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Exploring Microdiversity in Novel Kordia Sp. (Bacteroidetes) with Proteorhodopsin from the Tropical Indian Ocean Via Single Amplified Genomes

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Exploring Microdiversity in Novel Kordia Sp. (Bacteroidetes) with Proteorhodopsin from the Tropical Indian Ocean Via Single Amplified Genomes Research Collection Journal Article Exploring Microdiversity in Novel Kordia sp. (Bacteroidetes) with Proteorhodopsin from the Tropical Indian Ocean via Single Amplified Genomes Author(s): Royo-Llonch, Marta; Ferrera, Isabel; Cornejo-Castillo, Francisco M.; Sánchez, Pablo; Salazar Guiral, Guillem; Stepanauskas, Ramunas; González, José M.; Sieracki, Michael E.; Speich, Sabrina; Stemmann, Lars; Pedrós-Alió, Carlos; Acinas, Silvia G. Publication Date: 2017-07 Permanent Link: https://doi.org/10.3929/ethz-b-000371229 Originally published in: Frontiers in Microbiology 8, http://doi.org/10.3389/fmicb.2017.01317 Rights / License: Creative Commons Attribution 4.0 International This page was generated automatically upon download from the ETH Zurich Research Collection. For more information please consult the Terms of use. ETH Library fmicb-08-01317 July 21, 2017 Time: 15:22 # 1 ORIGINAL RESEARCH published: 25 July 2017 doi: 10.3389/fmicb.2017.01317 Exploring Microdiversity in Novel Kordia sp. (Bacteroidetes) with Proteorhodopsin from the Tropical Indian Ocean via Single Amplified Genomes Marta Royo-Llonch1, Isabel Ferrera1, Francisco M. Cornejo-Castillo1, Pablo Sánchez1, Guillem Salazar1, Ramunas Stepanauskas2, José M. González3, Michael E. Sieracki4, Sabrina Speich5, Lars Stemmann6, Carlos Pedrós-Alió7 and Silvia G. Acinas1,8* 1 Department of Marine Biology and Oceanography, Institut de Ciències del Mar, Consejo Superior de Investigaciones Edited by: Científicas, Barcelona, Spain, 2 Bigelow Laboratory for Ocean Sciences, East Boothbay, ME, United States, 3 Department of Roland Hatzenpichler, Microbiology, University of La Laguna, La Laguna, Spain, 4 National Science Foundation, Arlington, VA, United States, Montana State University, 5 École Normale Supérieure, Département de Géosciences, Laboratoire de Météorologie Dynamique, UMR 8539 United States ENS-CNRS- École Polytechnique, Paris, France, 6 Sorbonne Universités, UPMC Université Paris 06, CNRS, Laboratoire 7 Reviewed by: d’Océanographie de Villefranche (LOV) UMR7093, Observatoire Océanologique, Villefranche-sur-Mer, France, Systems Jayashree Ray, Biology Program, Centro Nacional de Biotecnologia, Consejo Superior de Investigaciones Científicas, Madrid, Spain, 8 Lawrence Berkeley National Departament de Genètica i de Microbiologia, Facultat de Biociències, Universitat Autònoma de Barcelona, Bellaterra, Spain Laboratory, United States Christian Rinke, Marine Bacteroidetes constitute a very abundant bacterioplankton group in the The University of Queensland, Australia oceans that plays a key role in recycling particulate organic matter and includes Albert Leopold Mueller, several photoheterotrophic members containing proteorhodopsin. Relatively few marine Stanford University, United States Bacteroidetes species have been described and, moreover, they correspond to cultured *Correspondence: Silvia G. Acinas isolates, which in most cases do not represent the actual abundant or ecologically [email protected] relevant microorganisms in the natural environment. In this study, we explored the microdiversity of 98 Single Amplified Genomes (SAGs) retrieved from the surface Specialty section: This article was submitted to waters of the underexplored North Indian Ocean, whose most closely related isolate Microbial Physiology and Metabolism, is Kordia algicida OT-1. Using Multi Locus Sequencing Analysis (MLSA) we found a section of the journal no microdiversity in the tested conserved phylogenetic markers (16S rRNA and 23S Frontiers in Microbiology rRNA genes), the fast-evolving Internal Transcribed Spacer and the functional markers Received: 10 February 2017 Accepted: 29 June 2017 proteorhodopsin and the beta-subunit of RNA polymerase. Furthermore, we carried Published: 25 July 2017 out a Fragment Recruitment Analysis (FRA) with marine metagenomes to learn about Citation: the distribution and dynamics of this microorganism in different locations, depths and Royo-Llonch M, Ferrera I, Cornejo-Castillo FM, Sánchez P, size fractions. This analysis indicated that this taxon belongs to the rare biosphere, Salazar G, Stepanauskas R, showing its highest abundance after upwelling-induced phytoplankton blooms and González JM, Sieracki ME, Speich S, sinking to the deep ocean with large organic matter particles. This uncultured Kordia Stemmann L, Pedrós-Alió C and Acinas SG (2017) Exploring lineage likely represents a novel Kordia species (Kordia sp. CFSAG39SUR) that contains Microdiversity in Novel Kordia sp. the proteorhodopsin gene and has a widespread spatial and vertical distribution. The (Bacteroidetes) with Proteorhodopsin from the Tropical Indian Ocean via combination of SAGs and MLSA makes a valuable approach to infer putative ecological Single Amplified Genomes. roles of uncultured abundant microorganisms. Front. Microbiol. 8:1317. doi: 10.3389/fmicb.2017.01317 Keywords: MLSA, SAGs, Bacteroidetes, Kordia, proteorhodopsin Frontiers in Microbiology| www.frontiersin.org 1 July 2017| Volume 8| Article 1317 fmicb-08-01317 July 21, 2017 Time: 15:22 # 2 Royo-Llonch et al. Single Amplified Genomes of Bacteroidetes INTRODUCTION The genus Kordia (Bacteroidetes, Flavobacteriaceae) contains representatives with isolation sources suggesting different The phylum Bacteroidetes is the third most abundant group of lifestyles and habitats: (i) marine surface seawater for Kordia bacteria in the oceans (Kirchman, 2002) but has been poorly antarctica (Baek et al., 2013), K. aquimaris (Hameed et al., 2013), studied at the species level compared to the two other main and K. algicida (Sohn et al., 2004), (ii) surface freshwater for marine microbial phyla, i.e., Proteobacteria and Cyanobacteria. K. zhangzhouensis (Lai et al., 2015), (iii) the interphase between Bacteroidetes is a cosmopolitan phylum that typically constitutes the ocean and a freshwater spring for K. jejudonensis (Park et al., between 4 and 22% of marine bacterioplankton cells (Glöckner 2014), (iv) the surface of the green alga Ulva sp. for K. ulvae (Qi et al., 1999; Cottrell and Kirchman, 2000; Alonso-Sáez et al., et al., 2016) or (v) the digestive tract of a marine polychaete for 2007; Ruiz-González et al., 2012; Lefort and Gasol, 2013; Acinas K. periserrulae (Choi et al., 2011). et al., 2014). The relative abundance of Bacteroidetes can reach Here we report the first MLSA analysis of the genus up to 53% and it often correlates with phytoplankton blooms Kordia, performed with 98 Single Amplified Genomes (SAGs) (Abell and Bowman, 2005; Fandino et al., 2005). Bacteroidetes from the genus Kordia that were retrieved from a seawater are proficient at the degradation of particulate organic matter sample from the North Indian Ocean, a location subjected (POM) (Cottrell and Kirchman, 2000; Gómez-Pereira et al., 2012; to seasonal monsoon winds and coastal upwelling events as Fernández-Gómez et al., 2013; Swan et al., 2013) and present well as open ocean oligotrophy. As a result, the microbial a generally high growth rate when substrate is available (e.g., community structure varies and large phytoplankton blooms are following phytoplankton blooms) (Kirchman, 2002; Ferrera et al., common, especially those formed by diatoms (Landry et al., 2011; Buchan et al., 2014). Some representatives contain the gene 1998). One characteristic feature of the North Indian Ocean coding for the light-dependent proton-pump proteorhodopsin, is the marked Oxygen Minimum Zone (OMZ) layered in the that has been shown to stimulate bacterial growth or work subsurface of the upwelling regions (Roullier et al., 2014). Even as a source of additional energy in the presence of light in though there have been studies of the bacterial community some strains (Gómez-Consarnau et al., 2007; Stepanauskas and composition of the Indian Ocean seawater (Sunagawa et al., Sieracki, 2007; González et al., 2008; Woyke et al., 2009; Martínez- 2015; Wang et al., 2016) and deep-sea sediments (Wu et al., García et al., 2012). Although Bacteroidetes can be found in the 2011; Khandeparker et al., 2014), the diversity and genomics free-living plankton size fraction, they seem to be predominantly of the Bacteroidetes populations remain poorly characterized particle-attached (DeLong et al., 1993; Schattenhofer et al., in this area. This is then a good opportunity to analyze 2009; Crespo et al., 2013; Díez-Vives et al., 2014; Salazar et al., whether micro-diversity exists in a particular Bacteroidetes 2015). taxon dominating after the phytoplankton bloom event. We Population genetics studies of marine Bacteroidetes are scarce, used the well-conserved ribosomal RNA genes, the fast- and have been generally conducted using very small populations evolving internal transcribed spacer (ITS) and the beta subunit of isolates or comparing several distant species (Fernández- DNA-directed RNA polymerase rpoB. We also screened these Gómez et al., 2013; Swan et al., 2013), giving a general genomes for a gene that can provide ecological information overview of common genotypic traits and differences above of the targeted population: proteorhodopsin (PR), which the species level. Single cell sequencing enables the retrieval of is present in ecologically relevant Bacteroidetes genomes discrete microbial genomes from natural samples. A direct link (González et al., 2008; Pinhassi et al., 2016). Fragment between phylogenetic markers and functional information from Recruitment Analysis (FRA) of metagenomic reads suggested single cells allows a finer resolution in microdiversity studies the preferred habitat and an estimated abundance
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