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Am. J. Trop. Med. Hyg., 70(2), 2004, pp. 221-224
Copyright © 2004 by The American Society of Tropical Medicine and Hygiene

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DETERMINATION OF THE PREVALENCE OF ENTAMOEBA HISTOLYTICA AND E. DISPAR IN THE PERNAMBUCO STATE OF NORTHEASTERN BRAZIL BY A POLYMERASE CHAIN REACTION

SANDRA M. B. PINHEIRO, ROSA M. CARNEIRO, IVANISE S. ACA, JOÃO I. IRMÃO, MARCOS A. MORAIS, JR., MARIA R. M. COIMBRA, AND LUIZ B. CARVALHO, JR.
Laboratório de Imunopatologia Keizo Asami; Departamento de Medicina Tropical; Departamento de Medicina Social; Departamento de Genética, e Departamento de Bioquímica, Universidade Federal de Pernambuco, Recife, Pernambuco, Brazil; Departamento de Pesca, Universidade Federal Rural de Pernambuco, Recife, Brazil

Previous studies using methods varying from traditional serologic tests to molecular biology techniques have shown that in northeastern Brazil, Entamoeba dispar was more prevalent than E. histolytica. In this study, the prevalence was established by using E. histolytica stool antigen detection kits and a polymerase chain reaction (PCR) with genomic DNA extracted from cultured trophozoites in all four-nuclei, amoeba-positive samples from a population living in Macaparana in northeastern Brazil. Among 1,437 stool samples analyzed, only 59 (4.1%) were positive for four nuclei amoeba. However, all of these samples were negative in an immunoenzymatic assay for the presence of E. histolytica-specific galactose adhesin. Of 59 cultivated samples, only 31 showed trophozoites. Extraction of DNA from these 31 samples, followed by the PCR, showed that 23 samples (74.19%) were positive for E. dispar and no amplification was observed for pathogenic E. histolytica. The remaining eight samples were negative for both species. These findings are consistent with those previously reported.


Received August 14, 2003. Accepted for publication October 7, 2003.

Acknowledgments: We thank Dr. Tsutomo Takeuchi (Department of Tropical Medicine and Parasitology of Keio University, Tokyo, Japan) for providing the primers and positive DNA controls. We also thank Dr. Seiki Kobayashi for helpful discussions during the development of this project.

Financial support: This work was supported by the Conselho Nacional de Desenvolvimento Cientifico e Technológico/Fundo Setorial do Petróleo e Gás Natural (grant number 463655/001), the Fundação de Amparo à Ciéncia e Tecnologia do Estado de Pernambuco (grant number 23-CBIO-08/00-01/01-6), and the Japan International Cooperation Agency.

Authors’ addresses: Sandra M. B. Pinheiro, Ivanise S. Aca, and João I. Irmão, Departamento de Medicina Tropical, Universidade Federal de Pernambuco, Campus Universitário, 50670-901, Recife, Pernambuco, Brazil. Rosa M. Carneiro, Departamento de Medicina Social, Universidade Federal de Pernambuco, Campus Universitário, 50670-901, Recife, Pernambuco, Brazil. Marcos A. Morais Jr., Departamento de Genética, Universidade Federal de Pernambuco, Campus Universitário, 50670-901, Recife, Pernambuco, Brazil. Maria R. M. Coimbra, Departamento de Pesca, Dom Manoel de Medeiros, Dois Irmãos, 52171-900, Universidade Federal Rural de Pernambuco, Recife, Brazil. Luiz B. Carvalho Jr., Departamento de Bioquímica, Laboratório de Imunopatologia Keizo Asami, Universidade Federal de Pernambuco, Campus Universitário, 50670-901, Recife, Pernambuco, Brazil.

Reprint requests: Luiz B. Carvalho Jr., Laboratório de Imunopatologia Keizo Asami, Universidade Federal de Pernambuco, Campus Universitário, 50670-901, Recife, Pernambuco, Brazil, Telephone: 55-81-3271-8484, Fax: 55-81-3271-8485, E-mail: lbcj{at}lika.ufpe.br.




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Copyright © 2004 by the American Society of Tropical Medicine and Hygiene.