菌毛
DNA
转化(遗传学)
细胞外
化学
生物物理学
氧化应激
生物化学
细菌
基因
氧化磷酸化
外源DNA
细胞生物学
微生物学
DNA损伤
辅因子
生物
基因表达调控
离子键合
DNA缩合
基因表达
抗生素
胞外聚合物
新月形茎杆菌
抗生素耐药性
作者
Qiting Xie,Huiming Tang,Huijie Lu,Lizhong Zhu
标识
DOI:10.1021/acs.est.6c02776
摘要
Natural transformation represents one of the major dissemination pathways of antibiotic resistance genes (ARGs) in the environment. It can be facilitated by heavy metals, which is traditionally attributed to the induction of oxidative stress and an SOS response. Here, we demonstrate an alternative mechanism involving type IV pili (T4P), the molecular machinery for extracellular DNA (eDNA) uptake. Specifically, 2 μM Cu(II) and Zn(II) significantly enhanced transformation in Acinetobacter baylyi by 28% and 46% (p < 0.05) and in soil communities by 51% and 74% (p < 0.05). T4P sensitively responded to the two metals at concentrations as low as 0.5 μM within 2 h, preceding any detectable oxidative stress responses. At the initial phase of T4P-mediated uptake (DNA binding), Cu(II) enhanced extracellular ARGs adhesion by inducing DNA condensation and strengthening T4P-DNA binding via ionic bridging. During the latter phase (DNA pulling), Zn(II) functioned as a cofactor for T4P ATPase, stimulating pilus extension-retraction dynamics to facilitate DNA transformation. At higher concentrations (8 μM), the CpiR-CpiA regulatory axis serves as a molecular brake, curtailing T4P dynamics by derepressing the PilB-inhibitor CpiA and thereby attenuating transformation enhancement. These findings reveal that Cu and Zn interfere with different phases of T4P-mediated DNA uptake, highlighting a previously unrecognized mechanism by which metals accelerate ARG dissemination in the environment.
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