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IgA 肾病与健康对照者的肠道和血液微生物组。

The Gut and Blood Microbiome in IgA Nephropathy and Healthy Controls.

机构信息

Division of Hospital Medicine, Department of Medicine, Johns Hopkins Bayview Medical Center, Baltimore, Maryland.

Division of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts.

出版信息

Kidney360. 2021 Jun 9;2(8):1261-1274. doi: 10.34067/KID.0000132021. eCollection 2021 Aug 26.

Abstract

BACKGROUND

IgA nephropathy (IgAN) has been associated with gut dysbiosis, intestinal membrane disruption, and translocation of bacteria into blood. Our study aimed to understand the association of gut and blood microbiomes in patients with IgAN in relation to healthy controls.

METHODS

We conducted a case-control study with 20 patients with progressive IgAN, matched with 20 healthy controls, and analyzed bacterial DNA quantitatively in blood using 16S PCR and qualitatively in blood and stool using 16S metagenomic sequencing. We conducted between-group comparisons as well as comparisons between the blood and gut microbiomes.

RESULTS

Higher median 16S bacterial DNA in blood was found in the IgAN group compared with the healthy controls group (7410 versus 6030 16S rDNA copies/l blood, =0.04). - and -Diversity in both blood and stool was largely similar between the IgAN and healthy groups. In patients with IgAN, in comparison with healthy controls, we observed higher proportions of the class Coriobacteriia and species of the genera , , and in blood, and species of the genera , , and some in stool. Taxa distribution were markedly different between the blood and stool samples of each subject in both IgAN and healthy groups, without any significant correlation between corresponding gut and blood phyla.

CONCLUSIONS

Important bacterial taxonomic differences, quantitatively in blood and qualitatively in both blood and stool samples, that were detected between IgAN and healthy groups warrant further investigation into their roles in the pathogenesis of IgAN. Although gut bacterial translocation into blood may be one of the potential sources of the blood microbiome, marked taxonomic differences between gut and blood samples in each subject in both groups confirms that the blood microbiome does not directly reflect the gut microbiome. Further research is needed into other possible sites of origin and internal regulation of the blood microbiome.

摘要

背景

IgA 肾病(IgAN)与肠道菌群失调、肠黏膜破坏和细菌易位入血有关。我们的研究旨在了解 IgAN 患者与健康对照者的肠道和血液微生物组之间的关联。

方法

我们进行了一项病例对照研究,纳入 20 例进展性 IgAN 患者和 20 例健康对照者,采用 16SPCR 定量分析血液中细菌 DNA,采用 16S 宏基因组测序定性分析血液和粪便中的细菌 DNA。我们进行了组间比较以及血液和肠道微生物组之间的比较。

结果

与健康对照组相比,IgAN 组患者血液中 16S 细菌 DNA 的中位数更高(7410 与 6030 16S rDNA 拷贝/l 血液,=0.04)。血液和粪便中的 - 和 - 多样性在 IgAN 组和健康组之间基本相似。与健康对照组相比,IgAN 患者血液中拟杆菌门和 、 、 属的种比例较高,粪便中 、 、 属的种和一些 属的种比例较高。在 IgAN 和健康组中,每个个体的血液和粪便样本中的分类群分布差异显著,血液和肠道的对应菌群之间没有明显的相关性。

结论

在 IgAN 和健康组之间,血液中存在重要的细菌分类差异(定量),血液和粪便样本中也存在定性差异,这表明它们在 IgAN 的发病机制中可能发挥作用。尽管肠道细菌易位入血可能是血液微生物组的潜在来源之一,但在两组中,每个个体的血液和粪便样本之间存在明显的分类群差异,这证实了血液微生物组并不直接反映肠道微生物组。需要进一步研究血液微生物组的其他可能来源和内部调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c59/8676391/6d0dee45f6d3/KID.0000132021absf1.jpg

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