Concerted Action of Two Formins in Gliding Motility and Host Cell Invasion by
The invasive forms of apicomplexan parasites share a conserved form of gliding motility that powers parasite migration across biological barriers, host cell invasion and egress from infected cells. Previous studies have established that the duration and direction of gliding motility are determined by actin polymerization; however, regulators of actin dynamics in apicomplexans remain poorly characterized. In the absence of a complete ARP2/3 complex, the formin homology 2 domain containing proteins and the accessory protein profilin are presumed to orchestrate actin polymerization during host cell invasion. Here, we have undertaken the biochemical and functional characterization of two Toxoplasma gondii formins and established that they act in concert as actin nucleators during invasion. The importance of TgFRM1 for parasite motility has been assessed by conditional gene disruption. The contribution of each formin individually and jointly was revealed by an approach based upon the expression of dominant mutants with modified FH2 domains impaired in actin binding but still able to dimerize with their respective endogenous formin. These mutated FH2 domains were fused to the ligand-controlled destabilization domain (DD-FKBP) to achieve conditional expression. This strategy proved unique in identifying the non-redundant and critical roles of both formins in invasion. These findings provide new insights into how controlled actin polymerization drives the directional movement required for productive penetration of parasites into host cells.
Vyšlo v časopise:
Concerted Action of Two Formins in Gliding Motility and Host Cell Invasion by. PLoS Pathog 6(10): e32767. doi:10.1371/journal.ppat.1001132
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.ppat.1001132
Souhrn
The invasive forms of apicomplexan parasites share a conserved form of gliding motility that powers parasite migration across biological barriers, host cell invasion and egress from infected cells. Previous studies have established that the duration and direction of gliding motility are determined by actin polymerization; however, regulators of actin dynamics in apicomplexans remain poorly characterized. In the absence of a complete ARP2/3 complex, the formin homology 2 domain containing proteins and the accessory protein profilin are presumed to orchestrate actin polymerization during host cell invasion. Here, we have undertaken the biochemical and functional characterization of two Toxoplasma gondii formins and established that they act in concert as actin nucleators during invasion. The importance of TgFRM1 for parasite motility has been assessed by conditional gene disruption. The contribution of each formin individually and jointly was revealed by an approach based upon the expression of dominant mutants with modified FH2 domains impaired in actin binding but still able to dimerize with their respective endogenous formin. These mutated FH2 domains were fused to the ligand-controlled destabilization domain (DD-FKBP) to achieve conditional expression. This strategy proved unique in identifying the non-redundant and critical roles of both formins in invasion. These findings provide new insights into how controlled actin polymerization drives the directional movement required for productive penetration of parasites into host cells.
Zdroje
1. DaherW
Soldati-FavreD
2009 Mechanisms controlling glideosome function in apicomplexans. Curr Opin Microbiol 12 408 414
2. DobrowolskiJM
SibleyLD
1996 Toxoplasma invasion of mammalian cells is powered by the actin cytoskeleton of the parasite. Cell 84 933 939
3. WetzelDM
HakanssonS
HuK
RoosD
SibleyLD
2003 Actin filament polymerization regulates gliding motility by apicomplexan parasites. Mol Biol Cell 14 396 406
4. MeissnerM
SchluterD
SoldatiD
2002 Role of Toxoplasma gondii myosin A in powering parasite gliding and host cell invasion. Science 298 837 840
5. AllenML
DobrowolskiJM
MullerH
SibleyLD
MansourTE
1997 Cloning and characterization of actin depolymerizing factor from Toxoplasma gondii. Mol Biochem Parasitol 88 43 52
6. SahooN
BeattyW
HeuserJ
SeptD
SibleyLD
2006 Unusual kinetic and structural properties control rapid assembly and turnover of actin in the parasite Toxoplasma gondii. Mol Biol Cell 17 895 906
7. SchmitzS
GraingerM
HowellS
CalderLJ
GaebM
2005 Malaria parasite actin filaments are very short. J Mol Biol 349 113 125
8. SchulerH
MuellerAK
MatuschewskiK
2005 Unusual properties of Plasmodium falciparum actin: new insights into microfilament dynamics of apicomplexan parasites. FEBS Lett 579 655 660
9. PaulAS
PollardTD
2009 Review of the mechanism of processive actin filament elongation by formins. Cell Motil Cytoskeleton 66 606 617
10. GordonJL
SibleyLD
2005 Comparative genome analysis reveals a conserved family of actin-like proteins in apicomplexan parasites. BMC Genomics 6 179
11. BaumJ
PapenfussAT
BaumB
SpeedTP
CowmanAF
2006 Regulation of apicomplexan actin-based motility. Nat Rev Microbiol 4 621 628
12. BaumJ
TonkinCJ
PaulAS
RugM
SmithBJ
2008 A malaria parasite formin regulates actin polymerization and localizes to the parasite-erythrocyte moving junction during invasion. Cell Host Microbe 3 188 198
13. PlattnerF
YarovinskyF
RomeroS
DidryD
CarlierMF
2008 Toxoplasma profilin is essential for host cell invasion and TLR11-dependent induction of an interleukin-12 response. Cell Host Microbe 3 77 87
14. GoodeBL
EckMJ
2007 Mechanism and function of formins in the control of actin assembly. Annu Rev Biochem 76 593 627
15. PruyneD
EvangelistaM
YangC
BiE
ZigmondS
2002 Role of formins in actin assembly: nucleation and barbed-end association. Science 297 612 615
16. SagotI
KleeSK
PellmanD
2002 Yeast formins regulate cell polarity by controlling the assembly of actin cables. Nat Cell Biol 4 42 50
17. BushellES
EckerA
SchlegelmilchT
GouldingD
DouganG
2009 Paternal effect of the nuclear formin-like protein MISFIT on Plasmodium development in the mosquito vector. PLoS Pathog 5 e1000539
18. MazumdarJ
EHW
MasekK
CAH
StriepenB
2006 Apicoplast fatty acid synthesis is essential for organelle biogenesis and parasite survival in Toxoplasma gondii. Proc Natl Acad Sci U S A 103 13192 13197
19. WichroskiMJ
MeltonJA
DonahueCG
TwetenRK
WardGE
2002 Clostridium septicum alpha-toxin is active against the parasitic protozoan Toxoplasma gondii and targets members of the SAG family of glycosylphosphatidylinositol-anchored surface proteins. Infect Immun 70 4353 4361
20. BozdechZ
LlinasM
PulliamBL
WongED
ZhuJ
2003 The transcriptome of the intraerythrocytic developmental cycle of Plasmodium falciparum. PLoS Biol 1 E5
21. HuynhMH
CarruthersVB
2006 Toxoplasma MIC2 is a major determinant of invasion and virulence. PLoS Pathog 2 e84
22. PringM
EvangelistaM
BooneC
YangC
ZigmondSH
2003 Mechanism of formin-induced nucleation of actin filaments. Biochemistry 42 486 496
23. RomeroS
Le ClaincheC
DidryD
EgileC
PantaloniD
2004 Formin is a processive motor that requires profilin to accelerate actin assembly and associated ATP hydrolysis. Cell 119 419 429
24. OtomoT
TomchickDR
OtomoC
PanchalSC
MachiusM
2005 Structural basis of actin filament nucleation and processive capping by a formin homology 2 domain. Nature 433 488 494
25. XuY
MoseleyJB
SagotI
PoyF
PellmanD
2004 Crystal structures of a Formin Homology-2 domain reveal a tethered dimer architecture. Cell 116 711 723
26. KovarDR
PollardTD
2004 Insertional assembly of actin filament barbed ends in association with formins produces piconewton forces. Proc Natl Acad Sci U S A 101 14725 14730
27. CopelandJW
CopelandSJ
TreismanR
2004 Homo-oligomerization is essential for F-actin assembly by the formin family FH2 domain. J Biol Chem 279 50250 50256
28. BanaszynskiLA
ChenLC
Maynard-SmithLA
OoiAG
WandlessTJ
2006 A rapid, reversible, and tunable method to regulate protein function in living cells using synthetic small molecules. Cell 126 995 1004
29. Herm-GotzA
Agop-NersesianC
MunterS
GrimleyJS
WandlessTJ
2007 Rapid control of protein level in the apicomplexan Toxoplasma gondii. Nat Methods 4 1003 1005
30. HarrisES
RouillerI
HaneinD
HiggsHN
2006 Mechanistic differences in actin bundling activity of two mammalian formins, FRL1 and mDia2. J Biol Chem 281 14383 14392
31. HakanssonS
MorisakiH
HeuserJ
SibleyLD
1999 Time-lapse video microscopy of gliding motility in Toxoplasma gondii reveals a novel, biphasic mechanism of cell locomotion. Mol Biol Cell 10 3539 3547
32. KovarDR
2006 Molecular details of formin-mediated actin assembly. Curr Opin Cell Biol 18 11 17
33. ChalkiaD
NikolaidisN
MakalowskiW
KleinJ
NeiM
2008 Origins and evolution of the formin multigene family that is involved in the formation of actin filaments. Mol Biol Evol 25 2717 2733
34. KursulaI
KursulaP
GanterM
PanjikarS
MatuschewskiK
2008 Structural basis for parasite-specific functions of the divergent profilin of Plasmodium falciparum. Structure 16 1638 1648
35. HelferE
NevalainenEM
NaumanenP
RomeroS
DidryD
2006 Mammalian twinfilin sequesters ADP-G-actin and caps filament barbed ends: implications in motility. EMBO J 25 1184 1195
36. DonaldRG
CarterD
UllmanB
RoosDS
1996 Insertional tagging, cloning, and expression of the Toxoplasma gondii hypoxanthine-xanthine-guanine phosphoribosyltransferase gene. Use as a selectable marker for stable transformation. J Biol Chem 271 14010 14019
37. KimK
SoldatiD
BoothroydJC
1993 Gene replacement in Toxoplasma gondii with chloramphenicol acetyltransferase as selectable marker. Science 262 911 914
38. MeissnerM
BrechtS
BujardH
SoldatiD
2001 Modulation of myosin A expression by a newly established tetracycline repressor-based inducible system in Toxoplasma gondii. Nucleic Acids Res 29 E115
39. DonaldRG
RoosDS
1993 Stable molecular transformation of Toxoplasma gondii: a selectable dihydrofolate reductase-thymidylate synthase marker based on drug-resistance mutations in malaria. Proc Natl Acad Sci U S A 90 11703 11707
40. AugustijnKD
KleemannR
ThompsonJ
KooistraT
CrawfordCE
2007 Functional characterization of the Plasmodium falciparum and P. berghei homologues of macrophage migration inhibitory factor. Infect Immun 75 1116 1128
41. de Koning-WardTF
JanseCJ
WatersAP
2000 The development of genetic tools for dissecting the biology of malaria parasites. Annu Rev Microbiol 54 157 185
42. WatersAP
ThomasAW
van DijkMR
JanseCJ
1997 Transfection of malaria parasites. Methods 13 134 147
43. BillkerO
DechampsS
TewariR
WenigG
Franke-FayardB
2004 Calcium and a calcium-dependent protein kinase regulate gamete formation and mosquito transmission in a malaria parasite. Cell 117 503 514
44. MoseleyJB
MaitiS
GoodeBL
2006 Formin proteins: purification and measurement of effects on actin assembly. Methods Enzymol 406 215 234
45. DingM
ClaytonC
SoldatiD
2000 Toxoplasma gondii catalase: are there peroxisomes in toxoplasma? J Cell Sci 113 Pt 13 2409 2419
46. MannT
BeckersC
2001 Characterization of the subpellicular network, a filamentous membrane skeletal component in the parasite Toxoplasma gondii. Mol Biochem Parasitol 115 257 268
47. HettmannC
HermA
GeiterA
FrankB
SchwarzE
2000 A dibasic motif in the tail of a class XIV apicomplexan myosin is an essential determinant of plasma membrane localization. Mol Biol Cell 11 1385 1400
48. HertzogM
van HeijenoortC
DidryD
GaudierM
CoutantJ
2004 The beta-thymosin/WH2 domain; structural basis for the switch from inhibition to promotion of actin assembly. Cell 117 611 623
49. BlumenscheinTM
FriedrichN
ChildsRA
SaourosS
CarpenterEP
2007 Atomic resolution insight into host cell recognition by Toxoplasma gondii. Embo J 26 2808 2820
Štítky
Hygiena a epidemiológia Infekčné lekárstvo LaboratóriumČlánok vyšiel v časopise
PLOS Pathogens
2010 Číslo 10
- Očkování proti virové hemoragické horečce Ebola experimentální vakcínou rVSVDG-ZEBOV-GP
- Parazitičtí červi v terapii Crohnovy choroby a dalších zánětlivých autoimunitních onemocnění
- Koronavirus hýbe světem: Víte jak se chránit a jak postupovat v případě podezření?
Najčítanejšie v tomto čísle
- Retroviral RNA Dimerization and Packaging: The What, How, When, Where, and Why
- Viral Replication Rate Regulates Clinical Outcome and CD8 T Cell Responses during Highly Pathogenic H5N1 Influenza Virus Infection in Mice
- Antimicrobial Peptides: Primeval Molecules or Future Drugs?
- Crystal Structure of DotD: Insights into the Relationship between Type IVB and Type II/III Secretion Systems