Molecular Epidemiological Survey of Cutaneous Leishmaniasis in Two Highly Endemic Metropolises of Iran, Application of FTA Cards for DNA Extraction From Giemsa-Stained Slides

被引:26
作者
Izadi, Shahrokh [1 ]
Mirhendi, Hossein [1 ,2 ]
Jalalizand, Niloufar [3 ]
Khodadadi, Hossein [4 ]
Mohebali, Mehdi [1 ]
Nekoeian, Shahram [5 ]
Jamshidi, Ali [6 ]
Ghatee, Mohammad Amin [6 ,7 ]
机构
[1] Univ Tehran Med Sci, Sch Publ Hlth, Dept Med Parasitol & Mycol, Tehran, Iran
[2] Isfahan Univ Med Sci, Sch Med, Dept Med Parasitol & Mycol, Esfahan, Iran
[3] Isfahan Hlth Res Ctr, Natl Hlth Res Ctr, Esfahan, Iran
[4] Shiraz Univ Med Sci, Dept Med Parasitol & Mycol, Sch Med, Shiraz, Iran
[5] Isfahan Prov Hlth Ctr, Cellular & Mol Dept, Esfahan, Iran
[6] Yasuj Univ Med Sci, Sch Med, Dept Med Parasitol & Mycol, Yasuj, Iran
[7] Yasuj Univ Med Sci, Cellular & Mol Res Ctr, Yasuj, Iran
关键词
Molecular Epidemiology; Extraction Method; Iran; Cutaneous leishmaniasis; VISCERAL LEISHMANIASIS; ISFAHAN-PROVINCE; CLINICAL-SAMPLES; DIAGNOSIS; PCR; IDENTIFICATION; TROPICA; FOCUS; HETEROGENEITY; AMPLIFICATION;
D O I
10.5812/jjm.32885
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: PCR has been used for confirmation of leishmaniasis in epid emiological studies, but complexity of DNA extraction and PCR approach has confined its routine use in developing countries. Objectives: In this study recent epidemiological situation of cutaneous leishmaniasis (CL) in two hyper-endemic metropolises of Shiraz and Isfahan in Iran was studied using DNA extraction by commercial FTA cards and kinetoplastid DNA (kDNA)-PCR amplification for detection/identification of Leishmania directly from stained skin scraping imprints. Patients and Methods: Fifty four and 30 samples were collected from clinically diagnosed CL patients referred to clinical laboratories of leishmaniasis control centers in Isfahan and Shiraz cities, respectively. The samples were examined by direct microscopy and then scrapings of the stained smears were applied to FTA cards and used directly as DNA source in a nested-PCR to amplify kDNA to detect and identify Leishamaia species. Results: Fifty four of 84(64.2%) slides obtained from patients had positive results microscopically, while 79/84 (94%) of slides had positive results by FTA card-nested-PCR. PCR and microscopy showed a sensitivity of 96.4% and 64.2% and specificity of l00% and 100%, respectively Interestingly Leishmania major as causative agent of zoonotic CL was identified in 100% and 90.7% of CL cases from Isfahan and Shiraz cities, respectively, but L. tropica was detected from only 93% of cases from Shiraz city. All cases from central regions of Shiraz were L. tropica and no CL case was found in Isfahan central areas. Conclusions: Filter paper-based DNA extraction can facilitate routine use of PCR for diagnosis of CL in research and diagnostic laboratories in Iran and countries with similar conditions. Epidemiologic changes including dominancy of L. major in suburbs of Shiraz and Isfahan metropolises where anthroponotic CL caused by L. tropica had been established, showed necessity of precise studies on CL epidemiology in old urban and newly added districts in the suburbs.
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页数:7
相关论文
共 48 条
[1]   Clinical diagnosis of cutaneous leishmaniasis: A comparison study between standardized graded direct microscopy and ITS1-PCR of Giemsa-stained smears [J].
Al-Jawabreh, A. ;
Schoenian, G. ;
Hamarsheh, O. ;
Presber, W. .
ACTA TROPICA, 2006, 99 (01) :55-61
[2]   Leishmaniasis Worldwide and Global Estimates of Its Incidence [J].
Alvar, Jorge ;
Velez, Ivan D. ;
Bern, Caryn ;
Herrero, Merce ;
Desjeux, Philippe ;
Cano, Jorge ;
Jannin, Jean ;
den Boer, Margriet .
PLOS ONE, 2012, 7 (05)
[3]  
[Anonymous], 2002, Wkly Epidemiol Rec, V77, P365
[4]   PCR detection and identification of Leishmania parasites in clinical specimens in Ecuador:: A comparison with classical diagnostic methods [J].
Aviles, H ;
Belli, A ;
Armijos, R ;
Monroy, FP ;
Harris, E .
JOURNAL OF PARASITOLOGY, 1999, 85 (02) :181-187
[5]   Diagnostic Performance of Filter Paper Lesion Impression PCR for Secondarily Infected Ulcers and Nonulcerative Lesions Caused by Cutaneous Leishmaniasis [J].
Boggild, Andrea K. ;
Ramos, Ana Pilar ;
Valencia, Braulio Mark ;
Veland, Nicolas ;
Calderon, Flor ;
Arevalo, Jorge ;
Low, Donald E. ;
Llanos-Cuentas, Alejandro .
JOURNAL OF CLINICAL MICROBIOLOGY, 2011, 49 (03) :1097-1100
[6]   Sensitivity and specificity of polymerase chain reaction in Giemsa-stained slides for diagnosis of visceral leishmaniasis in children [J].
Brustoloni, Yvone Maia ;
Lima, Rosimar Batista ;
da Cunha, Rivaldo Venancio ;
Dorval, Maria Elizabeth ;
Oshiro, Elisa Teruya ;
de Oliveira, Ana Lucia Lyrio ;
Pirmez, Claude .
MEMORIAS DO INSTITUTO OSWALDO CRUZ, 2007, 102 (04) :497-500
[7]  
Capelli G., 2004, Parassitologia (Rome), V46, P193
[8]   Cutaneous Leishmaniasis: Recent Developments in Diagnosis and Management [J].
de Vries, Henry J. C. ;
Reedijk, Sophia H. ;
Schallig, Henk D. F. H. .
AMERICAN JOURNAL OF CLINICAL DERMATOLOGY, 2015, 16 (02) :99-109
[9]   The increase in risk factors for leishmaniasis worldwide [J].
Desjeux, P .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 2001, 95 (03) :239-243
[10]   Leishmania (Viannia) subgenus kDNA amplification for the diagnosis of mucosal leishmaniasis [J].
Disch, J ;
Pedras, MJ ;
Orsini, M ;
Pirmez, C ;
de Oliveira, MC ;
Castro, M ;
Rabello, A .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2005, 51 (03) :185-190