MELICHEROVÁ, Janka, Veronika MAZOUROVÁ and Andrea VALIGUROVÁ. In vitro excystation of Cryptosporidium muris oocysts and viability of released sporozoites in different incubation media. Parasitology Research. Springer Berlin Heidelberg, vol. 115, No 3, p. 1113-1121. ISSN 0932-0113. doi:10.1007/s00436-015-4841-0. 2016.
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Basic information
Original name In vitro excystation of Cryptosporidium muris oocysts and viability of released sporozoites in different incubation media
Authors MELICHEROVÁ, Janka (703 Slovakia, belonging to the institution), Veronika MAZOUROVÁ (203 Czech Republic, belonging to the institution) and Andrea VALIGUROVÁ (703 Slovakia, guarantor, belonging to the institution).
Edition Parasitology Research, Springer Berlin Heidelberg, 2016, 0932-0113.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10600 1.6 Biological sciences
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 2.329
RIV identification code RIV/00216224:14310/16:00087850
Organization unit Faculty of Science
Doi http://dx.doi.org/10.1007/s00436-015-4841-0
UT WoS 000370868200021
Keywords (in Czech) kryptosporidie excystace oocysta sporozoit
Keywords in English cryptosporidia excystation oocyst sporozoite
Tags AKR, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Lucie Jarošová, DiS., učo 205746. Changed: 7/3/2018 10:32.
Abstract
This study aimed to evaluate and document the excystation process of Cryptosporidium muris oocysts in various incubation media, and to monitor the behaviour of excysting and freshly excysted sporozoites. A test of oocyst viability, using fluorescent double staining with fluorescein diacetate and propidium iodide, was performed prior to each experimental assay. Light microscope observations confirmed that relatively often only three sporozoites were released; the fourth one either left the oocyst later together with a residual body or remained trapped within the oocyst wall. These results suggest that successful oocyst excystation is not limited by the viability of all four sporozoites. Darkening of oocysts to opaque and their specific movement (the so-called oocyst dancing) preceded the final excystation and liberation of sporozoites, while the dormant oocysts appeared refractive. The process of excystation in C. muris is not gradual as generally described in cryptosporidia but very rapid in an eruptive manner. Experiments were performed using oocysts stored at 4 °C for various time periods, as well as oocysts freshly shed from host rodents (Mastomys coucha) of different ages. The most suitable medium supporting high excystation rate (76 %) and prolonged motility of sporozoites was RPMI 1640, enriched with 5 % bovine serum albumin (BSA). Our results emphasize that to reliably evaluate the success of in vitro excystation of cryptosporidia, not only the number of released sporozoites in a set time period should be taken into consideration but also their subsequent activity (motility), as it is expected to be essential for the invasion of host cells.
Links
GAP505/11/1163, research and development projectName: Protizánětlivá aktivita extraktů z rostlin Indonésie a jejich účinek na průběh oportunních parazitóz
Investor: Czech Science Foundation
7AMB14FR013, research and development projectName: Mechanizmus buněčného pohybu výtrusovců (Apicomplexa) (Acronym: MOTAP)
Investor: Ministry of Education, Youth and Sports of the CR
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