发展中国家肠炎相关关节炎患儿肠道微生物组及益生菌给药效果

A. Aggarwal, A. N. Sarangi, P. Gaur, Anuj Shukla, R. Aggarwal
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引用次数: 45

摘要

在亚洲,膝炎相关关节炎(ERA)是青少年特发性关节炎中最常见的一类。ERA与人白细胞抗原(HLA) - B27和亚临床肠道炎症密切相关。在HLA‐B27转基因大鼠模型中,肠道中拟杆菌的存在似乎会导致脊椎关节病(SpA)。因此,我们研究了ERA患儿的肠道菌群。研究了33例ERA患者和14例年龄匹配的健康对照者的粪便标本;没有人有任何胃肠道症状,或在前6周内接受过已知影响肠道运动或微生物群的药物。从每个标本中,对细菌16S rRNA V3区域的cDNA文库进行高通量、大规模平行测序。利用主坐标分析(PCoA)研究了样品间的关系,并比较了各组间不同细菌类群的丰度和α多样性。在8名患者中,经过12周的益生菌治疗后,重复粪便标本进行了研究。55份样本的高质量读数中位数(范围)为397 315(102 093-1 502 380)。在PCoA中,来自ERA的肠道微生物群比来自对照组的肠道微生物群分布更广。在患者中,拟杆菌科和肠杆菌科较对照组丰富,普氏菌科较对照组少。此外,在ERA患者中,拟杆菌属、肠球菌属和克雷伯氏菌属被过度代表,普雷沃氏菌属被低估。益生菌治疗导致普氏菌科的非显著性增加。ERA患者肠道生态失调,类杆菌增多,普雷沃氏菌减少。在一部分患者中补充益生菌并没有显著逆转这些变化。
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Gut microbiome in children with enthesitis‐related arthritis in a developing country and the effect of probiotic administration
In Asia, enthesitis‐related arthritis (ERA) is the most frequent category of juvenile idiopathic arthritis. ERA has a strong association with human leucocyte antigen (HLA)‐B27 and subclinical gut inflammation. In an HLA‐B27 transgenic rat model, the presence of Bacteroides bacteria in the gut appears to cause spondyloarthropathy (SpA). Thus, we studied gut microbiota in children with ERA. Stool specimens from 33 patients with ERA and 14 age‐matched healthy controls were studied; none had any gastrointestinal symptom, or had received a drug known to affect gut motility or microbiota in the preceding 6 weeks. From each specimen, a cDNA library for the V3 region of bacterial 16S rRNA was subjected to high‐throughput, massively parallel sequencing. Relationship of the specimens was studied using principal co‐ordinate analysis (PCoA), and abundances of various bacterial taxa and alpha diversity were compared between groups. In eight patients, a repeat faecal specimen was studied after 12 weeks of probiotic therapy. The 55 specimens yielded a median (range) of 397 315 (102 093–1 502 380) high‐quality reads each. In PCoA, gut microbiota from ERA showed a wider dispersion than those from controls. In patients, families Bacteroidaceae and Enterobacteriaceae were more abundant and Prevotellaceae were less abundant than in controls. Also, genera Bacteroides, Entercoccus and Klebsiella were over‐represented and genus Prevotella was under‐represented in ERA patients. Probiotic therapy led to a non‐significant increase in Prevotellaceae. Patients with ERA have a dysbiosis in the gut, with increased abundance of Bacteroides and reduction of Prevotella. Probiotic supplementation in a subset of patients did not reverse these changes significantly.
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