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Detection of Internal Transcribed Spacer 1 and hsp70 Genetic Markers Using Restriction Fragment Length Polymorphisms and Sequencing in Identification of Leishmania Species Causing Tegumentary Leishmaniasis in Brazil.
Delprete, Jaqueline Alves; de Almeida, Livia Vieira; Barros, Alessandra Moraes; Soler, Rita de Cássia; Bittencourt, Amanda Azevedo; Luna, Expedito José de Albuquerque; Lindoso, José Angelo Lauletta; Braz, Lúcia Maria Almeida.
Afiliação
  • Delprete JA; Departamento de Doenças Infecciosas e Parasitárias, Faculdade de Medicina da Universidade de São Paulo (FMUSP), São Paulo, Brazil.
  • de Almeida LV; Instituto de Infectologia Emílio Ribas, São Paulo, Brazil.
  • Barros AM; Instituto de Infectologia Emílio Ribas, São Paulo, Brazil.
  • Soler RC; Instituto de Infectologia Emílio Ribas, São Paulo, Brazil.
  • Bittencourt AA; Instituto de Infectologia Emílio Ribas, São Paulo, Brazil.
  • Luna EJA; Instituto de Infectologia Emílio Ribas, São Paulo, Brazil.
  • Lindoso JAL; Departamento de Medicina Preventiva, Faculdade de Medicina da Universidade de São Paulo (FMUSP), São Paulo, Brazil.
  • Braz LMA; Departamento de Doenças Infecciosas e Parasitárias, Faculdade de Medicina da Universidade de São Paulo (FMUSP), São Paulo, Brazil.
Am J Trop Med Hyg ; 110(1): 52-58, 2024 Jan 03.
Article em En | MEDLINE | ID: mdl-38081057
The identification of Leishmania species that cause tegumentary leishmaniasis (TL) is important for taxonomic and prognostic purposes. Molecular analysis using different Leishmania genomic targets is the most useful method for identifying Leishmania species. Therefore, we evaluated the performance of ribosomal RNA internal transcribed spacer 1 (ITS1) and heat shock protein (hsp70) genetic markers by polymerase chain reaction (PCR), followed by restriction fragment length polymorphism analysis (RFLP) and sequencing, for identification of Leishmania species. Samples from 84 Brazilian patients were amplified. Internal transcribed spacer 1 PCR followed by RFLP (HaeIII) [ITS1-RFLP (HaeIII)] identified 46.4% (39/84) of the samples as compatible with the Viannia subgenus. Internal transcribed spacer 1 PCR followed by sequencing (ITS1-sequencing) identified Leishmania (Viannia) braziliensis in 91.7% (77/84) of the TL samples, Leishmania (Leishmania) amazonensis in 3.6% (3/84), L. (V.) guyanensis in 2.4% (2/84), and L. (L.) infantum in 1.2% (1/84). One of the samples showed the same proportion of similarity with L. (V.) guyanensis and L. (V.) panamensis. hsp70 nested PCR followed by RFLP (HaeIII) [nested hsp70-RFLP (HaeIII)] identified 91.7% (77/84) of the samples as compatible with L. (V.) braziliensis/L. (V.) naiffi, 3.6% (3/84) with L. (L.) amazonensis, 1.2% (1/84) with L. (L.) infantum, and 3.6% (3/84) with L. (V.) guyanensis. hsp70 PCR followed by sequencing (hsp70-sequencing) identified L. (V.) braziliensis in 91.7% (77/84) of the TL samples, L. (L.) amazonensis in 3.6% (3/84), L. (V.) guyanensis in 3.6% (3/84), and L. (L.) infantum in 1.2% (1/84). Our findings clearly showed that nested hsp70-RFLP (HaeIII) is better than ITS1-RFLP (HaeIII) and that ITS1 or hsp70 PCR followed by sequencing was adequate for identifying Leishmania species. We also found that Leishmania (Viannia) braziliensis is the most common species causing TL in Brazil. Therefore, sequencing multiple target genes such as ITS1 and hsp 70 is more accurate than RFLP for identifying Leishmania species.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leishmania braziliensis / Leishmaniose / Leishmaniose Cutânea / Leishmania Limite: Humans País/Região como assunto: America do sul / Brasil Idioma: En Revista: Am J Trop Med Hyg Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Brasil

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leishmania braziliensis / Leishmaniose / Leishmaniose Cutânea / Leishmania Limite: Humans País/Região como assunto: America do sul / Brasil Idioma: En Revista: Am J Trop Med Hyg Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Brasil