Viral infection of Phaeocystis globosa impedes release of chitinous star‐like structures: quantification using single cell approaches. (1st August 2012)
- Record Type:
- Journal Article
- Title:
- Viral infection of Phaeocystis globosa impedes release of chitinous star‐like structures: quantification using single cell approaches. (1st August 2012)
- Main Title:
- Viral infection of Phaeocystis globosa impedes release of chitinous star‐like structures: quantification using single cell approaches
- Authors:
- Sheik, A. R.
Brussaard, C. P. D.
Lavik, G.
Foster, R. A.
Musat, N.
Adam, B.
Kuypers, M. M. M. - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Summary</title> <p> <italic>Phaeocystis globosa</italic> 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 <italic>P. globosa</italic> (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 <italic>P. globosa</italic> 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 <italic>P. globosa</italic> cultures was identical to the assimilation by the non‐infected cultures (33 µmol C l<sup>−1</sup>). However, single cell analysis showed that viral infection of <italic>P. globosa</italic> impedes the release of star‐like structures. Non‐infected cells transfer up to 44.5 µmol C l<sup>−1</sup> (36%) of cellular biomass in the form of star‐like structures, suggesting a vital role in the survival of <italic>P. globosa</italic> cells. We hypothesize that impediment of star‐like structures in infected<abstract abstract-type="main" xml:lang="en"> <title>Summary</title> <p> <italic>Phaeocystis globosa</italic> 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 <italic>P. globosa</italic> (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 <italic>P. globosa</italic> 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 <italic>P. globosa</italic> cultures was identical to the assimilation by the non‐infected cultures (33 µmol C l<sup>−1</sup>). However, single cell analysis showed that viral infection of <italic>P. globosa</italic> impedes the release of star‐like structures. Non‐infected cells transfer up to 44.5 µmol C l<sup>−1</sup> (36%) of cellular biomass in the form of star‐like structures, suggesting a vital role in the survival of <italic>P. globosa</italic> cells. We hypothesize that impediment of star‐like structures in infected <italic>P. globosa</italic> 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 <italic>P. globosa</italic> 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.</p> </abstract> … (more)
- Is Part Of:
- Environmental microbiology. Volume 15:Number 5(2013:May)
- Journal:
- Environmental microbiology
- Issue:
- Volume 15:Number 5(2013:May)
- Issue Display:
- Volume 15, Issue 5 (2013)
- Year:
- 2013
- Volume:
- 15
- Issue:
- 5
- Issue Sort Value:
- 2013-0015-0005-0000
- Page Start:
- 1441
- Page End:
- 1451
- Publication Date:
- 2012-08-01
- Subjects:
- Microbial ecology -- Periodicals
Environmental Microbiology -- Periodicals
579.17 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=1462-2912;screen=info;ECOIP ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1462-2920/issues ↗
http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=emi ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/j.1462-2920.2012.02838.x ↗
- Languages:
- English
- ISSNs:
- 1462-2912
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3791.522600
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3838.xml