TY - JOUR
T1 - Ecology and evolution of viruses infecting uncultivated SUP05 bacteria as revealed by single-cell- and meta-genomics
AU - Roux, Simon
AU - Hawley, Alyse K.
AU - Beltran, Monica Torres
AU - Scofeld, Melanie
AU - Schwientek, Patrick
AU - Stepanauskas, Ramunas
AU - Woyke, Tanja
AU - Hallam, Steven J.
AU - Sullivan, Matthew B.
N1 - Publisher Copyright:
© Roux et al.
PY - 2014/1/1
Y1 - 2014/1/1
N2 - Viruses modulate microbial communities and alter ecosystem functions. However, due to cultivation bottlenecks, specifc virus–host interaction dynamics remain cryptic. In this study, we examined 127 single-cell amplifed genomes (SAGs) from uncultivated SUP05 bacteria isolated from a model marine oxygen minimum zone (OMZ) to identify 69 viral contigs representing fve new genera within dsDNA Caudovirales and ssDNA Microviridae. Infection frequencies suggest that ∼1/3 of SUP05 bacteria is viral-infected, with higher infection frequency where oxygen-defciency was most severe. Observed Microviridae clonality suggests recovery of bloom-terminating viruses, while systematic co-infection between dsDNA and ssDNA viruses posits previously unrecognized cooperation modes. Analyses of 186 microbial and viral metagenomes revealed that SUP05 viruses persisted for years, but remained endemic to the OMZ. Finally, identifcation of virus-encoded dissimilatory sulfte reductase suggests SUP05 viruses reprogram their host's energy metabolism. Together, these results demonstrate closely coupled SUP05 virus–host co-evolutionary dynamics with the potential to modulate biogeochemical cycling in climate-critical and expanding OMZs.
AB - Viruses modulate microbial communities and alter ecosystem functions. However, due to cultivation bottlenecks, specifc virus–host interaction dynamics remain cryptic. In this study, we examined 127 single-cell amplifed genomes (SAGs) from uncultivated SUP05 bacteria isolated from a model marine oxygen minimum zone (OMZ) to identify 69 viral contigs representing fve new genera within dsDNA Caudovirales and ssDNA Microviridae. Infection frequencies suggest that ∼1/3 of SUP05 bacteria is viral-infected, with higher infection frequency where oxygen-defciency was most severe. Observed Microviridae clonality suggests recovery of bloom-terminating viruses, while systematic co-infection between dsDNA and ssDNA viruses posits previously unrecognized cooperation modes. Analyses of 186 microbial and viral metagenomes revealed that SUP05 viruses persisted for years, but remained endemic to the OMZ. Finally, identifcation of virus-encoded dissimilatory sulfte reductase suggests SUP05 viruses reprogram their host's energy metabolism. Together, these results demonstrate closely coupled SUP05 virus–host co-evolutionary dynamics with the potential to modulate biogeochemical cycling in climate-critical and expanding OMZs.
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U2 - 10.7554/eLife.03125.001
DO - 10.7554/eLife.03125.001
M3 - Article
C2 - 25171894
AN - SCOPUS:84922964128
SN - 2050-084X
VL - 2014
JO - eLife
JF - eLife
IS - 3
M1 - e03125
ER -