TY - JOUR
T1 - UV-inducible cellular aggregation of the hyperthermophilic archaeon Sulfolobus solfataricus is mediated by pili formation
AU - Froels, Sabrina
AU - Ajon, Malgorzata
AU - Wagner, Michaela
AU - Teichmann, Daniela
AU - Zolghadr, Behnam
AU - Folea, Mihaela
AU - Boekema, Egbert J.
AU - Driessen, Arnold J. M.
AU - Schleper, Christa
AU - Albers, Sonja-Verena
PY - 2008/11
Y1 - 2008/11
N2 - The hyperthermophilic archaeon Sulfolobus solfataricus has been shown to exhibit a complex transcriptional response to UV irradiation involving 55 genes. Among the strongest UV-induced genes was a putative pili biogenesis operon encoding a potential secretion ATPase, two pre-pilins, a putative transmembrane protein and a protein of unknown function. Electron microscopy and image reconstruction of UV-treated cells showed straight pili with 10 nm in diameter, variable in length, not bundled or polarized and composed of three evenly spaced helices, thereby clearly being distinguishable from archaeal flagella. A deletion mutant of SSO0120, the central type II/IV secretion ATPase, did not produce pili. It could be complemented by reintroducing the gene on a plasmid vector. We have named the operon ups operon for UV-inducible pili operon of Sulfolobus. Overexpression of the pre-pilins, Ups-A/B (SSO0117/0118) in Sulfolobus resulted in production of extremely long filaments. Pronounced cellular aggregation was observed and quantified upon UV treatment. This aggregation was a UV-dose-dependent, dynamic process, not inducible by other physical stressors (such as pH or temperature shift) but stimulated by chemically induced double-strand breaks in DNA. We hypothesize that pili formation and subsequent cellular aggregation enhance DNA transfer among Sulfolobus cells to provide increased repair of damaged DNA via homologous recombination.
AB - The hyperthermophilic archaeon Sulfolobus solfataricus has been shown to exhibit a complex transcriptional response to UV irradiation involving 55 genes. Among the strongest UV-induced genes was a putative pili biogenesis operon encoding a potential secretion ATPase, two pre-pilins, a putative transmembrane protein and a protein of unknown function. Electron microscopy and image reconstruction of UV-treated cells showed straight pili with 10 nm in diameter, variable in length, not bundled or polarized and composed of three evenly spaced helices, thereby clearly being distinguishable from archaeal flagella. A deletion mutant of SSO0120, the central type II/IV secretion ATPase, did not produce pili. It could be complemented by reintroducing the gene on a plasmid vector. We have named the operon ups operon for UV-inducible pili operon of Sulfolobus. Overexpression of the pre-pilins, Ups-A/B (SSO0117/0118) in Sulfolobus resulted in production of extremely long filaments. Pronounced cellular aggregation was observed and quantified upon UV treatment. This aggregation was a UV-dose-dependent, dynamic process, not inducible by other physical stressors (such as pH or temperature shift) but stimulated by chemically induced double-strand breaks in DNA. We hypothesize that pili formation and subsequent cellular aggregation enhance DNA transfer among Sulfolobus cells to provide increased repair of damaged DNA via homologous recombination.
KW - III SIGNAL PEPTIDES
KW - HALOBACTERIUM-SALINARUM
KW - ESCHERICHIA-COLI
KW - BIOFILM DEVELOPMENT
KW - IV PILI
KW - ACTINOBACILLUS-ACTINOMYCETEMCOMITANS
KW - PSEUDOMONAS-AERUGINOSA
KW - NONSPECIFIC ADHERENCE
KW - PYROCOCCUS-FURIOSUS
KW - FLAGELLAR FILAMENT
U2 - 10.1111/j.1365-2958.2008.06459.x
DO - 10.1111/j.1365-2958.2008.06459.x
M3 - Article
SN - 0950-382X
VL - 70
SP - 938
EP - 952
JO - Molecular Microbiology
JF - Molecular Microbiology
IS - 4
ER -