Abstract
Marine sponges often house small-molecule-producing symbionts extracellularly in their mesohyl, providing the host with a means of chemical defence against predation and microbial infection. Here, we report an intriguing case of chemically mediated symbiosis between the renieramycin-containing sponge Haliclona sp. and its herein discovered renieramycin-producing symbiont Candidatus Endohaliclona renieramycinifaciens. Remarkably, Ca. E. renieramycinifaciens has undergone extreme genome reduction where it has lost almost all necessary elements for free living while maintaining a complex, multi-copy plasmid-encoded biosynthetic gene cluster for renieramycin biosynthesis. In return, the sponge houses Ca. E. renieramycinifaciens in previously uncharacterized cellular reservoirs (chemobacteriocytes), where it can acquire nutrients from the host and avoid bacterial competition. This relationship is highly specific to a single clade of Haliclona sponges. Our study reveals intracellular symbionts as an understudied source for defence chemicals in the oldest-living metazoans and paves the way towards discovering similar systems in other marine sponges.
This is a preview of subscription content, access via your institution
Relevant articles
Open Access articles citing this article.
-
Microbes from Mum: symbiont transmission in the tropical reef sponge Ianthella basta
ISME Communications Open Access 27 September 2022
-
Genomic diversity and biosynthetic capabilities of sponge-associated chlamydiae
The ISME Journal Open Access 30 August 2022
-
Oceanographic setting influences the prokaryotic community and metabolome in deep-sea sponges
Scientific Reports Open Access 01 March 2022
Access options
Access Nature and 54 other Nature Portfolio journals
Get Nature+, our best-value online-access subscription
$29.99 / 30 days
cancel any time
Subscribe to this journal
Receive 12 digital issues and online access to articles
$119.00 per year
only $9.92 per issue
Rent or buy this article
Prices vary by article type
from$1.95
to$39.95
Prices may be subject to local taxes which are calculated during checkout






Data availability
The data that support the findings of this study are available from the corresponding author on request. The Ca. E. renieramycinifaciens genomes have been deposited to the IMG (Joint Genome Institute, Department of Energy) public repository, under IMG submission IDs 151197, 151198, 119799 and 119800.
References
Thomas, T. et al. Diversity, structure and convergent evolution of the global sponge microbiome. Nat. Commun. 7, 11870 (2016).
Hentschel, U., Piel, J., Degnan, S. M. & Taylor, M. W. Genomic insights into the marine sponge microbiome. Nat. Rev. Microbiol. 10, 641–654 (2012).
Nguyen, M. T., Liu, M. & Thomas, T. Ankyrin-repeat proteins from sponge symbionts modulate amoebal phagocytosis. Mol. Ecol. 23, 1635–1645 (2014).
Burgsdorf, I. et al. Lifestyle evolution in cyanobacterial symbionts of sponges. mBio 6, e00391-15 (2015).
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).
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).
Garate, L., Sureda, J., Agell, G. & Uriz, M. J. Endosymbiotic calcifying bacteria across sponge species and oceans. Sci. Rep. 7, 43674 (2017).
Zhang, F. et al. Phosphorus sequestration in the form of polyphosphate by microbial symbionts in marine sponges. Proc. Natl Acad. Sci. USA 112, 4381–4386 (2015).
Schmidt, E. W., Obraztsova, A. Y., Davidson, S., Faulkner, D. J. & Haygood, M. Identification of the antifungal peptide-containing symbiont of the marine sponge Theonella swinhoei as a novel delta-proteobacterium, “Candidatus Entotheonella palauensis”. Mar. Biol. 136, 969–977 (2000).
Wilson, M. C. et al. An environmental bacterial taxon with a large and distinct metabolic repertoire. Nature 506, 58–62 (2014).
Agarwal, V. et al. Metagenomic discovery of polybrominated diphenyl ether biosynthesis by marine sponges. Nat. Chem. Biol. 13, 537–543 (2017).
Blunt, J. W. et al. Marine natural products. Nat. Prod. Rep. 35, 8–53 (2018).
Amnuoypol, S. et al. Chemistry of renieramycins. Part 5. Structure elucidation of renieramycin-type derivatives O, Q, R, and S from thai marine sponge Xestospongia species pretreated with potassium cyanide. J. Nat. Prod. 67, 1023–1028 (2004).
Davidson, B. S. Renieramycin G, a new alkaloid from the sponge Xestospongia caycedoi. Tetrahedron Lett. 33, 3721–3724 (1992).
Oku, N., Matsunaga, S., van Soest, R. W., Fusetani, N. & Renieramycin, J. A highly cytotoxic tetrahydroisoquinoline alkaloid, from a marine sponge Neopetrosia sp. J. Nat. Prod. 66, 1136–1139 (2003).
Suwanborirux, K. et al. Chemistry of renieramycins. Part 3.(1) isolation and structure of stabilized renieramycin type derivatives possessing antitumor activity from Thai sponge Xestospongia species, pretreated with potassium cyanide. J. Nat. Prod. 66, 1441–1446 (2003).
Frincke, J. M. & Faulkner, D. J. Antimicrobial metabolites of the sponge Reniera sp. J. Am. Chem. Soc. 104, 265–269 (1982).
Lopanik, N. B. & Clay, K. Chemical defensive symbioses in the marine environment. Funct. Ecol. 28, 328–340 (2014).
Darumas, U., Chavanich, S. & Suwanborirux, K. Distribution patterns of the renieramycin-producing sponge, Xestospongia sp., and its association with other reef organisms in the gulf of Thailand. Zool. Stud. 46, 695–704 (2007).
Arai, T. et al. The structures of novel antibiotics, saframycin B and C. Tetrahedron Lett. 20, 2355–2358 (1979).
Arai, T., Takahashi, K., Nakahara, S. & Kubo, A. The structure of a novel antitumor antibiotic, saframycin A. Experientia 36, 1025–1027 (1980).
Irschik, H., Trowitzsch-Kienast, W., Gerth, K., Hofle, G. & Reichenbach, H. Saframycin Mx1, a new natural saframycin isolated from a myxobacterium. J. Antibiot. (Tokyo) 41, 993–998 (1988).
Ikeda, Y., Matsuki, H., Ogawa, T. & Munakata, T. Safracins, new antitumor antibiotics. II. Physicochemical properties and chemical structures. J. Antibiot. (Tokyo) 36, 1284–1289 (1983).
Ikeda, Y., Shimada, Y., Honjo, K., Okumoto, T. & Munakata, T. Safracins, new antitumor antibiotics. III. Biological activity. J. Antibiot. (Tokyo) 36, 1290–1294 (1983).
Rinehart, K. L. et al. Ecteinascidins 729, 743, 745, 759A, 759B, and 770: potent antitumor agents from the Caribbean tunicate Ecteinascidia turbinata. J. Org. Chem. 55, 4512–4515 (1990).
Rath, C. M. et al. Meta-omic characterization of the marine invertebrate microbial consortium that produces the chemotherapeutic natural product ET-743. ACS Chem. Biol. 6, 1244–1256 (2011).
Schofield, M. M., Jain, S., Porat, D., Dick, G. J. & Sherman, D. H. Identification and analysis of the bacterial endosymbiont specialized for production of the chemotherapeutic natural product ET-743. Environ. Microbiol. 17, 3964–3975 (2015).
Recine, F. et al. Update on the role of trabectedin in the treatment of intractable soft tissue sarcomas. OncoTargets Ther. 10, 1155–1164 (2017).
Pospiech, A., Cluzel, B., Bietenhader, J. & Schupp, T. A new Myxococcus xanthus gene cluster for the biosynthesis of the antibiotic saframycin Mx1 encoding a peptide synthetase. Microbiology 141, 1793–1803 (1995).
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).
Woodhouse, J. N., Fan, L., Brown, M. V., Thomas, T. & Neilan, B. A. Deep sequencing of non-ribosomal peptide synthetases and polyketide synthases from the microbiomes of Australian marine sponges. ISME J. 7, 1842–1851 (2013).
Fu, C.-Y. Biosynthesis of 3-hydroxy-5-methyl-O-methyltyrosine in the saframycin/safracin biosynthetic pathway. J. Microbiol. Biotechnol. 19, 439–446 (2009).
Velasco, A. et al. Molecular characterization of the safracin biosynthetic pathway from Pseudomonas fluorescens A2-2: designing new cytotoxic compounds. Mol. Microbiol. 56, 144–154 (2005).
Amann, R. I. et al. Combination of 16S rRNA-targeted oligonucleotide probes with flow cytometry for analyzing mixed microbial populations. Appl. Environ. Microbiol. 56, 1919–1925 (1990).
Daims, H., Bruhl, A., Amann, R., Schleifer, K. H. & Wagner, M. The domain-specific probe EUB338 is insufficient for the detection of all Bacteria: development and evaluation of a more comprehensive probe set. Syst. Appl. Microbiol. 22, 434–444 (1999).
Webster, N. S. et al. Same, same but different: symbiotic bacterial associations in GBR sponges. Front. Microbiol. 3, 444 (2012).
Checcucci, A. & Mengoni, A. The Integrated Microbial Genome resource of analysis. Methods Mol. Biol. 1231, 289–295 (2015).
Caporaso, J. G. et al. QIIME allows analysis of high-throughput community sequencing data. Nat. Methods 7, 335–336 (2010).
Lackner, G., Peters, E. E., Helfrich, E. J. & Piel, J. Insights into the lifestyle of uncultured bacterial natural product factories associated with marine sponges. Proc. Natl Acad. Sci. USA 114, E347–E356 (2017).
Mori, T. et al. Single-bacterial genomics validates rich and varied specialized metabolism of uncultivated Entotheonella sponge symbionts. Proc. Natl Acad. Sci. USA 115, 1718–1723 (2018).
Florez, L. V., Biedermann, P. H., Engl, T. & Kaltenpoth, M. Defensive symbioses of animals with prokaryotic and eukaryotic microorganisms. Nat. Prod. Rep. 32, 904–936 (2015).
Kwan, J. C. et al. Genome streamlining and chemical defense in a coral reef symbiosis. Proc. Natl Acad. Sci. USA 109, 20655–20660 (2012).
Lopera, J., Miller, I. J., McPhail, K. L. & Kwan, J. C. Increased biosynthetic gene dosage in a genome-reduced defensive bacterial symbiont. mSystems 2, e00096-17 (2017).
Engl, T. et al. Evolutionary stability of antibiotic protection in a defensive symbiosis. Proc. Natl Acad. Sci. USA 115, E2020–E2029 (2018).
Nakabachi, A. et al. Defensive bacteriome symbiont with a drastically reduced genome. Curr. Biol. 23, 1478–1484 (2013).
Maldonado, M. Intergenerational transmission of symbiotic bacteria in oviparous and viviparous demosponges, with emphasis on intracytoplasmically-compartmented bacterial types. J. Mar. Biol. Assoc. UK 87, 1701–1713 (2007).
Vacelet, J. & Donadey, C. Electron microscope study of the association between some sponges and bacteria. J. Exp. Mar. Biol. Ecol. 30, 301–314 (1977).
Uriz, M. J., Agell, G., Blanquer, A., Turon, X. & Casamayor, E. O. Endosymbiotic calcifying bacteria: a new cue to the origin of calcification in metazoa? Evolution 66, 2993–2999 (2012).
Schmieder, R. & Edwards, R. Quality control and preprocessing of metagenomic datasets. Bioinformatics 27, 863–864 (2011).
Bankevich, A. et al. SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing. J. Comput. Biol. 19, 455–477 (2012).
Kearse, M. et al. Geneious Basic: an integrated and extendable desktop software platform for the organization and analysis of sequence data. Bioinformatics 28, 1647–1649 (2012).
Langmead, B. & Salzberg, S. L. Fast gapped-read alignment with Bowtie 2. Nat. Methods 9, 357–359 (2012).
Li, H. et al. The sequence alignment/map format and SAMtools. Bioinformatics 25, 2078–2079 (2009).
Caporaso, J. G. et al. Ultra-high-throughput microbial community analysis on the Illumina HiSeq and MiSeq platforms. ISME J. 6, 1621–1624 (2012).
Magoc, T. & Salzberg, S. L. FLASH: fast length adjustment of short reads to improve genome assemblies. Bioinformatics 27, 2957–2963 (2011).
Edgar, R. C. MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res. 32, 1792–1797 (2004).
Price, M. N., Dehal, P. S. & Arkin, A. P. FastTree 2—approximately maximum-likelihood trees for large alignments. PLoS ONE 5, e9490 (2010).
Letunic, I. & Bork, P. Interactive Tree of Life (iTOL) v3: an online tool for the display and annotation of phylogenetic and other trees. Nucleic Acids Res. 44, W242–W245 (2016).
Albertsen, M. et al. Genome sequences of rare, uncultured bacteria obtained by differential coverage binning of multiple metagenomes. Nat. Biotechnol. 31, 533–538 (2013).
Srivastava, M. et al. The Amphimedon queenslandica genome and the evolution of animal complexity. Nature 466, 720–726 (2010).
Wickham, H. ggplot2: Elegant Graphics for Data Analysis (Springer, 2009).
Ludwig, W. et al. ARB: a software environment for sequence data. Nucleic Acids Res. 32, 1363–1371 (2004).
Schramm, A., Fuchs, B. M., Nielsen, J. L., Tonolla, M. & Stahl, D. A. Fluorescence in situ hybridization of 16S rRNA gene clones (clone-FISH) for probe validation and screening of clone libraries. Environ. Microbiol. 4, 713–720 (2002).
Wolfgang, M. C. et al. Conservation of genome content and virulence determinants among clinical and environmental isolates of Pseudomonas aeruginosa. Proc. Natl Acad. Sci. USA 100, 8484–8489 (2003).
Yamanaka, K. et al. Direct cloning and refactoring of a silent lipopeptide biosynthetic gene cluster yields the antibiotic taromycin A. Proc. Natl Acad. Sci. USA 111, 1957–1962 (2014).
Acknowledgements
We thank E. W. Schmidt, M. K. Harper-Ireland and C. Ireland at the University of Utah for providing samples Ren-PNG-07060, Ren-PNG-07113 and Ren-Pal-02, and the Republic of Palau, Papua New Guinea and the Republic of Indonesia as original sources for the sponge samples studied here. We thank M. K. Harper-Ireland and C. Ireland at the University of Utah for the underwater photograph of the Haliclona sponge shown in Fig. 1. We are grateful to C. DeCoste and the Molecular Biology Flow Cytometry Resource Facility (partially supported by the Cancer Institute of New Jersey Cancer Center Support Grant P30CA072720) for assistance with flow cytometry; P. Shao and the Molecular Biology Electron Microscopy Core Facility for assistance with TEM; G. Laevsky, the Molecular Biology Confocal Microscopy Core Facility (a Nikon Center of Excellence) and J. Zan for assistance with FISH and microscopy experiments; G. Hrebikova and A. Ploss for assistance with LCM; W. Wang and the Lewis Sigler Institute Sequencing Core Facility for assistance with high-throughput sequencing; M. Cahn for assistance with metagenomic data analysis; S. Chatterjee for general assistance; Y. Sugimoto and P. Chankhamjon for assistance with NMR and HPLC–HR-MS; and the rest of the Donia lab for useful discussions. We also thank the anonymous Nature Microbiology reviewer who suggested the name Ca. E. renieramycinifaciens for the symbiont discovered in this study. Funding for this project has been provided by Princeton University, and M.S.D. is funded by an NIH Director’s New Innovator Award (ID: 1DP2AI124441).
Author information
Authors and Affiliations
Contributions
M.D.T.-M. and M.S.D. designed the study. M.D.T.-M., J.N.B. and M.S.D. performed the experiments, analysed the data and wrote the manuscript.
Corresponding author
Ethics declarations
Competing interests
M.S.D. is a member of the Scientific Advisory Board for Deepbiome Therapeutics and a consultant for Flagship Pioneering.
Additional information
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary information
Supplementary Information
Supplementary Notes, Supplementary Tables 1–5, Supplementary Figures 1–9 and Supplementary References.
Rights and permissions
About this article
Cite this article
Tianero, M.D., Balaich, J.N. & Donia, M.S. Localized production of defence chemicals by intracellular symbionts of Haliclona sponges. Nat Microbiol 4, 1149–1159 (2019). https://doi.org/10.1038/s41564-019-0415-8
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1038/s41564-019-0415-8
This article is cited by
-
Genomic diversity and biosynthetic capabilities of sponge-associated chlamydiae
The ISME Journal (2022)
-
Strategies to access biosynthetic novelty in bacterial genomes for drug discovery
Nature Reviews Drug Discovery (2022)
-
Oceanographic setting influences the prokaryotic community and metabolome in deep-sea sponges
Scientific Reports (2022)
-
Microbes from Mum: symbiont transmission in the tropical reef sponge Ianthella basta
ISME Communications (2022)
-
Subcellular view of host–microbiome nutrient exchange in sponges: insights into the ecological success of an early metazoan–microbe symbiosis
Microbiome (2021)