HCAI, Fungal, AMR, AMU & Sepsis Division, UK Health Security Agency, London, UK.
Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Sci Rep. 2023 Feb 13;13(1):2500. doi: 10.1038/s41598-023-29530-y.
Plasmids are major vectors of bacterial antibiotic resistance, but understanding of factors associated with plasmid antibiotic resistance gene (ARG) carriage is limited. We curated > 14,000 publicly available plasmid genomes and associated metadata. Duplicate and replicate plasmids were excluded; where possible, sample metadata was validated externally (BacDive database). Using Generalised Additive Models (GAMs) we assessed the influence of 12 biotic/abiotic factors (e.g. plasmid genetic factors, isolation source, collection date) on ARG carriage, modelled as a binary outcome. Separate GAMs were built for 10 major ARG types. Multivariable analysis indicated that plasmid ARG carriage patterns across time (collection years), isolation sources (human/livestock) and host bacterial taxa were consistent with antibiotic selection pressure as a driver of plasmid-mediated antibiotic resistance. Only 0.42% livestock plasmids carried carbapenem resistance (compared with 12% human plasmids); conversely, tetracycline resistance was enriched in livestock vs human plasmids, reflecting known prescribing practices. Interpreting results using a timeline of ARG type acquisition (determined by literature review) yielded additional novel insights. More recently acquired ARG types (e.g. colistin and carbapenem) showed increases in plasmid carriage during the date range analysed (1994-2019), potentially reflecting recent onset of selection pressure; they also co-occurred less commonly with ARGs of other types, and virulence genes. Overall, this suggests that following acquisition, plasmid ARGs tend to accumulate under antibiotic selection pressure and co-associate with other adaptive genes (other ARG types, virulence genes), potentially re-enforcing plasmid ARG carriage through co-selection.
质粒是细菌抗生素耐药性的主要载体,但人们对与质粒抗生素耐药基因(ARG)携带相关的因素的了解有限。我们整理了超过 14000 个公开的质粒基因组及其相关元数据。排除了重复和复制质粒;在可能的情况下,外部验证了样本元数据(BacDive 数据库)。使用广义加性模型(GAMs),我们评估了 12 个生物/非生物因素(例如质粒遗传因素、分离源、收集日期)对 ARG 携带的影响,将其建模为二元结果。针对 10 种主要 ARG 类型分别构建了 GAMs。多变量分析表明,质粒 ARG 携带模式在时间(收集年份)、分离源(人类/牲畜)和宿主细菌分类群上与抗生素选择压力一致,这是质粒介导的抗生素耐药性的驱动因素。只有 0.42%的牲畜质粒携带碳青霉烯类耐药性(而 12%的人类质粒);相反,四环素耐药性在牲畜质粒中更为丰富,反映了已知的处方实践。通过文献综述确定的 ARG 类型获得时间线(通过文献综述确定)来解释结果,得出了其他新的见解。在分析的日期范围内(1994-2019 年),最近获得的 ARG 类型(如粘菌素和碳青霉烯)在质粒携带量上有所增加,这可能反映了最近开始出现选择压力;它们也与其他类型的 ARG 较少共同出现,与毒力基因也较少共同出现。总体而言,这表明在获得质粒 ARG 后,它们往往在抗生素选择压力下积累,并与其他适应性基因(其他 ARG 类型、毒力基因)共同关联,可能通过共同选择进一步增强质粒 ARG 的携带。