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  Yersinia enterocolitica type III secretion injectisomes form regularly spaced clusters, which incorporate new machines upon activation

Kudryashev, M., Diepold, A., Amstutz, M., Armitage, J. P., Stahlberg, H., & Cornelis, G. R. (2015). Yersinia enterocolitica type III secretion injectisomes form regularly spaced clusters, which incorporate new machines upon activation. Molecular Microbiology, 95(5), 875-884. doi:10.1111/mmi.12908.

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 Creators:
Kudryashev, Misha1, 2, Author           
Diepold, Andreas3, Author
Amstutz, Marlise2, Author
Armitage, Judith P.3, Author
Stahlberg, Henning1, Author
Cornelis, Guy R.1, 4, Author
Affiliations:
1Center for Cellular Imaging and NanoAnalytics (C-CINA), Biozentrum, University of Basel, 4058 Basel, Switzerland, ou_persistent22              
2Focal Area Infection Biology, Biozentrum, University of Basel, 4056 Basel, Switzerland, ou_persistent22              
3Department of Biochemistry, University of Oxford, South Parks Road, Oxford, OX1 3QU UK, ou_persistent22              
4Research Unit in Microorganism Biology, University of Namur, 61 rue de Bruxelles, 5000 Namur, Belgium, ou_persistent22              

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 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 Ca2+), the intensity of single spots significantly increased compared with non-secreting conditions (presence of Ca2+), 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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Language(s): eng - English
 Dates: 2014-12-122015-01-302015-03
 Publication Status: Issued
 Pages: 10
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1111/mmi.12908
PMID: 25524451
 Degree: -

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Title: Molecular Microbiology
  Other : Mol. Microbiol.
Source Genre: Journal
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Publ. Info: Oxford : Blackwell Science
Pages: - Volume / Issue: 95 (5) Sequence Number: - Start / End Page: 875 - 884 Identifier: ISSN: 0950-382X
CoNE: https://pure.mpg.de/cone/journals/resource/954925574950