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Appl. Environ. Microbiol., 08 1996, 2869-2874, Vol 62, No. 8
F Chen, CA Suttle and SM Short
Algal-virus-specific PCR primers were used to amplify DNA polymerase gene
(pol) fragments (683 to 689 bp) from the virus-sized fraction (0.02 to 0.2
microns) concentrated from inshore and offshore water samples collected
from the Gulf of Mexico. Algal-virus-like DNA pol genes were detected in
five samples collected from the surface and deep chlorophyll maximum. PCR
products from an offshore station were cloned, and the genetic diversity of
33 fragments was examined by restriction fragment length polymorphism and
sequence analysis. The five different genotypes or operational taxonomic
units (OTUs) that were identified on the basis of restriction fragment
length polymorphism banding patterns were present in different relative
abundances (9 to 34%). One clone from each OTU was sequenced, and
phylogenetic analysis showed that all of the OTUs fell within the family
Phycodnaviridae. Four of the OTUs fell within a group of viruses (MpV)
which infect the photosynthetic picoplankter Micromonas pusilla. The
genetic diversity among these genotypes was as large as that previously
found for MpV isolates from different oceans. The remaining genotype formed
its own clade between viruses which infect M. pusilla and Chrysochromulina
brevifilum. These results imply that marine virus communities contain a
diverse assemblage of MpV-like viruses, as well as other unknown members of
the Phycodnaviridae.
Copyright © 1996, American Society for Microbiology
Genetic diversity in marine algal virus communities as revealed by sequence analysis of DNA polymerase genes
Department of Marine Science, University of Texas at Austin, Port Aransas 78373-1267, USA. fchen2@uga.cc.uga.edu
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