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Viral Hijacking and Metabolic Reprogramming in Candidatus Pelagibacter ubique: Ecological Consequences of Phage-Driven “Zombification” in the Global Ocean

DOI: 10.4236/aim.2026.167015, PP. 273-287

Keywords: Candidatus Pelagibacter ubique, SAR11, Pelagiphages, Marine Viral Ecology, Metabolic Reprogramming, Auxiliary Metabolic Genes, Viral Shunt, Carbon Cycling, Ocean Biogeochemistry, Marine Microbiology, Host-Phage Interactions, Climate Change

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Abstract:

Candidatus Pelagibacter ubique, a dominant member of the SAR11 clade, is among the most abundant heterotrophic organisms in the global ocean and plays a central role in marine carbon cycling. Despite possessing one of the smallest genomes of any free-living organism, SAR11 thrives in oligotrophic marine environments through extensive genome streamlining, efficient nutrient acquisition systems, and specialized metabolic adaptations. However, SAR11 populations are subject to persistent viral predation by pelagiphages, a diverse group of bacteriophages that influence microbial mortality, evolution, and nutrient turnover throughout the oceans. This review examines current understanding of SAR11 physiology, pelagiphage infection dynamics, and the ecological consequences of infection-induced metabolic reprogramming. Particular emphasis is placed on viral manipulation of host metabolism, auxiliary metabolic genes, host resource allocation, and the role of phage-mediated lysis in the marine viral shunt. The term “zombification” is used here as a conceptual analogy describing a transient physiological state in which infected cells may remain metabolically active while cellular functions become increasingly redirected toward viral replication. While aspects of this phenomenon have been observed in marine phage-host systems, several proposed mechanisms remain incompletely resolved in SAR11-pelagiphage interactions and require further experimental investigation. We further examine how viral turnover of SAR11 biomass contributes to dissolved organic matter recycling, nutrient redistribution, and the regulation of oceanic carbon sequestration. Finally, emerging genomic, transcriptomic, and imaging technologies are discussed as tools for resolving outstanding questions concerning host-virus interactions in marine ecosystems. Understanding how pelagiphages alter the physiology and ecological function of SAR11 populations provides important insight into one of the most widespread biological interactions in the global ocean and its potential consequences under changing climatic conditions.

References

[1]  Giovannoni, S.J., Tripp, H.J., Givan, S., Podar, M., Vergin, K.L., Baptista, D., et al. (2005) Genome Streamlining in a Cosmopolitan Oceanic Bacterium. Science, 309, 1242-1245.
https://doi.org/10.1126/science.1114057
[2]  Giovannoni, S.J. (2017) SAR11 Bacteria: The Most Abundant Plankton in the Oceans. Annual Review of Marine Science, 9, 231-255.
https://doi.org/10.1146/annurev-marine-010814-015934
[3]  Giovannoni, S.J., Cameron Thrash, J. and Temperton, B. (2014) Implications of Streamlining Theory for Microbial Ecology. The ISME Journal, 8, 1553-1565.
https://doi.org/10.1038/ismej.2014.60
[4]  Wilhelm, S.W. and Suttle, C.A. (1999) Viruses and Nutrient Cycles in the Sea. BioScience, 49, 781-788.
https://doi.org/10.2307/1313569
[5]  Jover, L.F., Effler, T.C., Buchan, A., Wilhelm, S.W. and Weitz, J.S. (2014) The Elemental Composition of Virus Particles: Implications for Marine Biogeochemical Cycles. Nature Reviews Microbiology, 12, 519-528.
https://doi.org/10.1038/nrmicro3289
[6]  Suttle, C.A. (2007) Marine Viruses-Major Players in the Global Ecosystem. Nature Reviews Microbiology, 5, 801-812.
[7]  Zhao, Y., Temperton, B., Thrash, J.C., Schwalbach, M.S., Vergin, K.L., Landry, Z.C., et al. (2013) Abundant SAR11 Viruses in the Ocean. Nature, 494, 357-360.
https://doi.org/10.1038/nature11921
[8]  Choi, C.J., Qin, F., Cude, W.N. and Colleagues (2024) Globally Occurring Pelagiphage Infections Create Ribosome-Deprived Cells. Nature Microbiology, 9, 879-891.
[9]  Grote, J., Thrash, J.C., Huggett, M.J., Landry, Z.C., Carini, P., Giovannoni, S.J., et al. (2012) Streamlining and Core Genome Conservation among Highly Divergent Members of the SAR11 Clade. mBio, 3, e00252-12.
https://doi.org/10.1128/mbio.00252-12
[10]  Buchholz, H.H., Michelsen, M.L., Bola?os, L.M. and Colleagues (2022) Genome-Resolved Analyses Reveal Diverse Ecological Strategies among Pelagiphages in Marine Environments. ISME Journal, 16, 1821-1835.
[11]  Breitbart, M., Bonnain, C., Malki, K. and Sawaya, N.A. (2018) Phage Puppet Masters of the Marine Microbial Realm. Nature Microbiology, 3, 754-766.
https://doi.org/10.1038/s41564-018-0166-y
[12]  Thingstad, T.F. (2000) Elements of a Theory for the Mechanisms Controlling Abundance, Diversity, and Biogeochemical Role of Lytic Bacterial Viruses in Aquatic Systems. Limnology and Oceanography, 45, 1320-1328.
https://doi.org/10.4319/lo.2000.45.6.1320
[13]  Fuhrman, J.A. (1999) Marine Viruses and Their Biogeochemical and Ecological Effects. Nature, 399, 541-548.
https://doi.org/10.1038/21119

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