Related Experiment Video
Updated: Jan 23, 2026

Visualization of Pseudomonas aeruginosa within the Sputum of Cystic Fibrosis Patients
Published on: July 16, 2020
Codon-usage frequency mediated SNPs selection in lasR gene of cystic fibrosis Pseudomonas aeruginosa isolates
Huifang Qiu1, Yuanhao Li1, Weijun Dai1
1Integrative Microbiology Research Center, South China of Agricultural University, Guangzhou, 510642, China.
Abstract:
Pseudomonas aeruginosa is an opportunistic pathogen with high clinical relevance for hospital infections of patients. Accumulating DNA sequencing results of clinical P. aeruginosa isolates have revealed frequent mutations in lasR gene, which encodes the highest arches component of quorum-sensing system (QS). We analyzed the sequencing data of lasR gene from a large collection of cystic fibrosis (CF) P. aeruginosa isolates. Our systematical analyses revealed that single nucleotide polymorphisms (SNPs) selection in lasR gene were largely constrained by codon-usage frequency. As a whole, SNP-substituted codons encoding unconserved amino acid resulted in unfavored codons with relatively low codon-usage frequency, while those associating with conserved amino acid were not strictly regulated in such way. These SNPs substitutions gives rise to diverse functional LasR isoforms and contributes to the relative growth fitness of recombinant lasR variant strains. Our survey reveals a novel pattern of SNPs selections in lasR gene of CF isolates. Our findings could be served as a powerful resource for understanding adaptive mechanism of clinical isolates under environmental constrains and developing anti-bacteria drugs for CF patients.
Insights
Mutations in the lasR gene of Pseudomonas aeruginosa in cystic fibrosis patients are influenced by codon usage. These changes create diverse functional proteins, potentially aiding bacterial adaptation and offering targets for new drugs.
Area of Science:
- Microbiology
- Genetics
- Infectious Diseases
Background:
- Pseudomonas aeruginosa is a clinically significant opportunistic pathogen.
- Hospital-acquired infections frequently involve P. aeruginosa.
- Mutations in the quorum-sensing (QS) lasR gene are common in clinical isolates.
Purpose of the Study:
- To analyze lasR gene mutations in a large collection of cystic fibrosis (CF) P. aeruginosa isolates.
- To investigate the relationship between single nucleotide polymorphism (SNP) selection and codon usage frequency in the lasR gene.
- To understand the adaptive mechanisms of P. aeruginosa in CF patients.
Main Methods:
- Systematic analysis of DNA sequencing data from clinical P. aeruginosa isolates.
- Examination of lasR gene sequences from cystic fibrosis patient isolates.
- Correlation analysis between SNP-substituted codons and codon-usage frequency.
Main Results:
- SNP selection in the lasR gene is constrained by codon-usage frequency.
- Substitutions encoding unconserved amino acids often used less frequent codons.
- Conserved amino acid substitutions showed less strict regulation by codon usage.
- SNPs lead to diverse functional LasR protein variants, influencing growth fitness.
Conclusions:
- A novel pattern of SNPs in the lasR gene of CF isolates was identified.
- These findings provide insights into bacterial adaptive mechanisms under environmental pressures.
- The study offers potential targets for developing anti-bacterial drugs for CF patients.
Related Concept Videos
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
Cystic Fibrosis: Management
Sinus disease and chronic...
Frequency-dependent Selection
Comparing Copy Number Variations and SNPs
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
Nonsense-mediated mRNA Decay
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
Single Nucleotide Polymorphisms-SNPs

