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  4. Transient Shielding of Intimin and the Type III Secretion System of Enterohemorrhagic and Enteropathogenic Escherichia coli by a Group 4 Capsule

Transient Shielding of Intimin and the Type III Secretion System of Enterohemorrhagic and Enteropathogenic Escherichia coli by a Group 4 Capsule

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50379 Journal of Bacteriology-2008-Shifrin-5063.full.pdf (1.1 MB)
Date
2008
Author(s)
Shifrin, Yulia
Peleg, Adi
Ilan, Ophir
Nadler, Chen
Kobi, Simi
Baruch, Kobi
Yerushalmi, Gal
Berdichevsky, Tatiana
Altuvia, Shoshy
Elgrably-Weiss, Maya
Abe, Cecilia
Knutton, Stuart
Sasakawa, Chihiro
Ritchie, Jennifer M.
Waldor, Matthew K.
Rosenshine, Ilan
DOI
10.1128/JB.00440-08
Publisher
American Society for Microbiology
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Citation
Shifrin, Y., A. Peleg, O. Ilan, C. Nadler, S. Kobi, K. Baruch, G. Yerushalmi, et al. 2008. “Transient Shielding of Intimin and the Type III Secretion System of Enterohemorrhagic and Enteropathogenic Escherichia Coli by a Group 4 Capsule.” Journal of Bacteriology 190 (14): 5063–74. https://doi.org/10.1128/jb.00440-08.
Abstract
Enterohemorrhagic and enteropathogenic Escherichia coli (EHEC and EPEC, respectively) strains represent a major global health problem. Their virulence is mediated by the concerted activity of an array of virulence factors including toxins, a type III protein secretion system (TTSS), pili, and others. We previously showed that EPEC O127 forms a group 4 capsule (G4C), and in this report we show that EHEC O157 also produces a G4C, whose assembly is dependent on the etp, etk, and wzy genes. We further show that at early time points postinfection, these G4Cs appear to mask surface structures including intimin and the TTSS. This masking inhibited the attachment of EPEC and EHEC to tissue-cultured epithelial cells, diminished their capacity to induce the formation of actin pedestals, and attenuated TTSS-mediated protein translocation into host cells. Importantly, we found that Ler, a positive regulator of intimin and TTSS genes, represses the expression of the capsule-related genes, including etp and etk. Thus, the expression of TTSS and G4C is conversely regulated and capsule production is diminished upon TTSS expression. Indeed, at later time points postinfection, the diminishing capsule no longer interferes with the activities of intimin and the TTSS. Notably, by using the rabbit infant model, we found that the EHEC G4C is required for efficient colonization of the rabbit large intestine. Taken together, our results suggest that temporal expression of the capsule, which is coordinated with that of the TTSS, is required for optimal EHEC colonization of the host intestine.
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URI
http://nrs.harvard.edu/urn-3:HUL.InstRepos:41483568
Collection
HMS Scholarly Articles
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