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Characterization of Bacterial Differences Induced by Cleft-Palate-Related Spatial Heterogeneity

Background: Cleft palate (CP) patients have a higher prevalence of oral and respiratory tract bacterial infections than the general population. Nevertheless, characteristics of bacterial differences induced by CP-related anatomical heterogeneity are unknown. Methods: In this study, we systematically...

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Autores principales: Zhou, Fangjie, Su, Zhifei, Li, Qinyang, Wang, Renke, Liao, Ying, Zhang, Min, Li, Jiyao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9323727/
https://www.ncbi.nlm.nih.gov/pubmed/35890015
http://dx.doi.org/10.3390/pathogens11070771
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author Zhou, Fangjie
Su, Zhifei
Li, Qinyang
Wang, Renke
Liao, Ying
Zhang, Min
Li, Jiyao
author_facet Zhou, Fangjie
Su, Zhifei
Li, Qinyang
Wang, Renke
Liao, Ying
Zhang, Min
Li, Jiyao
author_sort Zhou, Fangjie
collection PubMed
description Background: Cleft palate (CP) patients have a higher prevalence of oral and respiratory tract bacterial infections than the general population. Nevertheless, characteristics of bacterial differences induced by CP-related anatomical heterogeneity are unknown. Methods: In this study, we systematically described the characteristics of bacteria in the oral and nasal niches in healthy children, CP children, healthy adolescents, CP adolescents, and postoperative adolescents by 454-pyrosequencing technology (V3–V6) to determine bacterial differences induced by CP. Results: Due to the CP-induced variations in spatial structure, the early establishment of microecology in CP children was different from that in healthy children. Nasal bacterial composition showed greater changes than in the saliva. Moreover, such discrepancy also appeared in CP and postoperative adolescents who had even undergone surgery > 10 years previously. Interestingly, we found by Lefse analysis that part of bacterial biomarkers in the nasal cavity of CP subjects was common oral flora, suggesting bacterial translocation between the oral and nasal niches. Therefore, we defined the oral–nasal translocation bacteria as O-N bac. By comparing multiple groups, we took the intersection sets of O-N bacs selected from CP children, CP adolescents, and postoperative adolescents as TS O-N bacs with time–character, including Streptococcus, Gemella, Alloprevotella, Neisseria, Rothia, Actinomyces, and Veillonella. These bacteria were at the core of the nasal bacterial network in CP subjects, and some were related to infectious diseases. Conclusions: CP would lead to significant and long-term differences in oral and nasal flora. TS O-N bacs migrating from the oral to the nasal might be the key stone causing nasal flora dysbiosis in the CP patients.
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spelling pubmed-93237272022-07-27 Characterization of Bacterial Differences Induced by Cleft-Palate-Related Spatial Heterogeneity Zhou, Fangjie Su, Zhifei Li, Qinyang Wang, Renke Liao, Ying Zhang, Min Li, Jiyao Pathogens Article Background: Cleft palate (CP) patients have a higher prevalence of oral and respiratory tract bacterial infections than the general population. Nevertheless, characteristics of bacterial differences induced by CP-related anatomical heterogeneity are unknown. Methods: In this study, we systematically described the characteristics of bacteria in the oral and nasal niches in healthy children, CP children, healthy adolescents, CP adolescents, and postoperative adolescents by 454-pyrosequencing technology (V3–V6) to determine bacterial differences induced by CP. Results: Due to the CP-induced variations in spatial structure, the early establishment of microecology in CP children was different from that in healthy children. Nasal bacterial composition showed greater changes than in the saliva. Moreover, such discrepancy also appeared in CP and postoperative adolescents who had even undergone surgery > 10 years previously. Interestingly, we found by Lefse analysis that part of bacterial biomarkers in the nasal cavity of CP subjects was common oral flora, suggesting bacterial translocation between the oral and nasal niches. Therefore, we defined the oral–nasal translocation bacteria as O-N bac. By comparing multiple groups, we took the intersection sets of O-N bacs selected from CP children, CP adolescents, and postoperative adolescents as TS O-N bacs with time–character, including Streptococcus, Gemella, Alloprevotella, Neisseria, Rothia, Actinomyces, and Veillonella. These bacteria were at the core of the nasal bacterial network in CP subjects, and some were related to infectious diseases. Conclusions: CP would lead to significant and long-term differences in oral and nasal flora. TS O-N bacs migrating from the oral to the nasal might be the key stone causing nasal flora dysbiosis in the CP patients. MDPI 2022-07-05 /pmc/articles/PMC9323727/ /pubmed/35890015 http://dx.doi.org/10.3390/pathogens11070771 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhou, Fangjie
Su, Zhifei
Li, Qinyang
Wang, Renke
Liao, Ying
Zhang, Min
Li, Jiyao
Characterization of Bacterial Differences Induced by Cleft-Palate-Related Spatial Heterogeneity
title Characterization of Bacterial Differences Induced by Cleft-Palate-Related Spatial Heterogeneity
title_full Characterization of Bacterial Differences Induced by Cleft-Palate-Related Spatial Heterogeneity
title_fullStr Characterization of Bacterial Differences Induced by Cleft-Palate-Related Spatial Heterogeneity
title_full_unstemmed Characterization of Bacterial Differences Induced by Cleft-Palate-Related Spatial Heterogeneity
title_short Characterization of Bacterial Differences Induced by Cleft-Palate-Related Spatial Heterogeneity
title_sort characterization of bacterial differences induced by cleft-palate-related spatial heterogeneity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9323727/
https://www.ncbi.nlm.nih.gov/pubmed/35890015
http://dx.doi.org/10.3390/pathogens11070771
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