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2.
Environ Microbiol ; 15(5): 1441-51, 2013 May.
Article in English | MEDLINE | ID: mdl-22857133

ABSTRACT

Phaeocystis globosa is an ecologically important bloom-forming phytoplankton, which sequesters substantial amounts of inorganic carbon and can form carbon-enriched chitinous star-like structures. Viruses infecting P. globosa (PgVs) play a significant regulatory role in population dynamics of the host species. However, the extent to which viruses alter host physiology and its carbon assimilation on single cell level is still largely unknown. This study demonstrates for the first time the impact of viral infection on carbon assimilation and cell morphology of individual axenic P. globosa cells using two single cell techniques: high resolution nanometre-scale Secondary-Ion Mass Spectrometry (nanoSIMS) approach and atomic force microscopy (AFM). Up until viral lysis (19 h post infection), the bulk carbon assimilation by infected P. globosa cultures was identical to the assimilation by the non-infected cultures (33 µmol C l(-1)). However, single cell analysis showed that viral infection of P. globosa impedes the release of star-like structures. Non-infected cells transfer up to 44.5 µmol C l(-1) (36%) of cellular biomass in the form of star-like structures, suggesting a vital role in the survival of P. globosa cells. We hypothesize that impediment of star-like structures in infected P. globosa cells may inactivate viral infectivity by forming flocculants after cell lysis. Moreover, we show that substantial amounts of newly produced viruses (≈ 68%) were attached to P. globosa cells prior to cell lysis. Further, we speculate that infected cells become more susceptible for grazing which provides potential reasons for the sudden disappearance of PgVs in the environment. The scenarios of enhanced grazing is at odds to the current perspective that viral infections facilitates microbial mediated processes by diverting host material away from the higher trophic levels.


Subject(s)
Chitin/metabolism , Haptophyta/virology , Viruses/metabolism , Biomass , Carbon/metabolism , Haptophyta/cytology , Phytoplankton/cytology , Phytoplankton/virology , Single-Cell Analysis , Water Microbiology
3.
Virology ; 341(1): 80-90, 2005 Oct 10.
Article in English | MEDLINE | ID: mdl-16081120

ABSTRACT

Twelve lytic viruses (PgV) infecting the marine unicellular eukaryotic harmful algal bloom species Phaeocystis globosa were isolated from the southern North Sea in 2000-2001 and partially characterized. All PgV isolates shared common phenotypic features with other algal viruses belonging to the family Phycodnaviridae and could be categorized in four different groups. Two main groups (PgV Group I and II) were discriminated based on particle size (150 and 100 nm respectively), genome size (466 and 177 kb) and structural protein composition. The lytic cycle showed a latent period of 10 h for PgV Group I and latent periods of 12 h and 16 h for PgV Group IIA and IIB. Host specificity and temperature sensitivity finally defined a fourth group (PgV Group IIC). Our results imply that viral infection plays an important role not only in P. globosa dynamics but also in the diversity of both host and virus community.


Subject(s)
Eukaryota/virology , Phycodnaviridae/isolation & purification , Phytoplankton/virology , Genome, Viral , Microscopy, Electron , Phenotype , Phycodnaviridae/genetics , Phycodnaviridae/growth & development , Phycodnaviridae/ultrastructure , Temperature , Viral Structural Proteins/isolation & purification
4.
Appl Environ Microbiol ; 70(6): 3700-5, 2004 Jun.
Article in English | MEDLINE | ID: mdl-15184176

ABSTRACT

Viruses infecting the harmful bloom-causing alga Phaeocystis globosa (Prymnesiophyceae) were readily isolated from Dutch coastal waters (southern North Sea) in 2000 and 2001. Our data show a large increase in the abundance of putative P. globosa viruses during blooms of P. globosa, suggesting that viruses are an important source of mortality for this alga. In order to examine genetic relatedness among viruses infecting P. globosa and other phytoplankton, DNA polymerase gene (pol) fragments were amplified and the inferred amino acid sequences were phylogenetically analyzed. The results demonstrated that viruses infecting P. globosa formed a closely related monophyletic group within the family Phycodnaviridae, with at least 96.9% similarity to each other. The sequences grouped most closely with others from viruses that infect the prymnesiophyte algae Chrysochromulina brevifilum and Chrysochromulina strobilus. Whether the P. globosa viruses belong to the genus Prymnesiovirus or form a separate group needs further study. Our data suggest that, like their phytoplankton hosts, the Chrysochromulina and Phaeocystis viruses share a common ancestor and that these prymnesioviruses and their algal host have coevolved.


Subject(s)
Eukaryota/virology , Phycodnaviridae/classification , Phycodnaviridae/isolation & purification , Phylogeny , Phytoplankton/virology , Animals , DNA-Directed DNA Polymerase/genetics , Molecular Sequence Data , Phycodnaviridae/genetics , Sequence Analysis, DNA
5.
Virology ; 319(2): 280-91, 2004 Feb 20.
Article in English | MEDLINE | ID: mdl-14980488

ABSTRACT

We report the isolation of the first double-stranded (ds) RNA virus in the family Reoviridae that infects a protist (microalga Micromonas pusilla, Prasinophyceae). The dsRNA genome was composed of 11 segments ranging between 0.8 and 5.8 kb, with a total size of approximately 25.5 kb. The virus (MpRNAV-01B) could not be assigned to the genus level because host type, genome size, and number of segments smaller than 2 kb did not correspond to either of the two existing 11-segmented dsRNA genera Rotavirus and Aquareovirus. MpRNAV-01B has a particle size of 65-80 nm, a narrow host range, a latent period of 36 h, and contains five major proteins (120, 95, 67, 53, and 32 kDa). MpRNAV-01B was stable to freeze-thawing, resistant to chloroform, ether, nonionic detergents, chelating and reducing agents. The virus was inactivated at temperatures above 35 degrees C and by ionic detergent, ethanol, acetone, and acidic conditions (pH 2-5).


Subject(s)
Chlorophyta/virology , RNA Viruses/isolation & purification , RNA, Double-Stranded , Chelating Agents/pharmacology , Chlorophyta/ultrastructure , Detergents/pharmacology , Genome, Viral , Hot Temperature , Hydrogen-Ion Concentration , Microscopy, Electron , Molecular Weight , RNA Viruses/drug effects , RNA Viruses/genetics , Reducing Agents/pharmacology , Species Specificity , Viral Structural Proteins/chemistry , Viral Structural Proteins/genetics , Virus Inactivation/drug effects , Virus Latency
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