Literature DB >> 11714518

Identification of indicator microorganisms using a standardized PNA FISH method.

H Perry-O'Keefe1, S Rigby, K Oliveira, D Sørensen, H Stender, J Coull, J J Hyldig-Nielsen.   

Abstract

A standardized fluorescent in situ hybridization (FISH) method using Peptide Nucleic Acid (PNA) probes for analysis of gram-negative and gram-positive bacteria, as well as yeast, has been developed. Fluorescently labeled PNA probes targeting specific rRNA sequences of Escherichia coli, Pseudomonas aeruginosa, Staphyloccocus aureus, Salmonella were designed, as well as PNA probes targeting eubacteria and eucarya. These PNA probes were evaluated by PNA FISH using 27 bacterial and 1 yeast species, representing both phylogenetically closely related species, as well as species important to both clinical and industrial settings. The S. aureus and P. aeruginosa PNA probes did not cross react with any of the organisms tested, whereas the E. coli PNA probe, as expected from sequence data, also detected Shigella species. The Salmonella PNA probe reacted with all of the 13 Salmonella strains, representing the 7 subspecies of Salmonella, however, it is also complementary to a few other bacterial species. The eubacteria- and eucarya-specific PNA probes detected all bacterial species and one yeast species, respectively. The general applicability of the PNA FISH method made simultaneous identification of multiple species, both gram-negative and gram-positive, in a mixed population an attractive possibility never accomplished using DNA probes. Four color images using differently labeled PNA probes showed simultaneous identification of E. coli, P. aeruginosa, S. aureus and Salmonella, thereby demonstrating the potential of multiplex FISH for various diagnostic applications within both clinical and industrial microbiology.

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Year:  2001        PMID: 11714518     DOI: 10.1016/s0167-7012(01)00303-7

Source DB:  PubMed          Journal:  J Microbiol Methods        ISSN: 0167-7012            Impact factor:   2.363


  42 in total

1.  Fluorescence in situ hybridization method using a peptide nucleic acid probe for identification of Salmonella spp. in a broad spectrum of samples.

Authors:  C Almeida; N F Azevedo; R M Fernandes; C W Keevil; M J Vieira
Journal:  Appl Environ Microbiol       Date:  2010-05-07       Impact factor: 4.792

2.  Use of DNA and peptide nucleic acid molecular beacons for detection and quantification of rRNA in solution and in whole cells.

Authors:  Chuanwu Xi; Michal Balberg; Stephen A Boppart; Lutgarde Raskin
Journal:  Appl Environ Microbiol       Date:  2003-09       Impact factor: 4.792

Review 3.  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

4.  Fluorescence in situ hybridization using peptide nucleic acid probes for rapid detection of Mycobacterium avium subsp. avium and Mycobacterium avium subsp. paratuberculosis in potable-water biofilms.

Authors:  Markku J Lehtola; Eila Torvinen; Ilkka T Miettinen; C William Keevil
Journal:  Appl Environ Microbiol       Date:  2006-01       Impact factor: 4.792

5.  Direct identification of major blood culture pathogens, including Pseudomonas aeruginosa and Escherichia coli, by a panel of fluorescence in situ hybridization assays using peptide nucleic acid probes.

Authors:  M Søgaard; H Stender; H C Schønheyder
Journal:  J Clin Microbiol       Date:  2005-04       Impact factor: 5.948

6.  Evaluation of in situ methods used to detect Mycobacterium avium subsp. paratuberculosis in samples from patients with Crohn's disease.

Authors:  Mangalakumari Jeyanathan; David C Alexander; Christine Y Turenne; Christiane Girard; Marcel A Behr
Journal:  J Clin Microbiol       Date:  2006-08       Impact factor: 5.948

7.  Improved in situ hybridization efficiency with locked-nucleic-acid-incorporated DNA probes.

Authors:  Kengo Kubota; Akiyoshi Ohashi; Hiroyuki Imachi; Hideki Harada
Journal:  Appl Environ Microbiol       Date:  2006-08       Impact factor: 4.792

8.  Development and application of a novel peptide nucleic acid probe for the specific detection of Cronobacter genomospecies (Enterobacter sakazakii) in powdered infant formula.

Authors:  C Almeida; N F Azevedo; C Iversen; S Fanning; C W Keevil; M J Vieira
Journal:  Appl Environ Microbiol       Date:  2009-03-06       Impact factor: 4.792

9.  Integration of FISH and Microfluidics.

Authors:  Célia F Rodrigues; Nuno F Azevedo; João M Miranda
Journal:  Methods Mol Biol       Date:  2021

10.  DNA mimics for the rapid identification of microorganisms by fluorescence in situ hybridization (FISH).

Authors:  Laura Cerqueira; Nuno F Azevedo; Carina Almeida; Tatiana Jardim; Charles William Keevil; Maria J Vieira
Journal:  Int J Mol Sci       Date:  2008-10-20       Impact factor: 5.923

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