Structural basis of the polar tube invasion machinery from microsporidia parasites
Project Number7R01AI147131-06
Former Number5R01AI147131-05
Contact PI/Project LeaderBHABHA, GIRA
Awardee OrganizationJOHNS HOPKINS UNIVERSITY
Description
Abstract Text
Project Summary/Abstract
Microsporidia are unicellular, fungal parasites with a wide host-range, from insects to humans. They are
emerging pathogens, classified as NIAID Category B opportunistic pathogens, and cause microsporidiosis in
immunocompromised patients. To gain entry into a target cell, microsporidia employ a remarkably unique and
specialized harpoon-like invasion machinery called the polar tube, which is conserved among microsporidial
species. While initially coiled neatly within the spore of the parasite, infection of a new cell begins with the rapid
extrusion of the polar tube from the spore on a fast timescale (< 2s), which anchors the spore to the host cell.
After it has been fired, the polar tube is thought to act as a conduit for the transfer of the infectious
“sporoplasm” into the target cell, where replication can begin. Early work has yielded global insights into this
process, and the molecular and structural underpinnings of the invasion process are ripe for exploration with
modern techniques, such as cryo electron microscopy. This work aims to address fundamental questions and
paradoxes in our understanding of the microsporidial polar tube machinery and how it drives invasion into host
cells. We will use a combined bottom-up (structural biology, biochemistry and other in vitro techniques on
purified proteins) and top-down (in vivo light microscopy, electron tomography) approach; the intersection of
these approaches will allow us to unravel the mechanistic biology of this unique invasion process. Here we
focus on three human pathogens: Anncaliia algerae, Encephalitozoon cuniculi and Encephalitozoon hellem.
The specific aims are 1) To characterize the dynamics of polar tube firing and movement of sporoplasm
through the tube using high-speed optical microscopy, and to comprehensively define the composition of the
polar tube using mass spectrometry; 2) To biochemically and structurally characterize the individual protein
components of the polar tube organelle using X-ray crystallography, single particle cryo electron microscopy
and protein-protein interaction assays; 3) To elucidate the overall architecture and packing of the polar tube in
the spore using structural cell biology techniques such as serial block face scanning electron microscopy
(SBFSEM) and cryo focused ion beam scanning electron microscopy (cryo FIB-SEM) followed by cryo electron
tomography (cryo ET).
Public Health Relevance Statement
Project Narrative
Microsporidia are unicellular, fungal parasites with a wide host-range, from insects to humans; they are
emerging pathogens, classified as NIAID Category B opportunistic pathogens, and cause microsporidiosis in
immunocompromised patients. To gain entry into a target cell, microsporidia employ a remarkably unique and
specialized harpoon-like invasion machine called the polar tube, which is conserved among microsporidial
species. Here we will focus on understanding the mechanism by which microsporidial parasites use this unique
organelle to initiate infection, which may provide broader insights into infection mechanisms used by other
eukaryotic parasites.
NIH Spending Category
No NIH Spending Category available.
Project Terms
3-DimensionalAcquired Immunodeficiency SyndromeAddressAnimalsArchitectureBiochemicalBiochemistryBiological AssayBiologyBiophysicsBombyxCategoriesCellsCellular biologyCiliaClassificationComplexCryo-electron tomographyCryoelectron MicroscopyDataDiseaseEncephalitozoon cuniculiEncephalitozoon hellemEnvironmentFaceFarmFishesFluorescent DyesFreezingGrowthHumanImageImmunocompromised HostIn SituIn VitroIndividualInfectionInsectaInvadedIonsLightMass Spectrum AnalysisMicroscopyMicrosporidiaMicrosporidiosisMicrotubulesModernizationMolecularMolecular ConformationMovementNamesNational Institute of Allergy and Infectious DiseaseOpticsOrganellesParasitesPatientsProcessProtein SubunitsProteinsProteomeReproduction sporesResolutionSamplingScanning Electron MicroscopySequence HomologySideSpeedStructureTechniquesThinnessTubeVisualizationWorkX-Ray Crystallographyburden of illnesselectron tomographyemerging pathogenexperimental studygenetic manipulationhuman pathogenin vivoinsightlight microscopylightspeedmortalityopportunistic pathogenorgan transplant recipientparticlepathogenprotein complexprotein protein interactionprotein purificationreconstructionstructural biology
National Institute of Allergy and Infectious Diseases
CFDA Code
855
DUNS Number
001910777
UEI
FTMTDMBR29C7
Project Start Date
01-March-2020
Project End Date
28-February-2026
Budget Start Date
01-April-2024
Budget End Date
28-February-2026
Project Funding Information for 2024
Total Funding
$530,241
Direct Costs
$323,811
Indirect Costs
$206,430
Year
Funding IC
FY Total Cost by IC
2024
National Institute of Allergy and Infectious Diseases
$530,241
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 7R01AI147131-06
Publications
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Outcomes
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Clinical Studies
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History
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