Literature DB >> 11543584

Rapid direct methods for enumeration of specific, active bacteria in water and biofilms.

G A McFeters1, B H Pyle, J T Lisle, S C Broadaway.   

Abstract

Conventional methods for detecting indicator and pathogenic bacteria in water may underestimate the actual population due to sublethal environmental injury, inability of the target bacteria to take up nutrients and other physiological factors which reduce bacterial culturability. Rapid and direct methods are needed to more accurately detect and enumerate active bacteria. Such a methodological advance would provide greater sensitivity in assessing the microbiological safety of water and food. The principle goal of this presentation is to describe novel approaches we have formulated for the rapid and simultaneous detection of bacteria plus the determination of their physiological activity in water and other environmental samples. The present version of our method involves the concentration of organisms by membrane filtration or immunomagnetic separation and combines an intracellular fluorochrome (CTC) for assessment of respiratory activity plus fluorescent-labelled antibody detection of specific bacteria. This approach has also been successfully used to demonstrate spatial and temporal heterogeneities of physiological activities in biofilms when coupled with cryosectioning. Candidate physiological stains include those capable of determining respiratory activity, membrane potential, membrane integrity, growth rate and cellular enzymatic activities. Results obtained thus far indicate that immunomagnetic separation can provide a high degree of sensitivity in the recovery of seeded target bacteria (Escherichia coli O157:H7) in water and hamburger. The captured and stained target bacteria are then enumerated by either conventional fluorescence microscopy or ChemScan(R), a new instrument that is very sensitive and rapid. The ChemScan(R) laser scanning instrument (Chemunex, Paris, France) provides the detection of individual fluorescently labelled bacterial cells using three emission channels in less than 5 min. A high degree of correlation has been demonstrated between results obtained with the ChemScan and traditional plate counts of mixed natural bacterial populations in water. The continuing evolution of these methods will be valuable in the rapid and accurate analysis of environmental samples.

Entities:  

Keywords:  NASA Discipline Environmental Health; Non-NASA Center

Mesh:

Substances:

Year:  1999        PMID: 11543584

Source DB:  PubMed          Journal:  Symp Ser Soc Appl Microbiol        ISSN: 1467-4734


  4 in total

1.  Comparison of fluorescence microscopy and solid-phase cytometry methods for counting bacteria in water.

Authors:  John T Lisle; Martin A Hamilton; Alan R Willse; Gordon A McFeters
Journal:  Appl Environ Microbiol       Date:  2004-09       Impact factor: 4.792

Review 2.  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

3.  A 96-well-plate-based optical method for the quantitative and qualitative evaluation of Pseudomonas aeruginosa biofilm formation and its application to susceptibility testing.

Authors:  Mathias Müsken; Stefano Di Fiore; Ute Römling; Susanne Häussler
Journal:  Nat Protoc       Date:  2010-07-29       Impact factor: 13.491

Review 4.  Revisiting the methods for detecting Mycobacterium tuberculosis: what has the new millennium brought thus far?

Authors:  Thales Alves Campelo; Paulo Rafael Cardoso de Sousa; Lucas de Lima Nogueira; Cristiane Cunha Frota; Paulo Renato Zuquim Antas
Journal:  Access Microbiol       Date:  2021-08-02
  4 in total

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