toll样受体2和4多态性与食物过敏儿童肠道微生物群的评估。

Mehmet Kılıç, Elif Beyazıt, Ebru Etem Önalan, Tuğçe Kaymaz, Erdal Taşkın
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引用次数: 0

摘要

背景:免疫系统和肠道微生物群之间的相互调节是通过几种机制实现的,包括在多种细胞类型上表达的toll样受体(TLRs)的参与。在这项研究中,我们旨在探索食物过敏和TLR基因多态性与肠道微生物群之间的关系。方法:在一个前瞻性队列中,将130名1-24个月大的鸡蛋和/或牛奶过敏婴儿的Toll样受体多态性频率和肠道微生物群中的一些细菌与110名非食物过敏对照进行比较。采用等位基因鉴别聚合酶链反应(PCR)方法对四种候选多态性(TLR2 rs189883/rs5743708和TLR4 rs4986790/rs4986791)进行基因分型。肠道微生物群分析是通过高通量测序实现的。结果:食物过敏患者TLR4 rs4986790(Asp299Gly)单核苷酸多态性(SNP)大小等位基因频率为0.788/0.212,对照组为0.719/0.280(p=0.017),各组基因型频率(AA、AG、GG)差异有统计学意义。肠道微生物群分析显示,食物过敏患者粪便中厚壁菌门增加。除了TLR4 rs4986791(Thr399lle)等位基因外,其他TLR多态性与儿童食物过敏无关。当肠道微生物群中的细菌与TLR2和TLR4基因多态性进行比较时;我们测定了TLR4 rs4986791 CT杂合基因型肠道微生物群中双歧杆菌浓度的统计学显著增加(p=0.004)。结论:本研究证明了TLR4基因多态性和肠道微生物群在食物过敏的发展中的部分作用。未来需要在这一领域开展工作,以阐明不同微生物菌株在调节肠道微生物群组成和功能以及TLR转录途径方面的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of toll-like receptors 2 and 4 polymorphism and intestinal microbiota in children with food allergies.

Background: Mutual regulation between immune system and gut microbiota is achieved through several mechanisms including the engagement of toll-like receptors (TLRs) which is expressed on numerous cell types. In this study we aimed to explore the association between food allergies and TLR gene polymorphisms in association with gut microbiota.

Methods: Toll-like receptors polymorphism frequencies and some bacteria in the gut microbiota in 130 infants aged 1-24 months with egg and/or milk allergy in a prospective cohort were compared with 110 non-food allergic controls. Four candidate polymorphisms (TLR2 rs1898830/rs5743708 and TLR4 rs4986790/rs4986791) were genotyped by allelic discrimination polymerase chain rection (PCR) method. Gut microbiota analysis was achieved by using high-throughput sequencing.

Results: The TLR4 rs4986790 (Asp299Gly) single nucleotide polymorphism (SNP) major/minor allele frequency was 0.788/0.212 in food allergy patients and 0.719/0.280 in controls (p=0.017). There was a statistically significant difference between groups in terms of genotype frequencies (AA, AG, GG). Gut microbiota analysis revealed increased Firmicutes phylum in stool of the patients with food allergy. Except for TLR4 rs4986791 (Thr399lle) allele, the other TLR polymorphisms were not associated with food allergies in children. When the bacteria in the intestinal microbiota and TLR2 and TLR4 gene polymorphisms were compared; we determined a statistically significant increase in Bifidobacterium concentration in the intestinal microbiota in TLR4 rs4986791 CT heterozygous genotype (p=0.004).

Conclusions: This study demonstrated a partial role of TLR4 gene polymorphism and gut microbiota in the development of food allergies. Future work in this area will be required to clarify the roles of different microbial strains that modulate gut microbiota composition and function in conjunction with TLR transcription pathways.

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