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dc.contributor.authorEchchakery, Mohamed
dc.contributor.authorChicharro, Carmen 
dc.contributor.authorBoussaa, S
dc.contributor.authorNieto, Javier 
dc.contributor.authorOrtega, Sheila 
dc.contributor.authorCarrillo, Eugenia 
dc.contributor.authorMoreno, Javier 
dc.contributor.authorBoumezzough, Ali
dc.date.accessioned2021-05-19T16:05:50Z
dc.date.available2021-05-19T16:05:50Z
dc.date.issued2020-01
dc.identifier.citationJ Vector Borne Dis. Jan-Mar 2020;57(1):71-77.es_ES
dc.identifier.issn0972-9062es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/12979
dc.description.abstractCutaneous leishmaniasis (CL) in Marrakesh-Safi region located in the central-south part of Morocco is a public health problem. This study assessed the efficiency of a microscopic examination method in establishing the diagnosis of CL and PCR for the characterization and identification of the circulating Leishmania strains in different CL foci of the study area. A total of 297 smears obtained from cutaneous lesions of suspected patients with CL were stained with May-Grünwald Giemsa (MGG) for microscopic examination. For each positive smear, genomic DNA was extracted and PCR-analysed, targeting the small subunit ribosomal ribonucleic acid (ssu rRNA) gene to detect Leishmania DNA. Then, the internal transcribed spacer 1 (ITS1) was amplified and sequenced in order to identify the Leishmania species. The sensitivity and specificity of the conventional microscopy with ssu rRNA gene were compared by Leishmania nested PCR (LnPCR) and ITS1 gene by ITS-PCR. A total of 257 smears were positive in the microscopic examination, i.e. the detection rate of amastigotes by optical microscopy was 86.53% (257/297). The LnPCR was found to have a specificity and a sensitivity of 100%, each. Interestingly, the sequencing results showed that 99.61% (256/257) of the isolates had Leishmania tropica and 0.39% (1/257) had L. infantum infection. Though, classical microscopic examination is useful and economical, it is not sensitive enough, especially in endemic regions where several Leishmania species coexist. In such situations, PCR constitutes a complementary method for the identification of the causal species. The results indicate that both the L. tropica (dominant) and L. infantum are the causative agents of CL in the Marrakesh-Safi region. The rate of CL infection is high in Imintanout, and Chichaoua provinces. Hence, early diagnosis and prompt treatment of CL patients is necessary to prevent its extension to neighboring localities.es_ES
dc.language.isoenges_ES
dc.publisherMedknow Publicationses_ES
dc.relation.isversionofPublisher's versiones_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.subjectCutaneous leishmaniasises_ES
dc.subjectITS-PCRes_ES
dc.subjectL. tropicaes_ES
dc.subjectLeishmania infantumes_ES
dc.subjectLnPCRes_ES
dc.subjectMoroccoes_ES
dc.subjectMicroscopic examinationes_ES
dc.titleMolecular identification of Leishmania tropica and L. infantum isolated from cutaneous human leishmaniasis samples in central Morocco.es_ES
dc.typeArtículoes_ES
dc.rights.licenseAtribución-NoComercial-CompartirIgual 4.0 Internacional*
dc.identifier.pubmedID33818459es_ES
dc.format.volume57es_ES
dc.format.number1es_ES
dc.format.page71-77es_ES
dc.identifier.doi10.4103/0972-9062.308804es_ES
dc.description.peerreviewedes_ES
dc.relation.publisherversionhttps://doi.org/10.4103/0972-9062.308804es_ES
dc.identifier.journalJournal of Vector Borne Diseaseses_ES
dc.repisalud.centroISCIII::Centro Nacional de Microbiologíaes_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES


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Atribución-NoComercial-CompartirIgual 4.0 Internacional
This item is licensed under a: Atribución-NoComercial-CompartirIgual 4.0 Internacional