NHC Key Laboratory of Food Safety Risk Assessment, China National Center for Food Safety Risk Assessment, Beijing, People's Republic of China.
UCD-Centre for Food Safety, School of Public Health, Physiotherapy and Sports Science, University College Dublin, Belfield, Dublin, Ireland.
J Antimicrob Chemother. 2019 Jul 1;74(7):1786-1794. doi: 10.1093/jac/dkz126.
Our aim was to determine the antimicrobial susceptibilities of 2862 Listeria monocytogenes cultured from various foods in China and to use WGS to characterize the antimicrobial resistance and virulence genotypes of those expressing a resistance phenotype.
The susceptibilities of 2862 L. monocytogenes were determined by broth microdilution. Twenty-eight L. monocytogenes were found to be resistant to one to four antibiotics. All 28 resistant isolates were subsequently sequenced using short-read high accuracy protocols. The corresponding genomes were assembled and further analysis was carried out using appropriate bioinformatics pipelines.
All 28 resistant L. monocytogenes were classified into five STs (ST3, ST8, ST9, ST155 and ST515). Both ST9 and ST155 were dominant and their genotypes correlated with their resistance phenotypes. All ST9 isolates were MDR and could be phylogenetically classified into two clusters. One was relatively close to clinical origins and one to food. Downstream analysis of the genetic contexts in which these resistance genotypes were found suggested that these may have been acquired from other bacteria by horizontal transfer or insertion into the chromosome. All isolates harboured Listeria pathogenicity island (LIPI)-1 and LIPI-2, and only two harboured LIPI-3.
This study reported on the antimicrobial susceptibilities of 2862 foodborne L. monocytogenes along with the genomic characterization of 28 resistant isolates, 11 of which expressed an MDR phenotype. These data showed that this bacterium can acquire resistance by horizontal gene transfer in and between species. This study may necessitate a re-evaluation of risk to public health, associated with this bacterial species.
本研究旨在测定中国 2862 株食品源性李斯特菌的药敏谱,并利用 WGS 对表现出耐药表型的菌株进行耐药性和毒力基因型分析。
采用肉汤微量稀释法测定 2862 株李斯特菌的药敏谱。28 株李斯特菌对 1 至 4 种抗生素耐药。对所有 28 株耐药分离株进行短读高通量测序。采用适当的生物信息学流程对相应的基因组进行组装和进一步分析。
28 株耐药李斯特菌均被分为 5 个 ST 型(ST3、ST8、ST9、ST155 和 ST515)。ST9 和 ST155 均为优势菌,其基因型与其耐药表型相关。所有 ST9 分离株均为 MDR,可分为两个聚类。一个聚类与临床来源较近,另一个聚类与食品来源较近。对这些耐药基因型所在的遗传背景进行下游分析表明,这些耐药基因可能是通过水平转移或插入染色体从其他细菌中获得的。所有分离株均携带李斯特菌致病性岛(LIPI)-1 和 LIPI-2,仅 2 株携带 LIPI-3。
本研究报道了 2862 株食源性李斯特菌的药敏谱,并对 28 株耐药分离株进行了基因组特征分析,其中 11 株表现出 MDR 表型。这些数据表明,该细菌可以通过种间和种内的水平基因转移获得耐药性。本研究可能需要重新评估与该细菌相关的公共健康风险。