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The Chlamydia-Secreted Protease CPAF Promotes Chlamydial Survival in the Mouse Lower Genital Tract.
Yang, Zhangsheng; Tang, Lingli; Shao, Lili; Zhang, Yuyang; Zhang, Tianyuan; Schenken, Robert; Valdivia, Raphael; Zhong, Guangming.
Affiliation
  • Yang Z; Department of Microbiology & Immunology, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
  • Tang L; Department of Clinic Diagnosis, Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
  • Shao L; Department of Microbiology & Immunology, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
  • Zhang Y; Department of Microbiology & Immunology, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
  • Zhang T; Department of Microbiology & Immunology, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
  • Schenken R; Department of Obstetrics and Gynecology, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
  • Valdivia R; Duke Molecular Genetics and Microbiology, Duke University School of Medicine, Durham, North Carolina, USA.
  • Zhong G; Department of Microbiology & Immunology, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA Zhongg@uthscsa.edu.
Infect Immun ; 84(9): 2697-702, 2016 09.
Article in En | MEDLINE | ID: mdl-27382018
ABSTRACT
Despite the extensive in vitro characterization of CPAF (chlamydial protease/proteasome-like activity factor), its role in chlamydial infection and pathogenesis remains unclear. We now report that a Chlamydia trachomatis strain deficient in expression of CPAF (L2-17) is no longer able to establish a successful infection in the mouse lower genital tract following an intravaginal inoculation. The L2-17 organisms were cleared from the mouse lower genital tract within a few days, while a CPAF-sufficient C. trachomatis strain (L2-5) survived in the lower genital tract for more than 3 weeks. However, both the L2-17 and L2-5 organisms maintained robust infection courses that lasted up to 4 weeks when they were directly delivered into the mouse upper genital tract. The CPAF-dependent chlamydial survival in the lower genital tract was confirmed in multiple strains of mice. Thus, we have demonstrated a critical role of CPAF in promoting C. trachomatis survival in the mouse lower genital tracts. It will be interesting to further investigate the mechanisms of the CPAF-dependent chlamydial pathogenicity.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Endopeptidases / Chlamydia Infections / Chlamydia trachomatis / Proteasome Endopeptidase Complex / Genitalia Limits: Animals / Female / Humans Language: En Journal: Infect Immun Year: 2016 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Endopeptidases / Chlamydia Infections / Chlamydia trachomatis / Proteasome Endopeptidase Complex / Genitalia Limits: Animals / Female / Humans Language: En Journal: Infect Immun Year: 2016 Document type: Article Affiliation country:
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