Feuillie Cécile, Valotteau Claire, Makart Lionel, Gillis Annika, Mahillon Jacques, Dufrêne Yves F
Louvain Institute of Biomolecular Science and Technology , Université catholique de Louvain , Croix du Sud, 4-5 , B-1348 Louvain-la-Neuve , Belgium.
Laboratory of Food and Environmental Microbiology, Earth and Life Institute , Université catholique de Louvain , B-1348 Louvain-la-Neuve , Belgium.
Nano Lett. 2018 Sep 12;18(9):5821-5826. doi: 10.1021/acs.nanolett.8b02463. Epub 2018 Aug 31.
Understanding the basic mechanisms of bacterial sexuality is an important topic in current microbiology and biotechnology. While classical methods used to study gene transfer provide information on whole cell populations, nanotechnologies offer new opportunities for analyzing the behavior of individual mating partners. We introduce an innovative atomic force microscopy (AFM) platform to study and mechanically control DNA transfer between single bacteria, focusing on the large conjugative pXO16 plasmid of the Gram-positive bacterium Bacillus thuringiensis. We demonstrate that the adhesion forces between single donor and recipient cells are very strong (∼2 nN). Using a mutant plasmid, we find that these high forces are mediated by a pXO16 aggregation locus that contains two large surface protein genes. Notably, we also show that AFM can be used to mechanically induce plasmid transfer between single partners, revealing that transfer is very fast (<15 min) and triggers major cell surface changes in transconjugant cells. We anticipate that the single-cell technology developed here will enable researchers to mechanically control gene transfer among a wide range of Gram-positive and Gram-negative bacterial species and to understand the molecular forces involved. Also, the method could be useful in nanomedicine for the design of antiadhesion compounds capable of preventing intimate cell-cell contacts, therefore providing a means to control the resistance and virulence of bacterial pathogens.
了解细菌性行为的基本机制是当前微生物学和生物技术领域的一个重要课题。虽然用于研究基因转移的传统方法能够提供关于整个细胞群体的信息,但纳米技术为分析单个交配伙伴的行为提供了新的机会。我们引入了一种创新的原子力显微镜(AFM)平台,用于研究并机械控制单个细菌之间的DNA转移,重点关注革兰氏阳性细菌苏云金芽孢杆菌的大型接合质粒pXO16。我们证明单个供体细胞与受体细胞之间的粘附力非常强(约2 nN)。使用突变质粒,我们发现这些高粘附力是由一个包含两个大型表面蛋白基因的pXO16聚集位点介导的。值得注意的是,我们还表明AFM可用于机械诱导单个伙伴之间的质粒转移,这表明转移非常迅速(<15分钟),并引发转接合细胞的主要细胞表面变化。我们预计,此处开发的单细胞技术将使研究人员能够机械控制多种革兰氏阳性和革兰氏阴性细菌物种之间的基因转移,并了解其中涉及的分子力。此外,该方法在纳米医学中可能有助于设计能够防止细胞间紧密接触的抗粘附化合物,从而提供一种控制细菌病原体耐药性和毒力的手段。