16S rRNA gene sequencing reveals the correlation between the gut microbiota and the susceptibility to pathological scars

被引:3
|
作者
Li, Ming [1 ,2 ,3 ,4 ]
Li, Minghao [1 ,2 ,3 ,4 ]
Dai, Yingting [1 ,2 ,3 ,4 ]
Li, Dang [5 ]
Yu, Han [6 ]
Liu, Jian [7 ]
Gao, Hangqi [1 ,2 ,3 ,4 ]
Zhong, Yi [1 ,2 ,3 ,4 ]
Huang, Mingquan [1 ,2 ,3 ,4 ]
Lin, Jing [1 ,2 ,3 ,4 ]
Xie, Yide [1 ,2 ,3 ,4 ]
Guo, Zhihui [1 ,2 ,3 ,4 ]
Chen, Xiaosong [1 ,2 ,3 ,4 ]
机构
[1] Fujian Med Univ, Dept Plast Surg & Regenerat Med, Union Hosp, Fuzhou, Peoples R China
[2] Fujian Med Univ, Dept Plast Surg, Fuzhou, Peoples R China
[3] Fujian Med Univ, Regenerat Med Inst, Fuzhou, Peoples R China
[4] Fujian Prov Univ, Engn Res Ctr Tissue & Organ Regenerat, Fuzhou, Peoples R China
[5] Fujian Med Univ, Nursing Dept, Union Hosp, Fuzhou, Peoples R China
[6] Pingtan Comprehens Expt Area Hosp, Dept Dermatol, Fuzhou, Peoples R China
[7] Fuzhou MineButy Clin, Fuzhou, Peoples R China
关键词
pathological scars; susceptibility; gut microbiota; 16S rRNA sequencing; dysbiosis; INFLAMMATION; HOMEOSTASIS; PROTECTS;
D O I
10.3389/fmicb.2023.1215884
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The gut microbiome profile in patients with pathological scars remains rarely known, especially those patients who are susceptible to pathological scars. Previous studies demonstrated that gut microbial dysbiosis can promote the development of a series of diseases via the interaction between gut microbiota and host. The current study aimed to explore the gut microbiota of patients who are prone to suffer from pathological scars. 35 patients with pathological scars (PS group) and 40 patients with normal scars (NS group) were recruited for collection of fecal samples to sequence the 16S ribosomal RNA (16S rRNA) V3-V4 region of gut microbiota. Alpha diversity of gut microbiota showed a significant difference between NS group and PS group, and beta diversity indicated that the composition of gut microbiota in NS and PS participants was different, which implied that dysbiosis exhibits in patients who are susceptible to pathological scars. Based on phylum, genus, species levels, we demonstrated that the changing in some gut microbiota (Firmicutes; Bacteroides; Escherichia coli, etc.) may contribute to the occurrence or development of pathological scars. Moreover, the interaction network of gut microbiota in NS and PS group clearly revealed the different interaction model of each group. Our study has preliminary confirmed that dysbiosis exhibits in patients who are susceptible to pathological scars, and provide a new insight regarding the role of the gut microbiome in PS development and progression.
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页数:10
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