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Genomic Characterization of Intestinal Colonizing Pseudomonas juntendi Strains Harboring bla VIM-2
Weidong Zhu1, Junli Zhang2, Ruishan Liu3
1Zhuji Affiliated Hospital of Wenzhou Medical University, Zhuji, Zhejiang Province, People's Republic of China.
Introduction:
To characterize the genomic architecture of carbapenemase-producing Pseudomonas juntendi harboring bla VIM-2, elucidate genetic mechanisms underlying carbapenem resistance, and evaluate mobile genetic element (MGE)-mediated dissemination pathways using Oxford Nanopore and Illumina sequencing were combined for hybrid genome assembly approaches.
Methods:
Hybrid Nanopore-Illumina whole-genome sequencing was applied on two P. juntendi isolates (L2353hy/L2891hy) recovered from distinct human fecal samples. L2353hy and L2891hy were identified as P. juntendi by ANI analysis. Comparative pangenomics identified resistance determinants and phylogenetic relationships, and SNP distances were calculated using SNP-dists. Plasmid profiles were verified using S1 nuclease pulsed-field gel electrophoresis (S1-PFGE).
Results:
Both strains exhibited a multidrug resistance profile, comprising 13 antimicrobial resistance genes (ARGs), including bla VIM-2, bla OXA-246, and tet(A). Core genome phylogeny demonstrated clonal propagation of two VIM-producing P. juntendi strains. Notably, these two isolates were closely linked to P. juntendi yb_3 (a fish intestinal isolate; Wenzhou, China).
Conclusion:
This study reports two clonally related P. juntendi strains harboring bla VIM-2 isolated from human fecal microbiota, expanding the genomic understanding of carbapenem-resistant P. juntendi. The close phylogenetic relationship between these human isolates and an animal-derived strain (P. juntendi yb_3) underscores bidirectional resistance gene flow at the human-animal interface. Our findings support a One Health-oriented surveillance approach to mitigate the dissemination of carbapenemase-producing pathogens.
Insights
Genomic analysis revealed two carbapenem-resistant Pseudomonas juntendi strains from human feces carrying blaVIM-2. These strains are clonally related and linked to an animal isolate, highlighting potential human-animal resistance gene flow.
Area of Science:
- Microbiology
- Genomics
- Antimicrobial Resistance
Background:
- Pseudomonas juntendi is an emerging pathogen.
- Carbapenem resistance poses a significant public health threat.
- Understanding the genomic basis of resistance is crucial for control.
Purpose of the Study:
- To characterize the genome of carbapenemase-producing P. juntendi harboring blaVIM-2.
- To elucidate mechanisms of carbapenem resistance.
- To evaluate mobile genetic element-mediated dissemination.
Main Methods:
- Hybrid whole-genome sequencing (Oxford Nanopore and Illumina).
- Comparative pangenomics and core genome phylogeny.
- S1 nuclease pulsed-field gel electrophoresis (S1-PFGE) for plasmid analysis.
Main Results:
- Two clonally related P. juntendi strains (L2353hy/L2891hy) from human feces identified.
- Strains harbored 13 antimicrobial resistance genes, including blaVIM-2, blaOXA-246, and tet(A).
- Human isolates showed close phylogenetic links to an animal-derived P. juntendi strain.
Conclusions:
- This study expands genomic understanding of carbapenem-resistant P. juntendi.
- Bidirectional resistance gene flow at the human-animal interface is suggested.
- A One Health approach is recommended for surveillance.
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