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Novel Molecular Markers Linked to Pseudomonas aeruginosa Epidemic High-Risk Clones
Wedad Nageeb1, Dina H Amin2, Zuhair M Mohammedsaleh3
1Medical Microbiology and Immunology Department, Faculty of Medicine, Suez Canal University, Ismailia 41111, Egypt.
Abstract:
The population structure of Pseudomonas aeruginosa is panmictic-epidemic in nature, with the prevalence of some high-risk clones. These clones are often linked to virulence, antibiotic resistance, and more morbidity. The clonal success of these lineages has been linked to acquisition and spread of mobile genetic elements. The main aim of the study was to explore other molecular markers that explain their global success. A comprehensive set of 528 completely sequenced P. aeruginosa genomes was analyzed. The population structure was examined using Multilocus Sequence Typing (MLST). Strain relationships analysis and diversity analysis were performed using the geoBURST Full Minimum Spanning Tree (MST) algorithm and hierarchical clustering. A phylogenetic tree was constructed using the Unweighted Pair Group Method with Arithmetic mean (UPGMA) algorithm. A panel of previously investigated resistance markers were examined for their link to high-risk clones. A novel panel of molecular markers has been identified in relation to risky clones including armR, ampR, nalC, nalD, mexZ, mexS, gyrAT83I, gyrAD87N, nalCE153Q, nalCS46A, parCS87W, parCS87L, ampRG283E, ampRM288R, pmrALeu71Arg, pmrBGly423Cys, nuoGA890T, pstBE89Q, phoQY85F, arnAA170T, arnDG206C, and gidBE186A. In addition to mobile genetic elements, chromosomal variants in membrane proteins and efflux pump regulators can play an important role in the success of high-risk clones. Finding risk-associated markers during molecular surveillance necessitates applying more infection-control precautions.
Insights
High-risk Pseudomonas aeruginosa clones, linked to antibiotic resistance and severe illness, owe their success to mobile genetic elements and novel chromosomal variants. Identifying these markers aids infection control.
Area of Science:
- Microbiology
- Genomics
- Epidemiology
Background:
- Pseudomonas aeruginosa exhibits a panmictic-epidemic population structure, characterized by prevalent high-risk clones.
- These successful clones are associated with increased virulence, antibiotic resistance, and patient morbidity.
- The spread of mobile genetic elements is a known factor contributing to the success of these lineages.
Purpose of the Study:
- To identify additional molecular markers responsible for the global success of high-risk Pseudomonas aeruginosa clones.
- To investigate the role of chromosomal variants beyond mobile genetic elements.
Main Methods:
- Analysis of 528 complete Pseudomonas aeruginosa genome sequences.
- Population structure assessed using Multilocus Sequence Typing (MLST).
- Strain relationships and diversity analyzed with geoBURST Full Minimum Spanning Tree (MST) and hierarchical clustering.
- Phylogenetic tree construction using the Unweighted Pair Group Method with Arithmetic mean (UPGMA) algorithm.
- Examination of known resistance markers and identification of novel markers.
Main Results:
- A novel panel of molecular markers associated with high-risk clones was identified, including chromosomal variants in genes such as armR, ampR, nalC, nalD, mexZ, gyrA, and parC.
- These novel markers include specific mutations like gyrAT83I, gyrAD87N, nalCE153Q, nalCS46A, parCS87W, parCS87L, ampRG283E, ampRM288R, pmrALeu71Arg, pmrBGly423Cys, nuoGA890T, pstBE89Q, phoQY85F, arnAA170T, arnDG206C, and gidBE186A.
- Chromosomal variants in membrane proteins and efflux pump regulators, in addition to mobile genetic elements, are crucial for the success of high-risk clones.
Conclusions:
- Chromosomal variants play a significant role in the success of high-risk Pseudomonas aeruginosa clones, complementing the impact of mobile genetic elements.
- The identified novel molecular markers provide valuable targets for understanding and tracking these successful, potentially dangerous clones.
- Early detection of risk-associated markers through molecular surveillance is essential for implementing enhanced infection-control measures.
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