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. 1999 Oct;65(10):4528-36.
doi: 10.1128/AEM.65.10.4528-4536.1999.

Diversity and abundance of Bolidophyceae (Heterokonta) in two oceanic regions

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Diversity and abundance of Bolidophyceae (Heterokonta) in two oceanic regions

L Guillou et al. Appl Environ Microbiol. 1999 Oct.

Abstract

The diversity and abundance of the Bolidophyceae (Heterokonta), a newly described picoplanktonic algal class which is a sister group to the diatoms, was assessed in the equatorial Pacific Ocean and in the Mediterranean Sea by culture isolation, molecular biology techniques, and pigment analyses. Eight strains of Bolidophyceae were isolated in culture from different mesotrophic and oligotrophic areas. The corresponding small subunit (SSU) rRNA gene sequences allowed us to design two probes specific for the Bolidophyceae. These probes have been used in natural samples (i) to selectively amplify and detect Bolidophyceae sequences and (ii) to quantify the relative abundance of Bolidophyceae within the picoeukaryote community. Sequences available to date indicate that the class Bolidophyceae comprises at least three different clades, two corresponding to the previously described species Bolidomonas pacifica and Bolidomonas mediterranea and the third one corresponding to a subspecies of B. pacifica. Amplification of the SSU rRNA gene from natural samples with universal primers and hybridization using a Bolidomonas-specific probe followed by a eukaryote-specific probe allowed us to estimate the contribution of the Bolidophyceae to the eukaryotic DNA in both Pacific and Mediterranean waters to be lower than 1%. Similarly, high-performance liquid chromatography analyses of fucoxanthin, the major carotenoid present in Bolidophyceae, indicated that less than 4% of the total chlorophyll a in the picoplanktonic fraction in the equatorial Pacific was due to Bolidophyceae. Consequently, although strains of Bolidophyceae have been isolated from samples collected at several stations, this new class seems to have been a minor component of the natural picoeukaryotic populations in the ecosystems investigated, at least during the periods sampled.

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Figures

FIG. 1
FIG. 1
Distance tree derived from an alignment of SSU rDNA sequences. Bootstrap values at internal branches (500 replicates; only values>70% divergent are displayed) correspond to result of NJ analysis (with a Kimura two-parameter correction)/result of maximum parsimony analysis (no. of sites, 883; no. of steps required, 988; tree length, 1.0743; residual sum squares, 0.0103). Asterisks indicate where branching orders differ between the two methods. Scale bar shows 0.1% divergence. The GenBank sequence accession numbers are as follows: OLI51105-15m env., AF167414; OLI2001-100m env, AF167413; A. bisexualis, M32705; Alexandrium tamarense, X54946; Amphidinium belauense, L13719; Asterionellopsis glacialis, X77701; Babesia rodhaini, M87565; B. paxillifer, M87325; B. mediterranea, AF123596; B. pacifica, AF123595; B. pacifica environmental sequences for OLI1103-15m env. and OLI51104-60m env., AF167156 and AF167157, respectively; B. pacifica var. eleuthera strains RCC210 RCC208, and RCC212, AF167153, AF167154, and AF167155, respectively; C. roenbergensis, L27633; E. huxleyi, M87327; Nannochloropsis salina, M87328; Ochromonas danica, M32704; Paraphysomonas vestita, Z28335; Pavlova salina, L34669; Pelagococcus subviridis, U14386; P. calceolata, U14389; Phaeocystis globosa, X77476; Prorocentrum micans, M14649; Prymnesium patilliferum, L34671; and Sarcocystis muris, M64244.
FIG. 2
FIG. 2
Alignment of the variable part of the SSU rRNAs from seven Bolidophyceae. This region corresponds to the E21-1 and E21-3 helices (for the model see reference 36). Asterisks show transversion events among the three strains.
FIG. 3
FIG. 3
Dot blots with the BOLI02 probe (top) and the general eukaryotic probe EUK 1209R (bottom) used successively on the same membrane. All spots were made in triplicate to better assess the variability of the hybridization method for a single sample. The upper left square of each panel corresponds to the positive control (B. pacifica DNA) deposited at different concentrations. The lower left square corresponds to 100 ng of DNAs from different negative controls. The middle part corresponds to 100-ng quantities of DNA amplified from Mediterranean Sea samples, each of them corresponding to a different row, as follows: row 1, MIN17 at 10 m; row 2, MIN17 at 60 m; row 3, MIN34 at 15 m; row 4, MIN34 at 50 m; and row 5, MIN44 at 20 m; row 6, MIN44 at 85 m; row 7, MIN52 at 20 m; and row 8, MIN52 at 70m. The right part of each panel corresponds to 100-ng quantities of DNA amplified from equatorial Pacific samples, each of them corresponding to a different row, as follows: row 1, OLI16 at 15 m; row 2, OLI16 at 75 m; row 3, OLI26 at 15 m; row 4, OLI26 at 60 m; row 5, OLI41 at 15 m; row 6, OLI41 at 75 m; row 7, OLI51 at 15 m; and row 8, OLI51 at 60 m.

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