The Chlamydia-Secreted Protease CPAF Promotes Chlamydial Survival in the Mouse Lower Genital Tract

Author:

Yang Zhangsheng1,Tang Lingli2,Shao Lili1,Zhang Yuyang1,Zhang Tianyuan1,Schenken Robert3,Valdivia Raphael4,Zhong Guangming1

Affiliation:

1. Department of Microbiology & Immunology, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA

2. Department of Clinic Diagnosis, Second Xiangya Hospital, Central South University, Changsha, Hunan, China

3. Department of Obstetrics and Gynecology, University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA

4. Duke Molecular Genetics and Microbiology, Duke University School of Medicine, Durham, North Carolina, USA

Abstract

ABSTRACT Despite the extensive in vitro characterization of CPAF ( c hlamydial p rotease/proteasome-like a ctivity f actor), 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.

Funder

HHS | National Institutes of Health

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

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