Abstract
Rapid developments in the field of whole genome sequencing (WGS) make in silico antimicrobial resistance (AMR) a target within reach. Campylobacter jejuni is a leading cause of foodborne infections in Israel with increasing rates of resistance. We applied WGS analysis to study the prevalence and genetic basis of AMR in 263 C. jejuni human and veterinary representative isolates retrieved from a national collection during 2003–2012. We evaluated the prediction of phenotypic AMR from genomic data. Genomes were screened by the NCBI AMRFinderPlus and the BioNumerics tools for acquired AMR genes and point mutations. The results were compared to phenotypic resistance determined by broth microdilution. The most prevalent resistant determinants were the multi-drug efflux transporter gene cmeABC (100%), the tetracycline resistance tet(O) gene (82.1%), the quinolone resistance gyrA T861 point mutation (75.7%), and the aadE streptomycin resistance gene. A variety of 12 known β lactam resistance genes (blaOXA variants) were detected in 241 (92%) isolates, the most prevalent being blaOXA−193, blaOXA−461, and blaOXA−580 (56, 16, and 7%, respectively). Other aminoglycoside resistance genes and the macrolide resistance point mutation were rare (<1%). The overall correlation rate between WGS-based genotypic prediction and phenotypic resistance was 98.8%, sensitivity, specificity, positive, and negative predictive values being 98.0, 99.3, 99.1, and 98.5%, respectively. wgMLST-based phylogeny indicated a high level of clonality and clustering among the studied isolates. Closely related isolates that were part of a genetic cluster (single linkage distance ≤ 15 alleles) based on wgMLST phylogeny mostly shared a homogenous AMR determinant profile. This was observed in 18 of 20 (90.0%) clusters within clonal complex-21, suggesting clonal expansion of resistant isolates. Strong association to lineage was noted for the aadE gene and the various blaOXA genes. High resistance rates to tetracycline and quinolones and a low resistance rate to macrolides were detected among the Israeli C. jejuni isolates. While a high genotypic-phenotypic correlation was found, some resistance phenotypes could not be predicted by the presence of AMR determinants, and particularly not the level of resistance. WGS-based prediction of antimicrobial resistance in C. jejuni requires further optimization in order to integrate this approach in the routine workflow of public health laboratories for foodborne surveillance.
Highlights
Whole genome sequencing (WGS) has revolutionized foodborne pathogen surveillance practices (Jagadeesan et al, 2019)
A total of 263 C. jejuni isolates were analyzed by whole genome sequencing (Supplementary Table 1)
AMRFinderPlus analysis detected a total of 21 genetic antimicrobial resistance (AMR) determinants among the 263 C. jejuni studied sequences
Summary
Whole genome sequencing (WGS) has revolutionized foodborne pathogen surveillance practices (Jagadeesan et al, 2019). This has become achievable due to the rapid developments in high-throughput sequencing technologies, allowing affordable, real-time, large-scale WGS of foodborne pathogens. This technology can produce a large amount of fast, highly accurate, and reliable information permitting species identification and typing, phylogenetic analyses, outbreak investigation, and determination of virulence and resistance traits as a one-stopshop (Motro and Moran-Gilad, 2017; Ribot et al, 2019). WGS is rapidly becoming the first line method for Campylobacter subtyping in many public health laboratories, mostly based on whole genome (wg) multilocus sequence typing (MLST) (wgMLST) and core genome MLST (cgMLST) (Nadon et al, 2017; Ribot et al, 2019)
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