Journal
APPLIED AND ENVIRONMENTAL MICROBIOLOGY
Volume 81, Issue 9, Pages 2995-3000Publisher
AMER SOC MICROBIOLOGY
DOI: 10.1128/AEM.03642-14
Keywords
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Categories
Funding
- Gordon and Betty Moore Foundation [GBMF3305]
- CNRS
- EMBL
- Genoscope/CEA
- VIB
- Stazione Zoologica Anton Dohrn
- UNIMIB
- ANR [POSEIDON/ANR-09-BLAN-0348, BIOMARKS/ANR-08-BDVA-003, PROMETHEUS/ANR-09-GENM-031, TARA-GIRUS/ANR-09-PCS-GENM-218]
- EU FP7 [287589]
- FWO
- BIO5
- Biosphere 2
- agnes b.
- Veolia Environment Foundation
- Region Bretagne
- World Courier
- Illumina
- Cap L'Orient
- EDF Foundation EDF Diversiterre
- FRB
- Prince Albert II de Monaco Foundation
- Etienne Bourgois
- captain and crew of the Tara schooner
- [GBMF2631]
- [GBMF3790]
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Viruses affect biogeochemical cycling, microbial mortality, gene flow, and metabolic functions in diverse environments through infection and lysis of microorganisms. Fundamental to quantitatively investigating these roles is the determination of viral abundance in both field and laboratory samples. One current, widely used method to accomplish this with aquatic samples is the filter mount method, in which samples are filtered onto costly 0.02-mu m-pore-size ceramic filters for enumeration of viruses by epifluorescence microscopy. Here we describe a cost-effective (ca. 500-fold-lower materials cost) alternative virus enumeration method in which fluorescently stained samples are wet mounted directly onto slides, after optional chemical flocculation of viruses in samples with viral concentrations of <5 x 10(7) viruses ml(-1). The concentration of viruses in the sample is then determined from the ratio of viruses to a known concentration of added microsphere beads via epifluorescence microscopy. Virus concentrations obtained by using this wet-mount method, with and without chemical flocculation, were significantly correlated with, and had precision equivalent to, those obtained by the filter mount method across concentrations ranging from 2.17 x 10(6) to 1.37 x 10(8) viruses ml(-1) when tested by using cultivated viral isolates and natural samples from marine and freshwater environments. In summary, the wet-mount method is significantly less expensive than the filter mount method and is appropriate for rapid, precise, and accurate enumeration of aquatic viruses over a wide range of viral concentrations (>= 1 x 10(6) viruses ml(-1)) encountered in field and laboratory samples.
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