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Appl. Environ. Microbiol., Jul 1995, 2506-2513, Vol 61, No. 7
N Simon, N LeBot, D Marie, F Partensky and D Vaulot
Because of their tiny size (0.2 to 2 microns), oceanic picophytoplanktonic
cells (either cultured strains or natural communities) are difficult to
identify, and some basic questions concerning their taxonomy, physiology,
and ecology are still largely unanswered. The present study was designed to
test the suitability of in situ hybridization with rRNA fluorescent probes
detected by flow cytometry for the identification of small photosynthetic
eukaryotes. Oligonucleotide probes targeted against regions of the 18S
rRNAs of Chlorophyta lineage (CHLO probe) and of non-Chlorophyta (NCHLO
probe) algal species were designed. The CHLO and NCHLO probes, which
differed by a single nucleotide, allowed discrimination of chlorophyte from
nonchlorophyte cultured strains. The sensitivity of each probe was
dependent upon the size of the cells and upon their growth stage. The mean
fluorescence was 8 to 80 times higher for specifically labeled than for
nonspecifically labeled cells in exponential growth phase, but it decreased
sharply in stationary phase. Such taxon-specific probes should increase the
applicability of flow cytometry for the rapid identification of cultured
pico- and nanoplanktonic strains, especially those that lack taxonomically
useful morphological features.
Copyright © 1995, American Society for Microbiology
Fluorescent in situ hybridization with rRNA-targeted oligonucleotide probes to identify small phytoplankton by flow cytometry
Centre National de la Recherche Scientifique, Roscoff, France.
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