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细菌性脑膜炎患儿及其健康家庭成员中TLR2、TLR4和TLR9单核苷酸多态性分析

Analysis of TLR2, TLR4, and TLR9 single nucleotide polymorphisms in children with bacterial meningitis and their healthy family members.

作者信息

Gowin Ewelina, Świątek-Kościelna Bogna, Kałużna Ewelina, Nowak Jerzy, Michalak Michał, Wysocki Jacek, Januszkiewicz-Lewandowska Danuta

机构信息

Department of Family Medicine, Poznań University of Medical Sciences, Przybyszewskiego 39, 60-355 Poznań, Poland.

Department of Molecular Pathology, Institute of Human Genetics, Polish Academy of Sciences, Poznań, Poland.

出版信息

Int J Infect Dis. 2017 Jul;60:23-28. doi: 10.1016/j.ijid.2017.04.024. Epub 2017 May 6.

DOI:10.1016/j.ijid.2017.04.024
PMID:28487240
Abstract

BACKGROUND

The aim was to analyse TLR2 rs5743708, TLR2 rs4696480, TLR4 rs4986790, TLR9 rs5743836, and TLR9 rs352140 single nucleotide polymorphisms (SNPs) in children with pneumococcal and meningococcal meningitis and their family members.

METHODS

The study group consisted of 39 children with bacterial meningitis (25 with meningococcal meningitis and 14 with pneumococcal meningitis) and 49 family members. Laboratory test results and the course of the diseases were analyzed. Genomic DNA was extracted from 1.2ml of peripheral blood in order to analyze the five SNPs.

RESULTS

Patients with pneumococcal and meningococcal meningitis showed a similar male/female ratio, mean age, and duration of symptoms. There were no statistically significant differences in biochemical markers between the two groups. All patients possessed at least one polymorphic variant of the analyzed SNPs. The most common SNP was TLR9 rs352140, detected in 89.7% of patients. No significant differences in SNP frequency were found between patients, family members, and the general population.

CONCLUSIONS

The allele frequencies in the population studied are in accordance with the literature data. The study did not find an association between the analyzed SNPs and susceptibility to bacterial meningitis. The role of SNPs in genes coding toll-like receptors and the interactions between them in controlling inflammation in the central nervous system needs further evaluation.

摘要

背景

目的是分析肺炎球菌性和脑膜炎球菌性脑膜炎患儿及其家庭成员中TLR2基因rs5743708、TLR2基因rs4696480、TLR4基因rs4986790、TLR9基因rs5743836和TLR9基因rs352140的单核苷酸多态性(SNP)。

方法

研究组由39例细菌性脑膜炎患儿(25例脑膜炎球菌性脑膜炎患儿和14例肺炎球菌性脑膜炎患儿)及其49名家庭成员组成。分析实验室检查结果和疾病病程。为分析这5个SNP从1.2ml外周血中提取基因组DNA。

结果

肺炎球菌性和脑膜炎球菌性脑膜炎患儿在男女比例、平均年龄和症状持续时间方面相似。两组间生化指标无统计学显著差异。所有患者均至少拥有所分析SNP中的一种多态性变体。最常见的SNP是TLR9基因rs352140,在89.7%的患者中检测到。患者、家庭成员和普通人群之间的SNP频率未发现显著差异。

结论

所研究人群中的等位基因频率与文献数据一致。该研究未发现所分析的SNP与细菌性脑膜炎易感性之间存在关联。SNP在编码Toll样受体的基因中的作用及其在控制中枢神经系统炎症中的相互作用需要进一步评估。

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