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Isolation and characterization of marine psychrophilic phage-host systems from Arctic sea ice

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Abstract

Phage-host systems from extreme cold environments have rarely been surveyed. This study is concerned with the isolation and characterization of three different phage-host systems from Arctic sea ice and melt pond samples collected north-west of Svalbard (Arctic). On the basis of 16S rDNA sequences, the three bacterial phage hosts exhibited the greatest similarity to the species Shewanella frigidimarina (96.0%), Flavobacterium hibernum (94.0%), and Colwellia psychrerythraea (98.4%), respectively. The host bacteria are psychrophilic with good growth at 0°C, resulting in a rapid formation of visible colonies at this temperature. The phages showed an even more pronounced adaptation to cold temperatures than the bacteria, with growth maxima below 14°C and good plaque formation at 0°C. Transmission electron microscopy (TEM) examinations revealed that the bacteriophages belonged to the tailed, double-stranded DNA phage families Siphoviridae and Myoviridae. All three phages were host-specific.

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References

  • Ausubel FM, et al (2001) Current protocols in molecular biology. Wiley: New York

  • Bergh O, Boersheim KY, Bratbak G, Heldal M (1989) High abundance of viruses found in aquatic environments. Nature 6233:467–468

    Article  Google Scholar 

  • Bird DF, Maranger R, Karl DM (1993) Palmer LTER: aquatic virus abundances near the Antarctic Peninsula. Antarct J US 28:234–235

    Google Scholar 

  • Bowman JP, McCammon SA, Brown MV, Nichols DS, McMeekin TA (1997) Diversity and association of psychrophilic bacteria in Antarctic sea ice. Appl Environ Microbiol 63:3068–3078

    CAS  PubMed  Google Scholar 

  • Bratbak G, Heldal M, Thingstad TF, Tuomi P (1996) Dynamics of virus abundance in coastal seawater. FEMS Microbiol Ecol 19:263–269

    Article  CAS  Google Scholar 

  • Brown MV, Bowman JP (2001) A molecular phylogenetic survey of sea-ice microbial communities (SIMCO). FEMS Microbiol Ecol 35:267–275

    Article  CAS  PubMed  Google Scholar 

  • Greer G (1983) Psychrotrophic Brocothrix thermospacta bacteriophages isolated from beef. Appl Environ Microbiol 46:245–251

    CAS  PubMed  Google Scholar 

  • Grossi SM, Kottmeier ST, Sullivan CW (1984) Sea ice microbial communities. III. Seasonal abundance of microalgae and associated bacteria, McMurdo Sound, Antarctica. Microb Ecol 10:231–242

    Google Scholar 

  • Grossmann S, Dieckmann G (1994) Bacterial standing stock, activity, and carbon production during formation and growth of sea ice in the Weddell Sea, Antarctica. Appl Environ Microbiol 60:2746–2753

    CAS  Google Scholar 

  • Guixa-Boixereu N, Vaque D, Gaso JM, Sanchez-Camara J, Pedros-Alio C (2002) Viral distribution and activity in Antarctic waters. Deep-Sea Res 49:827–845

    Google Scholar 

  • Helmke E, Weyland H (1995) Bacteria in sea ice and underlying water of the eastern Weddell Sea in midwinter. Mar Ecol Prog Ser 117:269–287

    Google Scholar 

  • Hofer JS, Sommaruga R (2001) Seasonal dynamics of viruses in an alpine lake: importance of filamentous forms. Aquat Microb Ecol 26:1–11

    Google Scholar 

  • Jiang SC, Kellogg CA, Paul JH (1998) Characterization of marine temperate phage-host systems isolated from Mamala Bay, Oahu, Hawaii. Appl Environ Microbiol 648:535–542

    Google Scholar 

  • Kepner RL Jr, Wharton RA Jr, Suttle CA (1998) Viruses in Antarctic lakes. Limnol Oceanogr 43:1754–1761

    PubMed  Google Scholar 

  • Kottmeier ST; Sullivan CW (1987) Late winter primary production and bacterial production in sea ice and seawater west of the Antarctic Peninsula. Mar Ecol Prog Ser 36:287–298

    Google Scholar 

  • Kottmeier ST, Grossi SM, Sullivan CW (1987) Sea ice microbial communities. VIII. Bacterial production in annual sea ice of McMurdo Sound, Antarctica. Mar Ecol Prog Ser 35:175–186

    Google Scholar 

  • Maidak BL, et al (1999) A new version of the RDP (Ribosomal Database Project). Nucleic Acids Res 27:171–173

    CAS  PubMed  Google Scholar 

  • Maranger R, Bird DF, Juniper SK (1994) Viral and bacterial dynamics in Arctic sea ice during the spring algal bloom near Resolute, NWT, Canada. Mar Ecol Prog Ser 111:121–127

    Google Scholar 

  • Marchant H, Davidson A, Wright S, Glazebrook J (2000) The distribution and abundance of viruses in the Southern Ocean during spring. Antarct Sci 12:414–417

    Google Scholar 

  • Moebus K (1991) Preliminary observations on the concentration of marine bacteriophages in the water around Helgoland. Helgol Wiss Meeresunters 45:411–422

    Google Scholar 

  • Moebus K, Nattkemper H (1983) Taxonomic investigations of bacteriophage sensitive bacteria isolated from marine waters. Helgol Meeresunters 36:357–373

    Google Scholar 

  • Morita RY (1975) Psychrophilic bacteria. Bact Rev 39:144–167

    CAS  Google Scholar 

  • Noble RT, Fuhrman JA (2000) Rapid virus production and removal as measured with fluorescently labeled viruses as tracers. Appl Environ Microbiol 66:3790–3797

    Article  CAS  PubMed  Google Scholar 

  • Olsen RH (1967) Isolation and growth of psychrophilic bacteriophage. Appl Microbiol 15:198

    CAS  PubMed  Google Scholar 

  • Oren A, Bratbak G, Heldal M (1997) Occurrence of virus-like particles in the Dead Sea. Extremophiles 1:143–149

    Article  CAS  PubMed  Google Scholar 

  • Pinhassi J, Zweifel UL, Hagstrom A (1997) Dominant marine bacterioplankton species found among colony-forming bacteria. Appl Environ Microbiol 63:3359–3366

    CAS  PubMed  Google Scholar 

  • Priddle J, Leakey R, Archer S, Murphy E (1996) Eukaryotic microbiota in the surface waters and sea ice of the Southern Ocean: aspects of physiology, ecology and biodiversity in a 'two-phase' system. Biodivers Cons 5:1473–1504

    Google Scholar 

  • Proctor LM, Fuhrman JA (1990) Viral mortality of marine cyanobacteria and bacteria. Nature 343:60–62

    Article  Google Scholar 

  • Rainey FA, Ward-Rainey N, Kroppenstedt RM, Stackebrandt E (1996) The genus Nocardiopsis represents a phylogenetically coherent taxon and a distinct actinomycete lineage: proposal of Nocardiopsaceae fam. nov. Int J Syst Bacteriol 46:1088–1092

    CAS  PubMed  Google Scholar 

  • Smith RE, Clement P (1990) Heterotrophic activity and bacterial productivity in assemblages of microbes from sea ice in the high Arctic. Polar Biol 10:351–357

    Google Scholar 

  • Smith DC, Steward GF, Azam F, Hollibaugh JT (1992) Virus and bacteria abundance in the Drake Passage during January and August 1991. Antarct J US 27:125–127

    Google Scholar 

  • Staley JT, Gosink JJ (1999) Poles apart: biodiversity and biogeography of sea ice bacteria. Annu Rev Microbiol 53:189–215

    CAS  PubMed  Google Scholar 

  • Steward FG, Smith DC, Azam F (1996) Abundance and production of bacteria and viruses in the Bering and Chukchi Seas. Mar Ecol Prog Ser 131:287–300

    Google Scholar 

  • Suttle CA, Chan AM, Cottrell MT (1990) Infection of phytoplankton by viruses and reduction of primary productivity. Nature 347:467–469

    Article  Google Scholar 

  • Tan TL (1997) Biolog metabolic fingerprints for clustering marine oligotrophic bacteria from polar regions In: Insam H, Rangers A (eds) Microbial communities: function versus structural approaches. Springer, Berlin Heidelberg New York, pp 161–170

  • Thomas DN, Dieckmann GS (2002) Antarctic sea ice habitat for extremophiles. Science 5555:641–644

    Article  Google Scholar 

  • Truong LV, Tuyen H, Helmke E, Binh LT, Schweder T (2001) Cloning and characterization of two cold-adapted pectate lyases from the marine Antarctic bacterium Pseudoalteromonas haloplanktis strain ANT/505. Extremophiles 5:35–44

    Article  CAS  PubMed  Google Scholar 

  • Vincent WF, Gibson JAE, Pienitz R, Villeneuve V (2000) Ice shelf microbial ecosystems in the high Arctic and implications for life on snowball earth. Naturwissenschaften 87:137–141

    CAS  PubMed  Google Scholar 

  • Wichels A, Biel SS, Gelderblom HR, Brinkhoff T, Muyzer G, Schütt C (1998) Bacteriophage diversity in the North Sea. Appl Environ Microbiol 64:4128–4133

    CAS  PubMed  Google Scholar 

  • Wommack KE, Colwell RR (2000) Virioplankton: viruses in aquatic ecosystems. Microbiol Mol Biol Rev 64:69–114

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgment

This work was supported by the Bundesministerium für Bildung und Forschung (03F0278B).

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Correspondence to Thomas Schweder.

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Communicated by K. Horikoshi

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Borriss, M., Helmke, E., Hanschke, R. et al. Isolation and characterization of marine psychrophilic phage-host systems from Arctic sea ice. Extremophiles 7, 377–384 (2003). https://doi.org/10.1007/s00792-003-0334-7

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  • DOI: https://doi.org/10.1007/s00792-003-0334-7

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