scholarly journals Faculty Opinions recommendation of Actin and an unconventional myosin motor, TgMyoF, control the organization and dynamics of the endomembrane network in Toxoplasma gondii.

Author(s):  
Markus Engstler ◽  
Brooke Morriswood
2021 ◽  
Vol 17 (2) ◽  
pp. e1008787
Author(s):  
Romain Carmeille ◽  
Porfirio Schiano Lomoriello ◽  
Parvathi M. Devarakonda ◽  
Jacob A. Kellermeier ◽  
Aoife T. Heaslip

Toxoplasma gondii is an obligate intracellular parasite that relies on three distinct secretory organelles, the micronemes, rhoptries, and dense granules, for parasite survival and disease pathogenesis. Secretory proteins destined for these organelles are synthesized in the endoplasmic reticulum (ER) and sequentially trafficked through a highly polarized endomembrane network that consists of the Golgi and multiple post-Golgi compartments. Currently, little is known about how the parasite cytoskeleton controls the positioning of the organelles in this pathway, or how vesicular cargo is trafficked between organelles. Here we show that F-actin and an unconventional myosin motor, TgMyoF, control the dynamics and organization of the organelles in the secretory pathway, specifically ER tubule movement, apical positioning of the Golgi and post-Golgi compartments, apical positioning of the rhoptries, and finally, the directed transport of Rab6-positive and Rop1-positive vesicles. Thus, this study identifies TgMyoF and actin as the key cytoskeletal components that organize the endomembrane system in T. gondii.


2020 ◽  
Author(s):  
Romain Carmeille ◽  
Aoife T. Heaslip

AbstractToxoplasma gondii is an obligate intracellular parasite that relies on three distinct secretory organelles, the micronemes, rhoptries and dense granules, for parasite survival and disease pathogenesis. Secretory proteins destined for these organelles are synthesized in the endoplasmic reticulum (ER) and sequentially trafficked through a highly polarized endomembrane network that consists of the Golgi and multiple post-Golgi compartments. Currently, little is known about how the parasite cytoskeleton controls the positioning of the organelles in this pathway, or how vesicular cargo is trafficked between organelles. Here we show that F-actin and an unconventional myosin motor, TgMyoF, control the dynamics and organization of the organelles in the secretory pathway, specifically ER tubule movement, apical positioning of the Golgi and post-Golgi compartments, apical positioning of the rhoptries and finally, the directed transport of Rab6-positive and Rop1-positive vesicles. Thus, this study identifies TgMyoF and actin as the key cytoskeletal components that organize the endomembrane system in T. gondii.Author SummaryEndomembrane trafficking is a vital cellular process in all eukaryotic cells. In most cases the molecular motors myosin, kinesin and dynein transport cargo including vesicles, organelles and transcripts along actin and microtubule filaments in a manner analogous to a train moving on its tracks. For the unicellular eukaryote Toxoplasma gondii, the accurate trafficking of proteins through the endomembrane system is vital for parasite survival and pathogenicity. However, the mechanisms of cargo transport in this parasite are poorly understood. In this study, we fluorescently labeled multiple endomembrane organelles and imaged their movements using live cell microscopy. We demonstrate that filamentous actin and an unconventional myosin motor named TgMyoF control both the positioning of organelles in this pathway and the movement of transport vesicles throughout the parasite cytosol. This data provides new insight into the mechanisms of cargo transport in this important pathogen and expands are understanding of the biological roles of actin in the intracellular phase of the parasite’s growth cycle.


mSphere ◽  
2021 ◽  
Vol 6 (3) ◽  
Author(s):  
Pramod K. Rompikuntal ◽  
Robyn S. Kent ◽  
Ian T. Foe ◽  
Bin Deng ◽  
Matthew Bogyo ◽  
...  

ABSTRACT Toxoplasma gondii is a widespread apicomplexan parasite that causes severe disease in immunocompromised individuals and the developing fetus. Like other apicomplexans, T. gondii uses an unusual form of substrate-dependent gliding motility to invade cells of its hosts and to disseminate throughout the body during infection. It is well established that a myosin motor consisting of a class XIVa heavy chain (TgMyoA) and two light chains (TgMLC1 and TgELC1/2) plays an important role in parasite motility. The ability of the motor to generate force at the parasite periphery is thought to be reliant upon its anchoring and immobilization within a peripheral membrane-bound compartment, the inner membrane complex (IMC). The motor does not insert into the IMC directly; rather, this interaction is believed to be mediated by the binding of TgMLC1 to the IMC-anchored protein, TgGAP45. Therefore, the binding of TgMLC1 to TgGAP45 is considered a key element in the force transduction machinery of the parasite. TgMLC1 is palmitoylated, and we show here that palmitoylation occurs on two N-terminal cysteine residues, C8 and C11. Mutations that block TgMLC1 palmitoylation completely abrogate the binding of TgMLC1 to TgGAP45. Surprisingly, the loss of TgMLC1 binding to TgGAP45 in these mutant parasites has little effect on their ability to initiate or sustain movement. These results question a key tenet of the current model of apicomplexan motility and suggest that our understanding of gliding motility in this important group of human and animal pathogens is not yet complete. IMPORTANCE Gliding motility plays a central role in the life cycle of T. gondii and other apicomplexan parasites. The myosin motor thought to power motility is essential for virulence but distinctly different from the myosins found in humans. Consequently, an understanding of the mechanism(s) underlying parasite motility and the role played by this unusual myosin may reveal points of vulnerability that can be targeted for disease prevention or treatment. We show here that mutations that uncouple the motor from what is thought to be a key structural component of the motility machinery have little impact on parasite motility. This finding runs counter to predictions of the current, widely held “linear motor” model of motility, highlighting the need for further studies to fully understand how apicomplexan parasites generate the forces necessary to move into, out of, and between cells of the hosts they infect.


2011 ◽  
Vol 39 (5) ◽  
pp. 1115-1119 ◽  
Author(s):  
Lisa M. Bond ◽  
Hemma Brandstaetter ◽  
James R. Sellers ◽  
John Kendrick-Jones ◽  
Folma Buss

In eukaryotes, the final steps in both the regulated and constitutive secretory pathways can be divided into four distinct stages: (i) the ‘approach’ of secretory vesicles/granules to the PM (plasma membrane), (ii) the ‘docking’ of these vesicles/granules at the membrane itself, (iii) the ‘priming’ of the secretory vesicles/granules for the fusion process, and, finally, (iv) the ‘fusion’ of vesicular/granular membranes with the PM to permit content release from the cell. Recent work indicates that non-muscle myosin II and the unconventional myosin motor proteins in classes 1c/1e, Va and VI are specifically involved in these final stages of secretion. In the present review, we examine the roles of these myosins in these stages of the secretory pathway and the implications of their roles for an enhanced understanding of secretion in general.


eLife ◽  
2015 ◽  
Vol 4 ◽  
Author(s):  
Teresa Nicolson

Two forms of an unconventional myosin motor protein have separate functions in the growth and maintenance of hair bundles in auditory hair cells.


2015 ◽  
Vol 11 (11) ◽  
pp. e1005268 ◽  
Author(s):  
Rajshekhar Y. Gaji ◽  
Derrick E. Johnson ◽  
Moritz Treeck ◽  
Mu Wang ◽  
Andy Hudmon ◽  
...  

2012 ◽  
Vol 154 (6) ◽  
pp. 251-255 ◽  
Author(s):  
F. C. Frey ◽  
E. A. Berger-Schoch ◽  
C. D. Herrmann ◽  
G. Schares ◽  
N. Müller ◽  
...  
Keyword(s):  

2019 ◽  
Vol 12 (4) ◽  
pp. 485-494
Author(s):  
Joaquim C. Rossini ◽  
Carolina S. Lopes ◽  
Fernanda P. Dirscherl ◽  
Deise A. O. Silva ◽  
José R. Mineo

2014 ◽  
Vol 14 (02) ◽  
pp. 101-106
Author(s):  
C. Feiterna-Sperling
Keyword(s):  

ZusammenfassungBei einer primären Toxoplasmose in der Schwangerschaft besteht für den Fetus das Risiko einer konnatalen Infektion durch diaplazentare Transmission von Toxoplasma gondii. Das Risiko einer fetalen Infektion nimmt dabei mit der Schwangerschaftsdauer zu, während die Schwere der Symptomatik mit zunehmendem Gestationsalter abnimmt. Bei den meisten infizierten Neugeborenen finden sich klinisch inapparente Infektionen, aber auch postnatal unauffällige Kinder sind einem Risiko von späteren Folgeschäden ausgesetzt. Neben neurologischen Entwicklungsstörungen ist vor allem das Risiko einer Retinochoroiditis von Bedeutung, die sich auch erst im späteren Leben manifestieren kann. Eine frühzeitige Erkennung einer Primärinfektion in der Schwangerschaft ist Voraussetzung, um durch eine frühzeitige anti-parasitäre Therapie, das Risiko einer fetalen Schädigung zu reduzieren. Durch eine post-natale Therapie kann vermutlich zusätzlich das Risiko der Langzeitkomplikationen gesenkt werden. Neugeborene mit Verdacht auf eine konnatale Toxoplasmose müssen sorgfältig hinsichtlich einer konnatalen Infektion untersucht werden und Säuglinge mit einer gesicherten Infektion benötigen langfristige Nachuntersuchungen hinsichtlich möglicher Spätschäden, insbesondere der Manifestation einer Retinochoroiditis.


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