Ling Zongxin, Liu Fengping, Shao Li, Cheng Yiwen, Li Lanjuan
Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.
Nursing School, Jiangsu Vocational College of Medicine, Yancheng, China.
Front Immunol. 2017 Aug 25;8:1032. doi: 10.3389/fimmu.2017.01032. eCollection 2017.
Evidence has shown that dysbiosis of the urinary microbiota existed in female type 2 diabetes mellitus (T2DM) patients. Perturbations of intestinal microbiota are linked to proinflammatory chemokine interleukin-8 (IL-8); however, the correlations between urinary microbiota and IL-8 are not well studied. Here, we investigated the associations between the altered urinary microbiota and urinary IL-8 in female T2DM patients. A modified four-tube midstream urine technique was used to collect urine specimens from 70 female T2DM patients and 70 matched healthy controls (HCs). Bacterial genomic DNA from urine specimens was isolated using magnetic beads and the urinary microbiota was assessed using Illumina MiSeq platform targeting on the 16S rRNA gene V3-V4 region. Urinary IL-8 was determined by enzyme linked immunosorbent assay. Subsequently, the T2DM patients were separated into urine IL-8 detectable (WIL8) and undetectable (NIL8) groups, and the composition of urinary microbiota between the two groups was compared. Meanwhile, the levels of IL-8 between the "≥HCs" group (those specific bacterial genera were more than or equal to the HCs) and the "<HCs" group (those specific bacterial genera were less than the HCs) was also compared. Of 70 urine samples from T2DM patients without urinary tract infections, 46 patients had detectable IL-8 in their urine (64.31 ± 70.43 pg/mL), while 24 patients had undetectable IL-8. Compared to the NIL8 group, 11 bacterial genera increased in the WIL8 group, including , etc., whereas 10 genera, such as , and decreased. One species of , increased obviously in the WIL8 group. The "≥HCs" group showed 17 genera increased and 16 genera decreased. In addition, 18 genera contributed to the presence of urinary IL-8 in T2DM patients, which explained 95.60% of the total variance of urinary microbiota. Our study demonstrated that dysbiosis of the urinary microbiota with several key bacteria was associated with urinary IL-8 in female T2DM patients, which might be useful to explore the interactions between urinary microbiota and inflammatory responses and shed light on novel diagnosis and therapy for urinary microbiota associated with infections in T2DM patients.
证据表明,女性2型糖尿病(T2DM)患者存在泌尿微生物群失调。肠道微生物群的紊乱与促炎趋化因子白细胞介素-8(IL-8)有关;然而,泌尿微生物群与IL-8之间的相关性尚未得到充分研究。在此,我们调查了女性T2DM患者中泌尿微生物群改变与尿IL-8之间的关联。采用改良的四管中段尿技术,从70例女性T2DM患者和70例匹配的健康对照(HCs)中收集尿液标本。使用磁珠从尿液标本中分离细菌基因组DNA,并使用针对16S rRNA基因V3-V4区域的Illumina MiSeq平台评估泌尿微生物群。通过酶联免疫吸附测定法测定尿IL-8。随后,将T2DM患者分为尿IL-8可检测(WIL8)组和不可检测(NIL8)组,并比较两组之间泌尿微生物群的组成。同时,还比较了“≥HCs”组(那些特定细菌属多于或等于HCs的组)和“<HCs”组(那些特定细菌属少于HCs的组)之间的IL-8水平。在70例无尿路感染的T2DM患者尿液样本中,46例患者尿液中IL-8可检测(64.31±70.43 pg/mL),而24例患者尿液中IL-8不可检测。与NIL8组相比,WIL8组中有11个细菌属增加,包括等,而10个属,如、和减少。一种,在WIL8组中明显增加。“≥HCs”组显示17个属增加,16个属减少。此外,18个属导致T2DM患者尿IL-8的存在,这解释了泌尿微生物群总变异的95.60%。我们的研究表明,女性T2DM患者中具有几种关键细菌的泌尿微生物群失调与尿IL-8有关,这可能有助于探索泌尿微生物群与炎症反应之间的相互作用,并为T2DM患者泌尿微生物群相关感染的新诊断和治疗提供线索。