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Fluorescence in situ hybridisation in Carnoy’s fixed tonsil tissue
Fluorescence in situ hybridisation (FISH) is a powerful molecular technique that enables direct visualisation of specific bacterial species. Few studies have established FISH protocols for tonsil tissue in Carnoy’s fixative, accordingly limiting its application to investigate the pathogenesis of ton...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9300673/ https://www.ncbi.nlm.nih.gov/pubmed/35858968 http://dx.doi.org/10.1038/s41598-022-16309-w |
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author | Clark, S. T. Waldvogel-Thurlow, S. Wagner Mackenzie, B. Douglas, R. G. Biswas, K. |
author_facet | Clark, S. T. Waldvogel-Thurlow, S. Wagner Mackenzie, B. Douglas, R. G. Biswas, K. |
author_sort | Clark, S. T. |
collection | PubMed |
description | Fluorescence in situ hybridisation (FISH) is a powerful molecular technique that enables direct visualisation of specific bacterial species. Few studies have established FISH protocols for tonsil tissue in Carnoy’s fixative, accordingly limiting its application to investigate the pathogenesis of tonsillar hyperplasia. Tonsil tissue from 24 children undergoing tonsillectomy for either recurrent tonsillitis or sleep-disordered breathing were obtained during a previous study. The specificity of each of the five FISH probes (Fusobacterium spp., Bacteroides spp., Streptococcus spp., Haemophilus influenzae and Pseudomonas spp.) were successfully optimised using pure and mixed bacterial isolates, and in Carnoy’s fixed tonsil tissue. Bacteroides spp. were present in 100% of patients with microcolonies. In comparison, the prevalence of Fusobacterium spp. was 93.8%, Streptococcus spp. 85.7%, H. influenzae 82.35% and Pseudomonas spp. 76.5%. Notable differences in the organisation of bacterial taxa within a single microcolony were also observed. This is the first study to establish a robust FISH protocol identifying multiple aerobic and anaerobic bacteria in Carnoy’s fixed tonsil tissue. This protocol provides a strong foundation for combining histological and microbiological analyses of Carnoy’s fixed tonsil samples. It may also have important implications on the analysis of microorganisms in other human tissues prepared using the same techniques. |
format | Online Article Text |
id | pubmed-9300673 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-93006732022-07-22 Fluorescence in situ hybridisation in Carnoy’s fixed tonsil tissue Clark, S. T. Waldvogel-Thurlow, S. Wagner Mackenzie, B. Douglas, R. G. Biswas, K. Sci Rep Article Fluorescence in situ hybridisation (FISH) is a powerful molecular technique that enables direct visualisation of specific bacterial species. Few studies have established FISH protocols for tonsil tissue in Carnoy’s fixative, accordingly limiting its application to investigate the pathogenesis of tonsillar hyperplasia. Tonsil tissue from 24 children undergoing tonsillectomy for either recurrent tonsillitis or sleep-disordered breathing were obtained during a previous study. The specificity of each of the five FISH probes (Fusobacterium spp., Bacteroides spp., Streptococcus spp., Haemophilus influenzae and Pseudomonas spp.) were successfully optimised using pure and mixed bacterial isolates, and in Carnoy’s fixed tonsil tissue. Bacteroides spp. were present in 100% of patients with microcolonies. In comparison, the prevalence of Fusobacterium spp. was 93.8%, Streptococcus spp. 85.7%, H. influenzae 82.35% and Pseudomonas spp. 76.5%. Notable differences in the organisation of bacterial taxa within a single microcolony were also observed. This is the first study to establish a robust FISH protocol identifying multiple aerobic and anaerobic bacteria in Carnoy’s fixed tonsil tissue. This protocol provides a strong foundation for combining histological and microbiological analyses of Carnoy’s fixed tonsil samples. It may also have important implications on the analysis of microorganisms in other human tissues prepared using the same techniques. Nature Publishing Group UK 2022-07-20 /pmc/articles/PMC9300673/ /pubmed/35858968 http://dx.doi.org/10.1038/s41598-022-16309-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article′s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article′s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Clark, S. T. Waldvogel-Thurlow, S. Wagner Mackenzie, B. Douglas, R. G. Biswas, K. Fluorescence in situ hybridisation in Carnoy’s fixed tonsil tissue |
title | Fluorescence in situ hybridisation in Carnoy’s fixed tonsil tissue |
title_full | Fluorescence in situ hybridisation in Carnoy’s fixed tonsil tissue |
title_fullStr | Fluorescence in situ hybridisation in Carnoy’s fixed tonsil tissue |
title_full_unstemmed | Fluorescence in situ hybridisation in Carnoy’s fixed tonsil tissue |
title_short | Fluorescence in situ hybridisation in Carnoy’s fixed tonsil tissue |
title_sort | fluorescence in situ hybridisation in carnoy’s fixed tonsil tissue |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9300673/ https://www.ncbi.nlm.nih.gov/pubmed/35858968 http://dx.doi.org/10.1038/s41598-022-16309-w |
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