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Published on: December 23, 2022
Functional analysis of the uropathogenic Escherichia coli R049 gene
Dongjing Yang1, Jie Dong1, Xu Su1
1Tianjin Centers for Disease Control and Prevention, Tianjin 300011, China.
Abstract:
The objective of this study was to determine the function of the novel uropathogenic Escherichia coli (UPEC) gene R049 during host infection. We infected the urinary tracts of mice with E. coli UPEC132 or the R049 deletion mutant UPEC132ΔR049.The mouse kidneys were harvested at 4 and 8h post-infection and screened for differentially expressed genes by microarray analysis. We identified 379 and 515 differentially expressed genes at 4 and 8 h post-infection, respectively. Thirty-four of these genes were associated with inflammatory and immune signaling pathways, including those related to mitogen-activated protein kinase signaling, leukocyte transendothelial migration, cytokine-cytokine receptor interaction, Toll-like receptor signaling, and apoptosis. Protein binding (GO 0005515) was the most prevalent molecular function in the Gene Ontology terms related to differentially expressed genes. In conclusion, R049 expression in UPEC132 is related to the early innate immune and inflammatory responses in UPEC-infected hosts. This work lays the foundation for further research on anti-infective immunity against UPEC.
Insights
The novel uropathogenic Escherichia coli (UPEC) gene R049 influences host immune responses during infection. Understanding R049 function is key for developing new treatments against UPEC.
Area of Science:
- Microbiology
- Immunology
- Genetics
Background:
- Uropathogenic Escherichia coli (UPEC) is a major cause of urinary tract infections.
- The specific functions of many UPEC genes during host infection remain poorly understood.
- Identifying virulence factors is crucial for developing targeted anti-infective strategies.
Purpose of the Study:
- To investigate the role of the novel UPEC gene R049 in host-pathogen interactions.
- To elucidate the impact of R049 on the host's early innate immune and inflammatory responses during infection.
Main Methods:
- Mouse model of urinary tract infection using wild-type UPEC and an R049 deletion mutant.
- Microarray analysis of differentially expressed genes in mouse kidneys at 4 and 8 hours post-infection.
- Gene Ontology (GO) term analysis to identify affected biological pathways and molecular functions.
Main Results:
- Microarray analysis revealed significant differential gene expression in response to UPEC infection.
- 379 and 515 differentially expressed genes were identified at 4 and 8 hours post-infection, respectively.
- Genes involved in inflammatory and immune signaling pathways (MAPK, leukocyte migration, cytokine interaction, TLR, apoptosis) were significantly affected, with protein binding being a prevalent molecular function.
Conclusions:
- R049 expression in UPEC is intrinsically linked to the host's early innate immune and inflammatory responses.
- This study provides a foundation for future research into anti-infective immunity against UPEC.
- Targeting R049 may represent a novel therapeutic approach for UPEC infections.
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