First Report of Colistin-Resistant Escherichia coli Carrying mcr-1 IncI2(delta) and IncX4 Plasmids from Camels ( Camelus dromedarius ) in the Gulf Region.
Akela GhazawiNikolaos StrepisFebin AnesDana YaaqeibAmal AhmedAysha AlHosaniMirah AlShehhiAshrat ManzoorIhab HabibNisar A WaniJohn Philip HaysMushtaq Ahmad KhanPublished in: Antibiotics (Basel, Switzerland) (2024)
Addressing the emergence of antimicrobial resistance (AMR) poses a significant challenge in veterinary and public health. In this study, we focused on determining the presence, phenotypic background, and genetic epidemiology of plasmid-mediated colistin resistance ( mcr ) in Escherichia coli bacteria isolated from camels farmed in the United Arab Emirates (UAE). Fecal samples were collected from 50 camels at a Dubai-based farm in the UAE and colistin-resistant Gram-negative bacilli were isolated using selective culture. Subsequently, a multiplex PCR targeting a range of mcr -genes, plasmid profiling, and whole-genome sequencing (WGS) were conducted. Eleven of fifty camel fecal samples (22%) yielded colonies positive for E. coli isolates carrying the mcr-1 gene on mobile genetic elements. No other mcr -gene variants and no chromosomally located colistin resistance genes were detected. Following plasmid profiling and WGS, nine E. coli isolates from eight camels were selected for in-depth analysis. E. coli sequence types (STs) identified included ST7, ST21, ST24, ST399, ST649, ST999, and STdaa2. Seven IncI2(delta) and two IncX4 plasmids were found to be associated with mcr-1 carriage in these isolates. These findings represent the first identification of mcr -1-carrying plasmids associated with camels in the Gulf region. The presence of mcr-1 in camels from this region was previously unreported and serves as a novel finding in the field of AMR surveillance.
Keyphrases
- escherichia coli
- klebsiella pneumoniae
- gram negative
- genome wide
- public health
- antimicrobial resistance
- copy number
- multidrug resistant
- biofilm formation
- genome wide identification
- dna methylation
- single cell
- gene expression
- pseudomonas aeruginosa
- bioinformatics analysis
- risk factors
- cancer therapy
- real time pcr
- candida albicans