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Polymerase chain reaction-based method for the identification of Leishmania (Viannia) braziliensis and Leishmania (Viannia) guyanensis in mucosal tissues conserved in paraffin
Prestes, Suzane Ribeiro; Guerra, Jorge Augusto de Oliveira; Romero, Gustavo Adolfo Sierra; Magalhaes, Laylah Kelre Costa; Santana, Rosa Amelia Gonçalves; Maciel, Marcel Gonçalves; Custódio, Ana; Barbosa, Maria das Graças Vale; Silveira, Henrique.
  • Prestes, Suzane Ribeiro; Universidade do Estado do Amazonas. Manaus. BR
  • Guerra, Jorge Augusto de Oliveira; Universidade do Estado do Amazonas. Manaus. BR
  • Romero, Gustavo Adolfo Sierra; Universidade do Estado do Amazonas. Manaus. BR
  • Magalhaes, Laylah Kelre Costa; Universidade do Estado do Amazonas. Manaus. BR
  • Santana, Rosa Amelia Gonçalves; Universidade do Estado do Amazonas. Manaus. BR
  • Maciel, Marcel Gonçalves; Universidade do Estado do Amazonas. Manaus. BR
  • Custódio, Ana; Universidade do Estado do Amazonas. Manaus. BR
  • Barbosa, Maria das Graças Vale; Universidade do Estado do Amazonas. Manaus. BR
  • Silveira, Henrique; Universidade do Estado do Amazonas. Manaus. BR
Rev. Soc. Bras. Med. Trop ; 48(5): 555-559, Sept.-Oct. 2015. graf
Article in English | LILACS | ID: lil-763336
ABSTRACT
ABSTRACT

INTRODUCTION:

In the Americas, mucosal leishmaniasis is primarily associated with infection by Leishmania (Viannia) braziliensis. However, Leishmania (Viannia) guyanensis is another important cause of this disease in the Brazilian Amazon. In this study, we aimed at detecting Leishmaniadeoxyribonucleic acid (DNA) within paraffin-embedded fragments of mucosal tissues, and characterizing the infecting parasite species.

METHODS:

We evaluated samples collected from 114 patients treated at a reference center in the Brazilian Amazon by polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) analyses.

RESULTS:

Direct examination of biopsy imprints detected parasites in 10 of the 114 samples, while evaluation of hematoxylin and eosin-stained slides detected amastigotes in an additional 17 samples. Meanwhile, 31/114 samples (27.2%) were positive for Leishmania spp. kinetoplast deoxyribonucleic acid (kDNA) by PCR analysis. Of these, 17 (54.8%) yielded amplification of the mini-exon PCR target, thereby allowing for PCR-RFLP-based identification. Six of the samples were identified as L. (V.) braziliensis, while the remaining 11 were identified as L. (V.) guyanensis.

CONCLUSIONS:

The results of this study demonstrate the feasibility of applying molecular techniques for the diagnosis of human parasites within paraffin-embedded tissues. Moreover, our findings confirm that L. (V.) guyanensisis a relevant causative agent of mucosal leishmaniasis in the Brazilian Amazon.
Subject(s)


Full text: Available Index: LILACS (Americas) Main subject: Leishmania braziliensis / Leishmaniasis, Mucocutaneous / Leishmania guyanensis / Mucous Membrane Type of study: Diagnostic study / Prognostic study Limits: Female / Humans / Male Country/Region as subject: South America / Brazil Language: English Journal: Rev. Soc. Bras. Med. Trop Journal subject: Tropical Medicine Year: 2015 Type: Article / Project document Affiliation country: Brazil Institution/Affiliation country: Universidade do Estado do Amazonas/BR

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Full text: Available Index: LILACS (Americas) Main subject: Leishmania braziliensis / Leishmaniasis, Mucocutaneous / Leishmania guyanensis / Mucous Membrane Type of study: Diagnostic study / Prognostic study Limits: Female / Humans / Male Country/Region as subject: South America / Brazil Language: English Journal: Rev. Soc. Bras. Med. Trop Journal subject: Tropical Medicine Year: 2015 Type: Article / Project document Affiliation country: Brazil Institution/Affiliation country: Universidade do Estado do Amazonas/BR