| Literature DB >> 31772596 |
Wei Xian Lin1, Xin Du1, Li Lin Yang1, Si Yun Chen1, Wei Yu Qiu1, Hai Wang Wu1, Guang Zhao2, Yi Hui Feng1, Qing Ying Yu1, He Tian1, Song Ping Luo1, Jie Gao3.
Abstract
Spleen-deficiency syndrome and damp-heat syndrome are the two most common syndromes of vaginitis in traditional Chinese medicine (TCM). Although it is known that the vaginal microbiota is closely associated with vaginitis, present studies have not fully elucidated the relationship between the composition of the vaginal microbiome and type of TCM syndrome because of the limitations in the present reductionist approaches. Samples of vaginal secretions were collected from patients with bacterial vaginitis and healthy subjects with spleen-deficiency syndrome and damp-heat syndrome, in order to analyze the constitution of the vaginal microflora using 16S rRNA sequencing methods that encompass taxonomic units, alpha diversity rarefaction curves, and principal component analyses. This prospective study indicated that there was a statistically significant difference in the composition of the vaginal microbiome between patients with spleen-deficiency syndrome and patients with damp-heat syndrome. Streptococcus was the dominant microbiota in patients with spleen-deficiency syndrome. This can serve as a biomarker for differentiating spleen-deficiency syndrome and damp-heat syndrome. In addition, as indicated by the findings on the samples, patients with bacterial vaginitis of dominant abundance in Pseudomonadaceae might be prone to manifest spleen-deficiency syndrome, while patients with bacterial vaginitis of dominant abundance in Prevotella might be prone to manifest damp-heat syndrome. These present findings can provide a new approach to acquire a scientific understanding of the syndromes of TCM, which in turn would benefit the development of personalized medicine, in terms of ancient medicine and complex biological systems.Entities:
Year: 2019 PMID: 31772596 PMCID: PMC6855005 DOI: 10.1155/2019/5456379
Source DB: PubMed Journal: Evid Based Complement Alternat Med ISSN: 1741-427X Impact factor: 2.629
Figure 1Study design flow chart.
Figure 2TCM tongue-coating appearance classification. (a, b) Typical tongue-coating of spleen-deficiency syndrome, pale tongue with teeth marks (red dotted) and white coating. (c, d) Typical tongue-coating of damp-heat syndrome, red tongue, and yellow greasy coating.
Comparison of symptoms of spleen-deficiency syndrome and damp-heat syndrome [13].
| Spleen-deficiency syndrome | Damp-heat syndrome | |
|---|---|---|
| Leucorrhea | White or pale yellow | Yellow |
| Tongue and coating | Tongue with tooth marks, pale tongue, white or greasy coating | Red tongue, yellow greasy |
| Other symptoms | Low voice and no desire to speak, lassitude, slow movement, loss of appetite, loose stool | Bit and greasy mouth, short and red urine |
General information of BV patients and healthy volunteers with the two different syndromes.
| Characteristics | Healthy volunteers | BV patients | ||
|---|---|---|---|---|
| Spleen-deficiency syndrome | Damp-heat syndrome | Spleen-deficiency syndrome | Damp-heat syndrome | |
| Number of samples | 8 | 8 | 8 | 8 |
| Age (mean ± SD) | 28.5 ± 4.14 | 29.13 ± 4.39 | 28.88 ± 2.36 | 29.38 ± 2.45 |
Figure 316S rRNA sequencing analysis and taxonomy classification of the vaginal microbiome at the genus level. (a) The flow chart of sequence preprocessing, quality control and chimera detection. (b) Relative abundance of dominant and rare genus in samples of healthy volunteers and BV patients. (c) Relative abundance of dominant and rare genus in samples with different TCM syndromes. (d) Relative abundance of dominant and rare genus in spleen-deficiency syndrome of healthy volunteers and BV samples. (e) Relative abundance of dominant and rare genus in damp-heat syndrome of healthy volunteers and BV samples. PE: paired-end, OTU: operational taxonomic units, BV: bacterial vaginitis.
Figure 4Alpha diversity rarefaction curves of samples based on species-level OTUs. (a) The rarefaction curves of different groups. (b) The rarefaction curves of different syndromes. (c) The rank abundance curves of different groups. (d) The rank abundance curves of different syndromes.
Figure 5PCoA of the dissimiliarities among bacterial community taxonomical structure using Unifrac distance. (a) PCoA plot of the samples among healthy and BV patients. (b) PCoA plot of the samples between spleen-deficiency syndrome and damp-heat syndrome. (c) PCoA plot of the healthy volunteers' samples between the two syndromes. (d) PCoA plot of the BV patients' samples between the two syndromes. (e) AMOVA results of the BV and normal control group by unweighted Unifrac distance. (f) AMOVA results of the BV and normal control group by weighted unifrac distance. PCoA: principal coordination analysis, AMOVA: analysis of molecular variance. (represents P ≤ 0.05, PC1 represents the first principal component, PC2 represents the second principal component).
Figure 6Heatmap representing the differences between the two syndromes and the two groups. (a) Heatmap of patients' samples with spleen-deficiency syndrome and damp-heat syndrome. (b) Heatmap of BV and normal control group.