Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/60589

TitleOptimizing locked nucleic acid/2-O-methyl-RNA fluorescence in situ hybridization (LNA/2OMe-FISH) procedure for bacterial detection
Author(s)Azevedo, Andreia S.
Sousa, Inês M.
Fernandes, R.
Azevedo, Nuno F.
Almeida, Carina
Issue date31-May-2019
PublisherPublic Library of Science
JournalPLoS ONE
CitationAzevedo, Andreia S.; Sousa, Inês M.; Fernandes, R.; Azevedo, Nuno F.; Almeida, Carina, Optimizing locked nucleic acid/2-O-methyl-RNA fluorescence in situ hybridization (LNA/2OMe-FISH) procedure for bacterial detection. PLoS One, 14(5), e0217689, 2019
Abstract(s)Despite the successful application of LNA/2OMe-FISH procedures for bacteria detection, there is a lack of knowledge on the properties that affect hybridization. Such information is crucial for the rational design of protocols. Hence, this work aimed to evaluate the effect of three essential factors on the LNA/2OMe hybridization stephybridization temperature, NaCl concentration and type and concentration of denaturant (formamide, ethylene carbonate and urea). This optimization was performed for 3 Gram-negative bacteria (Escherichia coli, Pseudomonas aeruginosa and Citrobacter freundii) and 2 Gram-positive bacteria (Enterococcus faecalis and Staphylococcus epidermidis), employing the response surface methodology and a Eubacteria probe. In general, it was observed that a high NaCl concentration is beneficial (from 2 M to 5 M), regardless of the denaturant used. Urea, formamide and ethylene carbonate are suitable denaturants for LNA/2OMe-FISH applications; but urea provides higher fluorescence intensities among the different bacteria, especially for gram-positive bacteria and for P. aeruginosa. However, a unique optimal protocol was not found for all tested bacteria. Despite this, the results indicate that a hybridization solution with 2 M of urea and 4 M of NaCl would be a proper starting point. Furthermore, a hybridization temperature around 62°C, for 14 bp probes with LNA monomers at every third position of 2?OMe and 64% of GC content, should be use in initial optimization of new LNA/2OMe-FISH protocols.
TypeArticle
URIhttp://hdl.handle.net/1822/60589
DOI10.1371/journal.pone.0217689
ISSN1932-6203
e-ISSN1932-6203
Publisher versionhttp://journals.plos.org/plosone/
Peer-Reviewedyes
AccessOpen access
Appears in Collections:CEB - Publicações em Revistas/Séries Internacionais / Publications in International Journals/Series

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