Importance of mobile genetic element immunity in numerically abundant Trichodesmium clades

dc.contributor.author Webb, Eric A.
dc.contributor.author Held, Noelle A.
dc.contributor.author Zhao, Yiming
dc.contributor.author Graham, Elaina D.
dc.contributor.author Conover, Asa E.
dc.contributor.author Semones, Jake
dc.contributor.author Lee, Michael D.
dc.contributor.author Feng, Yuanyuan
dc.contributor.author Fu, Fei-Xue
dc.contributor.author Saito, Mak A.
dc.contributor.author Hutchins, David A.
dc.date.accessioned 2023-09-28T19:45:38Z
dc.date.available 2023-09-28T19:45:38Z
dc.date.issued 2023-02-23
dc.description © The Author(s), 2023. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Webb, E. A., Held, N. A., Zhao, Y., Graham, E. D., Conover, A. E., Semones, J., Lee, M. D., Feng, Y., Fu, F.-X., Saito, M. A., & Hutchins, D. A. Importance of mobile genetic element immunity in numerically abundant Trichodesmium clades. ISME Communications, 3(1), (2023): 15, https://doi.org/10.1038/s43705-023-00214-y.
dc.description.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 Nfixing 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 CO-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.
dc.description.sponsorship This work was funded by NSF grants OCE 1657757 and OCE 1851222 to DAH, FXF, and EAW, OCE 1850719 to MAS, discretionary USC funds, and BIO2125191 to EAW.
dc.identifier.citation Webb, E. A., Held, N. A., Zhao, Y., Graham, E. D., Conover, A. E., Semones, J., Lee, M. D., Feng, Y., Fu, F.-X., Saito, M. A., & Hutchins, D. A. (2023). Importance of mobile genetic element immunity in numerically abundant Trichodesmium clades. ISME Communications, 3(1), 15.
dc.identifier.doi 10.1038/s43705-023-00214-y
dc.identifier.uri https://hdl.handle.net/1912/66934
dc.publisher Springer
dc.relation.uri https://doi.org/10.1038/s43705-023-00214-y
dc.rights Attribution 4.0 International *
dc.rights.uri http://creativecommons.org/licenses/by/4.0/ *
dc.title Importance of mobile genetic element immunity in numerically abundant Trichodesmium clades
dc.type Article
dspace.entity.type Publication
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