Microsporidian Spore Wall: Ultrastructural Findings on Encephalitozoon hellem Exospore

1996 ◽  
Vol 43 (3) ◽  
pp. 181-186 ◽  
Author(s):  
ELISA BIGLIARDI ◽  
MARIA GLORIA SELMI ◽  
PIETRO LUPETTI ◽  
SILVIA CORONA ◽  
SIMONETTA GATTI ◽  
...  
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.


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.


2006 ◽  
Vol 36 (3) ◽  
pp. 309-318 ◽  
Author(s):  
Isabelle Peuvel-Fanget ◽  
Valérie Polonais ◽  
Damien Brosson ◽  
Catherine Texier ◽  
Lauriane Kuhn ◽  
...  

1984 ◽  
Vol 43 (2) ◽  
pp. 276-277 ◽  
Author(s):  
Jeffrey C. Lord ◽  
Donald W. Wall

2005 ◽  
Vol 247 (1) ◽  
pp. 81-90 ◽  
Author(s):  
Damien Brosson ◽  
Lauriane Kuhn ◽  
Gérard Prensier ◽  
Christian P. Vivarès ◽  
Catherine Texier

Author(s):  
George Price ◽  
Lizardo Cerezo

Ultrastructural defects of ciliary structure have been known to cause recurrent sino-respiratory infection concurrent with Kartagener's syndrome. (1,2,3) These defects are also known to cause infertility in both males and females. (4) Overall, the defects are defined as the Immotile, or Dyskinetic Cilia Syndrome (DCS). Several ultrastructural findings have been described, including decreased number of cilia, multidirection orientation, fused and compound cilia, membrane blebs, excess matrix in the axoneme, missing outer tubular doublets, translocated doublets, defective radial spokes and dynein arms. A rare but noteworthy ultrastructural finding in DCS is the predominance of microvilli-like structures on the luminal surface of the respiratory epithelium. (5,6) These permanent surface modifications of the apical respiratory epithelium no longer resemble cilia but reflect the ultrastructure of stereocilia, similar to that found in the epidydimal epithelium. Like microvilli, stereocilia are devoid of microtubular ultrastructure in comparison with true cilia.


Author(s):  
S. F. Hayes ◽  
M. D. Corwin ◽  
T. G. Schwan ◽  
D. W. Dorward ◽  
W. Burgdorfer

Characterization of Borrelia burgdorferi strains by means of negative staining EM has become an integral part of many studies related to the biology of the Lyme disease organism. However, relying solely upon negative staining to compare new isolates with prototype B31 or other borreliae is often unsatisfactory. To obtain more satisfactory results, we have relied upon a correlative approach encompassing a variety EM techniques, i.e., scanning for topographical features and cryotomy, negative staining and thin sectioning to provide a more complete structural characterization of B. burgdorferi.For characterization, isolates of B. burgdorferi were cultured in BSK II media from which they were removed by low speed centrifugation. The sedimented borrelia were carefully resuspended in stabilizing buffer so as to preserve their features for scanning and negative staining. Alternatively, others were prepared for conventional thin sectioning and for cryotomy using modified procedures. For thin sectioning, the fixative described by Ito, et al.


Pathology ◽  
2001 ◽  
Vol 33 (3) ◽  
pp. 399-402 ◽  
Author(s):  
Leonardo D. Santos ◽  
Cyril S. K. C. Wong ◽  
Murray Killingsworth

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