A Critical Role for Toxoplasma gondii Vacuolar Protein Sorting VPS9 in Secretory Organelle Biogenesis and Host Infection
Accurate sorting of proteins to the three types of parasite-specific secretory organelles namely rhoptry, microneme and dense granule in Toxoplasma gondii is crucial for successful host cell invasion by this obligate intracellular parasite. Despite its tiny body architecture and limited trafficking...
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Published in | Scientific reports Vol. 6; no. 1; p. 38842 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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Nature Publishing Group UK
14.12.2016
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Abstract | Accurate sorting of proteins to the three types of parasite-specific secretory organelles namely rhoptry, microneme and dense granule in
Toxoplasma gondii
is crucial for successful host cell invasion by this obligate intracellular parasite. Despite its tiny body architecture and limited trafficking machinery,
T. gondii
relies heavily on transport of vesicles containing proteins, lipids and important virulence-like factors that are delivered to these secretory organelles. However, our understanding on how trafficking of vesicles operates in the parasite is still limited. Here, we show that the
T. gondii
vacuolar protein sorting 9 (
Tg
Vps9), has guanine nucleotide exchange factor (GEF) activity towards Rab5a and is crucial for sorting of proteins destined to secretory organelles. Our results illuminate features of
Tg
Vps9 protein as a key trafficking facilitator that regulates protein maturation, secretory organelle formation and secretion, thereby ensuring a primary role in host infection by
T. gondii
. |
---|---|
AbstractList | Accurate sorting of proteins to the three types of parasite-specific secretory organelles namely rhoptry, microneme and dense granule in
Toxoplasma gondii
is crucial for successful host cell invasion by this obligate intracellular parasite. Despite its tiny body architecture and limited trafficking machinery,
T. gondii
relies heavily on transport of vesicles containing proteins, lipids and important virulence-like factors that are delivered to these secretory organelles. However, our understanding on how trafficking of vesicles operates in the parasite is still limited. Here, we show that the
T. gondii
vacuolar protein sorting 9 (
Tg
Vps9), has guanine nucleotide exchange factor (GEF) activity towards Rab5a and is crucial for sorting of proteins destined to secretory organelles. Our results illuminate features of
Tg
Vps9 protein as a key trafficking facilitator that regulates protein maturation, secretory organelle formation and secretion, thereby ensuring a primary role in host infection by
T. gondii
. Abstract Accurate sorting of proteins to the three types of parasite-specific secretory organelles namely rhoptry, microneme and dense granule in Toxoplasma gondii is crucial for successful host cell invasion by this obligate intracellular parasite. Despite its tiny body architecture and limited trafficking machinery, T. gondii relies heavily on transport of vesicles containing proteins, lipids and important virulence-like factors that are delivered to these secretory organelles. However, our understanding on how trafficking of vesicles operates in the parasite is still limited. Here, we show that the T. gondii vacuolar protein sorting 9 ( Tg Vps9), has guanine nucleotide exchange factor (GEF) activity towards Rab5a and is crucial for sorting of proteins destined to secretory organelles. Our results illuminate features of Tg Vps9 protein as a key trafficking facilitator that regulates protein maturation, secretory organelle formation and secretion, thereby ensuring a primary role in host infection by T. gondii . Accurate sorting of proteins to the three types of parasite-specific secretory organelles namely rhoptry, microneme and dense granule in Toxoplasma gondii is crucial for successful host cell invasion by this obligate intracellular parasite. Despite its tiny body architecture and limited trafficking machinery, T. gondii relies heavily on transport of vesicles containing proteins, lipids and important virulence-like factors that are delivered to these secretory organelles. However, our understanding on how trafficking of vesicles operates in the parasite is still limited. Here, we show that the T. gondii vacuolar protein sorting 9 (TgVps9), has guanine nucleotide exchange factor (GEF) activity towards Rab5a and is crucial for sorting of proteins destined to secretory organelles. Our results illuminate features of TgVps9 protein as a key trafficking facilitator that regulates protein maturation, secretory organelle formation and secretion, thereby ensuring a primary role in host infection by T. gondii. Accurate sorting of proteins to the three types of parasite-specific secretory organelles namely rhoptry, microneme and dense granule in Toxoplasma gondii is crucial for successful host cell invasion by this obligate intracellular parasite. Despite its tiny body architecture and limited trafficking machinery, T. gondii relies heavily on transport of vesicles containing proteins, lipids and important virulence-like factors that are delivered to these secretory organelles. However, our understanding on how trafficking of vesicles operates in the parasite is still limited. Here, we show that the T. gondii vacuolar protein sorting 9 (TgVps9), has guanine nucleotide exchange factor (GEF) activity towards Rab5a and is crucial for sorting of proteins destined to secretory organelles. Our results illuminate features of TgVps9 protein as a key trafficking facilitator that regulates protein maturation, secretory organelle formation and secretion, thereby ensuring a primary role in host infection by T. gondii. Toxoplasma gondii is an important food and waterborne pathogen causing toxoplasmosis, a usually mild disease in immunocompetent humans that can turn into a major threat in immunocompromised patients and during primary infection of pregnant woman. T. gondii is a member of the Apicomplexa, a phylum of numerous medically important parasites causing life-threatening diseases in human and animals worldwide. The phylum is typified by specific secretory organelles called rhoptries, micronemes and dense granules that are essential for host cell invasion and host pathway modulation. In Toxoplasma, rhoptries contain two groups, termed rhoptry (ROP) and rhoptry neck (RON), of effector proteins some of which are virulence factors; whereas micronemes secrete MIC proteins that are involved in parasite gliding, host cell attachment and invasion 1,2. After invasion, dense granules discharge GRA proteins involved in parasitophorous vacuole (PV) formation and in hijacking host cell gene expression and metabolism 3. Despite having a single cell architecture, the parasite relies on active and abundant vesicle and protein trafficking. T. gondii and likely all Apicomplexa have reutilized classical endosomal and endocytic trafficking pathways more typical of higher eukaryotes towards building specialized secretory organelles that release parasite effectors to interplay with host cell signaling pathways as a way to take control over host immunity and ultimately to promote long-term parasitism 4–8. It is now well established that apicomplexan parasites operate an unconventional endosome-like system (ELC) to traffic proteins from the Golgi apparatus to rhoptries and micronemes 6–8. However, the mechanisms involved in endosome-like vesicle formation and delivery to the aforementioned organelles in general remain elusive. In mammalian cells, the endosomal system is used for the uptake of plasma membrane-associated components, which after passage through Rab5-positive early endosomes (EE) enter either Rab11A-positive recycling endosomes to return to the plasma membrane, or Rab7-positive late endosomes to be delivered to lysosomes (LE) 9 . |
ArticleNumber | 38842 |
Author | Hakimi, Mohamed-Ali Sakura, Takaya Bousquet, Hugo Sindikubwabo, Fabien Tomavo, Stanislas Langsley, Gordon Oesterlin, Lena K. Slomianny, Christian |
Author_xml | – sequence: 1 givenname: Takaya surname: Sakura fullname: Sakura, Takaya organization: Laboratory of Cellular and Molecular Biology of Toxoplasma, Université de Lille, Institut Pasteur de Lille, Center for Infection and Immunity of Lille, INSERM U 1019, CNRS UMR 8204 – sequence: 2 givenname: Fabien surname: Sindikubwabo fullname: Sindikubwabo, Fabien organization: Institute for Advanced Biosciences (IAB), INSERM U1209, CNRS UMR5309, Université Grenoble Alpes – sequence: 3 givenname: Lena K. surname: Oesterlin fullname: Oesterlin, Lena K. organization: Institut Curie, PSL Research University, CNRS UMR144, Molecular Mechanisms of Intracellular Transport Group – sequence: 4 givenname: Hugo surname: Bousquet fullname: Bousquet, Hugo organization: Institut Curie, PSL Research University, CNRS UMR144, Molecular Mechanisms of Intracellular Transport Group – sequence: 5 givenname: Christian surname: Slomianny fullname: Slomianny, Christian organization: Laboratory of Cell Physiology, INSERM U 1003, Université de Lille – sequence: 6 givenname: Mohamed-Ali surname: Hakimi fullname: Hakimi, Mohamed-Ali organization: Institute for Advanced Biosciences (IAB), INSERM U1209, CNRS UMR5309, Université Grenoble Alpes – sequence: 7 givenname: Gordon surname: Langsley fullname: Langsley, Gordon organization: Laboratoire de Biologie Cellulaire Comparative des Apicomplexes, INSERM U1016, CNRS UMR8104, Institut Cochin – sequence: 8 givenname: Stanislas surname: Tomavo fullname: Tomavo, Stanislas organization: Laboratory of Cellular and Molecular Biology of Toxoplasma, Université de Lille, Institut Pasteur de Lille, Center for Infection and Immunity of Lille, INSERM U 1019, CNRS UMR 8204 |
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26 J Rink (BFsrep38842_CR15) 2005; 122 H Stenmark (BFsrep38842_CR16) 2009; 10 JP Luzio (BFsrep38842_CR9) 2014; 6 JY Pan (BFsrep38842_CR19) 1995; 270 H Hama (BFsrep38842_CR23) 1999; 274 BFsrep38842_CR6 LO Sangaré (BFsrep38842_CR7) 2016; 7 MS Breinich (BFsrep38842_CR11) 2009; 19 SD Brydges (BFsrep38842_CR27) 2008; 100 MS Pieperhoff (BFsrep38842_CR12) 2013; 8 AL Paulsel (BFsrep38842_CR32) 2013; 288 DS Carney (BFsrep38842_CR22) 2006; 16 BFsrep38842_CR8 HJK Balderhaar (BFsrep38842_CR14) 2013; 126 |
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Snippet | Accurate sorting of proteins to the three types of parasite-specific secretory organelles namely rhoptry, microneme and dense granule in
Toxoplasma gondii
is... Accurate sorting of proteins to the three types of parasite-specific secretory organelles namely rhoptry, microneme and dense granule in Toxoplasma gondii is... Abstract Accurate sorting of proteins to the three types of parasite-specific secretory organelles namely rhoptry, microneme and dense granule in Toxoplasma... |
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SubjectTerms | 14 14/19 14/28 631/326/417 692/699/255 82 82/29 82/80 Biochemistry, Molecular Biology Cell Line Guanine Guanine nucleotide exchange factor Humanities and Social Sciences Humans Life Sciences Lipids multidisciplinary Organelles Parasites Protein transport Proteins Protozoa Protozoan Proteins - genetics Protozoan Proteins - metabolism Science Secretory Pathway Toxoplasma - genetics Toxoplasma - metabolism Toxoplasma - pathogenicity Toxoplasmosis - genetics Toxoplasmosis - metabolism Transport Vesicles - genetics Transport Vesicles - metabolism Vesicles Vesicular Transport Proteins - genetics Vesicular Transport Proteins - metabolism Virulence |
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Title | A Critical Role for Toxoplasma gondii Vacuolar Protein Sorting VPS9 in Secretory Organelle Biogenesis and Host Infection |
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