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CADD, a Chlamydia Protein That Interacts with Death Receptors*

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We report here the identification of a bacterial protein capable of interacting with mammalian death receptors in vitro and in vivo. The protein is encoded in the genome of Chlamydia trachomatis and has homologues in otherChlamydia species. This protein, which we refer to as “C hlamydia protein associating with death domains” (CADD), induces apoptosis in a variety of mammalian cell lines when expressed by transient gene transfection. Apoptosis induction can be blocked by Caspase inhibitors, indicating that CADD triggers cell death by engaging the host apoptotic machinery. CADD interacts with death domains of tumor necrosis factor (TNF) family receptors TNFR1, Fas, DR4, and DR5 but not with the respective downstream adaptors. In infected epithelial cells, CADD is expressed late in the infectious cycle of C. trachomatisand co-localizes with Fas in the proximity of the inclusion body. The results suggest a role for CADD modulating the apoptosis pathways of cells infected, revealing a new mechanism of host-pathogen interaction.

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Published, JBC Papers in Press, January 22, 2002, DOI 10.1074/jbc.C100693200

*

This work was supported by National Institutes of Health Grant CA68390 and Deutsche Krebshilfe/Mildred-Scheel-Stiftung Grant D/98/02293 (to F. S.-L.).The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

Both authors contributed equally to this work.