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Abnormal Blood Bacteriome, Gut Dysbiosis, and Progression to Severe Dengue Disease
Despite a well-known association between gut barrier defect (leaky gut) and several diseases, data on translocation of pathogen molecules, including bacterial DNA (blood bacteriome), lipopolysaccharide (LPS), and serum (1→3)-β-D-glucan (BG), from the gut to the blood circulation (gut translocation)...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9248029/ https://www.ncbi.nlm.nih.gov/pubmed/35782108 http://dx.doi.org/10.3389/fcimb.2022.890817 |
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author | Chancharoenthana, Wiwat Kamolratanakul, Supitcha Ariyanon, Wassawon Thanachartwet, Vipa Phumratanaprapin, Weerapong Wilairatana, Polrat Leelahavanichkul, Asada |
author_facet | Chancharoenthana, Wiwat Kamolratanakul, Supitcha Ariyanon, Wassawon Thanachartwet, Vipa Phumratanaprapin, Weerapong Wilairatana, Polrat Leelahavanichkul, Asada |
author_sort | Chancharoenthana, Wiwat |
collection | PubMed |
description | Despite a well-known association between gut barrier defect (leaky gut) and several diseases, data on translocation of pathogen molecules, including bacterial DNA (blood bacteriome), lipopolysaccharide (LPS), and serum (1→3)-β-D-glucan (BG), from the gut to the blood circulation (gut translocation) in dengue are still less studied. Perhaps, dengue infection might induce gut translocation of several pathogenic molecules that affect the disease severity. At the enrollment, there were 31 dengue cases in febrile and critical phases at 4.1 ± 0.3 days and 6.4 ± 1.1 days of illness, respectively, with the leaky gut as indicated by positive lactulose-to-mannitol excretion ratio. With blood bacteriome, the patients with critical phase (more severe dengue; n = 23) demonstrated more predominant abundance in Bacteroidetes and Escherichia spp. with the lower Bifidobacteria when compared with the healthy control (n = 5). Meanwhile, most of the blood bacteriome results in dengue with febrile stage (n = 8) were comparable to the control, except for the lower Bifidobacteria in dengue cases. Additionally, endotoxemia at the enrollment was demonstrated in five (62.5%) and 19 (82.6%) patients with febrile and critical phases, respectively, while serum BG was detectable in two (25%) and 20 (87%) patients with febrile and critical phases, respectively. There were higher peripheral blood non-classical monocytes and natural killer cells (NK cells) at the enrollment in patients with febrile phage than in the cases with critical stage. Then, non-classical monocytes (CD14(-)CD16(+)) and NK cells (CD56(+)CD16(-)) increased at 4 and 7 days of illness in the cases with critical and febrile stages, respectively, the elevation of LPS and/or BG in serum on day 7 was also associated with the increase in monocytes, NK cells, and cytotoxic T cells. In summary, enhanced Proteobacteria (pathogenic bacteria from blood bacteriomes) along with increased endotoxemia and serum BG (leaky gut syndrome) might be collaborated with the impaired microbial control (lower non-classical monocytes and NK cells) in the critical cases and causing more severe disease of dengue infection. |
format | Online Article Text |
id | pubmed-9248029 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92480292022-07-02 Abnormal Blood Bacteriome, Gut Dysbiosis, and Progression to Severe Dengue Disease Chancharoenthana, Wiwat Kamolratanakul, Supitcha Ariyanon, Wassawon Thanachartwet, Vipa Phumratanaprapin, Weerapong Wilairatana, Polrat Leelahavanichkul, Asada Front Cell Infect Microbiol Cellular and Infection Microbiology Despite a well-known association between gut barrier defect (leaky gut) and several diseases, data on translocation of pathogen molecules, including bacterial DNA (blood bacteriome), lipopolysaccharide (LPS), and serum (1→3)-β-D-glucan (BG), from the gut to the blood circulation (gut translocation) in dengue are still less studied. Perhaps, dengue infection might induce gut translocation of several pathogenic molecules that affect the disease severity. At the enrollment, there were 31 dengue cases in febrile and critical phases at 4.1 ± 0.3 days and 6.4 ± 1.1 days of illness, respectively, with the leaky gut as indicated by positive lactulose-to-mannitol excretion ratio. With blood bacteriome, the patients with critical phase (more severe dengue; n = 23) demonstrated more predominant abundance in Bacteroidetes and Escherichia spp. with the lower Bifidobacteria when compared with the healthy control (n = 5). Meanwhile, most of the blood bacteriome results in dengue with febrile stage (n = 8) were comparable to the control, except for the lower Bifidobacteria in dengue cases. Additionally, endotoxemia at the enrollment was demonstrated in five (62.5%) and 19 (82.6%) patients with febrile and critical phases, respectively, while serum BG was detectable in two (25%) and 20 (87%) patients with febrile and critical phases, respectively. There were higher peripheral blood non-classical monocytes and natural killer cells (NK cells) at the enrollment in patients with febrile phage than in the cases with critical stage. Then, non-classical monocytes (CD14(-)CD16(+)) and NK cells (CD56(+)CD16(-)) increased at 4 and 7 days of illness in the cases with critical and febrile stages, respectively, the elevation of LPS and/or BG in serum on day 7 was also associated with the increase in monocytes, NK cells, and cytotoxic T cells. In summary, enhanced Proteobacteria (pathogenic bacteria from blood bacteriomes) along with increased endotoxemia and serum BG (leaky gut syndrome) might be collaborated with the impaired microbial control (lower non-classical monocytes and NK cells) in the critical cases and causing more severe disease of dengue infection. Frontiers Media S.A. 2022-06-17 /pmc/articles/PMC9248029/ /pubmed/35782108 http://dx.doi.org/10.3389/fcimb.2022.890817 Text en Copyright © 2022 Chancharoenthana, Kamolratanakul, Ariyanon, Thanachartwet, Phumratanaprapin, Wilairatana and Leelahavanichkul https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology Chancharoenthana, Wiwat Kamolratanakul, Supitcha Ariyanon, Wassawon Thanachartwet, Vipa Phumratanaprapin, Weerapong Wilairatana, Polrat Leelahavanichkul, Asada Abnormal Blood Bacteriome, Gut Dysbiosis, and Progression to Severe Dengue Disease |
title | Abnormal Blood Bacteriome, Gut Dysbiosis, and Progression to Severe Dengue Disease |
title_full | Abnormal Blood Bacteriome, Gut Dysbiosis, and Progression to Severe Dengue Disease |
title_fullStr | Abnormal Blood Bacteriome, Gut Dysbiosis, and Progression to Severe Dengue Disease |
title_full_unstemmed | Abnormal Blood Bacteriome, Gut Dysbiosis, and Progression to Severe Dengue Disease |
title_short | Abnormal Blood Bacteriome, Gut Dysbiosis, and Progression to Severe Dengue Disease |
title_sort | abnormal blood bacteriome, gut dysbiosis, and progression to severe dengue disease |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9248029/ https://www.ncbi.nlm.nih.gov/pubmed/35782108 http://dx.doi.org/10.3389/fcimb.2022.890817 |
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