Microsporidian Spore/Sporoplasm Dynactin in Spraguea

2001 ◽  
Vol 201 (2) ◽  
pp. 245-246 ◽  
Author(s):  
Earl Weidner
Keyword(s):  
1997 ◽  
Vol 64 (1) ◽  
pp. 1-5 ◽  
Author(s):  
Elisa Bigliardi ◽  
Simonetta Gatti ◽  
Luciano Sacchi

1985 ◽  
Vol 100 (6) ◽  
pp. 1834-1838 ◽  
Author(s):  
J Pleshinger ◽  
E Weidner

The microsporidian spore extrusion apparatus activates with a calcium influx from Spraguea lophii spore wall/plasma membrane; this influx requires preconditioning with an extrasporular shift in medium pH to the alkaline in the presence of the polyanions mucin or polyglutamate. Undischarged S. lophii spores display calcium bound to the wall/plasma membrane with a characteristic calcium-chlorotetracycline fluorescence; this fluorescence declines significantly during spore discharge. S. lophii spores do not discharge when spore wall/plasma membrane calcium is removed with EGTA. Extrasporular mucin or polyglutamate and a pH shift to the alkaline appear to be necessary preconditions for the triggering of the influx of spore wall/plasma membrane-bound 45Ca2+. Ionophore A-23187 also effectively activates spore discharge without other extrasporular polyanions. Micromolar concentrations of the calcium antagonists lanthanum or verapamil prevent spore discharge, and micromolar concentrations of calmodulin inhibitors chlorpromazine and trifluroperazine prevent spore discharge. Calmodulin, visualized with a calmodulin antibody and a peroxidase conjugate, is localized particularly on the plasma membrane and the polaroplast membranes of the extrusion apparatus.


1994 ◽  
Vol 187 (2) ◽  
pp. 255-256 ◽  
Author(s):  
E. Weidner ◽  
S. B. Manale ◽  
S. K. Halonen ◽  
J. W. Lynn

1994 ◽  
Vol 41 (5) ◽  
pp. 464-468 ◽  
Author(s):  
EUGENIO FRIXIONE ◽  
LOURDES RUIZ ◽  
ALBERT H. UNDEEN

1976 ◽  
Vol 71 (1) ◽  
pp. 23-34 ◽  
Author(s):  
E Weidner

The extrusion apparatus of the microsporidian parasitic protozoan Nosema michaelis discharges an invasion (or polar) tube with a velocity suitalbe for piercing cells and injecting infective sporoplasm. The tube is composed of a polar tube protein (PTP) which consists of a single, low molecular weight polypeptide slightly smaller than chymotrypsinogen-A. Assembled PTP tubes resist dissociation in sodium dodecyl sulfate and brief exposures in media at extreme ends of the pH range; however, the tubes are reduced by mercaptoethanol and dithiothreitol. When acidified, mercaptoethanol-reduced PTP self-assembles into plastic, two-dimensional monolayers. Dithiothreitol-reduced PTP will not reassemble when acidified. Evidence is presented which indicates that PTP is assembled as a tube within the spore; that the ejected tube has plasticity during sporoplasm passage; and, finally, that the subunits within the tube polymer are bound together, in part, by interprotein disulfide linkages.


1982 ◽  
Vol 93 (3) ◽  
pp. 970-975 ◽  
Author(s):  
E Weidner ◽  
W Byrd

A swelling response by the polaroplast organelle initiated microsporidian invasion tube extrusions by Glugea hertwigi spores. The tumescence was induced by the displacement of internal calcium. Sodium citrate, phosphate, and the calcium ionophore A23187 were effective in initiating polaroplast swelling and spore discharge; however, the addition of external CaCl2 switched the expanded polaroplasts to a contracted state and blocked spore discharge. Unlike CaCl2, equivalent concentrations of KCl, NaCl, MgCl2, and BaCl2 did not induced polaroplast contraction, and spore discharge was not blocked. 45CaCl2 readily incorporated into spores with expanded polaroplasts; however, little calcium uptake was apparent in spores with contracted polaroplasts. Metallochromic arsenazo III yielded a color spectrum characteristic of the dye-Ca++ complex in the polaroplast region; furthermore, a membrane association with calcium was indicated by strong chlorotetracycline fluorescence within the polaroplast; this fluorescence was extinguished by pretreating spores with ionophore A23187. An association of the membrane with calcium was also indicated by a potassium ferrocyanide-osmium tetroxide technique. All evidence indicates that an internal calcium displacement is an important initial step in the swelling response of the polaroplast organelle.


2011 ◽  
Vol 79 (3) ◽  
pp. 1374-1385 ◽  
Author(s):  
Kaya Ghosh ◽  
Eddie Nieves ◽  
Patrick Keeling ◽  
Jean-Francois Pombert ◽  
Philipp P. Henrich ◽  
...  

ABSTRACTThe microsporidia are a diverse phylum of obligate intracellular parasites that infect all major animal groups and have been recognized as emerging human pathogens for which few chemotherapeutic options currently exist. These organisms infect every tissue and organ system, causing significant pathology, especially in immune-compromised populations. The microsporidian spore employs a unique infection strategy in which its contents are delivered into a host cell via the polar tube, an organelle that lies coiled within the resting spore but erupts with a force sufficient to pierce the plasma membrane of its host cell. Using biochemical and molecular approaches, we have previously identified components of the polar tube and spore wall of the Encephalitozoonidae. In this study, we employed a shotgun proteomic strategy to identify novel structural components of these organelles inEncephalitozoon cuniculi. As a result, a new component of theE. cuniculideveloping spore wall was identified. Surprisingly, using the same approach, a heretofore undescribed filamentous network within the lumen of the parasitophorous vacuole was discovered. This network was also present in the parasitophorous vacuole ofEncephalitozoon hellem. Thus, in addition to further elucidating the molecular composition of seminal organelles and revealing novel diagnostic and therapeutic targets, proteomic analysis-driven approaches exploring the spore may also uncover unknown facets of microsporidian biology.


1995 ◽  
Vol 188 (2) ◽  
pp. 128-135 ◽  
Author(s):  
E. Weidner ◽  
S. B. Manale ◽  
S. K. Halonen ◽  
J. W. Lynn

1993 ◽  
Vol 9 (11) ◽  
pp. 422-424 ◽  
Author(s):  
G.J. Leitch ◽  
G.S. Visvesvara ◽  
Q. He

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