Hostname: page-component-848d4c4894-jbqgn Total loading time: 0 Render date: 2024-06-20T14:58:18.748Z Has data issue: false hasContentIssue false

Induced encystment improves resistance to preservation and storage of Acanthamoeba castellanii

Published online by Cambridge University Press:  21 October 2008

S. J. CAMPBELL
Affiliation:
School of Engineering and Science, University of the West of Scotland, Paisley PA1 2BE, Scotland
P. R. INGRAM
Affiliation:
Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow G4 0NR, Scotland
C. W. ROBERTS
Affiliation:
Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow G4 0NR, Scotland
F. L. HENRIQUEZ*
Affiliation:
School of Engineering and Science, University of the West of Scotland, Paisley PA1 2BE, Scotland
*
*Corresponding author: School of Engineering and Science, University of the West of Scotland, Paisley PA1 2BE, Scotland. Tel: +01418483119. Fax: +01415484823. E-mail: fiona.henriquez@uws.ac.uk

Summary

Several conditions that allow the preservation, storage and rapid, efficient recovery of viable Acanthamoeba castellanii organisms were investigated. The viability of trophozoites (as determined by time to confluence) significantly declined over a period of 12 months when stored at −70°C using dimethyl sulfoxide (DMSO; 5 or 10%) as cryopreservant. As A. castellanii are naturally capable of encystment, studies were undertaken to determine whether induced encystment might improve the viability of organisms under a number of storage conditions. A. castellanii cysts stored in the presence of Mg2+ at 4°C remained viable over the study period, although time to confluence was increased from approximately 8 days to approximately 24 days over the 12-month period. Storage of cysts at −70°C with DMSO (5 or 10%) or 40% glycerol, but not 80% glycerol as cryopreservants increased their viability over the 12-month study period compared with those stored at room temperature. Continued presence of Mg2+ in medium during storage had no adverse effects and generally improved recovery of viable organisms. The present study demonstrates that A. castellanii can be stored as a non-multiplicative form inexpensively, without a need for cryopreservation, for at least 12 months, but viability is increased by storage at −70°C.

Type
Original Articles
Copyright
Copyright © 2008 Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Alejandre-Aguilar, R., Calvo-Mendez, L., Nogueda-Torres, B. and de la Jara-Alcocer, F. (1998). Maintenance of Acanthamoeba culbertsoni by cryopreservation. The Journal of Parasitology 84, 12611263.CrossRefGoogle ScholarPubMed
Gonzalez-Robles, A., Flores-Langarica, A., Omana-Molina, M. and Shibayama, M. (2001). Acanthamoeba castellanii: ultrastructure of trophozoites using fast free fixation. Journal of Electron Microscopy 50, 423427.CrossRefGoogle Scholar
Henriquez, F. L., Ingram, P. R., Muench, S. P., Rice, D. W. and Roberts, C. W. (2008). Molecular basis for resistance of Acanthamoeba tubulins to all major classes of antitubulin compounds. Antimicrobial Agents and Chemotherapy 52, 11331135.CrossRefGoogle ScholarPubMed
John, D. T., Eddy, P. L. and John, R. A. (1994). Cryopreservation of pathogenic free-living amebae. Folia Parasitologica 41, 110114.Google ScholarPubMed
John, D. T. and John, R. A. (1996). Viability of pathogenic Acanthamoeba and Naegleria and virulence of N. fowleri during long-term cryopreservation. Folia Parasitologica 43, 4346.Google Scholar
Marciano-Cabral, F. and Cabral, G. (2003). Acanthamoeba spp. as agents of disease in humans. Clinical Microbiology Reviews 16, 273307.CrossRefGoogle ScholarPubMed
Mattana, A., Biancu, G., Alberti, L., Accardo, A., Delogu, G., Fiori, P. L. and Cappuccinelli, P. (2004). In vitro evaluation of the effectiveness of the macrolide rokitamycin and chlorpromazine against Acanthamoeba castellanii. Antimicrobial Agents and Chemotherapy 48, 45204527.CrossRefGoogle ScholarPubMed
Mazur, T., Hadaś, E. and Iwanicka, I. (1995). The duration of the cyst stage and the viability and virulence of Acanthamoeba isolates. Tropical Medicine and Parasitology 46, 106108.Google ScholarPubMed
McBride, J., Ingram, P. I., Henriquez, F. L. and Roberts, C. W. (2005). Development of a colourimetric microtitre plate assay for assessment of anti-microbial agents against Acanthamoeba. Journal of Clinical Microbiology 43, 629634.CrossRefGoogle ScholarPubMed
McBride, J., Mullen, A. B., Carter, K. C. and Roberts, C. W. (2007). Differential cytotoxicity of phospholipid analogues to pathogenic Acanthamoeba species and mammalian cells. Journal of Antimicrobial Chemotherapy 60, 521525.CrossRefGoogle ScholarPubMed
Neff, R. J., Ray, S. A., Benton, W. F. and Wilborn, M. (1964). Induction of synchronous encystment (differentiation) in Acanthamoeba sp, Methods in Cell Physiology 1, 5583.CrossRefGoogle Scholar
Schuster, F. L. (2002). Cultivation of pathogenic and opportunistic free-living amebas. Clinical Microbiology Reviews 15, 342354.CrossRefGoogle ScholarPubMed
Schuster, F. L. and Visvesvara, G. S. (2004) Free living amoebae as opportunistic and non-opportunistic pathogens of humans and animals. International Journal for Parasitology 34, 10011027.CrossRefGoogle ScholarPubMed
Schuster, F. L. and Visvesvara, G. S. (1998). Efficacy of novel antimicrobials against clinical isolates of opportunistic amebas. Journal of Eukaryotic Microbiology 45, 612618.CrossRefGoogle ScholarPubMed
Seo, S. A., Yong, T. S. and Im, K. (1992). The maintenance of free-living amoebae by cryopreservation. The Korean Journal of Parasitology 30, 151153.CrossRefGoogle ScholarPubMed