Soriano-Lerma Ana, García-Burgos María, Barton Wiley, Alférez María José M, Crespo-Pérez Jorge Valentín, Soriano Miguel, López-Aliaga Inmaculada, Cotter Paul D, García-Salcedo José A
Department of Physiology (Faculty of Pharmacy, Campus Universitario de Cartuja), Institute of Nutrition and Food Technology "José Mataix Verdú", University of Granada, Granada, Spain; GENYO, Centre for Genomics and Oncological Research: Pfizer / University of Granada / Andalusian Regional Government, Granada, Spain; Instituto de Investigación Biosanitaria ibs, Granada, Spain.
Department of Physiology (Faculty of Pharmacy, Campus Universitario de Cartuja), Institute of Nutrition and Food Technology "José Mataix Verdú", University of Granada, Granada, Spain; GENYO, Centre for Genomics and Oncological Research: Pfizer / University of Granada / Andalusian Regional Government, Granada, Spain.
Biomed J. 2024 Dec;47(6):100701. doi: 10.1016/j.bj.2024.100701. Epub 2024 Jan 26.
Iron deficiency is the top leading cause of anaemia, whose treatment has been shown to deteriorate gut health. However, a comprehensive analysis of the intestinal barrier and the gut microbiome during iron deficiency anemia (IDA) has not been performed to date. This study aims to delve further into the analysis of these two aspects, which will mean a step forward minimising the negative impact of iron supplements on intestinal health.
IDA was experimentally induced in an animal model. Shotgun sequencing was used to analyse the gut microbiome in the colonic region, while the intestinal barrier was studied through histological analyses, mRNA sequencing (RNA-Seq), qPCR and immunofluorescence assays. Determinations of lipopolysaccharide (LPS) and bacteria-specific immunoglobulins were performed to assess microbial translocation.
Microbial metabolism in the colon shifted towards an increased production of certain amino acids, short chain fatty acids and nucleotides, with Clostridium species being enriched during IDA. Structural alterations of the colonic epithelium were shown by histological analysis. RNA-Seq revealed a downregulation of extracellular matrix-associated genes and proteins and an overall underdeveloped epithelium. Increased levels of serum LPS and an increased immune response against dysbiotic bacteria support an impairment in the integrity of the gut barrier during IDA.
IDA negatively impacts the gut microbiome and the intestinal barrier, triggering an increased microbial translocation. This study emphasizes the deterioration of gut health during IDA and the fact that it should be addressed when treating the disease.
缺铁是贫血的首要原因,已表明其治疗会损害肠道健康。然而,迄今为止尚未对缺铁性贫血(IDA)期间的肠道屏障和肠道微生物群进行全面分析。本研究旨在进一步深入分析这两个方面,这将意味着朝着尽量减少铁补充剂对肠道健康的负面影响迈出一步。
在动物模型中通过实验诱导缺铁性贫血。使用鸟枪法测序分析结肠区域的肠道微生物群,同时通过组织学分析、mRNA测序(RNA-Seq)、qPCR和免疫荧光测定研究肠道屏障。进行脂多糖(LPS)和细菌特异性免疫球蛋白的测定以评估微生物易位。
结肠中的微生物代谢转向某些氨基酸、短链脂肪酸和核苷酸产量增加,缺铁性贫血期间梭菌属物种富集。组织学分析显示结肠上皮的结构改变。RNA-Seq揭示细胞外基质相关基因和蛋白质下调以及上皮整体发育不全。血清LPS水平升高和对生态失调细菌的免疫反应增加支持缺铁性贫血期间肠道屏障完整性受损。
缺铁性贫血对肠道微生物群和肠道屏障产生负面影响,引发微生物易位增加。本研究强调缺铁性贫血期间肠道健康的恶化以及在治疗该疾病时应解决这一问题。