Figure 1. Ultrastructure of a Toxoplasma gondii tachyzoite. The conoid defines the apical end of the
parasite and is thought to be associated with the penetration of the host cell. Micronemes, rhoptries and dense
granules are the three major secretory organelles, found predominately at the apical end of the parasite.
Microneme proteins are released very early in the invasion process, facilitating host-cell binding and gliding
motility. Rhoptry proteins are also released during invasion, and can be detected within the lumen and membrane
of the newly generated parasitophorous vacuole (PV). Dense-granule proteins are released during and after
the formation of the PV, modifying the PV environment for intracellular survival and replication of the parasite.
The apicoplast is a plastid-like four-membrane organelle containing a 35 kb circular DNA. Most of the proteins
functioning within the organelle are encoded by the nucleus, and are specifically targeted to the apicoplast.
This targeting involves the secretory pathway, including the rough endoplasmic reticulum (ER) and a Golgi
body situated immediately apical to the nucleus. Targeted proteins have a bipartite N-terminal extension,
consisting of an ER signal sequence followed by a plastid transit peptide. T. gondii cells have a single nucleus
and a single mitochondrion. It is hypothesised that reliance on the mitochondrion for cellular metabolism differs
according to the life-cycle stage of the parasite