Literature DB >> 16395540

Bacterial abundance, activity, and viability in the eutrophic River Warnow, northeast Germany.

H M Freese1, U Karsten, R Schumann.   

Abstract

The River Warnow is the drinking water source for the city of Rostock. Its eutrophic status is accompanied by high amounts of bacteria, which may reach up to 24 x 10(6) cells mL(-1) as recorded during a seasonal study in 2002. Because the river is eutrophic and also heavily loaded with organic matter, this burden is a problem for drinking water purification, as it must be removed completely to not trigger new bacterial growth in the pipeline network. Therefore, restoration measures in the river have to be planned, and bacteria have to be favored as decomposers. That includes the investigation of the physiological state of bacteria in situ. Viable and active cells in the lower reaches of River Warnow were estimated using a broad set of methods. Intact bacteria were investigated by the LIVE/DEAD BacLight bacterial viability kit, containing a mixture of permeant and impermeant nucleic acid stains. Cells with ribosomes were visualized by fluorescence in situ hybridization with the EUB338 oligonucleotide probe. Intact cells and ribosome-containing bacteria represented 24% of total numbers stained by 4'6,-diamidino-2-phenylindole (DAPI) or 66 and 62%, respectively, in relation to all bacteria visualized by the LIVE/DEAD kit. Both fractions were considered as viable, although the fraction of RIB + bacteria is most likely underestimated by the protocol applied. 5-Cyano-2,3-ditolyltetrazolium chloride (CTC) was applied to mark respiring bacteria. The esterase substrate CellTracker Green 5-chloromethylfluorescein diacetate showed cells with intracellular hydrolytic activity. Whereas 1.5% of DAPI-stained bacteria were observed as respiring, 3.8% exhibited intracellular hydrolytic activity on average. If these active fractions were calculated as the percentages of intact cells, much higher fractions of 5.4% were respiring and 16% hydrolytic. Temperature was a main factor influencing total and viable cell numbers simultaneously. The results confirm that there are different states of viable and active cells in natural bacterioplankton communities. However, it remains unclear why fractions of viable and active cells were rather low in this eutrophic river in comparison to similar waters. We recommend to carefully address cells as viable in contrast to nonviable, i.e., dead. As viable cells may be active or inactive with respect to many different activities, e.g., substrate uptake, respiration, hydrolysis, and cell deviation, it is necessary to choose the method to visualize active cells according to the question to be answered.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16395540     DOI: 10.1007/s00248-005-0091-5

Source DB:  PubMed          Journal:  Microb Ecol        ISSN: 0095-3628            Impact factor:   4.552


  28 in total

1.  Comparative 16S rRNA analysis of lake bacterioplankton reveals globally distributed phylogenetic clusters including an abundant group of actinobacteria.

Authors:  F O Glöckner; E Zaichikov; N Belkova; L Denissova; J Pernthaler; A Pernthaler; R Amann
Journal:  Appl Environ Microbiol       Date:  2000-11       Impact factor: 4.792

2.  Resolution of viable and membrane-compromised bacteria in freshwater and marine waters based on analytical flow cytometry and nucleic acid double staining.

Authors:  G Grégori; S Citterio; A Ghiani; M Labra; S Sgorbati; S Brown; M Denis
Journal:  Appl Environ Microbiol       Date:  2001-10       Impact factor: 4.792

Review 3.  Direct estimate of active bacteria: CTC use and limitations.

Authors:  Véronique Créach; Anne Claire Baudoux; Georges Bertru; Bertrand Le Rouzic
Journal:  J Microbiol Methods       Date:  2003-01       Impact factor: 2.363

4.  Factors influencing the detection of bacterial cells using fluorescence in situ hybridization (FISH): A quantitative review of published reports.

Authors:  Thierry Bouvier; Paul A Del Giorgio
Journal:  FEMS Microbiol Ecol       Date:  2003-05-01       Impact factor: 4.194

5.  Hazards for the Rostock water supply from a tar-contaminated sediment in the river Warnow.

Authors:  F F Randow; T Hübener; G Merkel
Journal:  Toxicol Lett       Date:  1996-11       Impact factor: 4.372

6.  High abundance of viruses found in aquatic environments.

Authors:  O Bergh; K Y Børsheim; G Bratbak; M Heldal
Journal:  Nature       Date:  1989-08-10       Impact factor: 49.962

7.  Comparison of blue nucleic acid dyes for flow cytometric enumeration of bacteria in aquatic systems.

Authors:  P Lebaron; N Parthuisot; P Catala
Journal:  Appl Environ Microbiol       Date:  1998-05       Impact factor: 4.792

8.  Rapid fluorescence assessment of the viability of stressed Lactococcus lactis.

Authors:  C J Bunthof; S van den Braak; P Breeuwer; F M Rombouts; T Abee
Journal:  Appl Environ Microbiol       Date:  1999-08       Impact factor: 4.792

9.  Morphological and compositional changes in a planktonic bacterial community in response to enhanced protozoan grazing.

Authors:  K Jürgens; J Pernthaler; S Schalla; R Amann
Journal:  Appl Environ Microbiol       Date:  1999-03       Impact factor: 4.792

10.  Degradation of isooctane by Mycobacterium austroafricanum IFP 2173: growth and catabolic pathway.

Authors:  F Solano-Serena; R Marchal; S Heiss; J-P Vandecasteele
Journal:  J Appl Microbiol       Date:  2004       Impact factor: 3.772

View more
  17 in total

Review 1.  Selected fluorescent techniques for identification of the physiological state of individual water and soil bacterial cells - review.

Authors:  S Lew; M Lew; T Mieszczyński; J Szarek
Journal:  Folia Microbiol (Praha)       Date:  2010-05-19       Impact factor: 2.099

2.  New and fast method to quantify respiration rates of bacterial and plankton communities in freshwater ecosystems by using optical oxygen sensor spots.

Authors:  Mareike Warkentin; Heike M Freese; Ulf Karsten; Rhena Schumann
Journal:  Appl Environ Microbiol       Date:  2007-08-31       Impact factor: 4.792

3.  Labile and recalcitrant organic matter utilization by river biofilm under increasing water temperature.

Authors:  Irene Ylla; Anna M Romaní; Sergi Sabater
Journal:  Microb Ecol       Date:  2012-05-09       Impact factor: 4.552

4.  Substrate utilization profiles of bacterial strains in plankton from the River Warnow, a humic and eutrophic river in north Germany.

Authors:  Heike M Freese; Anja Eggert; Jay L Garland; Rhena Schumann
Journal:  Microb Ecol       Date:  2010-01       Impact factor: 4.552

5.  Bacterial activity and bacterioplankton diversity in the eutrophic River Warnow--direct measurement of bacterial growth efficiency and its effect on carbon utilization.

Authors:  Mareike Warkentin; Heike M Freese; Rhena Schumann
Journal:  Microb Ecol       Date:  2010-07-31       Impact factor: 4.552

6.  Short-term arsenic exposure reduces diatom cell size in biofilm communities.

Authors:  Laura Barral-Fraga; Soizic Morin; Marona D M Rovira; Gemma Urrea; Kit Magellan; Helena Guasch
Journal:  Environ Sci Pollut Res Int       Date:  2015-07-05       Impact factor: 4.223

7.  Agreement, precision, and accuracy of epifluorescence microscopy methods for enumeration of total bacterial numbers.

Authors:  Eun-Young Seo; Tae-Seok Ahn; Young-Gun Zo
Journal:  Appl Environ Microbiol       Date:  2010-01-22       Impact factor: 4.792

8.  Characterization of hydrogen peroxide-induced DNA release by Streptococcus sanguinis and Streptococcus gordonii.

Authors:  Jens Kreth; Hung Vu; Yongshu Zhang; Mark C Herzberg
Journal:  J Bacteriol       Date:  2009-08-14       Impact factor: 3.490

9.  Evaluating the flow-cytometric nucleic acid double-staining protocol in realistic situations of planktonic bacterial death.

Authors:  Tania Falcioni; Stefano Papa; Josep M Gasol
Journal:  Appl Environ Microbiol       Date:  2008-01-25       Impact factor: 4.792

10.  Use of propidium monoazide for live/dead distinction in microbial ecology.

Authors:  Andreas Nocker; Priscilla Sossa-Fernandez; Mark D Burr; Anne K Camper
Journal:  Appl Environ Microbiol       Date:  2007-06-22       Impact factor: 4.792

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.