This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Santillana-Hayat, M.
Right arrow Articles by Derouin, F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Santillana-Hayat, M.
Right arrow Articles by Derouin, F.

 Previous Article  |  Next Article 

Antimicrobial Agents and Chemotherapy, June 2002, p. 2049-2051, Vol. 46, No. 6
0066-4804/02/$04.00+0     DOI: 10.1128/AAC.46.6.2049-2051.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

Effects of Chemical and Physical Agents on Viability and Infectivity of Encephalitozoon intestinalis Determined by Cell Culture and Flow Cytometry

Maud Santillana-Hayat,1 Claudine Sarfati,1 Sandra Fournier,2 Françoise Chau,3 Raphaël Porcher,4 Jean-Michel Molina,2 and Francis Derouin1*

Parasitology-Mycology Laboratory,1 Department of Infectious Diseases,2 Department of Biostatistics, Saint-Louis Hospital, AP-HP and EA 3520, University of Paris 7,4 INSERM, Bichat Hospital, Paris, France3

Received 10 October 2001/ Returned for modification 27 November 2001/ Accepted 4 March 2002

We combined tissue culture and flow cytometry to assess the activities of various temperatures, chemicals, and disinfectants on the viability and infectivity of spores of Encephalitozoon intestinalis. Surfanios and benzalkonium chloride, disinfectants currently used in the hospital, were remarkably efficient in destroying spore viability and infectivity.


* Corresponding author. Mailing address: Laboratoire de Parasitologie-Mycologie, Saint-Louis Hospital, AP-HP, 1, Avenue Claude Vellefaux, 75475, Paris Cedex 10, France. Phone: 33 1 42 49 95 01. Fax: 33 1 42 49 48 03. E-mail: paracord{at}wanadoo.fr.


Antimicrobial Agents and Chemotherapy, June 2002, p. 2049-2051, Vol. 46, No. 6
0066-4804/02/$04.00+0     DOI: 10.1128/AAC.46.6.2049-2051.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Fenoy, S., Rueda, C., Higes, M., Martin-Hernandez, R., del Aguila, C. (2009). High-Level Resistance of Nosema ceranae, a Parasite of the Honeybee, to Temperature and Desiccation. Appl. Environ. Microbiol. 75: 6886-6889 [Abstract] [Full Text]  
  • Barbosa, J., Rodrigues, A. G., Pina-Vaz, C. (2009). Cytometric Approach for Detection of Encephalitozoon intestinalis, an Emergent Agent. CVI 16: 1021-1024 [Abstract] [Full Text]  
  • Menotti, J., Santillana-Hayat, M., Cassinat, B., Sarfati, C., Derouin, F., Molina, J.-M. (2005). Inhibitory Activity of Human Immunodeficiency Virus Aspartyl Protease Inhibitors against Encephalitozoon intestinalis Evaluated by Cell Culture-Quantitative PCR Assay. Antimicrob. Agents Chemother. 49: 2362-2366 [Abstract] [Full Text]  
  • Leiro, J., Cano, E., Ubeira, F. M., Orallo, F., Sanmartin, M. L. (2004). In Vitro Effects of Resveratrol on the Viability and Infectivity of the Microsporidian Encephalitozoon cuniculi. Antimicrob. Agents Chemother. 48: 2497-2501 [Abstract] [Full Text]  
  • Menotti, J., Cassinat, B., Sarfati, C., Liguory, O., Derouin, F., Molina, J.-M. (2003). Development of a Real-Time PCR Assay for Quantitative Detection of Encephalitozoon intestinalis DNA. J. Clin. Microbiol. 41: 1410-1413 [Abstract] [Full Text]