Abstract

An inhibitor of host cell lysophospholipid acyltransferase, an enzyme involved in lipid metabolism blocked growth of the obligate intracellular pathogen Chlamydia through its action on the transport of transferrin (Tf) via the slow pathway of recycling. A detailed characterization of this inhibition revealed that Tf accumulated in vesicles positive for Rab11, with a concomitant reduction in the level of Tf found within the transport intermediate Rab4/11 hybrid vesicles. The net result was the failure to be recycled to the plasma membrane. In chlamydiae-infected cells, the Tf-containing Rab11-positive vesicles were typically found intimately associated with the inclusion, and treatment with the inhibitor caused their accumulation, suggesting that the timely progression and completion of Tf recycling was necessary for proper chlamydial growth. Growth inhibition by the compound could be negated by the simple removal of the Tf-containing fraction of the serum, a further indication that accumulation of Tf around the chlamydial inclusion was deleterious to the pathogen. Thus, it appears that manipulating the slow recycling pathway can have biological consequences for Chlamydia and implies the need to regulate carefully the interaction of the inclusion with this host trafficking pathway.

Highlights

  • Chlamydia is a developmentally regulated bacterium that resides within its target host cell in a pathogen-defined protective niche called an inclusion (Hackstadt, 2000)

  • The unrelated compound U18666a, which affects a number of transport pathways due to its effects on cellular cholesterol homeostasis (Higgins et al, 1999), did not have observable effects on the inclusion phenotype and only minimal effects on inclusion forming units (IFU) yield

  • We examined the effects of FR179254 treatment on the subpopulation of Tf that localize around the chlamydial inclusion

Read more

Summary

Introduction

Chlamydia is a developmentally regulated bacterium that resides within its target host cell in a pathogen-defined protective niche called an inclusion (Hackstadt, 2000). The chlamydial inclusion displays selectivity in its interactions with the exocytic pathway by excluding vesicles containing glycoprotein cargo (Scidmore et al, 1996a). The significance of SM transport to the inclusion is unclear a recent report by Heuer et al (2009) demonstrated the role of infection-induced Golgi fragmentation in chlamydial growth, which correlated the fragmentation of the Golgi apparatus with enhanced SM transport to the inclusion. Inhibiting this process had only modest effects on chlamydial growth. Lipid droplets have been found inside chlamydial inclusions (Cocchiaro et al, 2008), the repertoire of organelles and vesicles with which Chlamydia interacts is likely to grow

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call