| Title | Host alpha-adducin is redistributed and localized to the inclusion membrane in chlamydia- and chlamydophila-infected cells. |
| Publication Type | Journal Article |
| Year of Publication | 2008 |
| Authors | Chu, HG, Weeks, SK, Gilligan, DM, Rockey, DD |
| Journal | Microbiology (Reading) |
| Volume | 154 |
| Issue | Pt 12 |
| Pagination | 3848-3855 |
| Date Published | 2008 Dec |
| ISSN | 1350-0872 |
| Keywords | Calmodulin-Binding Proteins, Chlamydia trachomatis, Chlamydophila, Chlamydophila pneumoniae, HeLa Cells, Host-Pathogen Interactions, Humans, Immunoblotting, Inclusion Bodies, Proto-Oncogene Proteins c-raf |
| Abstract |
A large-scale analysis of proteins involved in host-cell signalling pathways was performed using chlamydia-infected murine cells in order to identify host proteins that are differentially activated or localized following infection. Two proteins whose distribution was altered in Chlamydia trachomatis-infected cells relative to mock-infected cells were the actin-binding protein adducin and the regulatory kinase Raf-1. Immunoblot analysis with antibodies to both phosphorylated and non-phosphorylated forms of these proteins demonstrated that the abundance of each protein was markedly reduced in the cytosolic fraction of C. trachomatis- and Chlamydophila caviae-infected cells, but the total cellular protein abundance remained unaffected by infection. Fluorescence microscopy of chlamydia-infected cells using anti-alpha-adducin antibodies demonstrated labelling at or near the chlamydial inclusion membrane. Treatment of infected cells with nocodazole or cytochalasin D did not affect alpha-adducin that was localized to the margins of the inclusion. The demonstration of alpha-adducin and Raf-1 redistribution within cells infected by different chlamydiae provides novel opportunities for analysis of host-pathogen interactions in this system.
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| DOI | 10.1099/mic.0.2008/020941-0 |
| Alternate Journal | Microbiology (Reading) |
| PubMed ID | 19047752 |
| Grant List | AI031448 / AI / NIAID NIH HHS / United States AI48769 / AI / NIAID NIH HHS / United States |