2002
DOI: 10.1590/s0074-02762002000900011
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Polymerase chain reaction and restriction fragment length polymorphism of cytocrome oxidase subunit I used for differentiation of Brazilian Biomphalaria species intermediate host of Schistosoma mansoni

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Cited by 12 publications
(12 citation statements)
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“…A basic approach to develop such type test has been to employ universal PCR primers to amplify the COI gene and to subject the products to restriction fragment length polymorphism (RFPL) analysis (Vidigal et al. ; Caldeira et al. ; Thyssen et al.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…A basic approach to develop such type test has been to employ universal PCR primers to amplify the COI gene and to subject the products to restriction fragment length polymorphism (RFPL) analysis (Vidigal et al. ; Caldeira et al. ; Thyssen et al.…”
Section: Introductionmentioning
confidence: 99%
“…A basic approach to develop such type test has been to employ universal PCR primers to amplify the COI gene and to subject the products to restriction fragment length polymorphism (RFPL) analysis (Vidigal et al 2002;Caldeira et al 2003;Thyssen et al 2005). In addition, a large number of species-specific COI sequences (nearly 150,000 species) have now been submitted to public sequence databases such as GenBank or The Barcode of Life Data System (BOLD) for use in taxonomic and phylogenetic studies of insects (Kwong et al 2012;Ptaszy nska et al 2012;Smith et al 2012).…”
Section: Introductionmentioning
confidence: 99%
“…PCR-RFLP of the ITS region was used in the identification of species of the genus Lymnaea from different localities in Brazil and Argentina (Carvalho et al, 2004). The COI region was used in the differentiation of three species of Biomphalaria, which are the natural hosts of S. mansoni in Brazil (Vidigal et al, 2002b). The 16S region was employed in the identification of the native species of bivalves Crassostrea brasiliana (Lamarck, 1819) and C. rhizophorae (Guilding, 1828) and the introduced species C. gigas (Thunberg, 1793) (Pie et al, 2006b).…”
Section: Specific Dna Regionsmentioning
confidence: 99%
“…Fixed specimens were identified by means of comparative morphology of the reproductive organs and shells 11 12 13 15 . Total DNA was extracted from the foot of each snail using the Wizard Genomic DNA Purification Kit (Promega) 21 . The ITS2 region was amplified using the primers ITS2F (5'-CGTCCGTCTGAGGGTCGGTTTGC-3) 20 and ETTS1 (5 ' -TGCTTAAGTTCAGCGGGT-3') 7 anchored in the conserved extremities of the 5.8S and 28S ribosomal genes, respectively.…”
mentioning
confidence: 99%