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)...

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Main Authors: Wiwat Chancharoenthana, Supitcha Kamolratanakul, Wassawon Ariyanon, Vipa Thanachartwet, Weerapong Phumratanaprapin, Polrat Wilairatana, Asada Leelahavanichkul
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-06-01
Series:Frontiers in Cellular and Infection Microbiology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fcimb.2022.890817/full
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author Wiwat Chancharoenthana
Wiwat Chancharoenthana
Supitcha Kamolratanakul
Supitcha Kamolratanakul
Wassawon Ariyanon
Wassawon Ariyanon
Vipa Thanachartwet
Weerapong Phumratanaprapin
Polrat Wilairatana
Asada Leelahavanichkul
Asada Leelahavanichkul
author_facet Wiwat Chancharoenthana
Wiwat Chancharoenthana
Supitcha Kamolratanakul
Supitcha Kamolratanakul
Wassawon Ariyanon
Wassawon Ariyanon
Vipa Thanachartwet
Weerapong Phumratanaprapin
Polrat Wilairatana
Asada Leelahavanichkul
Asada Leelahavanichkul
author_sort Wiwat Chancharoenthana
collection DOAJ
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.
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spelling doaj.art-ea0b4092f9574acd83f92ab2defdf8512022-12-22T02:36:33ZengFrontiers Media S.A.Frontiers in Cellular and Infection Microbiology2235-29882022-06-011210.3389/fcimb.2022.890817890817Abnormal Blood Bacteriome, Gut Dysbiosis, and Progression to Severe Dengue DiseaseWiwat Chancharoenthana0Wiwat Chancharoenthana1Supitcha Kamolratanakul2Supitcha Kamolratanakul3Wassawon Ariyanon4Wassawon Ariyanon5Vipa Thanachartwet6Weerapong Phumratanaprapin7Polrat Wilairatana8Asada Leelahavanichkul9Asada Leelahavanichkul10Department of Clinical Tropical Medicine, Faculty of Tropical Medicine, Mahidol University, Bangkok, ThailandTropical Immunology and Translational Research Unit, Department of Clinical Tropical Medicine, Faculty of Tropical Medicine, Mahidol University, Bangkok, ThailandDepartment of Clinical Tropical Medicine, Faculty of Tropical Medicine, Mahidol University, Bangkok, ThailandTropical Immunology and Translational Research Unit, Department of Clinical Tropical Medicine, Faculty of Tropical Medicine, Mahidol University, Bangkok, ThailandCardiometabolic Centre, Department of Medicine, Bangkok Nursing Hospital, Bangkok, ThailandDepartment of Medicine, Banphaeo General Hospital, Samutsakhon, ThailandDepartment of Clinical Tropical Medicine, Faculty of Tropical Medicine, Mahidol University, Bangkok, ThailandDepartment of Clinical Tropical Medicine, Faculty of Tropical Medicine, Mahidol University, Bangkok, ThailandDepartment of Clinical Tropical Medicine, Faculty of Tropical Medicine, Mahidol University, Bangkok, ThailandImmunology Unit, Department of Microbiology, Faculty of Medicine, Chulalongkorn University, Bangkok, ThailandCenter of Excellence on Translational Research in Inflammation and Immunology (CETRII), Department of Microbiology, Chulalongkorn University, Bangkok, ThailandDespite 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.https://www.frontiersin.org/articles/10.3389/fcimb.2022.890817/fulldengue infectionimmunityleaky gut syndromelipopolysaccaridebeta-D-glucanmicrobiome & dysbiosis
spellingShingle Wiwat Chancharoenthana
Wiwat Chancharoenthana
Supitcha Kamolratanakul
Supitcha Kamolratanakul
Wassawon Ariyanon
Wassawon Ariyanon
Vipa Thanachartwet
Weerapong Phumratanaprapin
Polrat Wilairatana
Asada Leelahavanichkul
Asada Leelahavanichkul
Abnormal Blood Bacteriome, Gut Dysbiosis, and Progression to Severe Dengue Disease
Frontiers in Cellular and Infection Microbiology
dengue infection
immunity
leaky gut syndrome
lipopolysaccaride
beta-D-glucan
microbiome & dysbiosis
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 dengue infection
immunity
leaky gut syndrome
lipopolysaccaride
beta-D-glucan
microbiome & dysbiosis
url https://www.frontiersin.org/articles/10.3389/fcimb.2022.890817/full
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