Skip to main content
Log in

A Role for the Glycolipid Exoantigen (GLXA) in Chlamydial Infectivity

  • Published:
Current Microbiology Aims and scope Submit manuscript

Abstract

The chlamydial glycolipid exoantigen, GLXA, is associated with the bacterial membrane, intracellular inclusion, and can also be found secreted into the microenvironment of Chlamydia trachomatis-infected cells. The aim of this study was to investigate the function of GLXA in chlamydial pathogenesis. Pretreatment of HeLa 229 cells with affinity-purified GLXA resulted in a significant enhancement of chlamydial infectivity as determined by inclusion body enumeration. The GLXA-mediated enhancement was shown to be time- and dose-dependent and, more importantly, GLXA-specific, as the effect was abrogated by anti-GLXA antibody. In vitro neutralization assays on HEp-2 cells revealed that an anti-anti-idiotypic antibody to GLXA effectively reduced the infectivity of C. trachomatis, C. pneumoniae, and C. psittaci. In vivo, the co-inoculation of GLXA at the time of C. trachomatis serovar K intravaginal challenge of C3H/HeJ mice resulted in a significant increase in the numbers of shed organisms on days 4, 7, 14, 21, and 28. Taken together, these observations suggest that GLXA, both organism bound and secreted, is important in facilitating the initiation of infection.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Author information

Authors and Affiliations

Authors

Additional information

Received: 12 April 2002 / Accepted: 8 June 2002

Rights and permissions

Reprints and permissions

About this article

Cite this article

Vora, G., Stuart, E. A Role for the Glycolipid Exoantigen (GLXA) in Chlamydial Infectivity. Curr Microbiol 46, 0217–0223 (2003). https://doi.org/10.1007/s00284-002-3843-1

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00284-002-3843-1

Keywords

Navigation