Kittredge Heather A, Dougherty Kevin M, Evans Sarah E
W. K. Kellogg Biological Station, Department of Integrative Biology, Michigan State University, Hickory Corners, Michigan, USA.
Program in Ecology, Evolution, and Behavior, Michigan State University, East Lansing, Michigan, USA.
Appl Environ Microbiol. 2022 Apr 12;88(7):e0228021. doi: 10.1128/aem.02280-21. Epub 2022 Mar 24.
Antibiotic-resistant bacteria and the spread of antibiotic resistance genes (ARGs) pose a serious risk to human and veterinary health. While many studies focus on the movement of live antibiotic-resistant bacteria to the environment, it is unclear whether extracellular ARGs (eARGs) from dead cells can transfer to live bacteria to facilitate the evolution of antibiotic resistance in nature. Here, we use eARGs from dead, antibiotic-resistant Pseudomonas stutzeri cells to track the movement of eARGs to live P. stutzeri cells via natural transformation, a mechanism of horizontal gene transfer involving the genomic integration of eARGs. In sterile, antibiotic-free agricultural soil, we manipulated the eARG concentration, soil moisture, and proximity to eARGs. We found that transformation occurred in soils inoculated with just 0.25 μg of eDNA g soil, indicating that even low concentrations of soil eDNA can facilitate transformation (previous estimates suggested ∼2 to 40 μg eDNA g soil). When eDNA was increased to 5 μg g soil, there was a 5-fold increase in the number of antibiotic-resistant P. stutzeri cells. We found that eARGs were transformed under soil moistures typical of terrestrial systems (5 to 30% gravimetric water content) but inhibited at very high soil moistures (>30%). Overall, this work demonstrates that dead bacteria and their eARGs are an overlooked path to antibiotic resistance. More generally, the spread of eARGs in antibiotic-free soil suggests that transformation allows genetic variants to establish in the absence of antibiotic selection and that the soil environment plays a critical role in regulating transformation. Bacterial death can release eARGs into the environment. Agricultural soils can contain upwards of 10 ARGs g soil, which may facilitate the movement of eARGs from dead to live bacteria through a mechanism of horizontal gene transfer called natural transformation. Here, we track the spread of eARGs from dead, antibiotic-resistant Pseudomonas stutzeri cells to live antibiotic-susceptible P. stutzeri cells in sterile agricultural soil. Transformation increased with the abundance of eARGs and occurred in soils ranging from 5 to 40% gravimetric soil moisture but was lowest in wet soils (>30%). Transformants appeared in soil after 24 h and persisted for up to 15 days even when eDNA concentrations were only a fraction of those found in field soils. Overall, our results show that natural transformation allows eARGs to spread and persist in antibiotic-free soils and that the biological activity of eDNA after bacterial death makes environmental eARGs a public health concern.
抗生素耐药细菌及抗生素耐药基因(ARGs)的传播对人类和兽医健康构成严重威胁。虽然许多研究聚焦于活的抗生素耐药细菌向环境中的转移,但尚不清楚死细胞中的细胞外ARGs(eARGs)能否转移至活细菌,从而在自然环境中促进抗生素耐药性的演变。在此,我们利用来自死亡的、具有抗生素耐药性的斯氏假单胞菌细胞的eARGs,通过自然转化来追踪eARGs向活的斯氏假单胞菌细胞的转移,自然转化是一种水平基因转移机制,涉及eARGs的基因组整合。在无菌、无抗生素的农业土壤中,我们对eARG浓度、土壤湿度以及与eARGs的距离进行了调控。我们发现,在每克土壤仅接种0.25μg eDNA的土壤中就发生了转化,这表明即使是低浓度的土壤eDNA也能促进转化(先前的估计表明每克土壤约有2至40μg eDNA)。当eDNA增加到每克土壤5μg时,具有抗生素耐药性的斯氏假单胞菌细胞数量增加了5倍。我们发现,eARGs在陆地系统典型的土壤湿度条件下(重量含水量为5%至30%)会发生转化,但在土壤湿度非常高(>30%)时受到抑制。总体而言,这项研究表明,死细菌及其eARGs是抗生素耐药性的一条被忽视的途径。更普遍地说,eARGs在无抗生素土壤中的传播表明,转化使得遗传变异体在没有抗生素选择的情况下得以建立,并且土壤环境在调节转化过程中起着关键作用。细菌死亡可将eARGs释放到环境中。农业土壤中每克土壤可能含有超过10种ARGs,这可能通过一种名为自然转化的水平基因转移机制促进eARGs从死细菌向活细菌的转移。在此,我们在无菌农业土壤中追踪了eARGs从死亡的、具有抗生素耐药性的斯氏假单胞菌细胞向活的对抗生素敏感的斯氏假单胞菌细胞的传播。转化随着eARGs的丰度增加而增加,并且在重量土壤湿度为5%至40%的土壤中发生,但在湿润土壤(>30%)中最低。转化体在24小时后出现在土壤中,即使eDNA浓度仅为田间土壤中发现浓度的一小部分,也能持续存在长达15天。总体而言,我们的结果表明,自然转化使eARGs能够在无抗生素的土壤中传播和持续存在,并且细菌死亡后eDNA的生物活性使环境中的eARGs成为一个公共卫生问题。