Investigation of TLR2 and TLR4 Polymorphisms and Sepsis Susceptibility: Computational and Experimental Approaches.
Mohammed Y BehairyAli A AbdelrahmanEman Ali ToraihEmad El-Deen A IbrahimMarwa M AzabAnwar A SayedHany R HashemPublished in: International journal of molecular sciences (2022)
Toll-like receptors (TLR) play an eminent role in the regulation of immune responses to invading pathogens during sepsis. TLR genetic variants might influence individual susceptibility to developing sepsis. The current study aimed to investigate the association of genetic polymorphisms of the TLR2 and TLR4 with the risk of developing sepsis with both a pilot study and in silico tools. Different in silico tools were used to predict the impact of our SNPs on protein structure, stability, and function. Furthermore, in our prospective study, all patients matching the inclusion criteria in the intensive care units (ICU) were included and followed up, and DNA samples were genotyped using real-time polymerase chain reaction (RT-PCR) technology. There was a significant association between TLR2 Arg753Gln polymorphisms and sepsis under the over-dominant model ( p = 0.043). In contrast, we did not find a significant difference with the TLR4 Asp299Gly polymorphism with sepsis. However, there was a significant association between TLR4 Asp299Gly polymorphisms and Acinetobacter baumannii infection which is quite a virulent organism in ICU ( p = 0.001) and post-surgical cohorts ( p = 0.033). Our results conclude that the TLR2 genotype may be a risk factor for sepsis in adult patients.
Keyphrases
- toll like receptor
- immune response
- intensive care unit
- inflammatory response
- acute kidney injury
- septic shock
- nuclear factor
- end stage renal disease
- multidrug resistant
- mechanical ventilation
- chronic kidney disease
- magnetic resonance
- pseudomonas aeruginosa
- newly diagnosed
- gene expression
- computed tomography
- gram negative
- molecular docking
- small molecule
- single molecule
- peritoneal dialysis
- contrast enhanced
- protein protein