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Revista da Sociedade Brasileira de Medicina Tropical

Print version ISSN 0037-8682

Rev. Soc. Bras. Med. Trop. vol.44 no.5 Uberaba Sept./Oct. 2011  Epub Aug 19, 2011

http://dx.doi.org/10.1590/S0037-86822011005000049 

Evaluation of Leishmania (Leishmania) chagasi strains isolated from dogs originating from two visceral leishmaniasis-endemic areas in Brazil using multilocus enzyme electrophoresis

 

Avaliação de amostras de Leishmania (Leishmania) chagasi isoladas de cães oriundos de duas áreas endêmicas de leishmaniose visceral no Brasil através da eletroforese de isoenzimas

 

 

Carlos Eduardo Ribeiro CoutinhoI; Dilvani Oliveira SantosII; Cibele BaptistaI; Fabiano Borges FigueiredoIII; Maria de Fatima MadeiraI

ILaboratório de Vigilância em Leishmaniose, Instituto de Pesquisa Clínica Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro, RJ
IILaboratório de Biopatogêneses e Ativação Celular, Instituto de Biologia, Universidade Federal Fluminense, Niterói, RJ
IIILaboratório de Pesquisa Clínica em Dermatozoonoses em Animais Domésticos, Instituto de Pesquisa Clínica Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro, RJ

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ABSTRACT

INTRODUCTION: Domestic dogs are the most important reservoir in the peridomestic transmission cycle of Leishmania (Leishmania) chagasi. The genetic variability of subpopulations of this parasite circulating in dogs has not been thoroughly analyzed in Brazil, even though this knowledge has important implications in the clinical-epidemiological context.
METHODS: The objective of this study was to evaluate and compare the phenotypic variability of 153 L. chagasi strains isolated from dogs originating from the municipalities of Rio de Janeiro (n = 57) and Belo Horizonte (n = 96), where the disease is endemic. Strains isolated only from intact skin were selected and analyzed by multilocus enzyme electrophoresis using nine enzyme systems (6PG, GPI, NH1 and NH2, G6P, PGM, MDH, ME, and IDHNADP).
RESULTS: The electrophoretic profile was identical for all isolates analyzed and was the same as that of the L. chagasi reference strain (MHOM/BR/74/PP75). Phenetic analysis showed a similarity index of one for all strains, with the isolates sharing 100% of the characteristics analyzed.
CONCLUSIONS: The results demonstrate that the L. chagasi populations circulating in dogs from Rio de Janeiro and Belo Horizonte belong to a single zymodeme.

Keywords: Dog. Leishmania chagasi. Genetic variability. MLEE.


RESUMO

INTRODUÇÃO: Cães domésticos são considerados os reservatórios mais importantes no ciclo peridoméstico de transmissão de Leishmania (Leishmania) chagasi. No entanto, a variabilidade genética de sub-populações que circulam neste hospedeiro é ainda pouco explorada no Brasil, sendo tal conhecimento de grande importância no contexto clínico-epidemiológico.
MÉTODOS: O objetivo deste estudo foi avaliar e comparar a variabilidade fenotípica de 153 amostras de L. chagasi isoladas de cães oriundos dos municípios do Rio de Janeiro (n = 57) e Belo Horizonte (n = 96), onde a doença é endêmica. Foram selecionadas somente amostras isoladas de pele íntegra e analisadas por eletroforese de isoenzimas (MLEE) empregando nove sistemas enzimáticos (6PG, GPI, NH1 e NH2, G6P, PGM, MDH, ME, IDHNADP).
RESULTADOS: Todas as amostras analisadas apresentaram perfil eletroforético idêntico entre si e com a amostra de L. chagasi utilizada como referência neste estudo (MHOM/BR/74/PP75). A análise fenética demonstrou índice de similaridade igual a um para todas as amostras, revelando um compartilhamento de 100% dos caracteres avaliados.
CONCLUSÕES: A partir desses resultados, podemos inferir que as populações de L. chagasi que estão circulando nos cães do Rio de Janeiro e Belo Horizonte podem ser agrupadas em um único zimodema.

Palavras-chaves: Cão. Leishmania chagasi. Variabilidade genética. MLEE.


 

 

INTRODUCTION

Leishmaniases are diseases caused by different species of the genus Leishmania, including the subgenera Viannia and Leishmania1. Clinically, leishmaniasis can be divided into visceral leishmaniasis and tegumentary leishmaniasis, with both diseases presenting a broad spectrum of manifestations2,3.

In Brazil, Leishmania (Leishmania) chagasi [syn. Leishmania infantum] is the only agent that causes visceral leishmaniasis and is associated with the vector Lutzomyia longipalpis in most regions. Recently, Leishmania (Leishmania) chagasi has been detected in natural canine infections in areas unaffected by visceral leishmaniasis4.The role of the dog as a domestic reservoir in the transmission cycle of visceral leishmaniasis has been well established. The disease progresses slowly in this animal but shows an insidious onset and a variable spectrum of clinical manifestations. During more advanced stages of the disease, onychogryphosis, splenomegaly, lymphadenopathy, alopecia, dermatitis, skin ulcers, keratoconjunctivitis, a runny nose, anemia, apathy, diarrhea, intestinal hemorrhage, paw edema, vomiting, and hyperkeratosis are frequent findings5. However, the disease may remain latent in some cases and may even resolve spontaneously6.

The identity of the etiological agent of visceral leishmaniasis in the Americas has been the matter of numerous discussions7-9. For a long time, L. chagasi has been considered to be an autochthonous agent in the New World, and this hypothesis directed studies that genetically compared L. chagasi and L. infantum using isolates obtained from different hosts and by different methods10-13. In all studies cited, L. chagasi and L. infantum presented similar genetic profiles and were considered to be the same species. It is currently assumed that this parasite was introduced to South America during European colonization through dogs infected with L. infantum, the predominant species in Mediterranean countries, and that L. infantum adapted to new vectors and hosts14,15.

The correct classification of Leishmania parasites is fundamental for the establishment of control measures for the diseases caused by these organisms, and numerous tools are currently applied for this purpose. In this respect, multilocus enzyme electrophoresis (MLEE) is the reference standard for the identification of species of the genus Leishmania and is one of the methods most used for the characterization of species of this genus16-21. The characterization of isolates is important, especially in epidemiological surveillance studies, permitting the mapping of Leishmania species and variants that circulate in humans and animals in a given region. In addition, this characterization contributes to a better understanding of the factors related to these phenotypic variations, such as clinical characteristics, drug resistance, parasite virulence, preference for certain hosts, and association with certain immunosuppressive diseases.

In view of the importance of the domestic dog in the transmission cycle of L. chagasi and the importance of studies investigating the genetic variability of isolates circulating in this host, the objective of the present investigation was to evaluate and compare the phenotypic characteristics of 153 Leishmania strains isolated from dogs originating from two endemic areas in Brazil.

 

METHODS

The 153 isolates studied were obtained from the strain collection of the Laboratory of Leishmaniasis Surveillance (VigiLeish, IPEC/ FIOCRUZ). The strains isolated from dogs were obtained during epidemiological surveys carried out in the municipalities of Rio de Janeiro (Campo Grande, Guaratiba, Barra de Guaratiba, Barra da Tijuca, Jacarepaguá, Realengo and Bangu) during the period from 2000 to 2008 (RJ; n= 57) and Belo Horizonte (Barreiro, Centro Sul, Leste, Nordeste, Noroeste, Norte, Oeste, Pampulha and Lagoa de Pampulha) in 2004 (BH; n = 96). Both regions are located in southeastern Brazil. Only strains isolated from the intact skin of dogs presenting different clinical conditions were selected. First, the isolates were recovered from liquid nitrogen storage and expanded in Schneider's medium (Sigma) supplemented with 10% fetal bovine serum (Cultilab) and antibiotics (200 units/mL penicillin G potassium and 100 units/mL streptomycin) to obtain approximately 109 parasites. When in the exponential phase, the culture was pelleted by centrifugation, resuspended in appropriate buffer, and stored at -196ºC until isoenzyme electrophoresis.

Multilocus enzyme electrophoresis was performed on 1% gels according to previously described procedures17,22. Nine enzyme systems were used: glucose-6-phosphate dehydrogenase (G6PDH), 6-phosphogluconate dehydrogenase (6PGDH), glucose phosphate isomerase (GPI), nucleoside hydrolase (NH1 and NH2), phosphoglucomutase (PGM), malate dehydrogenase (MDH), malic enzyme (ME), and isocitrate dehydrogenase (IDH). The gels were analyzed by determining the electrophoretic mobility of the bands based on the standard positions of the following reference strains: Leishmania (Leishmania) chagasi (MHOM/BR/74/PP75), Leishmania (Viannia) braziliensis (MHOM/BR/75/M2903), and Leishmania (Leishmania) amazonensis (IFLA/BR/67/PH8).

The MLEE bands were compared using the simple matching coefficient of similarity, and the matrix was transformed into a dendrogram using the UPGMA algorithm23. Phenetic analysis was performed with the NTSYS-pc program, version 2.02 (Exeter Software, Setauket, NY, USA).

Ethical considerations

The collection of biological samples from the dogs was approved by the Ethics Committee on the Use of Animals of FIOCRUZ (CEUA/FIOCRUZ), license numbers P-286/06 and L-023/06.

 

RESULTS

All 153 canine isolates analyzed by MLEE demonstrated similar electrophoretic profiles, which were similar to that of the L. chagasi reference strain (MHOM/BR/74/PP75). No isoenzyme variants were observed among parasites isolated from Rio de Janeiro and Belo Horizonte. All isolates were classified into the same zymodeme, with a similarity index of one, demonstrating that all isolates studied shared 100% of the characteristics analyzed (Figure 1).

 

 

DISCUSSION

Visceral leishmaniasis is widely distributed in Brazil, with outbreaks occurring in urban areas, a fact highlighting the importance of the domestic dog in this context2,24,25. Clinically, dogs infected with L. chagasi can show a broad spectrum of manifestations or can remain asymptomatic, suggesting the circulation of distinct subpopulations of the parasite in these hosts. Because of this variation, studies investigating the genetic variability of strains isolated from dogs are extremely important but are scarce in the literature. Therefore, the objective of this study was to evaluate and compare the phenotypic characteristics of L. chagasi strains isolated from dogs originating from two endemic areas in Brazil.

In addition to being an effective method for the identification of Leishmania isolates, isoenzyme electrophoresis has various applications. One of the disadvantages of this technique is the need for previous isolation of the parasite to subsequently obtain a large culture volume, a fact that has contributed to the use of PCR-based methods in many studies26,27. However, the variability of parasites of the genus Leishmania has been widely studied by MLEE11,19,28.

In the present study, nine enzyme systems were used for the analysis of 153 L. chagasi strains isolated from animals originating from two endemic regions. These isolates presented identical electrophoretic profiles. This result demonstrates that the isolates originating from the two endemic regions showed no difference that could be associated with geographic area or host status, indicating complete homogeneity of this species. This fact has also been reported by other investigators who demonstrated the absence of enzyme polymorphisms in L. chagasi isolates11,29,30. In this respect, one interesting fact is the large heterogeneity observed among L. infantum strains, with the numerous zymodemes circulating naturally in different regions of the Old World31. MON-1 is the only zymodeme described for L. infantum that shows identity with L. chagasi in the Americas. This fact suggests that the introduction of L. chagasi to the American continent occurred at a single time point and that all strains in the Americas are derived from this zymodeme or that only this zymodeme found conditions that permitted the adaptation and propagation of the parasite. This fact may also explain the homogeneity of L. chagasi observed in this study and reported by other investigators12. The homogeneity of this species may also be related to the poor diversity of vertebrate and invertebrate hosts in the transmission cycle or to the fact that all isolates analyzed were obtained from a single anatomical site on the animals (intact skin), somehow standardizing subpopulations that show tropism for this site. Parasitism of intact skin of dogs infected with L. chagasi, which was described for the first time in the 1950s32, is one of the characteristics that renders the dog an important reservoir in the transmission cycle. This site has been used for the parasitological confirmation of seroreactive dogs, and the isolates for the present study were obtained from this site, demonstrating that the skin is an excellent target for the parasitological confirmation of canine visceral leishmaniasis33,34.

The present results demonstrate the low variability of L. chagasi. In addition, the findings demonstrate that the population of Leishmania parasites circulating in dogs from Rio de Janeiro and Belo Horizonte is extremely homogeneous and shares 100% of characteristics, revealing that the isolates analyzed in this study all belong to a single zymodeme.

 

ACKNOWLEDGMENTS

We thank Célia de Fatima Moreira Venâncio for technical assistance. This research is part of the Master Degree Dissertation in Clinical Research in Infectious Disease of Carlos Eduardo Ribeiro Coutinho in the Program of the Instituto de Pesquisa Clínica Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil.

 

CONFLICT OF INTEREST

The authors declare that there is no conflict of interest.

 

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Address to:
Dra. Maria de Fatima Madeira
Lab. Vigilância em Leishmanioses/IPEC/FIOCRUZ
Av. Brasil 4.365
21040-900 Rio de Janeiro, RJ, Brasil
Phone/fax: 55 21 3865-9541
e-mail: fatima.madeira@ipec.fiocruz.br

Received in 06/11/2010
Accepted in 19/04/2011

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