Skip to main content
. 2023 Oct 18;13:1281823. doi: 10.3389/fcimb.2023.1281823

Figure 1.

Figure 1

Developmental cycle of C. trachomatis. Important proteins expressed at different stages of the development cycle are shown with established transcription factors (italicised), T3SS effectors (bolded), and proteases (underlined). Infectious EBs (coloured green) adhere to and enter the host cell (coloured pink) using various adhesins (Ctad1, Pmps) and the T3SS. Once inside, EBs begin differentiation into replicative RBs (coloured blue). During the RB replication phase, host cell metabolites are used to facilitate the pathogen’s survival. After several rounds of replication, the RBs then asynchronously re-differentiate into EBs for exit via extrusion of the inclusion vacuole from the host cell or lysis of the host cell. The released EB progeny then restarts the infection cycle. Release of EBs (late stage) varies from 48 hours to 72 hours, depending on the serovar (asterisk). In atypical cycles, stressors trigger persistence, in which RBs (coloured green) pause replication and differentiate into long-surviving, stable ABs (coloured orange) and enter a stasis-like state until the stressor is removed. The ABs “detect” this change and re-differentiate back into replicative RBs to resume development. Figure produced with BioRender.