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CA88, a nuclear repetitive DNA sequence identified in Schistosoma mansoni, aids in the genotyping of nine Schistosoma species of medical and veterinary importance
Bahia, Diana; Rodrigues, Nilton B; Araújo, Flávio Marcos G; Romanha, Álvaro José; Ruiz, Jerônimo C; Johnston, David A; Oliveira, Guilherme.
  • Bahia, Diana; Universidade Federal de São Paulo. Escola Paulista de Medicina. Imunologia e Parasitologia. Departamento de Microbiologia. São Paulo. BR
  • Rodrigues, Nilton B; Instituto de Pesquisas René Rachou-Fiocruz. Belo Horizonte. BR
  • Araújo, Flávio Marcos G; Instituto de Pesquisas René Rachou-Fiocruz. Belo Horizonte. BR
  • Romanha, Álvaro José; Instituto de Pesquisas René Rachou-Fiocruz. Belo Horizonte. BR
  • Ruiz, Jerônimo C; Instituto de Pesquisas René Rachou-Fiocruz. Belo Horizonte. BR
  • Johnston, David A; The Natural History Museum. Department of Zoology. London. GB
  • Oliveira, Guilherme; Instituto de Pesquisas René Rachou-Fiocruz. Belo Horizonte. BR
Mem. Inst. Oswaldo Cruz ; 105(4): 391-397, July 2010. tab, ilus
Artículo en Inglés | LILACS | ID: lil-554803
ABSTRACT
CA88 is the first long nuclear repetitive DNA sequence identified in the blood fluke, Schistosoma mansoni. The assembled S. mansoni sequence, which contains the CA88 repeat, has 8,887 nucleotides and at least three repeat units of approximately 360 bp. In addition, CA88 also possesses an internal CA microsatellite, identified as SmBr18. Both PCR and BLAST analysis have been used to analyse and confirm the CA88 sequence in other S. mansoni sequences in the public database. PCR-acquired nuclear repetitive DNA sequence profiles from nine Schistosoma species were used to classify this organism into four genotypes. Included among the nine species analysed were five sequences of both African and Asian lineages that are known to infect humans. Within these genotypes, three of them refer to recognised species groups. A panel of four microsatellite loci, including SmBr18 and three previously published loci, has been used to characterise the nine Schistosoma species. Each species has been identified and classified based on its CA88 DNA fingerprint profile. Furthermore, microsatellite sequences and intra-specific variation have also been observed within the nine Schistosoma species sequences. Taken together, these results support the use of these markers in studying the population dynamics of Schistosoma isolates from endemic areas and also provide new methods for investigating the relationships between different populations of parasites. In addition, these data also indicate that Schistosoma magrebowiei is not a sister taxon to Schistosoma mattheei, prompting a new designation to a basal clade.
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Texto completo: Disponible Índice: LILACS (Américas) Asunto principal: Schistosoma / Secuencias Repetitivas de Ácidos Nucleicos / ADN de Helmintos / Repeticiones de Microsatélite Límite: Animales Idioma: Inglés Revista: Mem. Inst. Oswaldo Cruz Asunto de la revista: Medicina Tropical / Parasitología Año: 2010 Tipo del documento: Artículo / Documento de proyecto País de afiliación: Brasil / Reino Unido Institución/País de afiliación: Instituto de Pesquisas René Rachou-Fiocruz/BR / The Natural History Museum/GB / Universidade Federal de São Paulo/BR

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Texto completo: Disponible Índice: LILACS (Américas) Asunto principal: Schistosoma / Secuencias Repetitivas de Ácidos Nucleicos / ADN de Helmintos / Repeticiones de Microsatélite Límite: Animales Idioma: Inglés Revista: Mem. Inst. Oswaldo Cruz Asunto de la revista: Medicina Tropical / Parasitología Año: 2010 Tipo del documento: Artículo / Documento de proyecto País de afiliación: Brasil / Reino Unido Institución/País de afiliación: Instituto de Pesquisas René Rachou-Fiocruz/BR / The Natural History Museum/GB / Universidade Federal de São Paulo/BR