Abstract

Little is known regarding how the chronic Toxoplasma gondii cyst develops. Here, we investigated intravacuolar-network-associated dense granule (GRA) proteins GRA1, GRA2, GRA4, GRA6, GRA9, and GRA12 during cyst development in vitro after differentiation of the tachyzoite-stage parasitophorous vacuole. By day 1 postdifferentiation, GRA1, GRA4, GRA6, GRA9, and GRA12 colocalized with Dolichos biflorus agglutinin stain at the cyst periphery. In contrast, GRA2 remained in the cyst matrix. By day 2 postdifferentiation, coinciding with localization of GRA2 to the cyst periphery, GRA1, GRA4, GRA6, and GRA9 established a continuous matrix pattern in the cyst. In contrast, GRA2 and GRA12 were colocalized in prominent cyst matrix puncta throughout cyst development. While GRA2, GRA6, and GRA12 localized in outer and inner layers of the cyst wall, GRA1, GRA4, and GRA9 localized predominantly in the inner layers of the cyst wall. GRA2 and GRA12 were colocalized in the cyst wall by day 7 postdifferentiation. However, by day 10 postdifferentiation, GRA12 was relocalized from the cyst wall to puncta in the cyst matrix. Differentiation of Δgra2 parasites revealed a defect in the ability to establish a normal cyst matrix. In addition, the deletion of any intravacuolar-network-associated GRA protein, except GRA1, reduced the rate of accumulation of cyst wall proteins at the cyst periphery relative to the cyst interior. Our findings reveal dynamic patterns of GRA protein localization during cyst development and suggest that intravacuolar-network-associated GRA proteins regulate the formation and maturation of the cyst matrix and cyst wall structures.IMPORTANCEToxoplasma gondii establishes chronic infection in humans by forming thick-walled cysts that persist in the brain. If host immunity wanes, cysts reactivate to cause severe, and often lethal, toxoplasmic encephalitis. There is no available therapy to eliminate cysts or to prevent their reactivation. Moreover, how the vital and characteristic cyst matrix and cyst wall structures develop is poorly understood. Here, we visualized and tracked the localization of Toxoplasma intravacuolar-network-associated dense granule (GRA) proteins during cyst development in vitro Intravacuolar-network GRAs were present within the cyst matrix and at the cyst wall in developing cysts, and genetic deletion of intravacuolar-network-associated GRAs reduced the rate of accumulation of cyst wall material at the cyst periphery. Our results show that intravacuolar-network-associated GRAs, particularly GRA2 and GRA12, play dynamic and essential roles in the development and maturation of the cyst matrix and the cyst wall structures.

Highlights

  • Little is known regarding how the chronic Toxoplasma gondii cyst develops

  • Bar ϭ 5 ␮m. (D to J) Fluorescence intensity profiles of representative cysts shown in panel A were generated to quantify the location of GRA protein(s) relative to the cyst wall: Dolichos biflorus agglutinin (DBA) compared to GFPϩ bradyzoites (D), DBA compared to GRA1 (E), DBA compared to GRA2 (F), DBA compared to GRA4 (G), DBA compared to GRA6 (H), DBA compared to GRA9 (I), and DBA compared to GRA12 (J)

  • The dotted red vertical line indicates the middle of the cyst wall, which corresponds to the peak DBA fluorescence intensity. (K) Fluorescence intensities of DBA, GRA1, GRA2, GRA4, GRA6, GRA9, GRA12, and green fluorescent protein (GFP) were measured at the cyst periphery and within the cyst

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Summary

Introduction

Little is known regarding how the chronic Toxoplasma gondii cyst develops. Here, we investigated intravacuolar-network-associated dense granule (GRA) proteins GRA1, GRA2, GRA4, GRA6, GRA9, and GRA12 during cyst development in vitro after differentiation of the tachyzoite-stage parasitophorous vacuole. Our findings reveal dynamic patterns of GRA protein localization during cyst development and suggest that intravacuolar-network-associated GRA proteins regulate the formation and maturation of the cyst matrix and cyst wall structures. We visualized and tracked the localization of Toxoplasma intravacuolar-network-associated dense granule (GRA) proteins during cyst development in vitro. An established in vitro tachyzoite-to-bradyzoite differentiation method that exposes the tachyzoitestage PV to low CO2 and a medium with a higher pH [22, 23] triggers cyst development in vitro and produces mature orally infectious cysts from all cyst-competent type I, type II, type III, and exotic strain types [24]. A recent proteomic study of the cyst wall revealed that certain dense granule (GRA) proteins were localized in the mature cyst wall 8 days after differentiation of tachyzoite-stage PVs in vitro [29]

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