Marine & Environmental Sciences Faculty Articles

Document Type

Article

Publication Date

6-26-2018

Publication Title

mBio

Keywords

Bioluminescence, Evolution, Genome reduction, Symbiosis, Transposons

ISSN

2150-7511

Volume

9

Issue/No.

3

First Page

e01033-18

Abstract

Diverse marine fish and squid form symbiotic associations with extracellular bioluminescent bacteria. These symbionts are typically free-living bacteria with large genomes, but one known lineage of symbionts has undergone genomic reduction and evolution of host dependence. It is not known why distinct evolutionary trajectories have occurred among different luminous symbionts, and not all known lineages previously had genome sequences available. In order to better understand patterns of evolution across diverse bioluminescent symbionts, we de novo sequenced the genomes of bacteria from a poorly studied interaction, the extracellular symbionts from the “lures” of deep-sea ceratioid anglerfishes. Deep-sea anglerfish symbiont genomes are reduced in size by about 50% compared to free-living relatives. They show a striking convergence of genome reduction and loss of metabolic capabilities with a distinct lineage of obligately host-dependent luminous symbionts. These losses include reductions in amino acid synthesis pathways and abilities to utilize diverse sugars. However, the symbiont genomes have retained a number of categories of genes predicted to be useful only outside the host, such as those involved in chemotaxis and motility, suggesting that they may persist in the environment. These genomes contain very high numbers of pseudogenes and show massive expansions of transposable elements, with transposases accounting for 28 and 31% of coding sequences in the symbiont genomes. Transposon expansions appear to have occurred at different times in each symbiont lineage, indicating either independent evolutions of reduction or symbiont replacement. These results suggest ongoing genomic reduction in extracellular luminous symbionts that is facilitated by transposon proliferations.

Comments

Copyright © 2018 Hendry et al.

This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.

inline-supplementary-material-10.pdf (241 kB)
Supplemental Materials and Methods

ORCID ID

0000-0002-1637-4125

DOI

10.1128/mBio.01033-18

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