Charles-Orszag Arthur, van Wolferen Marleen, Lord Samuel J, Albers Sonja-Verena, Mullins R Dyche
Department of Cellular and Molecular Pharmacology, Howard Hughes Medical Institute, University of California, San Francisco, San Francisco, CA, United States.
Molecular Biology of Archaea, Faculty of Biology, Institute of Biology II, University of Freiburg, Freiburg, Germany.
bioRxiv. 2023 Aug 4:2023.08.04.552066. doi: 10.1101/2023.08.04.552066.
Type IV pili are ancient and widespread filamentous organelles found in most bacterial and archaeal phyla where they support a wide range of functions, including substrate adhesion, DNA uptake, self aggregation, and cell motility. In most bacteria, PilT-family ATPases disassemble adhesion pili, causing them to rapidly retract and produce twitching motility, important for surface colonization. As archaea do not possess homologs of PilT, it was thought that archaeal pili cannot retract. Here, we employ live-cell imaging under native conditions (75°C and pH 2), together with automated single-cell tracking, high-temperature fluorescence imaging, and genetic manipulation to demonstrate that exhibits bona fide twitching motility, and that this behavior depends specifically on retractable adhesion pili. Our results demonstrate that archaeal adhesion pili are capable of retraction in the absence of a PilT retraction ATPase and suggests that the ancestral type IV pilus machinery in the last universal common ancestor (LUCA) relied on such a bifunctional ATPase for both extension and retraction.
IV型菌毛是一种古老且广泛存在的丝状细胞器,存在于大多数细菌和古菌门类中,支持多种功能,包括底物黏附、DNA摄取、自我聚集和细胞运动。在大多数细菌中,PilT家族ATP酶会拆解黏附菌毛,使其迅速缩回并产生颤动运动,这对表面定殖很重要。由于古菌不具备PilT的同源物,因此人们认为古菌菌毛无法缩回。在此,我们在自然条件(75°C和pH 2)下进行活细胞成像,并结合自动单细胞追踪、高温荧光成像和基因操作,以证明 表现出真正的颤动运动,且这种行为特别依赖于可缩回的黏附菌毛。我们的结果表明,古菌黏附菌毛在没有PilT缩回ATP酶的情况下能够缩回,并表明最后共同祖先(LUCA)中的祖先IV型菌毛机制依赖于这种双功能ATP酶进行伸展和缩回。