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Published on: June 3, 2018
Clinical emergence of a novel sequence type (ST3672) NDM-1-producing Vibrio parahaemolyticus in foodborne disease
Chengpei Ni1, Jiancheng Wang2, Chao Yang2
1The Affiliated Wuxi Center for Disease Control and Prevention of Nanjing Medical University, Wuxi Center for Disease Control and Prevention, Wuxi, China.
Background:
This study characterized a newly identified ST3672-type Vibrio parahaemolyticus (V. parahaemolyticus) strain (VP1434), isolated directly from a patient involved in a food poisoning outbreak, highlighting its rare multidrug resistance (MDR) phenotype. The objectives were to investigate its resistance mechanisms, elucidate its evolutionary relationships, and assess its pathogenicity.
Methods:
The VP1434 isolate was analyzed as follows: (1) Antimicrobial susceptibility was tested against 29 antibiotics, and plasmid conjugation experiments verified drug resistance in recipient strains post-transfer. (2) Whole-genome sequencing was used to characterize its genomic features, including plasmid sequences and inter-plasmid relationships. (3) Evolutionary tracing of VP1434 and the plasmid pVP1434-NDM was performed by constructing phylogenetic trees. (4) Virulence factors (VFs) were identified via the Virulence Factor Database, and pathogenicity was assessed through mouse infection.
Results:
The strain demonstrated a concerning MDR profile, exhibiting resistance to all tested β-lactam antibiotics. Additionally, it displayed resistance to sulfonamides and aminoglycosides, with intermediate susceptibility to tetracyclines. Plasmid conjugation experiments showed the bla NDM-1-harboring plasmid was transferable to VP0577, and transconjugants also showed MDR. Whole-genome sequencing identified a bla NDM-1-carrying plasmid harboring multiple resistance genes, which fully explaining its phenotypic resistance to at least four classes of antibiotics. Phylogenetic analysis placed VP1434 on a distinct branch within the maximum-likelihood tree constructed from global V. parahaemolyticus isolates, while the closest relative of the blaNDM-1 -harboring plasmid was identified in a shrimp-derived V. parahaemolyticus strain. VP1434 was found to harbor 185 VFs, including tlh and trh, but lacked the key pathogenicity determinant tdh. In mouse infection experiments, strain VP1434 (tdh-/trh+ ) exhibited significantly higher lethality than environmental isolates (tdh-/trh- ), suggesting TRH plays a significant role in pathogenicity even in the absence of TDH.
Conclusion:
This first report of bla NDM-1-positive clinical V. parahaemolyticus reveals plasmid-mediated MDR emergence in human infections. Its unexpected virulence without classical toxins indicates evolutionary adaptation, necessitating diagnostic updates and strengthened surveillance.
Insights
A multidrug-resistant Vibrio parahaemolyticus strain (VP1434) carrying the blaNDM-1 gene emerged from a food poisoning outbreak. This strain shows unexpected virulence, highlighting the need for updated diagnostics and surveillance for emerging infectious diseases.
Area of Science:
- Microbiology and Infectious Diseases
- Genomics and Molecular Evolution
- Antimicrobial Resistance
Background:
- A novel ST3672-type Vibrio parahaemolyticus (V. parahaemolyticus) strain (VP1434) was isolated from a patient during a food poisoning outbreak.
- This strain exhibited a rare multidrug resistance (MDR) phenotype, prompting further investigation into its resistance mechanisms, evolutionary origins, and pathogenicity.
- The emergence of MDR V. parahaemolyticus poses a significant public health threat, necessitating a comprehensive understanding of its genetic basis and virulence.
Purpose of the Study:
- To characterize the antimicrobial resistance mechanisms of the newly identified MDR V. parahaemolyticus strain VP1434.
- To elucidate the evolutionary relationships of strain VP1434 and its resistance plasmids within the V. parahaemolyticus population.
- To assess the pathogenicity of strain VP1434 and identify contributing virulence factors.
Main Methods:
- Antimicrobial susceptibility testing against 29 antibiotics.
- Plasmid conjugation experiments to confirm the transferability of resistance.
- Whole-genome sequencing for genomic characterization, including plasmid analysis and phylogenetic tree construction.
- Identification of virulence factors (VFs) using the Virulence Factor Database.
- Mouse infection models to evaluate pathogenicity.
Main Results:
- Strain VP1434 displayed MDR, including resistance to all tested β-lactam antibiotics, sulfonamides, and aminoglycosides.
- Whole-genome sequencing identified a transferable blaNDM-1-carrying plasmid responsible for resistance to at least four antibiotic classes.
- Phylogenetic analysis revealed VP1434's distinct evolutionary position and identified a closely related plasmid in a shrimp-derived V. parahaemolyticus.
- VP1434 possessed 185 VFs, including trh but lacking tdh, and exhibited significantly higher lethality in mice compared to environmental isolates, indicating TRH's role in virulence.
Conclusions:
- This study reports the first blaNDM-1-positive clinical V. parahaemolyticus, signifying the emergence of plasmid-mediated MDR in human infections.
- The strain's virulence in the absence of the classical tdh toxin suggests evolutionary adaptation and highlights the need for updated diagnostic approaches.
- Strengthened surveillance for MDR V. parahaemolyticus is crucial to monitor and control the spread of resistant and virulent strains.
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