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Functional analysis of the YopE GTPase-activating protein (GAP) activity of Yersinia pseudotuberculosis

Aili, Margareta (author)
Umeå universitet,Institutionen för molekylärbiologi (Teknisk-naturvetenskaplig fakultet),Wolf-Watz
Isaksson, Elin L (author)
Umeå universitet,Institutionen för molekylärbiologi (Teknisk-naturvetenskaplig fakultet),Wolf-Watz
Hallberg, Bengt (author)
Umeå universitet,Patologi
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Wolf-Watz, Hans (author)
Umeå universitet,Institutionen för molekylärbiologi (Teknisk-naturvetenskaplig fakultet),Wolf-Watz
Rosqvist, Roland (author)
Umeå universitet,Institutionen för molekylärbiologi (Teknisk-naturvetenskaplig fakultet),Rosqvist
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 (creator_code:org_t)
Wiley, 2006
2006
English.
In: Cellular Microbiology. - : Wiley. - 1462-5814 .- 1462-5822. ; 8:6, s. 1020-1033
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • YopE of Yersinia pseudotuberculosis inactivates three members of the small RhoGTPase family (RhoA, Rac1 and Cdc42) in vitro and mutation of a critical arginine abolishes both in vitro GTPase-activating protein (GAP) activity and cytotoxicity towards HeLa cells, and renders the pathogen avirulent in a mouse model. To understand the functional role of YopE, in vivo studies of the GAP activity in infected eukaryotic cells were conducted. Wild-type YopE inactivated Rac1 as early as 5 min after infection whereas RhoA was down regulated about 30 min after infection. No effect of YopE was found on the activation state of Cdc42 in Yersinia-infected cells. Single-amino-acid substitution mutants of YopE revealed two different phenotypes: (i) mutants with significantly lowered in vivo GAP activity towards RhoA and Rac1 displaying full virulence in mice, and (ii) avirulent mutants with wild-type in vivo GAP activity towards RhoA and Rac1. Our results show that Cdc42 is not an in vivo target for YopE and that YopE interacts preferentially with Rac1, and to a lesser extent with RhoA, during in vivo conditions. Surprisingly, we present results suggesting that these interactions are not a prerequisite to establish infection in mice. Finally, we show that avirulent yopE mutants translocate YopE in about sixfold higher amount compared with wild type. This raises the question whether YopE's primary function is to sense the level of translocation rather than being directly involved in downregulation of the host defence.

Keyword

Animals
Bacterial Outer Membrane Proteins/*analysis/genetics/*physiology
Bacterial Translocation/physiology
DNA; Bacterial/analysis/genetics
Down-Regulation/physiology
Female
GTPase-Activating Proteins/*analysis/*physiology
Gene Expression Regulation; Bacterial
Hela Cells
Humans
L-Lactate Dehydrogenase/metabolism
Mice
Mice; Inbred C57BL
Mutation
Substrate Specificity
Virulence
Yersinia pseudotuberculosis/*chemistry/pathogenicity/*physiology
cdc42 GTP-Binding Protein/analysis/genetics/physiology
rac1 GTP-Binding Protein/analysis/genetics/physiology
rhoA GTP-Binding Protein/analysis/genetics/physiology

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