AJTMH Transactions of the Royal Society of Tropical Medicine and Hygiene
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am. J. Trop. Med. Hyg., 79(6), 2008, pp. 839-842
Copyright © 2008 by The American Society of Tropical Medicine and Hygiene

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
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Alborzi, A.
Right arrow Articles by Ziyaeyan, M.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Alborzi, A.
Right arrow Articles by Ziyaeyan, M.

Detection of Leishmania infantum Kinetoplast DNA in the Whole Blood of Asymptomatic Individuals by PCR-ELISA and Comparison with Other Infection Markers in Endemic Areas, Southern Iran

Abdolvahab Alborzi*, Bahman Pourabbas, Frahad Shahian, Jalal Mardaneh, Gholam R. Pouladfar, AND Mazyar Ziyaeyan
Professor Alborzi Clinical Microbiology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran

Visceral leishmaniasis (VL), caused by Leishmania infantum, is endemic in southern Iran. To detect asymptomatic individuals, we used kinetoplast DNA (kDNA) polymerase chain reaction (PCR)-ELISA methods on 388 blood samples of healthy persons in two endemic loci and compared the results with the leishmanin skin test (LST) and the immunofluorescent antibody test (IFAT). kDNA PCR, LST, and IFAT were positive in 95 (24.5%), 132 (34%), and 212 (54.6%) cases, respectively. Fifty-five (21.4%) individuals that were LST negative were PCR positive. All PCR-positive individuals had a titer of ≥ 1:20, whereas 45% of those that were IFAT positive were PCR positive. For a reliable index of prevalence rate of infection, LST alone is not sufficient and needs to be accompanied by PCR-ELISA. The high rate of kDNA-positive results may indicate the possibility of humans being a reservoir and source of transmission. In endemic areas, kDNA PCR-ELISA is not a reliable test for the diagnosis of active VL.


Received February 18, 2008. Accepted for publication August 8, 2008.

Acknowledgments: The authors thank H. Khajehei, PhD, for valuable assistance and cooperation in copyediting the manuscript.

* Address correspondence to Abdolvahab Alborzi, Professor Alborzi Clinical Microbiology Research Center, Nemazi Hospital, Shiraz, Iran. E-mail: alborziiraj2004{at}yahoo.com

Authors’ addresses: Abdolvahab Alborzi, Bahman Pourabbas, Fra-had Shahian, Jalal Mardaneh, Gholam R. Pouladfar, and Mazyar Ziyaeyan, Professor Alborzi Clinical Microbiology Research Center, Nemazi Hospital, Shiraz, Iran, Tel: 98-711-6470205, Fax: 98-711-6287071, E-mails: alborziiraj2004{at}yahoo.com, bpourabbas{at}yahoo.com, farhadwww{at}yahoo.com, jalalmardaneh{at}yahoo.com, pooladfar{at}yahoo.com, and ziyaeyan{at}gmail.com.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2008 by the American Society of Tropical Medicine and Hygiene.