Importance of mobile genetic element immunity in numerically abundant Trichodesmium clades

Author:

Webb Eric A1ORCID,Held Noelle A23ORCID,Zhao Yiming1ORCID,Graham Elaina D1ORCID,Conover Asa E1,Semones Jake1,Lee Michael D4,Feng Yuanyuan5,Fu Fei-xue1,Saito Mak A2ORCID,Hutchins David A1ORCID

Affiliation:

1. Marine and Environmental Biology, Department of Biological Sciences, University of Southern California , Los Angeles, CA 90089, USA

2. Department of Marine Chemistry and Geochemistry, Woods Hole Oceanographic Institution , Woods Hole, MA 02543, USA

3. Department of Earth, Atmospheric, and Planetary Sciences, Massachusetts Institute of Technology , Cambridge, MA 02139, USA

4. Blue Marble Space Institute of Science, NASA Ames Research Center , Mountain View, CA 94035, USA

5. College of Marine and Environmental Sciences, Tianjin University of Science and Technology , Tianjin 300457, China

Abstract

Abstract The colony-forming cyanobacteria Trichodesmium spp. are considered one of the most important nitrogen-fixing genera in the warm, low nutrient ocean. Despite this central biogeochemical role, many questions about their evolution, physiology, and trophic interactions remain unanswered. To address these questions, we describe Trichodesmium pangenomic potential via significantly improved genomic assemblies from two isolates and 15 new >50% complete Trichodesmium metagenome-assembled genomes from hand-picked, Trichodesmium colonies spanning the Atlantic Ocean. Phylogenomics identified ~four N2 fixing clades of Trichodesmium across the transect, with T. thiebautii dominating the colony-specific reads. Pangenomic analyses showed that all T. thiebautii MAGs are enriched in COG defense mechanisms and encode a vertically inherited Type III-B Clustered Regularly Interspaced Short Palindromic Repeats and associated protein-based immunity system (CRISPR-Cas). Surprisingly, this CRISPR-Cas system was absent in all T. erythraeum genomes, vertically inherited by T. thiebautii, and correlated with increased signatures of horizontal gene transfer. Additionally, the system was expressed in metaproteomic and transcriptomic datasets and CRISPR spacer sequences with 100% identical hits to field-assembled, putative phage genome fragments were identified. While the currently CO2-limited T. erythraeum is expected to be a ‘winner’ of anthropogenic climate change, their genomic dearth of known phage resistance mechanisms, compared to T. thiebautii, could put this outcome in question. Thus, the clear demarcation of T. thiebautii maintaining CRISPR-Cas systems, while T. erythraeum does not, identifies Trichodesmium as an ecologically important CRISPR-Cas model system, and highlights the need for more research on phage-Trichodesmium interactions.

Funder

NSF | GEO | Division of Ocean Sciences

NSF | Directorate for Biological Sciences

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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