TY - JOUR
T1 - Viral metabolic reprogramming in marine ecosystems
AU - Hurwitz, Bonnie L.
AU - U'Ren, Jana M.
N1 - Funding Information:
BLH was supported by the Gordon Betty Moore Foundation under award #4491. The authors thank two anonymous reviewers for their helpful suggestions.
Publisher Copyright:
© 2016 Elsevier Ltd.
PY - 2016/6/1
Y1 - 2016/6/1
N2 - Marine viruses often contain host-derived metabolic genes (i.e., auxiliary metabolic genes; AMGs), which are hypothesized to increase viral replication by augmenting key steps in host metabolism. Currently described AMGs encompass a wide variety of metabolic functions, including amino acid and carbohydrate metabolism, energy production, and iron-sulfur cluster assembly and modification, and their community-wide gene content and abundance vary as a function of environmental conditions. Here, we describe different AMGs classes, their hypothesized role in redirecting host carbon metabolism, and their ecological importance. Focusing on metagenomic ocean surveys, we propose a new model where a suite of phage-encoded genes activate host pathways that respond rapidly to environmental cues, presumably resulting in rapid changes to host metabolic flux for phage production.
AB - Marine viruses often contain host-derived metabolic genes (i.e., auxiliary metabolic genes; AMGs), which are hypothesized to increase viral replication by augmenting key steps in host metabolism. Currently described AMGs encompass a wide variety of metabolic functions, including amino acid and carbohydrate metabolism, energy production, and iron-sulfur cluster assembly and modification, and their community-wide gene content and abundance vary as a function of environmental conditions. Here, we describe different AMGs classes, their hypothesized role in redirecting host carbon metabolism, and their ecological importance. Focusing on metagenomic ocean surveys, we propose a new model where a suite of phage-encoded genes activate host pathways that respond rapidly to environmental cues, presumably resulting in rapid changes to host metabolic flux for phage production.
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U2 - 10.1016/j.mib.2016.04.002
DO - 10.1016/j.mib.2016.04.002
M3 - Review article
C2 - 27088500
AN - SCOPUS:84962854177
SN - 1369-5274
VL - 31
SP - 161
EP - 168
JO - Current Opinion in Microbiology
JF - Current Opinion in Microbiology
ER -