Flow cytometric enumeration of marine viral populations at low abundances
Flow cytometric enumeration of marine viral populations at low abundances
Flow cytometric enumeration has advanced our ability to analyze aquatic virus samples and thereby our understanding of the ecological role viruses play in the oceans. However, low virus abundances are underestimated using the current flow cytometry (FCM) protocol. Our results revealed that low dilutions (<30-fold) not only decreased the total virus count but also limited the ability to differentiate between virus clusters. Here we report a simple and efficient method optimization for improving virus counts and optical resolution at low abundances. Raising the pH of the Tris-EDTA (TE) buffer to 8.2 successfully countered the effect of insufficient buffering capacity at low dilutions, which is caused by the higher proportion of acidic glutaraldehyde fixative in the final sample. The higher buffer pH did not interfere with virus counts at higher dilutions. We therefore recommend amendment of the standard FCM aquatic virus enumeration protocol using a TE buffer with pH 8.2 as a simple and efficient improvement.
203-209
Mojica, Kda
ac345072-6952-48c4-9ab8-8a36d5c36d25
Evans, C.
222540af-62ce-4843-87ea-e73a2480f6a7
Brussaard, Cpd
aea5e56b-944f-46cb-b845-d9546d87d458
23 January 2014
Mojica, Kda
ac345072-6952-48c4-9ab8-8a36d5c36d25
Evans, C.
222540af-62ce-4843-87ea-e73a2480f6a7
Brussaard, Cpd
aea5e56b-944f-46cb-b845-d9546d87d458
Mojica, Kda, Evans, C. and Brussaard, Cpd
(2014)
Flow cytometric enumeration of marine viral populations at low abundances.
Aquatic Microbial Ecology, 71 (3), .
(doi:10.3354/ame01672).
Abstract
Flow cytometric enumeration has advanced our ability to analyze aquatic virus samples and thereby our understanding of the ecological role viruses play in the oceans. However, low virus abundances are underestimated using the current flow cytometry (FCM) protocol. Our results revealed that low dilutions (<30-fold) not only decreased the total virus count but also limited the ability to differentiate between virus clusters. Here we report a simple and efficient method optimization for improving virus counts and optical resolution at low abundances. Raising the pH of the Tris-EDTA (TE) buffer to 8.2 successfully countered the effect of insufficient buffering capacity at low dilutions, which is caused by the higher proportion of acidic glutaraldehyde fixative in the final sample. The higher buffer pH did not interfere with virus counts at higher dilutions. We therefore recommend amendment of the standard FCM aquatic virus enumeration protocol using a TE buffer with pH 8.2 as a simple and efficient improvement.
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Published date: 23 January 2014
Organisations:
Ocean Biochemistry & Ecosystems, National Oceanography Centre
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Local EPrints ID: 406871
URI: http://eprints.soton.ac.uk/id/eprint/406871
ISSN: 0948-3055
PURE UUID: a838c2ee-9da2-45b2-b858-17c99be2ee9c
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Date deposited: 25 Mar 2017 02:02
Last modified: 15 Mar 2024 12:55
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Author:
Kda Mojica
Author:
C. Evans
Author:
Cpd Brussaard
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