JEQ Grow Your Career With ASA
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Published online 23 June 2008
Published in J Environ Qual 37:1583-1588 (2008)
DOI: 10.2134/jeq2007.0474
© 2008 American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America
677 S. Segoe Rd., Madison, WI 53711 USA
This Article
Right arrow Figures Only
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
Google Scholar
Right arrow Articles by Ahmed, W.
Right arrow Articles by Gardner, T.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ahmed, W.
Right arrow Articles by Gardner, T.
Agricola
Right arrow Articles by Ahmed, W.
Right arrow Articles by Gardner, T.
Related Collections
Right arrow Surface Water Quality
Right arrow Water Quality
Right arrow Water Pollution

TECHNICAL REPORTS

Surface Water Quality

Evaluation of the Host-Specificity and Prevalence of Enterococci Surface Protein (esp) Marker in Sewage and its Application for Sourcing Human Fecal Pollution

W. Ahmeda,*, J. Stewartb, D. Powellc and T. Gardnera

a Dep. of Natural Resources and Water, Queensland 4068, Australia
b BMT WBM Pty Ltd, Queensland 4004, Australia
c Faculty of Science, Health and Education, Univ. of the Sunshine Coast, Maroochydore DC 4558, Queensland, Australia

* Corresponding author (Warish.Ahmed{at}nrw.qld.gov.au).

Received for publication September 6, 2007. The suitability of the enterococci surface protein (esp) marker to detect human fecal pollution was evaluated by testing 197 fecal samples from 13 host groups in Southeast Queensland, Australia. Overall, this marker was detected in 90.5% of sewage and septic system samples and could not be detected in any fecal samples from 12 animal host groups. The sensitivity of the esp primer to detect the human-specific esp marker in sewage and septic samples was 100 and 67%, respectively. The overall specificity of this marker to distinguish between human and animal fecal pollution was 100%. Its prevalence in sewage was also determined by testing samples from the raw sewage, secondary effluent, and treated effluent of a sewage treatment plant (STP) over five consecutive days. Of the 15 samples tested, 12 (80%) were found to be positive for this marker. In contrast, it was not found in three samples from the treated effluent and these samples did not contain any culturable enterococci. The PCR limit of detection of this marker in freshwater samples was up to dilution 1 x 10–4 and the number of culturable enterococci at this dilution was 4.8 x 101 ± 7.0 x 10° colony forming unit (CFU). The utility of this marker was evaluated by testing water samples from three non-sewered catchments in Pine Rivers in Southeast Queensland. Of the 13 samples tested, eight were positive for this marker with the number of enterococci ranging between 1.8 x 103 to 8.5 x 103 CFU per 100 mL of water. Based on the results, it can be concluded that the esp marker appears to be sewage specific and could be used as a reliable marker to detect human fecal pollution in surface waters in Southeast Queensland, Australia.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
The SCI Journals Agronomy Journal Crop Science
Journal of Natural Resources
and Life Sciences Education
Vadose Zone Journal
Soil Science Society of America Journal Journal of Plant Registrations The Plant Genome
Copyright © 2008 by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America.