Eukaryotic Cell
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Eukaryotic Cell, March 2008, p. 509-517, Vol. 7, No. 3
1535-9778/08/$08.00+0     doi:10.1128/EC.00316-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Glycogen Phosphorylase in Acanthamoeba spp.: Determining the Role of the Enzyme during the Encystment Process Using RNA Interference{triangledown}

Jacob Lorenzo-Morales,1 Jarmila Kliescikova,2 Enrique Martinez-Carretero,1 Luis Miguel De Pablos,3 Bronislava Profotova,2 Eva Nohynkova,2 Antonio Osuna,3 and Basilio Valladares1*

University Institute of Tropical Diseases and Public Health of the Canary Islands, University of La Laguna, Tenerife, Canary Islands, Spain,1 Department of Tropical Medicine, First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic,2 Institute of Biotechnology, Department of Parasitology, University of Granada, Campus de Fuentenueva 18071, Granada, Spain3

Received 27 August 2007/ Accepted 18 January 2008

Acanthamoeba infections are difficult to treat due to often late diagnosis and the lack of effective and specific therapeutic agents. The most important reason for unsuccessful therapy seems to be the existence of a double-wall cyst stage that is highly resistant to the available treatments, causing reinfections. The major components of the Acanthamoeba cyst wall are acid-resistant proteins and cellulose. The latter has been reported to be the major component of the inner cyst wall. It has been demonstrated previously that glycogen is the main source of free glucose for the synthesis of cellulose in Acanthamoeba, partly as glycogen levels fall during the encystment process. In other lower eukaryotes (e.g., Dictyostelium discoideum), glycogen phosphorylase has been reported to be the main tool used for glycogen breakdown in order to maintain the free glucose levels during the encystment process. Therefore, it was hypothesized that the regulation of the key processes involved in the Acanthamoeba encystment may be similar to the previously reported regulation mechanisms in other lower eukaryotes. The catalytic domain of the glycogen phosphorylase was silenced using RNA interference methods, and the effect of this phenomenon was assessed by light and electron microscopy analyses, calcofluor staining, expression zymogram assays, and Northern and Western blot analyses of both small interfering RNA-treated and control cells. The present report establishes the role of glycogen phosphorylase during the encystment process of Acanthamoeba. Moreover, the obtained results demonstrate that the enzyme is required for cyst wall assembly, mainly for the formation of the cell wall inner layer.


* Corresponding author. Mailing address: University Institute of Tropical Diseases and Public Health of the Canary Islands, University of La Laguna, Avda. Astrofísico Fco. Sánchez, S/N, 38203 La Laguna, Tenerife, Canary Islands, Spain. Phone: 34922318486. Fax: 34922318514. E-mail: bvallada{at}ull.es

{triangledown} Published ahead of print on 25 January 2008.


Eukaryotic Cell, March 2008, p. 509-517, Vol. 7, No. 3
1535-9778/08/$08.00+0     doi:10.1128/EC.00316-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.







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