Home LiteratureArticle Details
PMID: 11260599 Published · ppublish English Evaluation Study Journal Article Research Support, Non-U.S. Gov't

A new approach to determine the genetic diversity of viable and active bacteria in aquatic ecosystems.

Cytometry ·Vol. 43 ·No. 4 ·2001-04-01 ·Pages 314-21

Bernard L, Courties C, Duperray C, Schäfer H, Muyzer G, Lebaron P

Abstract

Discrimination among viable, active, and inactive cells in aquatic ecosystems is of great importance to understand which species participate in microbial processes. In this study, a new approach combining flow cytometry (FCM), cell sorting, and molecular analyses was developed to compare the diversity of viable cells determined by different methods with the diversity of total cells and active cells. Total bacteria were determined by SYBR-II staining. Viable bacteria were determined in water samples from different sites by plate count techniques and by the direct viable count (DVC) method. Substrate-responsive cells (i.e., DVC(+) cells) were distinguished from nonresponsive cells (i.e., DVC(-) cells) by FCM and sorted. The genetic diversity of the sorted cell fraction was compared with the diversity of the total microbial community and with that of the culturable cell fraction by denaturing gradient gel electrophoresis (DGGE) of polymerase chain reaction (PCR)-amplified 16S rDNA fragments. The same approach was applied to a seawater sample enriched with nutrients. In this case, actively respiring cells (CTC+) were also enumerated by FCM, sorted, and analyzed by DGGE. The diversity of viable cells varied depending on the methods (traditional culture or DVC) used for viability assessment. Some phylotypes detected in the fraction of viable cells were not detectable at the community level (from total DNA). Similar results were found for actively respiring cells. Inversely, some phylotypes found at the community level were not found in viable and active cell-sorted fractions. It suggests that diversity determined at the community level includes nonactive and nonviable cells. This new approach allows investigation of the genetic diversity of viable and active cells in aquatic ecosystems. The diversity determined from sorted cells provides relevant ecological information and uncultured organisms can also be detected. New investigations in the field of microbial ecology such as the identification of species able to maintain cellular activity under environmental changes or in the presence of toxic compounds are now possible.

MeSH Terms
Bacteria/classification,genetics Bacterial Physiological Phenomena Colony Count, Microbial/methods DNA, Bacterial/analysis DNA, Ribosomal/analysis Ecosystem Electrophoresis, Agar Gel/methods Flow Cytometry/methods Polymerase Chain Reaction Reproducibility of Results Seawater/microbiology Stem Cells Water Microbiology
Chemicals
DNA, Bacterial DNA, Ribosomal
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Bernard L
Observatoire Océanologique, Université Pierre et Marie Curie, Institut National des Sciences de l'Univers, Banyuls-sur-Mer, France.
Courties C
Duperray C
Schäfer H
Muyzer G
Lebaron P
Article Info
Journal
Cytometry
Abbr.
Cytometry
ISSN
0196-4763
Published
2001-04-01
Pages
314-21
Language
English
Region
United States
NLM ID
8102328
Subset
IM
External Links
PubMed source
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com