Community analysis of the bacterial assemblages in the winter cover and pelagic layers of a high mountain lake by in situ hybridization
- 1 June 1996
- journal article
- Published by American Society for Microbiology in Applied and Environmental Microbiology
- Vol. 62 (6) , 2138-44
- https://doi.org/10.1128/aem.62.6.2138-2144.1996
Abstract
The bacterial community structure in the winter cover and pelagic zone of a high mountain lake was analyzed by in situ hybridization with fluorescently labeled rRNA-targeted oligonucleotide probes. Cells fixed on membrane filters were hybridized with a probe specific for the domain Bacteria as well as with probes for the alpha, beta, and gamma subclasses of the class Proteobacteria and the Cytophaga-Flavobacterium group. The fraction of bacteria detectable after hybridization with the bacterial probe EUB ranged from 40 to 81% of 4(prm1),6-diamidino-2-phenylindole (DAPI) counts. The bacterial assemblage varied considerably between and within different habitats (snow, slush, and lake water) but was in most cases dominated by members of the beta subclass (6.5 to 116% of bacteria detectable with probe EUB). The sum of bacteria hybridizing with group-specific probes was usually lower than the fraction detectable with probe EUB. Image analysis was used to characterize morphology and the size-specific biomass distribution of bacterial assemblages, which clearly separated the three habitats. Although the measured secondary production parameters and the fraction of 2-(p-iodophenyl)-3-(p-nitrophenyl)-5-phenyltetrazolium chloride-reducing bacteria varied by more than an order of magnitude in the different slush and pelagic layers, detectability with the fluorescent probe EUB was constantly high. Physiological strategies of bacteria under nutrient limitation and at low temperatures are discussed in the context of the ribosome content of single cells. This study confirms the suitability of fluorescently labeled rRNA-targeted probes for the characterization of bacterial population structures even in oligotrophic habitats.Keywords
This publication has 20 references indexed in Scilit:
- Physiological assessment of bacteria using fluorochromesJournal of Microbiological Methods, 1995
- Estimating the Growth Rate of Slowly Growing Marine Bacteria from RNA ContentApplied and Environmental Microbiology, 1993
- Use of rRNA fluorescence in situ hybridization for measuring the activity of single cells in young and established biofilmsApplied and Environmental Microbiology, 1993
- How do non-differentiating bacteria adapt to starvation?Antonie van Leeuwenhoek, 1993
- Identification of single bacterial cells using digoxigenin-labelled, rRNA-targeted oligonucleotidesJournal of General Microbiology, 1991
- Genetic diversity in Sargasso Sea bacterioplanktonNature, 1990
- Effect of Growth Rate and Starvation-Survival on Cellular DNA, RNA, and Protein of a Psychrophilic Marine BacteriumApplied and Environmental Microbiology, 1989
- Phylogenetic Stains: Ribosomal RNA-Based Probes for the Identification of Single CellsScience, 1989
- The Transient Phase Between Growth and Nongrowth of Heterotrophic Bacteria, with Emphasis on the Marine EnvironmentAnnual Review of Microbiology, 1987
- A tentative direct microscopic method for counting living marine bacteriaCanadian Journal of Microbiology, 1979