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Dissemination of pHK01-like incompatibility group IncFII plasmids encoding CTX-M-14 in Escherichia coli from human
1Department of Microbiology, University of Hong Kong, Pokfulam Road, Pokfulam, Hong Kong, China. plho@hkucc.hku.hk
Abstract:
Few studies have compared CTX-M encoding plasmids identified in different ecological sources. This study aimed to analyze and compare the molecular epidemiology of plasmids encoding CTX-M-14 among strains from humans and animals. The CTX-M-14 encoding plasmids in 160 Escherichia coli isolates from animal faecal (14 pigs, 16 chickens, 12 cats, 8 cattle, 5 dogs and 3 rodents), human faecal (45 adults and 20 children) and human urine (37 adults) sources in 2002-2010 were characterized by molecular methods. The replicon types of the CTX-M-14 encoding plasmids were IncFII (n=61), I1-Iγ (n=24), other F types (n=23), B/O (n=10), K (n=6), N (n=3), A/C (n=1), HI1 (n=1), HI2 (n=1) and nontypeable (n=30). The genetic environment, ISEcp1 -bla(CTX-M-14) - IS903 was found in 89.7% (52/58), 87.7% (57/65) and 86.5% (32/37) of the animal faecal, human faecal and human urine isolates, respectively. Subtyping of the 61 IncFII incompatibility group plasmids by replicon sequence typing, plasmid PCR-restriction fragment length polymorphism and marker genes (yac, malB, eitA/eitC and parB/A) profiles showed that 31% (18/58), 30.6% (20/65) and 37.8% (14/37) of the plasmids originating from animal faecal, human faecal and human urine isolates, respectively, were pHK01-like. These 52 pHK01-like plasmids originated from diverse human (20 faecal isolates from 2002, 2007 to 2008, 14 urinary isolates from 2004) and animal (all faecal, 1 cattle, 1 chicken, 5 pigs, 9 cats, 1 dog, 1 rodent from 2008 to 2010) sources. In conclusion, this study highlights the importance of the IncFII group, pHK01-like plasmids in the dissemination of CTX-M-14 among isolates from diverse sources.
Insights
The IncFII group, specifically pHK01-like plasmids, are crucial for spreading the CTX-M-14 gene among Escherichia coli from both human and animal sources. This highlights the importance of tracking these plasmids across different environments.
Area of Science:
- Microbiology
- Molecular Epidemiology
- Antimicrobial Resistance
Background:
- CTX-M enzymes are a major cause of extended-spectrum beta-lactamase (ESBL) production in Enterobacteriaceae.
- Few studies have comparatively analyzed CTX-M encoding plasmids from diverse ecological niches.
- Understanding plasmid epidemiology is vital for controlling the spread of antimicrobial resistance.
Purpose of the Study:
- To compare the molecular epidemiology of CTX-M-14 encoding plasmids in Escherichia coli from human and animal sources.
- To characterize the genetic environment and replicon types of these plasmids.
- To identify common plasmid lineages disseminating CTX-M-14 across different hosts.
Main Methods:
- Molecular characterization of 160 Escherichia coli isolates from animal and human faecal and human urine samples.
- Plasmid replicon typing, genetic environment analysis (ISEcp1-blaCTX-M-14-IS903), and IncFII plasmid subtyping.
- Replicon sequence typing, PCR-restriction fragment length polymorphism, and marker gene profiling for IncFII plasmids.
Main Results:
- The IncFII incompatibility group was the most prevalent type (n=61) among CTX-M-14 encoding plasmids.
- The genetic structure ISEcp1-blaCTX-M-14-IS903 was conserved across animal, human faecal, and human urine isolates.
- A significant proportion of IncFII plasmids were identified as pHK01-like, originating from both human and animal sources.
Conclusions:
- The IncFII group, particularly pHK01-like plasmids, plays a significant role in the dissemination of CTX-M-14.
- The findings underscore the interconnectedness of human and animal reservoirs in the spread of CTX-M-14.
- Effective control strategies for CTX-M-14 require a One Health approach targeting diverse sources.
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