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Temporal proteomic profiling of Chlamydia trachomatis–infected HeLa‐229 human cervical epithelial cells
Authors:Grace Min Yi Tan  Hui Jing Lim  Tee Cian Yeow  Elaheh Movahed  Chung Yeng Looi  Rishein Gupta  Bernard P. Arulanandam  Sazaly Abu Bakar  Negar Shafiei Sabet  Li‐Yen Chang  Won Fen Wong
Affiliation:1. Department of Medical Microbiology, Tropical Infectious Disease Research and Education Centre, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia;2. Department of Pharmacology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia;3. Center of Excellence in Infection Genomics, South Texas Center For Emerging Infectious Diseases, University of Texas at San Antonio, Texas, USA;4. Faculty of Medicine, SEGi University, Petaling Jaya, Malaysia
Abstract:Chlamydia trachomatis is the leading causative agent of bacterial sexually transmitted infections worldwide which can lead to female pelvic inflammatory disease and infertility. A greater understanding of host response during chlamydial infection is essential to design intervention technique to reduce the increasing incidence rate of genital chlamydial infection. In this study, we investigated proteome changes in epithelial cells during C. trachomatis infection by using an isobaric tags for relative and absolute quantitation (iTRAQ) labeling technique coupled with a liquid chromatography‐tandem mass spectrometry (LC‐MS3) analysis. C. trachomatis (serovar D, MOI 1)–infected HeLa‐229 human cervical carcinoma epithelial cells (at 2, 4 and 8 h) showed profound modifications of proteome profile which involved 606 host proteins. MGST1, SUGP2 and ATXN10 were among the top in the list of the differentially upregulated protein. Through pathway analysis, we suggested the involvement of eukaryotic initiation factor 2 (eIF2) and mammalian target of rapamycin (mTOR) in host cells upon C. trachomatis infection. Network analysis underscored the participation of DNA repair mechanism during C. trachomatis infection. In summary, intense modifications of proteome profile in C. trachomatis–infected HeLa‐229 cells indicate complex host‐pathogen interactions at early phase of chlamydial infection.
Keywords:Cervical epithelial cells  Chlamydia trachomatis  Mass spectrometry  Proteome expression  Sexual transmitted infection
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