Assessing Viral Abundance and Community Composition in Four Contrasting Regions of the Southern Ocean

• Published in: Life
• Main Authors: Ana Sotomayor-Garcia, Maria Montserrat Sala, Isabel Ferrera, Marta Estrada, Evaristo Vázquez-Domínguez, Mikhail Emelianov, Pau Cortés, Cèlia Marrasé, Eva Ortega-Retuerta, Sdena Nunes, Yaiza M. Castillo, Maria Serrano Cuerva, Marta Sebastián, Manuel Dall’Osto, Rafel Simó, Dolors Vaqué
• Format: Text
• Language: English
• Published: Multidisciplinary Digital Publishing Institute 2020
• Subjects: viral abundance; viral community composition; prokaryotes; phytoplankton; environmental variables; secondary metabolic compounds; Southern Ocean; Antarctic Ocean; Antarctic Peninsula; Antarctic; South Orkney Islands; South Georgia Island; Anvers; Anvers Island; Antarc*
• Online Access: https://doi.org/10.3390/life10070107

We explored how changes of viral abundance and community composition among four contrasting regions in the Southern Ocean relied on physicochemical and microbiological traits. During January–February 2015, we visited areas north and south of the South Orkney Islands (NSO and SSO) characterized by low temperature and salinity and high inorganic nutrient concentration, north of South Georgia Island (NSG) and west of Anvers Island (WA), which have relatively higher temperatures and lower inorganic nutrient concentrations. Surface viral abundance (VA) was highest in NSG (21.50 ± 10.70 × 106 viruses mL−1) and lowest in SSO (2.96 ± 1.48 × 106 viruses mL−1). VA was positively correlated with temperature, prokaryote abundance and prokaryotic heterotrophic production, chlorophyll a, diatoms, haptophytes, fluorescent organic matter, and isoprene concentration, and was negatively correlated with inorganic nutrients (NO3−, SiO42−, PO43−), and dimethyl sulfide (DMS) concentrations. Viral communities determined by randomly amplified polymorphic DNA–polymerase chain reaction (RAPD-PCR) were grouped according to the sampling location, being more similar within them than among regions. The first two axes of a canonical correspondence analysis, including physicochemical (temperature, salinity, inorganic nutrients—NO3−, SiO42−, and dimethyl sulfoniopropionate -DMSP- and isoprene concentrations) and microbiological (chlorophyll a, haptophytes and diatom, and prokaryote abundance and prokaryotic heterotrophic production) factors accounted for 62.9% of the variance. The first axis, temperature-related, accounted for 33.8%; the second one, salinity-related, accounted for 29.1%. Thus, different environmental situations likely select different hosts for viruses, leading to distinct viral communities.