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Systemic hematogenous dissemination of mouse oral candidiasis is induced by oral mucositis
The causes of fungemia include immunosuppression and neutropenia stemming from diverse factors as well as the placement of central venous catheters. However, the relationship between fungemia and the oral cavity has not been substantiated. In this study, we explored the pathological conditions of Ca...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Japan
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6153985/ https://www.ncbi.nlm.nih.gov/pubmed/29797142 http://dx.doi.org/10.1007/s10266-018-0366-1 |
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author | Katagiri, Hiroki Fukui, Kayoko Nakamura, Kenjirou Tanaka, Akira |
author_facet | Katagiri, Hiroki Fukui, Kayoko Nakamura, Kenjirou Tanaka, Akira |
author_sort | Katagiri, Hiroki |
collection | PubMed |
description | The causes of fungemia include immunosuppression and neutropenia stemming from diverse factors as well as the placement of central venous catheters. However, the relationship between fungemia and the oral cavity has not been substantiated. In this study, we explored the pathological conditions of Candida albicans—derived oral candidiasis in a mouse model, which always develops oral mucositis as a complication. In oral candidiasis, the hyphae of C. albicans are believed to primarily invade the stratum granulosum, but not the subepithelium, of the mucous membrane. We provide histological evidence that in concomitant oral mucositis, the hyphae infiltrate the subepithelium and blood vessels. Blood cultures and tissue samples revealed the onset of fungemia only in the mucositis-induced groups. Positive numbers of colony-forming units were found in groups A (chemotherapy), B (chemotherapy + mucositis) and C (mucositis), but were highest in group B. Some organs revealed positive CFU in groups B and C. The presence of fungal DNA in blood plasma and tissue was confirmed by PCR. The fungal DNA frequency was significantly higher in the mucositis group when compared with the non-mucositis group. The results suggest that fungi first invade the subepithelium and then the blood vessels, from which they disseminate throughout the body, and that oral mucositis is an important risk factor for fungemia. This study clearly demonstrates the relationship between oral mucositis, fungemia, and the potential systemic fungal dissemination, which has not been previously proven. Our findings highlight the importance of oral care for patients at risk of fungemia. |
format | Online Article Text |
id | pubmed-6153985 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-61539852018-10-04 Systemic hematogenous dissemination of mouse oral candidiasis is induced by oral mucositis Katagiri, Hiroki Fukui, Kayoko Nakamura, Kenjirou Tanaka, Akira Odontology Original Article The causes of fungemia include immunosuppression and neutropenia stemming from diverse factors as well as the placement of central venous catheters. However, the relationship between fungemia and the oral cavity has not been substantiated. In this study, we explored the pathological conditions of Candida albicans—derived oral candidiasis in a mouse model, which always develops oral mucositis as a complication. In oral candidiasis, the hyphae of C. albicans are believed to primarily invade the stratum granulosum, but not the subepithelium, of the mucous membrane. We provide histological evidence that in concomitant oral mucositis, the hyphae infiltrate the subepithelium and blood vessels. Blood cultures and tissue samples revealed the onset of fungemia only in the mucositis-induced groups. Positive numbers of colony-forming units were found in groups A (chemotherapy), B (chemotherapy + mucositis) and C (mucositis), but were highest in group B. Some organs revealed positive CFU in groups B and C. The presence of fungal DNA in blood plasma and tissue was confirmed by PCR. The fungal DNA frequency was significantly higher in the mucositis group when compared with the non-mucositis group. The results suggest that fungi first invade the subepithelium and then the blood vessels, from which they disseminate throughout the body, and that oral mucositis is an important risk factor for fungemia. This study clearly demonstrates the relationship between oral mucositis, fungemia, and the potential systemic fungal dissemination, which has not been previously proven. Our findings highlight the importance of oral care for patients at risk of fungemia. Springer Japan 2018-05-24 2018 /pmc/articles/PMC6153985/ /pubmed/29797142 http://dx.doi.org/10.1007/s10266-018-0366-1 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Katagiri, Hiroki Fukui, Kayoko Nakamura, Kenjirou Tanaka, Akira Systemic hematogenous dissemination of mouse oral candidiasis is induced by oral mucositis |
title | Systemic hematogenous dissemination of mouse oral candidiasis is induced by oral mucositis |
title_full | Systemic hematogenous dissemination of mouse oral candidiasis is induced by oral mucositis |
title_fullStr | Systemic hematogenous dissemination of mouse oral candidiasis is induced by oral mucositis |
title_full_unstemmed | Systemic hematogenous dissemination of mouse oral candidiasis is induced by oral mucositis |
title_short | Systemic hematogenous dissemination of mouse oral candidiasis is induced by oral mucositis |
title_sort | systemic hematogenous dissemination of mouse oral candidiasis is induced by oral mucositis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6153985/ https://www.ncbi.nlm.nih.gov/pubmed/29797142 http://dx.doi.org/10.1007/s10266-018-0366-1 |
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