A preliminary study on the mutation of TLR4 gene in patients with invasive aspergillosis
10.16571/j.cnki.1008-8199.2015.09.010
- VernacularTitle:侵袭性曲霉病患者 Toll 样受体4基因变异的初步研究
- Author:
Chen CHEN
;
Xiaoyong XU
;
Hao XIE
;
Huiming SUN
;
Fei CHEN
;
Ming FANG
;
Beilei ZHAO
- Publication Type:Journal Article
- Keywords:
Invasive aspergillosis;
Toll-like receptor 4;
Genetic sequencing;
Genetic variation
- From:
Journal of Medical Postgraduates
2015;(9):944-948
- CountryChina
- Language:Chinese
-
Abstract:
Objective Toll-like receptor ( TLR) gene family is the most important pathogen recognition receptor and animal experiment have found TLR4 mice is inclined to infect aspergillosis ( IA) .The study was to investigate the variation of TLR4 gene in Chinese Han nationality and its relation with the susceptibility of IA. Methods 25 patients diagnosed with proven IA from June 2011 to December 2012 in our hospital were enrolled, among which 17 were males.Their average age was 52.4 ±12.3, and 12 pa-tients had underlying diseases, the others had no underlying diseases.The control group consisted of 103 normal persons, among which 70 were males.Their average age was 56.0 ±17.2.All of the subjects were Chinese Han population.DNA was extracted from periph-eral blood.Polymerase chain reaction ( PCR) was applied to amplify the coding sequence of TLR4 gene followed by sequencing.The sequencing result was compared with TLR4 coding sequence in NCBI GenBank along with the analysis on amino acid change caused by genetic mutation and its effect on protein function.Comparison analysis was made on genetic mutation rate between IA group and con-trol group. Results Two missense mutations,TLR4 219 C>G and 1420 C>T, were identified in TLR4.The prediction result of protein structure showed 219 C>G resulted in the change of functional area for TLR4 to recognize pathogen and 1420 C>T caused no change in domains.The variation rate of TLR4 in IA group was 8%( 2/25 ) and both the patients had no underlying diseases. No mutation has been founded in control group and the difference between two groups was of statistical significance (P=0.037). Conclusion Two missense mutations (219 C>G and 1420 C>T) have been detec-ted in encoding area of TLR4 gene of IA patients.Variation in the cod-ing region of TLR4 gene may increase the susceptibility to IA.
