Abstract
Many archaea display swimming motility in liquid medium, which is empowered by the archaellum. Directional movement requires a functional archaellum and a sensing system, such as the chemotaxis system that is used by Euryarchaea. Two well-studied models are the euryarchaeon Haloferax volcanii and the crenarchaeon Sulfolobus acidocaldarius. In this chapter we describe two methods to analyze their swimming behavior and directional movement: (a) time-lapse microscopy under native temperatures and (b) spotting on semi-solid agar or gelrite plates. Whereas the first method allows for deep analysis of swimming behavior, the second method is suited for high throughput comparison of multiple strains.
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References
Jarrell KF, Albers S-V (2012) The archaellum: an old motility structure with a new name. Trends Microbiol 20:307–312. https://doi.org/10.1016/j.tim.2012.04.007
Albers S-V, Jarrell KF (2018) The Archaellum: an update on the unique archaeal motility structure. Trends Microbiol 26:351–362. https://doi.org/10.1016/j.tim.2018.01.004
Lassak K, Neiner T, Ghosh A et al (2012) Molecular analysis of the crenarchaeal flagellum. Mol Microbiol 83:110–124. https://doi.org/10.1111/j.1365-2958.2011.07916.x
Chaban B, Ng SY, Kanbe M et al (2007) Systematic deletion analyses of the fla genes in the flagella operon identify several genes essential for proper assembly and function of flagella in the archaeon, Methanococcus maripaludis. Mol Microbiol 66:596–609. https://doi.org/10.1111/j.1365-2958.2007.05913.x
Kokoeva MV, Oesterhelt D (2000) BasT, a membrane-bound transducer protein for amino acid detection in Halobacterium salinarum. Mol Microbiol 35:647–656
Kokoeva MV, Storch K-F, Klein C, Oesterhelt D (2002) A novel mode of sensory transduction in archaea: binding protein-mediated chemotaxis towards osmoprotectants and amino acids. EMBO J 21:2312–2322. https://doi.org/10.1093/emboj/21.10.2312
Storch KF, Rudolph J, Oesterhelt D (1999) Car: a cytoplasmic sensor responsible for arginine chemotaxis in the archaeon Halobacterium salinarum. EMBO J 18:1146–1158. https://doi.org/10.1093/emboj/18.5.1146
Quax TEF, Albers S-V, Pfeiffer F (2018) Taxis in archaea. Emerg Top Life Sci 2:535–546. https://doi.org/10.1042/etls20180089
Quax TEF, Altegoer F, Rossi F et al (2018) Structure and function of the archaeal response regulator CheY. Proc Natl Acad Sci U S A 115:E1259–E1268. https://doi.org/10.1073/pnas.1716661115
Rudolph J, Oesterhelt D (1996) Deletion analysis of the che operon in the archaeon Halobacterium salinarium. J Mol Biol 258:548–554. https://doi.org/10.1006/jmbi.1996.0267
Kinosita Y, Uchida N, Nakane D, Nishizaka T (2016) Direct observation of rotation and steps of the archaellum in the swimming halophilic archaeon Halobacterium salinarum. Nat Microbiol 1:16148. https://doi.org/10.1038/nmicrobiol.2016.148
Shahapure R, Driessen RP, Haurat MF et al (2014) The archaellum: a rotating type IV pilus. Mol Microbiol 91:716–723. https://doi.org/10.1111/mmi.12486
Ding Y, Lau Z, Logan SM et al (2016) Effects of growth conditions on archaellation and N-glycosylation in Methanococcus maripaludis. Microbiology 162:339–350
Faguy DM, Jarrell KF, Kuzio J, Kalmokoff ML (1994) Molecular analysis of archaeal flagellins: similarity to the type IV pilin–transport superfamily widespread in bacteria. Can J Microbiol 40:67–71
Mukhopadhyay B, Johnson EF, Wolfe RS (2000) A novel pH2 control on the expression of flagella in the hyperthermophilic strictly hydrogenotrophic methanarchaeaon Methanococcus jannaschii. Proc Natl Acad Sci U S A 97:11522–11527
Hendrickson EL, Liu Y, Rosas-Sandoval G et al (2008) Global responses of Methanococcus maripaludis to specific nutrient limitations and growth rate. J Bacteriol 190:2198–2205. https://doi.org/10.1128/JB.01805-07
Weidenbach K, Ehlers C, Kock J et al (2008) Insights into the NrpR regulon in Methanosarcina mazei Gö1. Arch Microbiol 190:319–332. https://doi.org/10.1007/s00203-008-0369-3
Lassak K, Peeters E, Wróbel S, Albers SV (2013) The one-component system ArnR: a membrane-bound activator of the crenarchaeal archaellum. Mol Microbiol 88:125–139. https://doi.org/10.1111/mmi.12173
Esquivel RN, Pohlschroder M (2014) A conserved type IV pilin signal peptide H-domain is critical for the post-translational regulation of flagella-dependent motility. Mol Microbiol 93:494–504
Henche A, Ghosh A, Yu X et al (2012) Structure and function of the adhesive type IV pilus of S ulfolobus acidocaldarius. Environ Microbiol 14:3188–3202
Meyer BH, Peyfoon E, Dietrich C et al (2013) Agl16, a thermophilic glycosyltransferase mediating the last step of N-glycan biosynthesis in the thermoacidophilic crenarchaeon Sulfolobus acidocaldarius. J Bacteriol 195:2177–2186
Jarrell KF, Ding Y, Meyer BH et al (2014) N-linked glycosylation in archaea: a structural, functional, and genetic analysis. Microbiol Mol Biol Rev 78:304–341
Bischof LF, Haurat MF, Albers S-V (2019) Two membrane-bound transcription factors regulate expression of various type-IV-pili surface structures in Sulfolobus acidocaldarius. PeerJ 7:e6459
Hoffmann L, Anders K, Bischof LF et al (2019) Structure and interactions of the archaeal motility repression module ArnA-ArnB that modulates archaellum gene expression in Sulfolobus acidocaldarius. J Biol Chem 294(18):7460–7471
Ye X, Vogt MS, Van Der Does C et al (2020) The phosphatase PP2A interacts with ArnA and ArnB to regulate the oligomeric state and the stability of the ArnA/B complex. Front Microbiol 11:1849. https://doi.org/10.3389/fmicb.2020.01849
Li L, Banerjee A, Bischof LF et al (2017) Wing phosphorylation is a major functional determinant of the Lrs14-type biofilm and motility regulator AbfR1 in Sulfolobus acidocaldarius. Mol Microbiol 105:777–793. https://doi.org/10.1111/mmi.13735
Reimann J, Lassak K, Khadouma S et al (2012) Regulation of archaella expression by the FHA and von Willebrand domain-containing proteins ArnA and ArnB in Sulfolobus acidocaldarius. Mol Microbiol 86:24–36. https://doi.org/10.1111/j.1365-2958.2012.08186.x
Ye X, Van Der Does C, Albers S-V (2020) SaUspA, the universal stress protein of Sulfolobus acidocaldarius stimulates the activity of the PP2A phosphatase and is involved in growth at high salinity. Front Microbiol 11:598821
Ding Y, Nash J, Berezuk A et al (2016) Identification of the first transcriptional activator of an archaellum operon in a euryarchaeon. Mol Microbiol 102:54–70. https://doi.org/10.1111/mmi.13444
Li Z, Kinosita Y, Rodriguez-Franco M et al (2019) Positioning of the motility machinery in halophilic archaea. MBio 10:e00377-19. https://doi.org/10.1128/mBio.00377-19
Li Z, Rodriguez-Franco M, Albers SV et al (2020) The switch complex ArlCDE connects the chemotaxis system and the archaellum. Mol Microbiol 114(3):468–479. https://doi.org/10.1111/mmi.14527
Ducret A, Quardokus EM, Brun YV (2016) MicrobeJ, a tool for high throughput bacterial cell detection and quantitative analysis. Nat Microbiol 1:16077. https://doi.org/10.1038/nmicrobiol.2016.77
Schindelin J, Arganda-Carreras I, Frise E et al (2012) Fiji: an open-source platform for biological-image analysis. Nat Methods 9:676–682. https://doi.org/10.1038/nmeth.2019
Tittes C, Schwarzer S, Pfeiffer F et al (2021) Cellular and genomic properties of Haloferax gibbonsii LR2–5, the host of euryarchaeal virus HFTV1. Front Microbiol 12:625599. https://doi.org/10.1101/2020.10.26.354720
Schwarzer S, Rodriguez-Franco M, Oksanen HM, Quax TEF (2021) Growth phase dependent cell shape of Haloarcula. Microorganisms 9:1–14. https://doi.org/10.3390/microorganisms9020231
Acknowledgments
This work was supported by an Emmy Noether grant (411069969) from the DFG (German Research Foundation) to T.E.F.Q. M.P. received funding from the AL1206/4-3 Grant from the DFG. M.v.W. was supported by the Momentum grant 94933 from the Volkswagen Foundation. X.Y. received support from the Life? Grant Az 96727 from the Volkswagen Foundation.
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Patro, M., van Wolferen, M., Ye, X., Albers, SV., Quax, T.E.F. (2022). Methods to Analyze Motility in Eury- and Crenarchaea. In: Ferreira-Cerca, S. (eds) Archaea. Methods in Molecular Biology, vol 2522. Humana, New York, NY. https://doi.org/10.1007/978-1-0716-2445-6_25
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DOI: https://doi.org/10.1007/978-1-0716-2445-6_25
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