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Gut Microbiota Alternation in Disease Progression of Neurosyphilis

BACKGROUND: The gut microbiota plays an important role in the development of neurological disorders such as Parkinson’s disease and Alzheimer’s disease. However, studies on the gut microbiota of patients with neurosyphilis (NS) were rarely reported. METHODS: In this study, we collected fecal samples...

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Autores principales: Wang, Guixuan, Zou, Danyang, Lu, Xinying, Gu, Xin, Cheng, Yuanyuan, Qi, Tengfei, Cheng, Yanchun, Yu, Junjun, Ye, Meiping, Zhou, Pingyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9673944/
https://www.ncbi.nlm.nih.gov/pubmed/36406865
http://dx.doi.org/10.2147/IDR.S389155
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author Wang, Guixuan
Zou, Danyang
Lu, Xinying
Gu, Xin
Cheng, Yuanyuan
Qi, Tengfei
Cheng, Yanchun
Yu, Junjun
Ye, Meiping
Zhou, Pingyu
author_facet Wang, Guixuan
Zou, Danyang
Lu, Xinying
Gu, Xin
Cheng, Yuanyuan
Qi, Tengfei
Cheng, Yanchun
Yu, Junjun
Ye, Meiping
Zhou, Pingyu
author_sort Wang, Guixuan
collection PubMed
description BACKGROUND: The gut microbiota plays an important role in the development of neurological disorders such as Parkinson’s disease and Alzheimer’s disease. However, studies on the gut microbiota of patients with neurosyphilis (NS) were rarely reported. METHODS: In this study, we collected fecal samples from 62 syphilis patients, including 39 with NS and 23 with non-NS. Among the NS patients, 18 were general paresis (GP). The white blood cell counts, protein concentrations, and Venereal Disease Research Laboratory test positive rates of cerebrospinal fluid from patients in NS or GP group were significantly higher than those from patients in non-NS group. 16S ribosomal RNA sequencing results revealed that the alpha and beta diversities of the gut microbiota were similar between NS and non-NS patients or GP and non-NS patients. RESULTS: Linear discriminant analysis with effect size (LEfSe) analysis showed that some taxa, such as Coprobacter, were increased in both NS group and GP group, compared with non-NS group. Besides, the clade of Akkermansia was also overrepresented in GP Patients. Meanwhile, some taxa such as Clostridia_UCG-014 and SC-I-84 were underrepresented in NS patients. The abundances of class Bacilli and genus Alloprevotella were decreased in GP patients. Among them, the abundances of some taxa such as Coprobacter and Akkermansia have been reported to be associated with other neuropsychiatric disorders. CONCLUSION: Our findings suggest that the alternation of the gut microbiota in NS patients may contribute to the course of NS, which will deepen our understanding of NS.
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spelling pubmed-96739442022-11-19 Gut Microbiota Alternation in Disease Progression of Neurosyphilis Wang, Guixuan Zou, Danyang Lu, Xinying Gu, Xin Cheng, Yuanyuan Qi, Tengfei Cheng, Yanchun Yu, Junjun Ye, Meiping Zhou, Pingyu Infect Drug Resist Original Research BACKGROUND: The gut microbiota plays an important role in the development of neurological disorders such as Parkinson’s disease and Alzheimer’s disease. However, studies on the gut microbiota of patients with neurosyphilis (NS) were rarely reported. METHODS: In this study, we collected fecal samples from 62 syphilis patients, including 39 with NS and 23 with non-NS. Among the NS patients, 18 were general paresis (GP). The white blood cell counts, protein concentrations, and Venereal Disease Research Laboratory test positive rates of cerebrospinal fluid from patients in NS or GP group were significantly higher than those from patients in non-NS group. 16S ribosomal RNA sequencing results revealed that the alpha and beta diversities of the gut microbiota were similar between NS and non-NS patients or GP and non-NS patients. RESULTS: Linear discriminant analysis with effect size (LEfSe) analysis showed that some taxa, such as Coprobacter, were increased in both NS group and GP group, compared with non-NS group. Besides, the clade of Akkermansia was also overrepresented in GP Patients. Meanwhile, some taxa such as Clostridia_UCG-014 and SC-I-84 were underrepresented in NS patients. The abundances of class Bacilli and genus Alloprevotella were decreased in GP patients. Among them, the abundances of some taxa such as Coprobacter and Akkermansia have been reported to be associated with other neuropsychiatric disorders. CONCLUSION: Our findings suggest that the alternation of the gut microbiota in NS patients may contribute to the course of NS, which will deepen our understanding of NS. Dove 2022-11-14 /pmc/articles/PMC9673944/ /pubmed/36406865 http://dx.doi.org/10.2147/IDR.S389155 Text en © 2022 Wang et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Wang, Guixuan
Zou, Danyang
Lu, Xinying
Gu, Xin
Cheng, Yuanyuan
Qi, Tengfei
Cheng, Yanchun
Yu, Junjun
Ye, Meiping
Zhou, Pingyu
Gut Microbiota Alternation in Disease Progression of Neurosyphilis
title Gut Microbiota Alternation in Disease Progression of Neurosyphilis
title_full Gut Microbiota Alternation in Disease Progression of Neurosyphilis
title_fullStr Gut Microbiota Alternation in Disease Progression of Neurosyphilis
title_full_unstemmed Gut Microbiota Alternation in Disease Progression of Neurosyphilis
title_short Gut Microbiota Alternation in Disease Progression of Neurosyphilis
title_sort gut microbiota alternation in disease progression of neurosyphilis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9673944/
https://www.ncbi.nlm.nih.gov/pubmed/36406865
http://dx.doi.org/10.2147/IDR.S389155
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