Recent evidence suggests that viruses play an influential role within
the marine microbial food web. To understand this role, it is importan
t to determine rates and mechanisms of virus removal and degradation,
We used plaque assays to examine the decay of infectivity in lab-grown
viruses seeded into natural seawater. The rates of loss of infectivit
y of native viruses from Santa Monica Bay and of nonnative viruses fro
m the North Sea in the coastal seawater of Santa Monica Bay were deter
mined. Viruses were seeded into fresh seawater that had been pretreate
d in various ways: filtration with a 0.2-mu m-pore-size filter to remo
ve organisms, heat to denature enzymes, and dissolved organic matter e
nrichment to reconstitute enzyme activity, Seawater samples were then
incubated in full sunlight, in the dark, or under glass to allow parti
tioning of causative agents of virus decay, Solar radiation always res
ulted in increased rates of loss of virus infectivity, Virus isolates
which are native to Santa Monica Bay consistently degraded more slowly
in full sunlight in untreated seawater (decay ranged from 4.1 to 7.2%
h(-1)) than nonnative marine bacteriophages which were isolated from
the North Sea (decay ranged from 6.6 to 11.1% h(-1)). All phages demon
strated susceptibility to degradation by heat-labile substances, as he
at treatment reduced the decay rates to about 0.5 to 2.0% h(-1) in the
dark, Filtration reduced decay rates by various amounts, averaging 20
%. Heat-labile, high-molecular-weight dissolved material (>30 kDa, pro
bably enzymes) appeared responsible for about 1/5 of the maximal decay
, Solar radiation was responsible for about 1/3 to 2/3 of the maximal
decay of nonnative viruses and about 1/4 to 1/3 of that of the native
viruses, suggesting evolutionary adaptation to local light levels. Our
results suggest that sunlight is an important contributing factor to
virus decay but also point to the significance of particles and dissol
ved substances in seawater.