Abstract:
:Yersinia species pathogenic to humans have been extensively characterized with respect to type III secretion and its essential role in virulence. This study concerns the twin arginine translocation (Tat) pathway utilized by gram-negative bacteria to secrete folded proteins across the bacterial inner membrane into the periplasmic compartment. We have shown that the Yersinia Tat system is functional and required for motility and contributes to acid resistance. A Yersinia pseudotuberculosis mutant strain with a disrupted Tat system (tatC) was, however, not affected in in vitro growth or more susceptible to high osmolarity, oxidative stress, or high temperature, nor was it impaired in type III secretion. Interestingly, the tatC mutant was severely attenuated via both the oral and intraperitoneal routes in the systemic mouse infection model and highly impaired in colonization of lymphoid organs like Peyer's patches and the spleen. Our work highlights that Tat secretion plays a key role in the virulence of Y. pseudotuberculosis.
journal_name
Infect Immunjournal_title
Infection and immunityauthors
Lavander M,Ericsson SK,Bröms JE,Forsberg Adoi
10.1128/IAI.74.3.1768-1776.2006keywords:
subject
Has Abstractpub_date
2006-03-01 00:00:00pages
1768-76issue
3eissn
0019-9567issn
1098-5522pii
74/3/1768journal_volume
74pub_type
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