Abstract

The bacterial genus Endozoicomonas was commonly detected in healthy corals in many coral-associated bacteria studies in the past decade. Although, it is likely to be a core member of coral microbiota, little is known about its ecological roles. To decipher potential interactions between bacteria and their coral hosts, we sequenced and investigated the first culturable endozoicomonal bacterium from coral, the E. montiporae CL-33T. Its genome had potential sign of ongoing genome erosion and gene exchange with its host. Testosterone degradation and type III secretion system are commonly present in Endozoicomonas and may have roles to recognize and deliver effectors to their hosts. Moreover, genes of eukaryotic ephrin ligand B2 are present in its genome; presumably, this bacterium could move into coral cells via endocytosis after binding to coral's Eph receptors. In addition, 7,8-dihydro-8-oxoguanine triphosphatase and isocitrate lyase are possible type III secretion effectors that might help coral to prevent mitochondrial dysfunction and promote gluconeogenesis, especially under stress conditions. Based on all these findings, we inferred that E. montiporae was a facultative endosymbiont that can recognize, translocate, communicate and modulate its coral host.

Highlights

  • The bacterial genus Endozoicomonas was first proposed by Kurahashi and Yokota (2007)

  • We noticed that a previously released E. montiporae genome (Neave et al, 2014) had the same limitation, which was attributed to sequence assemblies being greatly affected by numerous repeat sequences

  • Instead of catalase, we identified another type of H2O2-removing enzyme, the thiol peroxidases (Tpx), that could be secreted via T3SS in pathogenic bacteria Vibrio

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Summary

Introduction

The bacterial genus Endozoicomonas was first proposed by Kurahashi and Yokota (2007). In the draft genome of the coral Acropora digitifera, open reading frames were detected in two regions located inside the scaffold 125 and 132 that resembled the mucin protein of N. vectensis and contained putative N-glycosylation sites. No similar homologs related to enzymes of the two reactions were detected in Endozoicomonas genomes, suggesting the bacteria might not be able to deeply decompose their host mucus.

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