Abstract

Background Chlamydia trachomatis is the etiological agent of trachoma the world's leading cause of infectious blindness. Here, we investigate whether protracted clearance of a primary infection in nonhuman primates is attributable to antigenic variation or related to the maturation of the anti-chlamydial humoral immune response specific to chlamydial antigens.Methodology/Principal FindingsGenomic sequencing of organisms isolated throughout the protracted primary infection revealed that antigenic variation was not related to the inability of monkeys to efficiently resolve their infection. To explore the maturation of the humoral immune response as a possible reason for delayed clearance, sera were analyzed by radioimmunoprecipitation using intrinsically radio-labeled antigens prepared under non-denaturing conditions. Antibody recognition was restricted to the antigenically variable major outer membrane protein (MOMP) and a few antigenically conserved antigens. Recognition of MOMP occurred early post-infection and correlated with reduction in infectious ocular burdens but not with infection eradication. In contrast, antibody recognition of conserved antigens, identified as PmpD, Hsp60, CPAF and Pgp3, appeared late and correlated with infection eradication. Partial immunity to re-challenge was associated with a discernible antibody recall response against all antigens. Antibody recognition of PmpD and CPAF was destroyed by heat treatment while MOMP and Pgp3 were partially affected, indicating that antibody specific to conformational epitopes on these proteins may be important to protective immunity.Conclusions/SignificanceOur findings suggest that delayed clearance of chlamydial infection in NHP is not the result of antigenic variation but rather a consequence of the gradual maturation of the C. trachomatis antigen-specific humoral immune response. However, we cannot conclude that antibodies specific for these proteins play the primary role in host protective immunity as they could be surrogate markers of T cell immunity. Collectively, our results argue that an efficacious subunit trachoma vaccine might require a combination of these antigens delivered in their native conformation.

Highlights

  • The obligate intracellular bacterial parasite Chlamydia trachomatis is the causative agent of blinding trachoma and sexually transmitted diseases

  • We investigated whether delayed clearance of a primary infection in nonhuman primates was attributable to antigenic variation or related to gradual changes in the humoral immune response specific to chlamydial antigens

  • In this study we investigated whether a long-duration but selflimiting ocular C. trachomatis infection in nonhuman primate (NHP) primates was related to antigenic drift or whether gradual maturation of the host antibody mediated immune response was required to eradicate the infection

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Summary

Introduction

The obligate intracellular bacterial parasite Chlamydia trachomatis is the causative agent of blinding trachoma and sexually transmitted diseases. Serovars A, B, Ba, and C are the etiological agents of trachoma [2], the global impact of which is significant. Designated by the WHO as one of the major neglected tropical diseases [3] it is the world’s leading cause of preventable blindness, primarily afflicting populations in developing nations [4]. Though chronicity of infection is frequently believed to relate to constant exposure and reinfection, the pathogenesis of trachoma is not fully understood. Chlamydia trachomatis is the etiological agent of trachoma the world’s leading cause of infectious blindness. We investigate whether protracted clearance of a primary infection in nonhuman primates is attributable to antigenic variation or related to the maturation of the anti-chlamydial humoral immune response specific to chlamydial antigens

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