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Updated: Apr 19, 2026

Analysis of Yersinia enterocolitica Effector Translocation into Host Cells Using Beta-lactamase Effector Fusions
Published on: October 13, 2015
Yersinia enterocolitica type III secretion injectisomes form regularly spaced clusters, which incorporate new
Mikhail Kudryashev1, Andreas Diepold, Marlise Amstutz
1Center for Cellular Imaging and NanoAnalytics (C-CINA), Biozentrum, University Basel, WRO-1058, Mattenstrasse 26, Basel, 4058, Switzerland; Focal Area Infection Biology, Biozentrum, University of Basel, Klingelbergstrasse 50/70, Basel, 4056, Switzerland.
Abstract:
Bacterial type III secretion systems or injectisomes are multiprotein complexes directly transporting bacterial effector proteins into eukaryotic host cells. To investigate the distribution of injectisomes in the bacterium and the influence of activation of the system on that distribution, we combined in vivo fluorescent imaging and high-resolution in situ visualization of Yersinia enterocolitica injectisomes by cryo-electron tomography. Fluorescence microscopy showed the injectisomes as regularly distributed spots around the bacterial cell. Under secreting conditions (absence of Ca(2+) ), the intensity of single spots significantly increased compared with non-secreting conditions (presence of Ca(2+) ), in line with an overall up-regulation of expression levels of all components. Single injectisomes observed by cryo-electron tomography tended to cluster at distances less than 100 nm, suggesting that the observed fluorescent spots correspond to evenly distributed clusters of injectisomes, rather than single injectisomes. The up-regulation of injectisome components led to an increase in the number of injectisomes per cluster rather than the formation of new clusters. We suggest that injectisome clustering may allow more effective secretion into the host cells.
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