribution of symbionts across the Porifera, we constructed a global bipartite network using the associations between OTUs and individual sponge species. The structure of this network differs greatly from what would be expected if connections between sponges and OTUs were randomly assigned (Fig. 6). This suggests that assembly mechanisms (such as ecological and evolutionary processes) are behind the structure of this network of interactions, as has been suggested for other types of networks of ecological interactions25.
The cumulative probability of finding an OTU in the network with k or less-associated hosts revealed a skewed degree distribution following a truncated power-law with an exponential cutoff at 7.44, almost half the number of host species an OTU is expected to interact with (the average number of hosts a given OTU is found in is 12.13) (Fig. 6). This shows that the majority of symbiont OTUs have a small number of connections and only a few OTUs are very well connected. The majority of OTUs are thus specialists (that is, found in only one or a few sponge species), while only a few are truly cosmopolitan (that is, found across many sponge species). Importantly, the degree distribution for the subset of OTUs belonging to previously defined sponge-specific sequence clusters follows the same distribution as the whole (see below).
The cumulative probability of finding a sponge host with k or less-associated OTUs also follows a skewed degree distribution with exponential decay. A large fraction (>50%) of species harbour a symbiont diversity between ∼60 and ∼1,800 distinct taxa, while a small fraction of sponge species can harbour up to ∼7,000 OTUs (see also above). Skewed degree distributions have been identified in several types of ecological networks, and are linked to important properties of ecological communities, such as their robustness to species loss and their stability over time25. Our results suggest that ecological communities formed between microbial symbionts and their sponge hosts display similar patterns, which may be linked to their ability to maintain important functions at both the host and ecosystem levels12.
To further investigate the specialization of OTUs in our interaction network, we analysed how consistently they are found across individual replicates of any given host species. Both highly specialized (defined here as those found in less than five different host species) and generalist OTUs (defined here as those found in more than 50 different host species) are present in a large fraction of the biological replicates of their respective host species (Fig. 7; Supplementary Fig. 2). In contrast, a large proportion of OTUs with an intermediate degree of host association (between 5 and 50 host species) can be considered as opportunistic taxa, associated with only a few biological replicates of multiple host species. Thus, symbiont communities within the phylum Porifera are characterized by a combination of highly generalist and truly specialist community members. Our analysis showed that generalists are cosmopolitan not only qualitatively (that is, present in a large number of species), but also quantitatively (that is, consistently present in a large fraction of individuals of those host species). To our knowledge, such patterns have not previously been observed for ecological networks, as it has traditionally been difficult to undertake repeated measures of many individuals across multiple host species.
Generalist symbionts comprise the core sponge microbiome
Considering the existence of generalist (that is, cosmopolitan) sponge OTUs, we queried their relative contribution to the core microbiome of any individual species. Here we define a core membership as any OTU that is present in at least 85% of the replicates for any single host species. To effectively model population dynamics of these OTUs, we identified host species with a sufficiently large number of replicates (here ≥47) across the entire data set. We identified five host species (Carteriospongia foliascens, Cliona delitrix, Ircinia oros, Ircinia variabilis and Sarcotragus fasciculatus) that fit this requirement and observed cores ranging in size from 7 to 20 OTUs. The proportion of OTUs with a certain degree (number of connections to different sponge species) or higher, and the frequency distribution of degrees were compared for all OTUs present in the global bipartite network and the aggregated subset of OTUs present in all five core microbiomes (Fig. 8). The core OTUs aggregated from all five sponge species showed an uneven distribution of degree frequencies. Core OTUs are primarily generalist and cosmopolitan (high degree) OTUs, while specialist (low degree) and intermediate degree OTUs are under-represented. This shows that highly connected OTUs in the global bipartite network also tend to comprise a larger fraction of the core for each of the host species investigated here.
Strong density dependence and weak, unidirectional interactions
Of particular interest is whether these core OTUs and their local interactions are important for the overall dynamics of the symbiont populations within each host species. For instance, density dependence (that is, the growth rate of a population is controlled by its density) has a strong effect on community dynamics, with stabilizing effects on population fluctuations26. To disentangle the complex nature of microbe–microbe interactions within our five sponge hosts described above, we applied a statistical framework27 that models population dynamics of the Lotka–Volterra type and allows us to decouple the variation in relative abundance of populations into contributions of (i) inter-specific interactions, (ii) density dependence and (iii) environmental stochasticity. Population dynamics are sensitive to both non-modelled environmental stochasticity and modelled fluctuating environmental conditions27. However, in this study, the environment is considered as fixed due to replicates being sampled from similar environments during the same time period (see Supplementary Data 2 and also (ref. 28) for temporal stability of symbionts in Ircinia oros, Ircinia variabilis and Sarcotragus fasciculatus), hence population dynamics are considered to be influenced solely by environmental stochastic processes and species interactions.
Density-dependent processes were found to explain the majority of variation in the relative abundance of core OTUs across biological replicates, followed by stochastic mechanisms (Supplementary Table 1). Only a small proportion of variance (3–8% across hosts) is explained by inter-specific interactions (Supplementary Table 1). It should, however, be noted that the contribution of inter-specific interactions may be larger because we are missing those interactions excluded from the cores (that is, interactions with more opportunistic OTUs).
Although inter-specific interactions contribute little to the dynamics of the core microbiomes, it is still important to investigate the nature and strength of these interactions as, for example, antagonism (that is, competition) and mutualism are known to differ in how they affect population and community stability29. Both empirical and theoretical studies in community ecology demonstrate that distributions skewed towards many weak and a few strong interactions enhance both population and community stability, and may arise during the assembly of persistent communities30,31. Similarly, mutualism or skewed interactions only affecting one interacting partner (that is, amensalism and commensalism) have been shown to promote diversity and lead to community stability32,33.
A number of indices were calculated for each core microbiome (Supplementary Table 2). Despite some variability in OTU number and linkages across different hosts, connectance (defined as the fraction of realized links among all possible links) was consistently low, ranging between 4.5 and 7.5%. We find that all cores are characterized by very few strong and many weak interactions (Supplementary Fig. 3). Moreover, cores are distingished by a mixture of positive and negative interactions with amensalism and commensalism as a signature rather than competition and/or mutualism (Fig. 9 illustrates this using the example of Ircinia oros; see Supplementary Figs 4–7 for further details and other sponge species). Across hosts, we observe that the most probable links are generally negative, although as the core size increases, the fraction of positive inter-specific interactions increases. Interestingly, we find that some OTUs, which are highly connected in the global bacteria-sponge (bipartite) network, are also highly connected within the core network. This suggests that OTUs that are present in a large number of different host species tend to be important for population dynamics within each particular host.
The low connectance, weak, and amensal and/or commensal interactions, together with strong density dependence found in most sponge species, suggest that symbiont communities in the phylum Porifera have stable cores. However, whether these stable cores play a role in the dynamics of remaining OTUs within individual microbiomes, and more importantly, whether this stability guarantees the homoeostasis of host functionality requires further investigation.
Sponge microbiomes are enriched in specific sequence clusters
Many of the microbes inhabiting sponges have previously been found to fall into monophyletic clusters of ‘sponge-specific’ or ‘sponge- and coral-specific’ 16S rRNA gene sequences, with these clusters spanning 14 bacterial and archaeal phyla9,12,14,34. The ecological and evolutionary significance of these monophyletic clusters remains unclear, yet it is noteworthy that this phenomenon has not been reported outside the phylum Porifera. Over 43% of all sponge-derived sequences from this global sponge analysis were assigned to previously defined monophyletic sponge-specific clusters. However, using deep sequencing and our extensive sampling, 2.7% of seawater sequences and 8.7% of sediment sequences were also assigned to these clusters, demonstrating some clusters are not strictly ‘sponge-specific’, but better described as ‘sponge-enriched’ (Supplementary Fig. 8)35. Importantly, these clusters contain generalists, specialists and opportunists (Fig. 7) indicating that the sponge-specific/enriched microbial sequence clusters have evolved multiple times, either early (that is, core) or late (that is, specialists and opportunists) in the assembly of symbiont communities.
Host phylogeny and identity structure symbiont communities
Environmental and host factors are known to influence the composition of host-associated communities12,36,37; however, the impact of host evolutionary history on the structure and composition of symbiont comunities has only recently been explored37. Considering the phylogenetic breadth of sponge species sampled here, we were able to evaluate the relationship between host phylogeny and microbial diversity. Diversity was assessed using the inverse Simpson’s index (D), while Blomberg’s K was calculated using the phylosignal function in the R package picante38 (Fig. 10; see Methods for details). K values of 1 correspond to a random process, values closer to zero correspond to patterns of convergent or random evolution and values >1 indicate phylogenetic conservatism38. We observed a significant value of K for the inverse Simpson’s index (K=0.151, P=0.027), supporting a significant host evolutionary signal. Pagel’s lambda39 was calculated to further compare the similarity of covariances among species with the covariances expected, given a random process. The lambda value of 0.216 (AICc=623.3; with λ fixed at 0, AICc =627.0) was significantly larger than what would be expected if there was no phylogenetic signal. Combined, these findings indicate a significant signal of convergent evolution in community structure, whereby sponges hosting more diverse communities are more phylogenetically related than expected by chance.
Beta-diversity analysis of symbiont communities (using Bray–Curtis distance) also indicated significant differences among species, with the factor ‘host species’ accounting for ∼64% of the observed variation among specimens. A partial Mantel test showed that host phylogeny was significantly correlated with Bray–Curtis distance (r=0.442, R2=0.195, P=0.001), as was host identity (r=0.706, R2=0.498, P=0.001). Testing for the effect of host phylogeny given host identity greatly reduced the explanatory power of host phylogeny (r=0.223, R2=0.050, P=0.001), although host phylogeny still had a significant effect.
Overall, the evolutionary history of the host plays a significant role in structuring the diversity of symbiont communities, but only a minor role in structuring community composition (that is, identity of microbial symbionts), where host identity (reflective of species-level forces) is the more important determinant. Thus, the evolutionary history of the host exerts a significant influence on microbial diversity despite strong selective forces for divergent microbiome composition, which might be critical for niche differentiation among closely related hosts40.
This global microbiome survey of an early-diverging metazoan phylum has revealed that sponges are a reservoir of exceptional microbial diversity and a major contributor to the total microbial diversity found in the world’s oceans. Across the Porifera, symbiont communities exhibit little commonality in species composition or structure although a number of emerging properties related to community organization are evident. For instance, sponge symbiont communities are characterized by a predominance of both specialists and generalists (as opposed to opportunists) and the core microbiomes are characterized by generalist symbionts with an under-representation of specialists. These communities represent dynamic systems, with the interacting members featuring all possible ecological interaction types (positive, negative and neutral)41. The sign and strength of species interactions among community members has previously been shown to be highly dynamic and contingent on species composition, species densities and the environment42. Here we show that the core symbiont communities in sponges are strongly density dependent, have few and weak interactions, low connectance, and amensal and/or commensal interactions indicative of stable core symbionts within the Porifera30,31,32,33. Perhaps surprisingly, symbionts that appear to be phylogenetically unique to sponges (that is, having previously been defined as ‘sponge-specific’) did not disproportionally contribute to the core microbiome or to any class of symbionts (that is, specialist, generalist or opportunist), indicating that symbiont communities have independently assembled or evolved across the Porifera and that convergent forces have resulted in the analogous community organization and interactions10. Although the evolutionary history of the host is undoubtedly a driving force in this process, we show here that host phylogeny primarily impacts the complexity rather than the composition of the symbiont community. These findings further support a model of convergent evolution in symbiont communities across the entire host phylum10.
Sampling and sample processing
Samples were taken and processed according to the standard operating procedures to ensure maximum comparability. In brief, at least three different specimens of each sponge species were collected into sterile bags and species identities were confirmed by microscopic examination of morphological characters following established protocols (for example, as reviewed in ref. 43). Specimens were either processed directly or after freezing, depending on logistical constraints of each sampling event. Specimens were cleaned of external growth (for example, barnacles), washed three times with sterile seawater to remove planktonic or loosely associated microorganisms and cut into small pieces from which a random sub-sample of pieces was used for subsequent DNA extraction. Sediment samples were collected under water in close proximity to sponges. Sediments were scooped into sterile containers using sterile spatulas to avoid laboratory contamination. Seawater was drained from the containers on surfacing and prior to freezing. Sponges and sediment samples were immediately frozen and kept on dry ice or at −80 °C until further processing. DNA was extracted from ∼0.25 g of sponge tissue or sediment using the PowerSoil DNA Extraction kit (MoBio) according to the Earth Microbiome Project standard protocols (http://press.igsb.anl.gov/earthmicrobiome/emp-standard-protocols/dna-extraction-protocol/). Microbial communities in seawater were collected by passing 2 l of seawater through 0.2 μm Sterivex filters and DNA was extracted from the filters as previously described13. Samples were extracted at laboratories at the Australian Institute of Marine Sciences (Townsville, Australia), the University of Wuerzburg (Germany) or the Nova Southeastern University (Dania Beach, FL, USA) to minimize shipment of frozen specimens. Aliquots of the specimens and DNA were kept at the three locations (and are available on request) and an aliquot of the extracted DNA was shipped to the University of Colorado, Bolder, CO, USA for sequencing of the 16S rRNA gene using standard procedures of the Earth Microbiome Project (http://www.earthmicrobiome.org/emp-standard-protocols/16s/). Briefly, the V4 region of the 16S rRNA gene was amplified using the primer 515f–806rB and sequenced using the HiSeq2500 platform (Illumina)44.
Analysis of sequencing data
We processed Illumina reads in mothur v.1.31.2 (ref. 45). First, quality-filtered, demultiplexed fastq sequences were trimmed according to quality (using the trim.seqs command: parameters qwindowaverage=30, qwindowsize=5, maxambig=0, maxhomop=8, minlength=100). Files were reduced to non-identical sequences (unique.seqs and count.seqs) to minimize computational effort. Non-redundant sequences were aligned (align.seqs: flip=t) to a trimmed reference SILVA 102 (ref. 46) bacteria database (pcr.seqs: start=11894, end=25319, keepdots=F), which was provided by mothur47. Only sequences that were aligned to the expected position were kept (screen.seqs: start=1968, end=4411; filter.seqs: vertical=T, trump=.). Aligned reads were reduced to non-redundant sequences (unique.seqs). Chimeric sequences were detected using Uchime (chimera.uchime: dereplicate=t)48, and filtered out (remove.seqs). Pairwise distances between aligned sequences were calculated (dist.seqs: cutoff=0.05) and used for clustering. Prior to clustering, aligned sequences were phylogenetically classified based on the trimmed SILVA database (classify.seqs)49. Sequences were clustered (cluster.split: fasta=, count=, taxonomy=, splitmethod=classify, taxlevel=4, cutoff=0.03, hard=t, method=furthest) and converted to.shared file format (make.shared:list=, count=, label=0.03). Finally, OTU representative sequences were retrieved based on the distance among the cluster sequences (get.oturep: list=, label=0.03, fasta=, count=) and were further classified based on SILVA, Greengenes (version gg_13_5_99 from May 2013), and RDP taxonomies (classify.seqs: fasta=, template=, taxonomy=, cutoff=60)46,50,51. Furthermore, Fastq sequences from additional samples (n=340) that were generated at a later time point (using the same sequencing procedure as described above) were processed with the same pipeline. These sequences were integrated into the shared file using QIIME 1.8 (ref. 52), based on their similarity to the OTU representative sequences (parallel_pick_otus_uclust_ref.py: --similarity 0.985 --optimal_uclust). Sequences that were not similar to the OTU representative sequences were separately clustered with mothur and integrated into the previous files (.shared and taxonomy files). The integrated OTU table (.shared file) was filtered to remove low-abundance sequences (sequences <0.001% across the whole data set) and chloroplasts (according to SILVA or Greengenes). In addition, counts from seawater-like OTUs (>0.01% across all seawater samples) were removed from sponge samples. File manipulation and processing was carried out with python scripts (http://www.python.org). OTU tables are available in Supplementary Data 4.
Calculation of community metrics
Rarefaction curves were generated using the R package vegan 2.2-1 (ref. 53). Inter-sample rarefaction curves were generated by mothur (rarefaction.shared). Distances of the samples in a group (sponge species, seawater or sediment) and their respective group centroids were calculated based on Bray–Curtis distances by the function betadisper from the vegan package in R (ref. 53). Richness indicators (Chao, Ace, Sobs) were also calculated with vegan. Nonmetric multidimensional scaling was calculated with vegan package based on Hellinger transformed OTU counts54. Taxonomic profiles were obtained based on Greengenes, which provided more phylum-level assignments than the SILVA or RDP databases. Briefly, percentage OTU counts were averaged by species/environment with the R package analogue 0.16-0 (ref. 55). Phylum percentages were calculated by summing averaged OTU percentages. Bray–Curtis dissimilarities were calculated and heatmap was obtained using the package pheatmap 1.0.7 (ref. 56).
Sponge-bacteria bipartite network analysis
A bipartite interaction network was constructed using the presence of specific OTUs within each of the sponge species in the data set. OTUs were considered part of the network only if they were found in at least 25 distinct samples from the whole data set. In this bipartite host–microbe interaction network, nodes represent sponge species (on one side) and OTUs (on the other); and links among them represent the presence of an OTU in the microbial community of the sponges to which it is linked. The network was constructed using a software script developed in R using the package igraph 0.7.1 (ref. 57) and interrogated using statistical tools to describe its properties.
The degree distribution of sponges and OTUs was analysed to assess the heterogeneity of the network in terms of node connectivity. Degree distributions depict the statistical probability distribution of finding nodes with a certain degree (number of other nodes it is connected to). A variant of the degree distribution was employed: the cumulative degree distribution, which has the same probability distribution, but shows the probability of finding nodes with that degree or less. These probability distributions (one for the OTUs and another for the sponges) were obtained using the cumsum function in R (ref. 58). In addition, we fitted truncated power law and exponential functions to the OTUs and sponges cumulative degree distributions, respectively. This was achieved using the non-linear least squares (nls) function provided by R. This analysis reveals the pattern of connectivity between sponges and OTUs and facilitates determination of the balance between generalist and specialist species. The thresholds for specialism and generalism were chosen arbitrarily, but following basic requirements for this type of network analysis. First, neither of the groups contains the parameter that provides the characteristic scale at which the exponential cutoff occurs in the truncated power-law distribution. In our case, this value is 7.44 (Pc(k)=k−0.32 × e−(k/7.44)), so specialists need to have a number of links below that threshold, and generalist species should have a number of links that is several times this number—for this purpose we selected seven times this number. Second, the average number of links in the specialist and generalist groups should be very different from the mean number of links in the network, and the difference in this ratio (mean group/mean network) should be similar for both groups. The mean number of network links is 12.13, the mean number of links for specialists is 2.5 and for generalists is 60, with specialists thus having a mean number of links ∼4.47 times smaller than the average, and generalists 4.66 times larger than the mean.
The relationship between the fraction of samples within which a given OTU is found for a particular sponge species versus the total number of sponges in which that OTU was found (degree of the OTU in the network) was also assessed. This was achieved by obtaining the fraction of sponge samples in which a given OTU was found out of all the samples available for the sponge hosts to which that OTU is connected in the host–microbe network. This information was plotted against the degree of the OTU. To better visualize this relationship a smoothing spline was fitted using the smooth.spline function provided by R. This relationship is used to analyse the true shape of specialisation versus generalism in ecological networks.
Bacteria–bacteria network analysis
For the bacteria–bacteria network analysis, we focused on host species with more than 47 individual replicates. If more than 47 replicates were available, we randomly subsampled 47 replicates. Cores were created for each host species by extracting OTUs occurring in at least 85% of the 47 replicates and were further filtered by removing OTUs with a relative abundance <0.01. This was done by using filter.shared(minpercentsamples=85, minpercent=1, makerare=f) in mothur v.1.31.2. The statistical model developed in ref. 27 for inferring interactions from temporal series data was adapted to substitute time for space such that spatial replicates for each host were used rather than temporal samples. If we denote ni,m as the natural logarithm of Ni,m, then on a natural logarithmic scale we have the number of sequences of core OTU i in replicate m within any given host species described by
where ri and ki represent the intrinsic growth rate and the carrying capacity of OTU i, respectively, αi,j represent the interaction coefficient between OTU i and j and expresses the per capita effect of OTU j on the growth rate of OTU j from replicate m−1 to replicate m. Finally, ɛi,m represents the effect of unexplained, latent, stochastic noise on the population dynamics of species i. The time-series is modelled using a Poisson distribution, where yi,m denotes the observed number of sequences of OTU i in replicate m
where log(Nm) and Πm represent offsets to model rates instead of counts. Both correspond to the total abundance in replicate m, but the latter is treated as a random normal variable with a mean of zero and a s.d. of 100.
ri is assumed to be ∼N(0, 10), while ki∼Exp(1) to limit ki to positive values.
The total variance Vi of individual OTU abundances can be decomposed into additive contributions from inter-specific interactions, density-dependence and stochasticity, respectively,
where vi,i is the stationary variance for ni. From this, the proportion of variation attributed to each source of variability can be calculated (see ref. 27 for details).
We used Gibbs variable selection method59 to constrain the model to only use inter-specific interaction coefficients, αi,j, for which there are strong support in the data. This is achieved by introducing a binary indicator variable γi,j for i≠j, and assuming γi,j∼Bernoulli(P), such that γi,j=1 when species j is included in the dynamics of species i, and γi,j=0 otherwise. Where there is low support for the inter-specific interaction in the data, γi,j=0, and the interaction is excluded from the model. When γi,j=1, αi,j is freely estimated from the data. A P of 0.1 was selected as we do not expect more than 10% of all possible inter-specific interactions to be realized.
We use Markov chain Monte Carlo simulation methods in R using the runjags package60 to sample from the joint posterior distribution of the model parameters. We ran 10 independent chains with dispersed initial values for 5e6 iterations, discarding the first 2e6 samples of each chain as burn-in and thinned the remainder to every 50th sample. We evaluated convergence of model parameters by visually inspecting trace and density plots. In addition, to ensure good mixing of αi,j we calculated the number of jumps γi,j did between its two states (0 and 1).
Finally, to build the representative networks, we analysed the interaction and sign structure of the posterior distribution for the interaction coefficient αi,j. αi,j is a full probability distribution, hence it contains the probability of OTU j having a non-zero per capita effect on the growth of OTU i (interaction strength), and vice versa. Using all information in αi,j, we constructed a representative network for each host species as a mean of visualizing the most ‘credible’ network structure. This was done by mapping the posterior average number of links onto αi,j, and in doing so, extracting the links with the highest probability of non-zero interactions. This was done by custom-written R scripts. As a way of validating the structure of each representative network, we compared the connectance of each representative network with the posterior average connectance for αi,j for each host species. The representative networks was plotted using the igraph package57 in R.
Identification of sponge-specific and sponge/coral-specific clusters
A representative sequence from each OTU was taxonomically assigned using a BLAST61 search against a curated ARB-SILVA database containing 178 previously identified sponge-specific clusters (SC) and 32 sponge/coral-specific clusters (SCC)14. For each BLAST search, the 10 best hits were aligned to determine sequence similarities. The most similar OTU sequence to the respective reference sequence within the database was then assigned (or otherwise) to an SC or SCC based on the application of a 75% similarity threshold (that is, a sequence read was only assigned to a cluster if it was more similar to the members of that cluster than to sequences outside the cluster and its similarity to the most similar sequence within that cluster was above 75%). In cases where the assignment of the most similar sequences was inconsistent, a majority rule was applied, and the OTU sequence was only assigned to an SC or SCC if at least 60% of the reference sequences were affiliated with this cluster.
Phylogenetic analysis of host species and correlation with symbiont communities
Our phylogenetic analysis considered 61 sponge species for which at least one of three gene sequences (small subunit of nuclear ribosomal RNA [18S], large subunit of nuclear ribosomal RNA [28S] or mitochondrial cytochrome oxidase subunit 1 [cox1]) could be obtained from GenBank. For 39 of the 61 species (64%), sponge gene sequences were also obtained from at least one identical specimen collected for the current study. The biologists who collected specimens were very familiar with sponge taxonomy and identification, and we intentionally focused our study on easily recognized and common taxa to avoid misidentification. Some genetic markers used for sponge taxonomy are easier to sequence than others and here we used all available data for the most frequently used markers for sponge molecular systematics.
For each gene, sequences were aligned using the default options of MAFFT 7.017 (ref. 62). Each alignment was analysed using the Gblocks Server63 to eliminate non-conserved regions; the resulting three alignments were then concatenated using the Geneious software (version 6.1.8, Biomatters Limited). The phylogeny was constructed with MrBayes version 3.2.1 (ref. 64), using the computational resources provided by CIPRES65. Within MrBayes, five partitions (18S, 28S and the three codon positions of cox1) were specified and separate general time reversible models of evolution for each partition were estimated, incorporating a gamma distribution of substitution rates among sites and a proportion of invariant sites (GTR+I+G) as suggested by ref. 66. The Homoscleromorpha Pseudocorticium jarrei and Plakortis halichondrioides (the only non-Demospongiae sponges of the taxon set) were constrained as an outgroup and the independent gamma rates relaxed-clock model with a birth–death process was implemented. The phylogenetic analysis included three parallel runs of 10 million generations, each utilizing four Markov chains and sampling every 100 generations. At the end of the runs, we assessed convergence by the average s.d. of split frequencies, which was 0.03, and the potential scale reduction factors of all parameters, which ranged from 1.00 to 1.01. Following a burn-in of 25%, the trees sampled by each of the three runs were summarized into a consensus tree. The diversity of OTUs associated with each host species was evaluated by calculating OTU richness, the Shannon index of diversity, and the inverse Simpson index of diversity. All indices demonstrated clear differences among sponge species (P<0.001). Beta-diversity analysis was conducted by calculating the Bray–Curtis distance among specimens, and testing for host species differences in this distance using the function adonis in the R package vegan53.
Processed sequences can be downloaded from the following portal: http://qiita.microbio.me (Study ID 10346). Sequence data have been deposited in the BioProject database under accession code PRJEB11983 and in the European Nucleotide Archive under accession code ERP013416. The authors declare that all other data supporting the findings of this study are available within the article and its Supplementary Information files.
How to cite this article: Thomas, T. et al. Diversity, structure and convergent evolution of the global sponge microbiome. Nat. Commun. 7:11870 doi: 10.1038/ncomms11870 (2016).
Kau, A. L., Ahern, P. P., Griffin, N. W., Goodman, A. L. & Gordon, J. I. Human nutrition, the gut microbiome and the immune system. Nature 474, 327–336 (2011).
Tkacz, A. & Poole, P. Role of root microbiota in plant productivity. J. Exp. Botany 66, 2167–2175 (2015).
Cabreiro, F. & Gems, D. Worms need microbes too: microbiota, health and aging in Caenorhabditis elegans. EMBO Mol. Med. 5, 1300–1310 (2013).
McFall-Ngai, M. et al. Animals in a bacterial world, a new imperative for the life sciences. Proc. Natl Acad. Sci. USA 110, 3229–3236 (2013).
Hacquard, S. et al. Microbiota and host nutrition across plant and animal kingdoms. Cell Host Microbe 17, 603–616 (2015).
Hentschel, U., Piel, J., Degnan, S. M. & Taylor, M. W. Genomic insights into the marine sponge microbiome. Nat. Rev. Microbiol. 10, 641–654 (2012).
Taylor, M. W., Thacker, R. W. & Hentschel, U. Genetics. Evolutionary insights from sponges. Science (New York, N.Y.) 316, 1854–1855 (2007).
Yin, Z. et al. Sponge grade body fossil with cellular resolution dating 60 Myr before the Cambrian. Proc. Natl Acad. Sci. USA 112, E1453–E1460 (2015).
Taylor, M. W. et al. 'Sponge-specific' bacteria are widespread (but rare) in diverse marine environments. ISME J. 7, 438–443 (2013).
Fan, L. et al. Functional equivalence and evolutionary convergence in complex communities of microbial sponge symbionts. Proc. Natl Acad. Sci. USA 109, E1878–E1887 (2012).
de Goeij, J. M. et al. Surviving in a marine desert: the sponge loop retains resources within coral reefs. Science (New York, N.Y.) 342, 108–110 (2013).
Taylor, M. W., Radax, R., Steger, D. & Wagner, M. Sponge-associated microorganisms: evolution, ecology, and biotechnological potential. Microbiol. Mol. Biol. Rev. 71, 295–347 (2007).
Webster, N. S. et al. Deep sequencing reveals exceptional diversity and modes of transmission for bacterial sponge symbionts. Environ. Microbiol. 12, 2070–2082 (2010).
Simister, R. L., Deines, P., Botté, E. S., Webster, N. S. & Taylor, M. W. Sponge‐specific clusters revisited: a comprehensive phylogeny of sponge‐associated microorganisms. Environ. Microbiol. 14, 517–524 (2012).
Human Microbiome Project Consortium. Structure, function and diversity of the healthy human microbiome. Nature 486, 207–214 (2012).
Gilbert, J. A., Jansson, J. K. & Knight, R. The Earth Microbiome project: successes and aspirations. BMC Biol. 12, 69 (2014).
Thacker, R. W. & Freeman, C. J. Sponge-microbe symbioses: recent advances and new directions. Adv. Mar. Biol. 62, 57 (2012).
Vrijenhoek, R. C. in The Vent and Seep Biota 15–49Springer (2010).
Dethlefsen, L., McFall-Ngai, M. & Relman, D. A. An ecological and evolutionary perspective on human-microbe mutualism and disease. Nature 449, 811–818 (2007).
Schmitt, S. et al. Assessing the complex sponge microbiota: core, variable and species-specific bacterial communities in marine sponges. ISME J. 6, 564–576 (2012).
Reveillaud, J. et al. Host-specificity among abundant and rare taxa in the sponge microbiome. ISME J. 8, 1198–1209 (2014).
Zinger, L. et al. Global patterns of bacterial beta-diversity in seafloor and seawater ecosystems. PLoS ONE 6, e24570 (2011).
Sunagawa, S. et al. Structure and function of the global ocean microbiome. Science (New York, N.Y.) 348, 1261359 (2015).
Van Soest, R. W. M. et al. Global diversity of sponges (Porifera). PLoS ONE 7, e35105 (2012).
Montoya, J. M., Pimm, S. L. & Sole, R. V. Ecological networks and their fragility. Nature 442, 259–264 (2006).
Henderson, P. A. & Magurran, A. E. Direct evidence that density-dependent regulation underpins the temporal stability of abundant species in a diverse animal community. Proc. R. Soc. Lond. B, Biol. Sci. 281, 20141336 (2014).
Mutshinda, C. M., O'Hara, R. B. & Woiwod, I. P. What drives community dynamics? Proc. R. Soc. Lond. B, Biol. Sci. 276, 2923–2929 (2009).
Erwin, P. M., Pita, L., López-Legentil, S. & Turon, X. Stability of sponge-associated bacteria over large seasonal shifts in temperature and irradiance. Appl. Environ. Microbiol. 78, 7358–7368 (2012).
Thébault, E. & Fontaine, C. Stability of ecological communities and the architecture of mutualistic and trophic networks. Science (New York, N.Y.) 329, 853–856 (2010).
McCann, K. S. The diversity–stability debate. Nature 405, 228–233 (2000).
Rooney, N. & McCann, K. S. Integrating food web diversity, structure and stability. Trends Ecol. Evol. 27, 40–46 (2012).
Bastolla, U. et al. The architecture of mutualistic networks minimizes competition and increases biodiversity. Nature 458, 1018–1020 (2009).
Lurgi, M., Montoya, D. & Montoya, J. M. The effects of space and diversity of interaction types on the stability of complex ecological networks. Theor. Ecol. 1–11 (2015).
Hentschel, U. et al. Molecular evidence for a uniform microbial community in sponges from different oceans. Appl. Environ. Microbiol. 68, 4431–4440 (2002).
Moitinho-Silva, L. et al. Specificity and transcriptional activity of microbiota associated with low and high microbial abundance sponges from the Red Sea. Mol. Ecol. 23, 1348–1363 (2014).
Costello, E. K., Stagaman, K., Dethlefsen, L., Bohannan, B. J. & Relman, D. A. The application of ecological theory toward an understanding of the human microbiome. Science (New York, N.Y.) 336, 1255–1262 (2012).
Easson, C. G. & Thacker, R. W. Phylogenetic signal in the community structure of host-specific microbiomes of tropical marine sponges. Front. Microbiol. 5, 532 (2014).
Kembel, S. W. et al. Picante: R tools for integrating phylogenies and ecology. Bioinformatics 26, 1463–1464 (2010).
Harmon, L. J., Weir, J. T., Brock, C. D., Glor, R. E. & Challenger, W. GEIGER: investigating evolutionary radiations. Bioinformatics 24, 129–131 (2008).
Freeman, C. J., Easson, C. G. & Baker, D. M. Metabolic diversity and niche structure in sponges from the Miskito Cays, Honduras. PeerJ 2, e695 (2014).
Faust, K. & Raes, J. Microbial interactions: from networks to models. Nat. Rev. Microbiol. 10, 538–550 (2012).
Ramsey, M. M., Rumbaugh, K. P. & Whiteley, M. Metabolite cross-feeding enhances virulence in a model polymicrobial infection. PLoS Pathog 7, e1002012 (2011).
Hooper, J. N. & Van Soest, R. W. Systema Porifera. A Guide to the Classification of Sponges Springer (2002).
Caporaso, J. G. et al. Global patterns of 16 S rRNA diversity at a depth of millions of sequences per sample. Proc. Natl Acad. Sci. USA 108, 4516–4522 (2011).
Schloss, P. D. et al. Introducing mothur: open-source, platform-independent, community-supported software for describing and comparing microbial communities. Appl. Environ. Microbiol. 75, 7537–7541 (2009).
Quast, C. et al. The SILVA ribosomal RNA gene database project: improved data processing and web-based tools. Nucleic Acids Res. gks1219 41, D590–D596 (2012).
Quast, C. et al. The SILVA ribosomal RNA gene database project: improved data processing and web-based tools. Nucleic Acids Res. 41, D590–D596 (2013).
Edgar, R. C., Haas, B. J., Clemente, J. C., Quince, C. & Knight, R. UCHIME improves sensitivity and speed of chimera detection. Bioinformatics 27, 2194–2200 (2011).
Wang, Q., Garrity, G. M., Tiedje, J. M. & Cole, J. R. Naive Bayesian classifier for rapid assignment of rRNA sequences into the new bacterial taxonomy. Appl. Environ. Microbiol. 73, 5261–5267 (2007).
Cole, J. R. et al. Ribosomal Database Project: data and tools for high throughput rRNA analysis. Nucleic Acids Res. 42, D633–D642 (2014).
DeSantis, T. Z. et al. Greengenes, a chimera-checked 16 S rRNA gene database and workbench compatible with ARB. Appl. Environ. Microbiol. 72, 5069–5072 (2006).
Caporaso, J. G. et al. QIIME allows analysis of high-throughput community sequencing data. Nat. Methods 7, 335–336 (2010).
Dixon, P. & Palmer, M. VEGAN, a package of R functions for community ecology. J. Veg. Sci. 14, 927–930 (2003).
Legendre, P. & Gallagher, E. D. Ecologically meaningful transformations for ordination of species data. Oecologia 129, 271–280 (2001).
Simpson, G. L. Analogue Methods in Palaeoecology: Using the analogue Package. J. Stat. Softw. 22, 1–29 (2007).
Kolde, R. Pheatmap: pretty heatmaps. R Package Version 61, 1–7 (2012).
Csardi, G. & Nepusz, T. The igraph software package for complex network research. InterJ. Complex Syst. 1695, 1–9 (2006).
Gentleman, R., Ihaka, R. & Leisch, F. R: A Language and Environment for Statistical Computing Vienna (2003).
O'Hara, R. B. & Sillanpää, M. J. A review of Bayesian variable selection methods: what, how and which. Bayesian Anal. 4, 85–117 (2009).
Denwood, M. runjags: An R package providing interface utilities, parallel computing methods and additional distributions for MCMC models in JAGS. J. Stat. Softw (in review) http://runjags.sourceforge.net (2013).
Altschul, S. F. et al. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 25, 3389–3402 (1997).
Katoh, K., Misawa, K., Kuma, K. & Miyata, T. MAFFT: a novel method for rapid multiple sequence alignment based on fast Fourier transform. Nucleic Acids Res. 30, 3059–3066 (2002).
Castresana, J. Selection of conserved blocks from multiple alignments for their use in phylogenetic analysis. Mol. Biol. Evol. 17, 540–552 (2000).
Ronquist, F. et al. MrBayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space. Syst. Biol. 61, 539–542 (2012).
Miller, M. A., Pfeiffer, W. & Schwartz, T. in Gateway Computing Environments Workshop (GCE) 1–8IEEE (2010).
Huelsenbeck, J. P. & Rannala, B. Frequentist properties of Bayesian posterior probabilities of phylogenetic trees under simple and complex substitution models. Syst. Biol. 53, 904–913 (2004).
T.T. and N.S.W. were funded through Australian Research Council Future Fellowships FT140100197 and FT120100480, respectively. S.L.L. and P.M.E. were funded by the Spanish Government project MARSYMBIOMICS CTM2013-43287-P. R.C. was funded by the Portuguese Foundation for Science and Technology through the Investigator Grant IF/01076/2014 and the project UID/Multi/04326/2013. C.G.E. and R.W.T. were supported by grants from the US National Science Foundation (DEB-0829986 and DEB-1208340). A.C.-F. was supported by the UNESCO L’Oréal Fellowship for Young Women in Science. U.H. and L.M.S. received funding from the EU- FP7 Program (KBBE.2012.3.2-01; grant no. 311932; SeaBioTech). J.M.M. was supported by the French Laboratory of Excellence Project ‘TULIP’ (ANR-10-LABX-41; ANR-11-IDEX-002-02) and by a Region Midi-Pyrénées Project (CNRS 121090). We thank Professor Russell Hill and members of his laboratory for providing samples and hosting a community data analysis workshop as part of the 2nd International Symposium for Sponge Microbiology. We also thank Emmanuelle Botte and Christine Gernert for DNA extractions and the Earth Microbiome Project for sequencing and sample preparation.
The authors declare no competing financial interests.
Supplementary Figures 1-8 and Supplementary Tables 1-2 (PDF 2584 kb)
Diversity and richness of sponge species. (XLS 64 kb)
Metadata for sponge samples analysed in the current study. (XLS 280 kb)
Representative sequences and taxonomy of OTUs. (TXT 26162 kb)
OTU cluster and their counts across samples. (TXT 88009 kb)
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Thomas, T., Moitinho-Silva, L., Lurgi, M. et al. Diversity, structure and convergent evolution of the global sponge microbiome. Nat Commun 7, 11870 (2016). https://doi.org/10.1038/ncomms11870
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