Title
Detection and species identification of Leishmania DNA from filter paper lesion impressions for patients with american cutaneous leishmaniasis
Date Issued
01 January 2010
Access level
open access
Resource Type
journal article
Author(s)
Universidad Peruana Cayetano Heredia
Universidad Peruana Cayetano Heredia
Universidad Peruana Cayetano Heredia
Universidad Peruana Cayetano Heredia
Universidad Peruana Cayetano Heredia
Abstract
Background. Traditional detection of Leishmania from ulcers involves collection of invasive specimens that cause discomfort, require technical expertise, and carry risks of invasive procedures. We compared traditional diagnostic methods with a molecular noninvasive filter paper-based method for the diagnosis of cutaneous leishmaniasis. Methods. Consecutive patients presenting to the Leishmania Clinic at Hospital Nacional Cayetano Heredia were enrolled. Polymerase chain reaction (PCR) was performed on lesion scrapings, aspirates, and filter paper impressions. The reference standard was any 2 of 5 tests positive: smear, aspirate culture, invasive-specimen PCR (scrapings and aspirates), filter paper PCR, and leishmanin skin test. Outcome measures were sensitivity and specificity. Leishmania speciation was performed by PCR-restriction fragment length polymorphism (RFLP) of positive specimens. Results. Forty-five patients with 66 lesions were enrolled. Of 52 lesions diagnosed as cutaneous leishmaniasis, 50 were positive by PCR of invasive specimens versus 48 by PCR of filter papers (P = .930). Sensitivity and specificity of PCR on invasively obtained specimens were 94.2% (95% confidence interval [CI], 87.9%-100%) and 92.9% (95% CI, 79.4%-100%). Sensitivity and specificity of filter paper PCR were 92.3% (95% CI, 85.1%-99.5%) and 100%. Culture, smear, and leishmanin skin test all had inferior sensitivities, compared with PCR of invasive or noninvasive specimens (P < .001). Of 50 specimens positive by PCR, 19 had sufficient DNA for PCR-RFLP analysis. Conclusions. Filter paper PCR constitutes a sensitive and specific alternative to traditional diagnostic assays. This novel, rapid, well-tolerated method has the potential for widespread use in the field and in pediatric populations where traditional specimen collection is most difficult to perform, and can potentially be used for rapid species identification. © 2009 by the Infectious Diseases Society of America. All rights reserved.
Volume
50
Issue
1
OCDE Knowledge area
Enfermedades infecciosas
Scopus EID
2-s2.0-72049095106
PubMed ID
Source
Clinical Infectious Diseases
ISSN of the container
10584838
Source funding
Royal College of Physicians and Surgeons of Canada
Sources of information: Directorio de Producción Científica Scopus