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Application of a novel rpoC1-RFLP approach reveals that marine Prochlorococcus populations in the atlantic gyres are composed of greater microdiversity than previously described
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Jameson, Eleanor, Joint, Ian, 1947-, Mann, Nicholas H. and Muehling, Martin. (2008) Application of a novel rpoC1-RFLP approach reveals that marine Prochlorococcus populations in the atlantic gyres are composed of greater microdiversity than previously described. Microbial Ecology, Vol.55 (No.1). pp. 141-151. ISSN 0095-3628
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Official URL: http://dx.doi.org/10.1007/s00248-007-9259-5
Abstract
To elucidate the degree of microdiversity within the genus Prochlorococcus, novel Prochlorococcus-specific polymerase chain reaction (PCR) primers were developed for the rpoC1 gene, which encodes the ribonucleic acid (RNA) polymerase core subunit. The size of the PCR fragment (925 bp) coupled with high sequence variation within the rpoC1 fragments (70-99% sequence similarity, 16S ribosomal RNA sequences show greater than 97% sequence similarity) meant that it was possible to distinguish Prochlorococcus strains by restriction fragment length polymorphism (RFLP) analysis. Clone libraries were constructed from environmental deoxyribonucleic acid samples from two stations, one in the northern and one in the southern oligotrophic gyre of the Atlantic Ocean. These were screened to determine the microdiversity of Prochlorococcus populations using this high-resolution high-throughput analysis approach. RFLP analysis of the clone libraries from the two gyre sites revealed that the two Prochlorococcus populations had a high degree of microdiversity with 40 and 52 different RFLP-type clones among the 143 clones tested for both the northern and southern gyres, respectively. Phylogenetic analysis of the nucleotide sequences of the RFLP types not only showed that it contained representatives of each of the currently recognized Prochlorococcus clades (based on the internal transcribed spacer region as molecular marker) but also led to the discovery of a previously unseen genetic microdiversity. This level of diversity was greater at the southern gyre site compared to the northern gyre site. Moreover, the high genetic resolution approach also revealed that there are two putative novel lineages within the HL I clade. Analyses of further samples by producing clone libraries from different geographic origins is likely to reveal further diversity and novel lineages within Prochlorococcus.
| Item Type: | Journal Article |
|---|---|
| Subjects: | Q Science > QH Natural history > QH301 Biology Q Science > QR Microbiology |
| Divisions: | Faculty of Science > Life Sciences (2010- ) > Biological Sciences ( -2010) |
| Library of Congress Subject Headings (LCSH): | Cyanobacteria -- Phylogeny, Cyanobacteria -- Variation -- Atlantic Ocean, Microbial diversity, Polymerase chain reaction, Polymerase chain reaction -- Diagnostic use |
| Journal or Publication Title: | Microbial Ecology |
| Publisher: | Springer New York LLC |
| ISSN: | 0095-3628 |
| Date: | January 2008 |
| Volume: | Vol.55 |
| Number: | No.1 |
| Number of Pages: | 11 |
| Page Range: | pp. 141-151 |
| Identification Number: | 10.1007/s00248-007-9259-5 |
| Status: | Peer Reviewed |
| Publication Status: | Published |
| Access rights to Published version: | Restricted or Subscription Access |
| Funder: | Natural Environment Research Council (Great Britain) (NERC) |
| Grant number: | NER/S/A/2003/11883A (NERC) |
| References: | 1. Ahlgren, N, Rocap, G, Chisholm, SW (2006) Measurement of Prochlorococcus ecotypes using real-time polymerase chain reaction reveals different abundances of genotypes with similar light physiologies. Environ Microbiol 8: 441–454 2. Bouman, HA, Ulloa, O, Scanlan, DJ, Zwirglmaier, K, Li, WKW, Platt, T et al (2006) Oceanographic basis of the global surface distribution of Prochlorococcus ecotypes. Science 312: 918–921 3. Chao, A (1984) Nonparametric estimation of the number of classes in a population. Scand J Statis 11: 265–270 4. Ferris, MJ, Palenik, B (1998) Niche adaptation in ocean cyanobacteria. Nature 396: 226–228 5. Guillou, L, Jacquet, S, Chre´tiennot-Dinet,MJ, Vaulot,D(2001) Grazing impact of two small heterotrophic flagellates on Prochlorococcus and Synechococcus. Aquat Microb Ecol 26: 201–207 6. Heck, KL Jr, Van Belle, G, Simberloff, D (1975) Explicit calculation of the rarefaction diversity measurement and the determination of sufficient sample size. Ecology 56: 1459–1461 7. Heiman, M (1997) Webcutter 2.0. http://www.firstmarket.com/ cutter/cut2.html 8. Herut, B, Zohary, T, Krom, MD, Mantoura, RFC, Pitta, P, Psarra, S, et al (2005) Response of east Mediterranean surface water to Saharan dust: on-board microcosm experiment and field observations. Deep-Sea Res Part 2 52: 3024–3040 9. Holland, SM (2003) aRarefactWin. http://www.uga.edu/~strata/ software/Software.html 10. Hurlbert, SH (1971) The nonconcept of species diversity: a critique and alternative parameters. Ecology 52: 577–586 11. Johnson, ZI, Zinser, ER, Coe, A, McNulty, NP, Woodward, EMS, Chisholm, SW (2006) Niche partitioning among Prochlorococcus ecotypes along ocean-scale environmental gradients. Science 311: 1737–1740 12. Ludwig, W, Strunk, O, Westram, R, Richter, L, Meier, H, Yadhukumar, et al (2004) ARB: a software environment for sequence data. Nucleic Acids Res 32: 1363–1371 13. Mann, EL, Ahlgren, N, Moffett, JW, Chisholm, SW (2002) Copper toxicity and cyanobacteria ecology in the Sargasso Sea. Limnol Oceanogr 47: 976–988 14. Moore, LR, Goericke, R, Chisholm, SW (1995) Comparative physiology of Synechococcus and Prochlorococcus: influence of light and temperature on growth, pigments, fluorescence and absorptive properties. Mar Ecol Prog Ser 116: 259–275 15. Moore, LR, Rocap, G, Chisholm, SW (1998) Physiology and molecular phylogeny of coexisting Prochlorococcus ecotypes. Nature 393: 464–467 16. Moore, LR, Post, AF, Rocap, G, Chisholm, SW (2002) Utilization of different nitrogen sources by the marine cyanobacteria Prochlorococcus and Synechococcus. Limnol Oceanogr 47: 989–996 17. Mu¨hling, M, Fuller, NJ, Millard, A, Somerfield, PJ, Marie, D, Wilson, WH, Scanlan, DJ, Post, AF, Joint, I, Mann, NH (2005) Genetic diversity of marine Synechococcus and co-occurring cyanophage communities: evidence for viral control of phytoplankton. Environ Microbiol 7: 499–508 18. Mu¨hling, M, Fuller, NJ, Millard, A, Somerfield, PJ, Post, AF, Wilson, WH, Scanlan, DJ, Joint, I, Mann, NH (2006) High resolution genetic diversity studies of marine Synechococcus using rpoC1-based restriction fragment length polymorphism. Aquat Microb Ecol 45: 263–275 19. Palenik, B (1994) Cyanobacterial community structure as seen from RNA polymerase gene sequence analysis. Appl Environ Microbiol 60: 3212–3219 20. Partensky, F, Hess, WR, Vaulot, D (1999) Prochlorococcus, a marine photosynthetic prokaryote of global significance. Microbiol Mol Biol Rev 63: 106–127 21. Penno, S, Lindell, D, Post, AF (2006) Diversity of Synechococcus and Prochlorococcus populations determined from DNA sequences of the N-regulatory gene ntcA. Environ Microbiol 8: 1200 22. Rocap, G, Distel, DL, Waterbury, JB, Chisholm, SW (2002) Resolution of Prochlorococcus and Synechococcus ecotypes by using 16S–23S ribosomal DNA Internal Transcribed Spacer sequences. Appl Environ Microbiol 68: 1180–1191 23. Rocap, G, Larimer, FW, Lamerdin, J, Malfatti, S, Chain, P, Ahlgren, N et al (2003) Genome divergence in two Prochlorococcus ecotypes reflects oceanic niche differentiation. Nature 424: 1042– 1047 24. Scanlan, DJ, West, NJ (2002) Molecular ecology of the marine cyanobacterial genera Prochlorococcus and Synechococcus. FEMS Microbiol Ecol 40: 1–12 25. Shen, T-J, Chao, A, Lin, C-H (2003) Predicting the number of new species in further taxonomic sampling. Ecology 84: 798–804 26. Sullivan, MB, Waterbury, JB, Chisholm, SW (2003) Cyanophage infecting the oceanic cyanobacterium, Prochlorococcus. Nature 424: 1047–1051 27. Suttle, CA (2000) Cyanophages and their role in the ecology of cyanobacteria. In: Whitton, BA, Potts, M (eds) The ecology of cyanobacteria: their diversity in time and space. Kluwer, London, UK, pp 563–589 28. Urbach, E, Chisholm, SW (1998) Genetic diversity in Prochlorococcus populations flow cytometrically sorted from the Sargasso Sea and Gulf Stream. Limnol Oceanogr 43: 1615–1630 29. West, NJ, Scanlan, DJ (1999) Niche-partitioning of Prochlorococcus in a Stratified Water Column in the Eastern North Atlantic Ocean. Appl Environ Microbiol 65: 2585–2591 30. Zinser, ER, Coe, A, Johnson, ZI, Martiny, AC, Fuller, NJ, Scanlan, DJ, Chisholm, SW (2006) Prochlorococcus ecotype abundances in the North Atlantic Ocean as revealed by an improved quantitative PCR method. Appl Environ Microbiol 72: 723–732 31. Zubkov,MV, Tarran, GA (2005) Amino acid uptake of Prochlorococcus spp. in surface waters across the South Atlantic Subtropical Front. Aquat Microb Ecol 40: 241–249 |
| URI: | http://wrap.warwick.ac.uk/id/eprint/30786 |
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