16S Rrna Gene Metabarcoding Indicates Species-Characteristic

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16S Rrna Gene Metabarcoding Indicates Species-Characteristic 16S rRNA Gene Metabarcoding Indicates Species-Characteristic Microbiomes in Deep-Sea Benthic Foraminifera Iines Salonen, Panagiota-Myrsini Chronopoulou, Hidetaka Nomaki, Dewi Langlet, Masashi Tsuchiya, Karoliina Koho To cite this version: Iines Salonen, Panagiota-Myrsini Chronopoulou, Hidetaka Nomaki, Dewi Langlet, Masashi Tsuchiya, et al.. 16S rRNA Gene Metabarcoding Indicates Species-Characteristic Microbiomes in Deep- Sea Benthic Foraminifera. Frontiers in Microbiology, Frontiers Media, 2021, 12, pp.694406. 10.3389/fmicb.2021.694406. hal-03306215 HAL Id: hal-03306215 https://hal.archives-ouvertes.fr/hal-03306215 Submitted on 29 Jul 2021 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. ORIGINAL RESEARCH published: 27 July 2021 doi: 10.3389/fmicb.2021.694406 16S rRNA Gene Metabarcoding Indicates Species-Characteristic Microbiomes in Deep-Sea Benthic Foraminifera Iines S. Salonen 1,2*, Panagiota-Myrsini Chronopoulou 1, Hidetaka Nomaki 2, Dewi Langlet 2,3,4, Masashi Tsuchiya 5 and Karoliina A. Koho 1 1 Ecosystems and Environment Research Program, University of Helsinki, Helsinki, Finland, 2 SUGAR, X-star, Japan Agency of Marine-Earth Science and Technology (JAMSTEC), Yokosuka, Japan, 3 UMR 8187 - LOG - Laboratoire d’Océanologie et de Géosciences, Université de Lille - CNRS, Université du Littoral Côte d’Opale, Station Marine de Wimereux, Lille, France, 4 Evolution, Cell Biology, and Symbiosis Unit, Okinawa Institute of Science and Technology, Okinawa, Japan, 5 Research Institute for Global Change (RIGC), Japan Agency of Marine-Earth Science and Technology (JAMSTEC), Yokosuka, Japan Foraminifera are unicellular eukaryotes that are an integral part of benthic fauna in many marine ecosystems, including the deep sea, with direct impacts on benthic biogeochemical cycles. In these systems, different foraminiferal species are known to have a distinct vertical Edited by: distribution, i.e., microhabitat preference, which is tightly linked to the physico-chemical Francisco J. A. Nascimento, Stockholm University, Sweden zonation of the sediment. Hence, foraminifera are well-adapted to thrive in various conditions, Reviewed by: even under anoxia. However, despite the ecological and biogeochemical significance of Amir Szitenberg, foraminifera, their ecology remains poorly understood. This is especially true in terms of the Dead Sea and Arava Science Center – Dead Sea Branch, Israel composition and diversity of their microbiome, although foraminifera are known to harbor Fatma Gomaa, diverse endobionts, which may have a significant meaning to each species’ survival strategy. Woods Hole Oceanographic In this study, we used 16S rRNA gene metabarcoding to investigate the microbiomes of five Institution, United States different deep-sea benthic foraminiferal species representing differing microhabitat preferences. *Correspondence: Iines S. Salonen The microbiomes of these species were compared intra- and inter-specifically, as well as with [email protected] the surrounding sediment bacterial community. Our analysis indicated that each species was characterized with a distinct, statistically different microbiome that also differed from the Specialty section: This article was submitted to surrounding sediment community in terms of diversity and dominant bacterial groups. We were Aquatic Microbiology, also able to distinguish specific bacterial groups that seemed to be strongly associated with a section of the journal Frontiers in Microbiology particular foraminiferal species, such as the family Marinilabiliaceae for Chilostomella ovoidea Received: 13 April 2021 and the family Hyphomicrobiaceae for Bulimina subornata and Bulimina striata. The presence Accepted: 06 July 2021 of bacterial groups that are tightly associated to a certain foraminiferal species implies that Published: 27 July 2021 there may exist unique, potentially symbiotic relationships between foraminifera and bacteria Citation: that have been previously overlooked. Furthermore, the foraminifera contained chloroplast Salonen IS, Chronopoulou P-M, Nomaki H, Langlet D, Tsuchiya M and reads originating from different sources, likely reflecting trophic preferences and ecological Koho KA (2021) 16S rRNA Gene characteristics of the different species. This study demonstrates the potential of 16S rRNA Metabarcoding Indicates Species- Characteristic Microbiomes in gene metabarcoding in resolving the microbiome composition and diversity of eukaryotic Deep-Sea Benthic Foraminifera. unicellular organisms, providing unique in situ insights into enigmatic deep-sea ecosystems. Front. Microbiol. 12:694406. doi: 10.3389/fmicb.2021.694406 Keywords: foraminifera, unicellular eukaryotes, sediment, deep sea, endobionts, metabarcoding Frontiers in Microbiology | www.frontiersin.org 1 July 2021 | Volume 12 | Article 694406 Salonen et al. Microbiomes of Deep-Sea Benthic Foraminifera INTRODUCTION faster in sediments than the deep-dwellers (Kitazato, 1988; Ernst et al., 2002). In contrast, deep infaunal species, which can Benthic foraminifera are single-celled eukaryotes, widespread live below oxygen penetration depth, react slower to the fresh in global oceans and particularly abundant in deep-sea sediments, organic matter inputs (Nomaki et al., 2005, 2006). This may accounting for up to 50% or more of the total eukaryotic be due to their suspected longer life cycle, during which they biomass in places (Snider et al., 1984; Gooday et al., 1992). are likely to rely on deposit-feeding and consumption of degraded They are important consumers of phytodetritus Gooday,( 1988; organic matter instead of fresh phytodetritus (Goldstein and Ohga and Kitazato, 1997; Moodley et al., 2002), experimentally Corliss, 1994; Ohga and Kitazato, 1997; Schmiedl et al., 2004). shown to consume carbon faster than metazoans (Nomaki However, the exact feeding preferences of foraminifera, especially et al., 2005). Part of their ecological success in the benthic on species level, are poorly resolved due to the difficulty of environment may be attributed to their ability to thrive in examining them in situ. New molecular approaches, such as the low-oxygen environments (e.g., Moodley and Hess, 1992; metabarcoding, can provide new insights on foraminiferal ecology Bernhard, 1993; Jorissen et al., 1995; Moodley et al., 1997; and their feeding preferences (Chronopoulou et al., 2019). Langlet et al., 2013). Adaptations to hypoxia may include, for In marine science, the research on microbiomes has rapidly example, the wide-spread ability of foraminifera to accumulate increased during the last decade, but host-associated microbiome and respire nitrate (Risgaard-Petersen et al., 2006; Piña-Ochoa research is still mainly focused on multicellular and larger et al., 2009), as well as their capability to reduce metabolism, animals, such as sponges and corals, instead of single-celled suspend reproduction, and enter a state of dormancy organisms (Trevathan-Tackett et al., 2019). In the case of (LeKieffre et al., 2017; Koho et al., 2018; Richirt et al., 2020). foraminifera, previous studies on their intracellular bacterial A yet unresolved link in deep-sea foraminiferal ecology and communities have been mainly based on transmission electron environmental adaptation is the composition and role of their microscopy (TEM) observations (e.g., Bernhard et al., 2018; associated microbiomes. Benthic foraminifera are known to Koho et al., 2018). However, the current molecular ecology develop endobiotic relationships and close associations with tools, such as DNA metabarcoding, offer new, efficient ways prokaryotes (e.g., Bernhard, 2003; Bernhard et al., 2006, 2018), to investigate the diversity and composition of microbiomes which may include denitrifiers (Bernhard et al., 2011), sulphur of the unicellular foraminifera (e.g., Bird et al., 2017; cycle-related bacteria (Tsuchiya et al., 2015; Salonen et al., Prazeres et al., 2017; Salonen et al., 2019). 2019), Cyanobacteria (Prazeres et al., 2017), or even In this study, we applied the definition of microbiome by methanotrophs (Bernhard and Panieri, 2018). The endobiotic Trevathan-Tackett et al. (2019), stating that microbiome is a relationships between foraminifera and bacteria have been consortium of intracellular bacteria derived from genetic material, hypothesized to provide the host with metabolic flexibility, to investigate the microbiome of deep-sea foraminifera with alternative carbon assimilation pathways, and enhanced nutrient/ variable microhabitat distributions. We utilized a DNA organic compound cycling, enabling them to not only survive metabarcoding approach based on 16S rRNA gene to investigate but also flourish in the harsh benthic environment Bernhard( the microbiome characteristics of deep-sea foraminifera in terms et al., 2011; Bird et al., 2017; Prazeres et al., 2017; Tsuchiya of intracellular bacterial and chloroplast composition. et al., 2018; Salonen et al., 2019). Despite the ecological importance Comparison was also made with the surrounding bacterial of microbiome in foraminiferal
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