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Published September 6, 2016 | Supplemental Material + Published
Journal Article Open

Stepwise metamorphosis of the tubeworm Hydroides elegans is mediated by a bacterial inducer and MAPK signaling

Abstract

Diverse animal taxa metamorphose between larval and juvenile phases in response to bacteria. Although bacteria-induced metamorphosis is widespread among metazoans, little is known about the molecular changes that occur in the animal upon stimulation by bacteria. Larvae of the tubeworm Hydroides elegans metamorphose in response to surface-bound Pseudoalteromonas luteoviolacea bacteria, producing ordered arrays of phage tail-like metamorphosis-associated contractile structures (MACs). Sequencing the Hydroides genome and transcripts during five developmental stages revealed that MACs induce the regulation of groups of genes important for tissue remodeling, innate immunity, and mitogen-activated protein kinase (MAPK) signaling. Using two MAC mutations that block P. luteoviolacea from inducing settlement or metamorphosis and three MAPK inhibitors, we established a sequence of bacteria-induced metamorphic events: MACs induce larval settlement; then, particular properties of MACs encoded by a specific locus in P. luteoviolacea initiate cilia loss and activate metamorphosis-associated transcription; finally, signaling through p38 and c-Jun N-terminal kinase (JNK) MAPK pathways alters gene expression and leads to morphological changes upon initiation of metamorphosis. Our results reveal that the intricate interaction between Hydroides and P. luteoviolacea can be dissected using genomic, genetic, and pharmacological tools. Hydroides' dependency on bacteria for metamorphosis highlights the importance of external stimuli to orchestrate animal development. The conservation of Hydroides genome content with distantly related deuterostomes (urchins, sea squirts, and humans) suggests that mechanisms of bacteria-induced metamorphosis in Hydroides may have conserved features in diverse animals. As a major biofouling agent, insight into the triggers of Hydroides metamorphosis might lead to practical strategies for fouling control.

Additional Information

© 2016 National Academy of Sciences. Freely available online through the PNAS open access option. Edited by Linda Z. Holland, University of California, San Diego, La Jolla, CA, and accepted by Editorial Board Member Nancy Knowlton July 13, 2016 (received for review February 24, 2016). Published online before print August 22, 2016. We thank Heather Maughan for providing constructive feedback and editing the manuscript. The authors acknowledge support from Piotr Szwedziak, Peter Tittmann, and ScopeM at ETH Zürich. Experiments were carried out in the laboratories of N.J.S., M.P., D.K.N., and at the Millard and Muriel Jacobs Genome Facility at Caltech. This work was supported by grants from the Office of Naval Research (N00014-14-1-0340 to N.J.S. and D.K.N.; N00014-16-1-2135 to N.J.S.), Swiss National Science Foundation (31003A_152878 to M.P.), ETH Zürich (ETH-45 15-1 to M.P.), and the Helmut Horten Foundation (to M.P.). N.J.S. and I.A. contributed equally to this work. Author contributions: N.J.S., I.A., J.M.M., M.P., and D.K.N. designed research; N.J.S., I.A., and J.M.M. performed research; N.J.S., I.A., J.M.M., M.P., and D.K.N. analyzed data; and N.J.S., I.A., and D.K.N. wrote the paper. The authors declare no conflict of interest. This article is a PNAS Direct Submission. L.Z.H. is a Guest Editor invited by the Editorial Board. Data deposition: The raw sequence reads reported in this paper have been deposited in the National Center for Biotechnology Information Sequence Read Archive (SRA) database [accession nos. SRP067980 (genome) and SRP067899 (transcriptome)]. The whole-genome shotgun project reported in this paper has been deposited in the DNA Data Bank of Japan (DDBJ)/European Molecular Biology Laboratory (EMBL)/GenBank database (accession no. LQRL00000000, version LQRL01000000). This article contains supporting information online at www.pnas.org/lookup/suppl/doi:10.1073/pnas.1603142113/-/DCSupplemental.

Attached Files

Published - PNAS-2016-Shikuma-10097-102.pdf

Supplemental Material - pnas.1603142113.sapp.pdf

Supplemental Material - pnas.1603142113.sd01.xlsx

Supplemental Material - pnas.1603142113.sd02.xlsx

Supplemental Material - pnas.1603142113.sd03.txt

Supplemental Material - pnas.1603142113.sd04.txt

Supplemental Material - pnas.1603142113.sm01.avi

Supplemental Material - pnas.1603142113.sm02.avi

Supplemental Material - pnas.201603142SI.pdf

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