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 Nelson, K. L.
Right arrow Articles by Darby, J. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Nelson, K. L.
Right arrow Articles by Darby, J. L.
Agricola
Right arrow Articles by Nelson, K. L.
Right arrow Articles by Darby, J. L.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, December 2001, p. 5453-5459, Vol. 67, No. 12
0099-2240/01/$04.00+0   DOI: 10.1128/AEM.67.12.5453-5459.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Inactivation of Viable Ascaris Eggs by Reagents during Enumeration

Kara L. Nelson1,* and Jeannie L. Darby2

Department of Civil and Environmental Engineering, University of California, Berkeley, California 94720,1 and Department of Civil and Environmental Engineering, University of California, Davis, California 956162

Received 10 May 2001/Accepted 19 September 2001

Various reagents commonly used to enumerate viable helminth eggs from wastewater and sludge were evaluated for their potential to inactivate Ascaris eggs under typical laboratory conditions. Two methods were used to enumerate indigenous Ascaris eggs from sludge samples. All steps in the methods were the same except that in method I a phase extraction step with acid-alcohol (35% ethanol in 0.1 N H2SO4) and diethyl ether was used whereas in method II the extraction step was avoided by pouring the sample through a 38-µm-mesh stainless steel sieve that retained the eggs. The concentration of eggs and their viability were lower in the samples processed by method I than in the samples processed by method II by an average of 48 and 70%, respectively. A second set of experiments was performed using pure solutions of Ascaris suum eggs to elucidate the effect of the individual reagents and relevant combination of reagents on the eggs. The percentages of viable eggs in samples treated with acid-alcohol alone and in combination with diethyl ether or ethyl acetate were 52, 27, and 4%, respectively, whereas in the rest of the samples the viability was about 80%. Neither the acid nor the diethyl ether alone caused any decrease in egg viability. Thus, the observed inactivation was attributed primarily to the 35% ethanol content of the acid-alcohol solution. Inactivation of the eggs was prevented by limiting the direct exposure to the extraction reagents to 30 min and diluting the residual concentration of acid-alcohol in the sample by a factor of 100 before incubation. Also, the viability of the eggs was maintained if the acid-alcohol solution was replaced with an acetoacetic buffer. None of the reagents used for the flotation step of the sample cleaning procedure (ZnSO4, MgSO4, and NaCl) or during incubation (0.1 N H2SO4 and 0.5% formalin) inactivated the Ascaris eggs under the conditions studied.


* Corresponding author. Mailing address: Department of Civil and Environmental Engineering, University of California, Berkeley, CA 94720-1710. Phone: (510) 643-5023. Fax (510) 642-7483. E-mail: nelson{at}ce.berkeley.edu.


Applied and Environmental Microbiology, December 2001, p. 5453-5459, Vol. 67, No. 12
0099-2240/01/$04.00+0   DOI: 10.1128/AEM.67.12.5453-5459.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Collick, A. S., Inglis, S., Wright, P., Steenhuis, T. S., Bowman, D. D. (2007). Inactivation of Ascaris suum in a Biodrying Compost System. J. Environ. Qual. 36: 1528-1533 [Abstract] [Full Text]  
  • Pecson, B. M., Barrios, J. A., Johnson, D. R., Nelson, K. L. (2006). A Real-Time PCR Method for Quantifying Viable Ascaris Eggs Using the First Internally Transcribed Spacer Region of Ribosomal DNA. Appl. Environ. Microbiol. 72: 7864-7872 [Abstract] [Full Text]