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      The oral microbiome in alcohol use disorder: a longitudinal analysis during inpatient treatment

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          ABSTRACT

          Background

          Alcohol use disorder (AUD)-induced disruption of oral microbiota can lead to poor oral health; there have been no studies published examining the longitudinal effects of alcohol use cessation on the oral microbiome.

          Aim

          To investigate the oral microbiome during alcohol cessation during inpatient treatment for AUD.

          Methods

          Up to 10 oral tongue brushings were collected from 22 AUD patients during inpatient treatment at the National Institutes of Health. Alcohol use history, smoking, and periodontal disease status were measured. Oral microbiome samples were sequenced using 16S rRNA gene sequencing.

          Results

          Alpha diversity decreased linearly during treatment across the entire cohort ( P = 0.002). Alcohol preference was associated with changes in both alpha and beta diversity measures. Characteristic tongue dorsum genera from the Human Microbiome Project such as Streptococcus, Prevotella, Veillonella and Haemophilus were highly correlated in AUD. Oral health-associated genera that changed longitudinally during abstinence included Actinomyces, Capnocytophaga, Fusobacterium, Neisseria and Prevotella.

          Conclusion

          The oral microbiome in AUD is affected by alcohol preference. Patients with AUD often have poor oral health but abstinence and attention to oral care improve dysbiosis, decreasing microbiome diversity and periodontal disease-associated genera while improving acute oral health.

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          Most cited references57

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          Structure, Function and Diversity of the Healthy Human Microbiome

          Studies of the human microbiome have revealed that even healthy individuals differ remarkably in the microbes that occupy habitats such as the gut, skin, and vagina. Much of this diversity remains unexplained, although diet, environment, host genetics, and early microbial exposure have all been implicated. Accordingly, to characterize the ecology of human-associated microbial communities, the Human Microbiome Project has analyzed the largest cohort and set of distinct, clinically relevant body habitats to date. We found the diversity and abundance of each habitat’s signature microbes to vary widely even among healthy subjects, with strong niche specialization both within and among individuals. The project encountered an estimated 81–99% of the genera, enzyme families, and community configurations occupied by the healthy Western microbiome. Metagenomic carriage of metabolic pathways was stable among individuals despite variation in community structure, and ethnic/racial background proved to be one of the strongest associations of both pathways and microbes with clinical metadata. These results thus delineate the range of structural and functional configurations normal in the microbial communities of a healthy population, enabling future characterization of the epidemiology, ecology, and translational applications of the human microbiome.
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            Microbial complexes in subgingival plaque

            Journal of Clinical Periodontology, 25(2), 134-144
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              Gut microbiota dysbiosis contributes to the development of hypertension

              Background Recently, the potential role of gut microbiome in metabolic diseases has been revealed, especially in cardiovascular diseases. Hypertension is one of the most prevalent cardiovascular diseases worldwide, yet whether gut microbiota dysbiosis participates in the development of hypertension remains largely unknown. To investigate this issue, we carried out comprehensive metagenomic and metabolomic analyses in a cohort of 41 healthy controls, 56 subjects with pre-hypertension, 99 individuals with primary hypertension, and performed fecal microbiota transplantation from patients to germ-free mice. Results Compared to the healthy controls, we found dramatically decreased microbial richness and diversity, Prevotella-dominated gut enterotype, distinct metagenomic composition with reduced bacteria associated with healthy status and overgrowth of bacteria such as Prevotella and Klebsiella, and disease-linked microbial function in both pre-hypertensive and hypertensive populations. Unexpectedly, the microbiome characteristic in pre-hypertension group was quite similar to that in hypertension. The metabolism changes of host with pre-hypertension or hypertension were identified to be closely linked to gut microbiome dysbiosis. And a disease classifier based on microbiota and metabolites was constructed to discriminate pre-hypertensive and hypertensive individuals from controls accurately. Furthermore, by fecal transplantation from hypertensive human donors to germ-free mice, elevated blood pressure was observed to be transferrable through microbiota, and the direct influence of gut microbiota on blood pressure of the host was demonstrated. Conclusions Overall, our results describe a novel causal role of aberrant gut microbiota in contributing to the pathogenesis of hypertension. And the significance of early intervention for pre-hypertension was emphasized. Electronic supplementary material The online version of this article (doi:10.1186/s40168-016-0222-x) contains supplementary material, which is available to authorized users.
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                Author and article information

                Journal
                J Oral Microbiol
                J Oral Microbiol
                Journal of Oral Microbiology
                Taylor & Francis
                2000-2297
                1 December 2021
                2022
                1 December 2021
                : 14
                : 1
                : 2004790
                Affiliations
                [a ]Translational Biobehavioral and Health Disparities Branch, National Institutes of Health, Clinical Center; , Bethesda, MD, USA
                [b ]Center for Scientific Review, National Institutes of Health; , Bethesda, Md, USA;
                [c ]National Institutes of Health, Clinical Center; , Bethesda, MD, USA
                [d ]Office of the Clinical Director, Laboratory of Neurogenetics, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health; , Bethesda, Md, USA
                Author notes
                CONTACT Jj Barb barbj@ 123456nih.gov National Institutes of Health, Clinical Center, Bethesda; , Md, USA
                [+]

                This work was conducted while Dr. Brooks was an employee of the NIH Clinical Center (2020).

                The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

                Author information
                https://orcid.org/0000-0003-3022-0154
                Article
                2004790
                10.1080/20002297.2021.2004790
                8648028
                34880965
                1664b044-7956-4704-9339-64f48adf7a9e
                © 2021 Informa UK Limited, trading as Taylor & Francis

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                Page count
                Figures: 5, Tables: 1, References: 58, Pages: 15
                Categories
                Research Article
                Original Article

                Microbiology & Virology
                oral microbiome,alcohol use disorder,ion torrent,16s rrna,boas,periodontal disease,hmp

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