
Phylogenetic Analysis of Members of the Phycodnaviridae Virus Family, Using Amplified Fragments of the Major Capsid Protein Gene
Author(s) -
Jens Borggaard Larsen,
Aud Larsen,
Gunnar Bratbak,
Ruth Anne Sandaa
Publication year - 2008
Publication title -
applied and environmental microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.552
H-Index - 324
eISSN - 1070-6291
pISSN - 0099-2240
DOI - 10.1128/aem.02548-07
Subject(s) - biology , phylogenetic tree , amplicon , capsid , genome , gene , genetics , virus , genetic diversity , human virome , phylogenetics , metagenomics , population , polymerase chain reaction , demography , sociology
Algal viruses are considered ecologically important by affecting host population dynamics and nutrient flow in aquatic food webs. Members of the familyPhycodnaviridae are also interesting due to their extraordinary genome size. Few algal viruses in thePhycodnaviridae family have been sequenced, and those that have been have few genes in common and low gene homology. It has hence been difficult to design general PCR primers that allow further studies of their ecology and diversity. In this study, we screened the nine type I core genes of the nucleocytoplasmic large DNA viruses for sequences suitable for designing a general set of primers. Sequence comparison between members of thePhycodnaviridae family, including three partly sequenced viruses infecting the prymnesiophytePyramimonas orientalis and the haptophytesPhaeocystis pouchetii andChrysochromulina ericina (Pyramimonas orientalis virus 01B [PoV-01B],Phaeocystis pouchetii virus 01 [PpV-01], andChrysochromulina ericina virus 01B [CeV-01B], respectively), revealed eight conserved regions in the major capsid protein (MCP). Two of these regions also showed conservation at the nucleotide level, and this allowed us to design degenerate PCR primers. The primers produced 347- to 518-bp amplicons when applied to lysates from algal viruses kept in culture and from natural viral communities. The aim of this work was to use the MCP as a proxy to infer phylogenetic relationships and genetic diversity among members of thePhycodnaviridae family and to determine the occurrence and diversity of this gene in natural viral communities. The results support the current legitimate genera in thePhycodnaviridae based on alga host species. However, while placing the mimivirus in close proximity to the type species, PBCV-1, ofPhycodnaviridae along with the three new viruses assigned to the family (PoV-01B, PpV-01, and CeV-01B), the results also indicate that the coccolithoviruses and phaeoviruses are more diverged from this group. Phylogenetic analysis of amplicons from virus assemblages from Norwegian coastal waters as well as from isolated algal viruses revealed a cluster of viruses infecting members of the prymnesiophyte and prasinophyte alga divisions. Other distinct clusters were also identified, containing amplicons from this study as well as sequences retrieved from the Sargasso Sea metagenome. This shows that closely related sequences of this family are present at geographically distant locations within the marine environment.