Detection and discrimination of biofilm populations using locked nucleic acid/2'-O-methyl-RNA fluorescence in situ hybridization (LNA/2'OMe-FISH)
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Publication Date: | 2015 |
Other Authors: | , , , , |
Format: | Article |
Language: | eng |
Source: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Download full: | https://hdl.handle.net/1822/37908 |
Summary: | Multispecies biofilms are the dominant form of biofilms found in Nature. The application of fluorescence in situ hybridization (FISH)-based techniques to the discrimination of biofilm populations might contribute to the understanding of microorganism interactions in these structures, and might allow the development of efficient strategies to prevent or minimize biofilm-associated diseases. This work presents the first study that develops, optimizes and validates a multiplex FISH procedure using locked nucleic acid (LNA) and 2-O-methyl RNA (2OMe) oligonucleotides probes for the in vitro discrimination within mixed populations. As a case study, Escherichia coli, the major cause of urinary tract infections (UTIs), and three other atypical colonizers of urinary catheters (Delftia tsuruhatensis, Achromobacter xylosoxidans and Burkholderia fungorum) with unproven pathogenic potential, were selected. Specific probes for these species were designed and optimized for specific hybridization in multiplex experiments. Results showed that the LNA/2OMe-FISH method performed well in multiplex experiments and presented a good correlation with total and cultivability counts, regardless of the cells physiological state. In fact, the method was also able to report variations of viable but non-cultivable populations. Further analysis of mixed biofilm structures by confocal laser scanning microscopy provided a clear discrimination in three dimensions between the location of the different populations. |
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Detection and discrimination of biofilm populations using locked nucleic acid/2'-O-methyl-RNA fluorescence in situ hybridization (LNA/2'OMe-FISH)BiofilmsDNAMicrobial GrowthRNALNA/2'OMe-FISHConfocal laser scanning microscopyScience & TechnologyMultispecies biofilms are the dominant form of biofilms found in Nature. The application of fluorescence in situ hybridization (FISH)-based techniques to the discrimination of biofilm populations might contribute to the understanding of microorganism interactions in these structures, and might allow the development of efficient strategies to prevent or minimize biofilm-associated diseases. This work presents the first study that develops, optimizes and validates a multiplex FISH procedure using locked nucleic acid (LNA) and 2-O-methyl RNA (2OMe) oligonucleotides probes for the in vitro discrimination within mixed populations. As a case study, Escherichia coli, the major cause of urinary tract infections (UTIs), and three other atypical colonizers of urinary catheters (Delftia tsuruhatensis, Achromobacter xylosoxidans and Burkholderia fungorum) with unproven pathogenic potential, were selected. Specific probes for these species were designed and optimized for specific hybridization in multiplex experiments. Results showed that the LNA/2OMe-FISH method performed well in multiplex experiments and presented a good correlation with total and cultivability counts, regardless of the cells physiological state. In fact, the method was also able to report variations of viable but non-cultivable populations. Further analysis of mixed biofilm structures by confocal laser scanning microscopy provided a clear discrimination in three dimensions between the location of the different populations.This work was funded by FEDER funds through the Operational Programme for Competitiveness Factors - COMPETE, ON.2 - O Novo Norte -North Portugal Regional Operational Programme and National Funds through FCT - Foundation for Science and Technology under the projects: PEst-C/EQB/UI0511, NORTE-07-0124-FEDER-000025 - RL2_ Environment & Health and Project "DNA mimics" PIC/IC/82815/2007; PhD Fellowship [SFRH/BD/82663/2011]; and Postdoctoral Fellowship [SFRH/BPD/74480/2010]. The authors would like to thank to M. Fenice and A. Steinbuchel for kindly providing the D. tsuruhatensis BM90 and A. xylosoxidans B3 strains, respectively.Elsevier B.V.Universidade do MinhoAzevedo, AndreiaAlmeida, CarinaPereira, BrunoMadureira, PedroWengel, JesperAzevedo, N. F.2015-12-152015-12-15T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/1822/37908engAzevedo, Andreia S.; Almeida, Carina; Pereira, Bruno; Madureira, Pedro; Wengel, Jesper; Azevedo, Nuno F., Detection and discrimination of biofilm populations using Locked Nucleic Acid/2-O-Methyl-RNA Fluorescence In Situ Hybridization (LNA/2OMe-FISH). Biochemical Engineering Journal, 104, 64-73, 20151369-703X1369-703X10.1016/j.bej.2015.04.024http://www.elsevier.com/locate/issn/1369703Xinfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-04-12T05:19:24Zoai:repositorium.sdum.uminho.pt:1822/37908Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T16:23:21.515171Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
dc.title.none.fl_str_mv |
Detection and discrimination of biofilm populations using locked nucleic acid/2'-O-methyl-RNA fluorescence in situ hybridization (LNA/2'OMe-FISH) |
title |
Detection and discrimination of biofilm populations using locked nucleic acid/2'-O-methyl-RNA fluorescence in situ hybridization (LNA/2'OMe-FISH) |
spellingShingle |
Detection and discrimination of biofilm populations using locked nucleic acid/2'-O-methyl-RNA fluorescence in situ hybridization (LNA/2'OMe-FISH) Azevedo, Andreia Biofilms DNA Microbial Growth RNA LNA/2'OMe-FISH Confocal laser scanning microscopy Science & Technology |
title_short |
Detection and discrimination of biofilm populations using locked nucleic acid/2'-O-methyl-RNA fluorescence in situ hybridization (LNA/2'OMe-FISH) |
title_full |
Detection and discrimination of biofilm populations using locked nucleic acid/2'-O-methyl-RNA fluorescence in situ hybridization (LNA/2'OMe-FISH) |
title_fullStr |
Detection and discrimination of biofilm populations using locked nucleic acid/2'-O-methyl-RNA fluorescence in situ hybridization (LNA/2'OMe-FISH) |
title_full_unstemmed |
Detection and discrimination of biofilm populations using locked nucleic acid/2'-O-methyl-RNA fluorescence in situ hybridization (LNA/2'OMe-FISH) |
title_sort |
Detection and discrimination of biofilm populations using locked nucleic acid/2'-O-methyl-RNA fluorescence in situ hybridization (LNA/2'OMe-FISH) |
author |
Azevedo, Andreia |
author_facet |
Azevedo, Andreia Almeida, Carina Pereira, Bruno Madureira, Pedro Wengel, Jesper Azevedo, N. F. |
author_role |
author |
author2 |
Almeida, Carina Pereira, Bruno Madureira, Pedro Wengel, Jesper Azevedo, N. F. |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Universidade do Minho |
dc.contributor.author.fl_str_mv |
Azevedo, Andreia Almeida, Carina Pereira, Bruno Madureira, Pedro Wengel, Jesper Azevedo, N. F. |
dc.subject.por.fl_str_mv |
Biofilms DNA Microbial Growth RNA LNA/2'OMe-FISH Confocal laser scanning microscopy Science & Technology |
topic |
Biofilms DNA Microbial Growth RNA LNA/2'OMe-FISH Confocal laser scanning microscopy Science & Technology |
description |
Multispecies biofilms are the dominant form of biofilms found in Nature. The application of fluorescence in situ hybridization (FISH)-based techniques to the discrimination of biofilm populations might contribute to the understanding of microorganism interactions in these structures, and might allow the development of efficient strategies to prevent or minimize biofilm-associated diseases. This work presents the first study that develops, optimizes and validates a multiplex FISH procedure using locked nucleic acid (LNA) and 2-O-methyl RNA (2OMe) oligonucleotides probes for the in vitro discrimination within mixed populations. As a case study, Escherichia coli, the major cause of urinary tract infections (UTIs), and three other atypical colonizers of urinary catheters (Delftia tsuruhatensis, Achromobacter xylosoxidans and Burkholderia fungorum) with unproven pathogenic potential, were selected. Specific probes for these species were designed and optimized for specific hybridization in multiplex experiments. Results showed that the LNA/2OMe-FISH method performed well in multiplex experiments and presented a good correlation with total and cultivability counts, regardless of the cells physiological state. In fact, the method was also able to report variations of viable but non-cultivable populations. Further analysis of mixed biofilm structures by confocal laser scanning microscopy provided a clear discrimination in three dimensions between the location of the different populations. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-12-15 2015-12-15T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://hdl.handle.net/1822/37908 |
url |
https://hdl.handle.net/1822/37908 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Azevedo, Andreia S.; Almeida, Carina; Pereira, Bruno; Madureira, Pedro; Wengel, Jesper; Azevedo, Nuno F., Detection and discrimination of biofilm populations using Locked Nucleic Acid/2-O-Methyl-RNA Fluorescence In Situ Hybridization (LNA/2OMe-FISH). Biochemical Engineering Journal, 104, 64-73, 2015 1369-703X 1369-703X 10.1016/j.bej.2015.04.024 http://www.elsevier.com/locate/issn/1369703X |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
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openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier B.V. |
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Elsevier B.V. |
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