Authors

S. Jiwani; Y. Wang; G. C. Dowd; A. Gianfelice; P. Pichestapong; B. Gavicherla; N. Vanbennekom;K. Ireton

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Abbreviated Journal Title

Infect. Immun.

Keywords

PROTEIN-KINASE-C; PLECKSTRIN HOMOLOGY DOMAINS; NUCLEOTIDE-EXCHANGE; FACTOR; GTPASE-ACTIVATING PROTEINS; PHOSPHATIDYLINOSITOL 3-KINASE; ACTIN; CYTOSKELETON; ENDOCYTIC TRAFFICKING; GLUCOSE-TRANSPORT; EPITHELIAL-CELLS; MAMMALIAN-CELLS; Immunology; Infectious Diseases

Abstract

The bacterial pathogen Listeria monocytogenes causes food-borne illnesses resulting in gastroenteritis, meningitis, or abortion. Listeria promotes its internalization into some human cells through binding of the bacterial surface protein InlB to the host receptor tyrosine kinase Met. The interaction of InlB with the Met receptor stimulates host signaling pathways that promote cell surface changes driving bacterial uptake. One human signaling protein that plays a critical role in Listeria entry is type IA phosphoinositide 3-kinase (PI 3-kinase). The molecular mechanism by which PI 3-kinase promotes bacterial internalization is not understood. Here we perform an RNA interference (RNAi)-based screen to identify components of the type IA PI 3-kinase pathway that control the entry of Listeria into the human cell line HeLa. The 64 genes targeted encode known upstream regulators or downstream effectors of type IA PI 3-kinase. The results of this screen indicate that at least 9 members of the PI 3-kinase pathway play important roles in Listeria uptake. These 9 human proteins include a Rab5 GTPase, several regulators of Arf or Rac1 GTPases, and the serine/threonine kinases phosphoinositide-dependent kinase 1 (PDK1), mammalian target of rapamycin (mTor), and protein kinase C-zeta. These findings represent a key first step toward understanding the mechanism by which type IA PI 3-kinase controls bacterial internalization.

Journal Title

Infection and Immunity

Volume

80

Issue/Number

3

Publication Date

1-1-2012

Document Type

Article

Language

English

First Page

1252

Last Page

1266

WOS Identifier

WOS:000300621600038

ISSN

0019-9567

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