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 inScientific reports Vol. 6; no. 1; p. 38842
Main Authors Sakura, Takaya, Sindikubwabo, Fabien, Oesterlin, Lena K., Bousquet, Hugo, Slomianny, Christian, Hakimi, Mohamed-Ali, Langsley, Gordon, Tomavo, Stanislas
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 14.12.2016
Nature Publishing Group
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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
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  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
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  givenname: Fabien
  surname: Sindikubwabo
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  givenname: Lena K.
  surname: Oesterlin
  fullname: Oesterlin, Lena K.
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  givenname: Hugo
  surname: Bousquet
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  givenname: Mohamed-Ali
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  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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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
URI https://link.springer.com/article/10.1038/srep38842
https://www.ncbi.nlm.nih.gov/pubmed/27966671
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https://search.proquest.com/docview/1852679113
https://inserm.hal.science/inserm-01472213
https://pubmed.ncbi.nlm.nih.gov/PMC5155228
Volume 6
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