PCR-RAPD and PCR-RFLP polymorphisms detected in Anopheles cruzii (Diptera, Culicidae)

Detalhes bibliográficos
Autor(a) principal: Calado,Daniéla
Data de Publicação: 2006
Outros Autores: Navarro-Silva,Mario Antonio, Sallum,Maria Anice Mureb
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Revista brasileira de entomologia (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0085-56262006000300014
Resumo: The aim of the present study was to examine genetic variability in populations of An. cruzii by employing PCR-RAPD and PCR-RFLP markers. All analyses were carried out using individuals of the F1 generation of wild caught females obtained in Santa Catarina State (Florianópolis and São Francisco do Sul), Paraná State (Morretes, Paranaguá and Guaratuba) and São Paulo State (Cananéia). In the PCR-RAPD experiments, seven primers were used for comparisons within and among populations. The restriction profile of the ITS2 including a fragment of both 5.8S and 28S regions of the rDNA was obtained with the enzymes BstUI, HaeIII, TaqI, HhaI, Sau96I, HinfI, HincII and NruI. The PCR-RAPD method detected a large number of polymorphic bands. Genetic distance among populations of An. cruzii varied from 0,0214 to 0,0673, suggesting that all individuals used in the analyses belong to a single species. The number of migrants per generation (Nm) was 4.3, showing the existence of gene flow among populations. The restriction profile of the ITS2, 5.8S and 28S gene regions was similar in all An. cruzii samples, whereas the results obtained by using HhaI and NruI are indicative that the individuals analyzed have nucleotide sequences distinct from those of An. cruzii samples from Peruíbe and Juquiazinho deposited in GenBank.
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spelling PCR-RAPD and PCR-RFLP polymorphisms detected in Anopheles cruzii (Diptera, Culicidae)Anophelinaegenetic variabilityITS2molecular markersThe aim of the present study was to examine genetic variability in populations of An. cruzii by employing PCR-RAPD and PCR-RFLP markers. All analyses were carried out using individuals of the F1 generation of wild caught females obtained in Santa Catarina State (Florianópolis and São Francisco do Sul), Paraná State (Morretes, Paranaguá and Guaratuba) and São Paulo State (Cananéia). In the PCR-RAPD experiments, seven primers were used for comparisons within and among populations. The restriction profile of the ITS2 including a fragment of both 5.8S and 28S regions of the rDNA was obtained with the enzymes BstUI, HaeIII, TaqI, HhaI, Sau96I, HinfI, HincII and NruI. The PCR-RAPD method detected a large number of polymorphic bands. Genetic distance among populations of An. cruzii varied from 0,0214 to 0,0673, suggesting that all individuals used in the analyses belong to a single species. The number of migrants per generation (Nm) was 4.3, showing the existence of gene flow among populations. The restriction profile of the ITS2, 5.8S and 28S gene regions was similar in all An. cruzii samples, whereas the results obtained by using HhaI and NruI are indicative that the individuals analyzed have nucleotide sequences distinct from those of An. cruzii samples from Peruíbe and Juquiazinho deposited in GenBank.Sociedade Brasileira De Entomologia2006-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0085-56262006000300014Revista Brasileira de Entomologia v.50 n.3 2006reponame:Revista brasileira de entomologia (Online)instname:Sociedade Brasileira De Entomologia (SBE)instacron:SBE10.1590/S0085-56262006000300014info:eu-repo/semantics/openAccessCalado,DaniélaNavarro-Silva,Mario AntonioSallum,Maria Anice Murebeng2006-10-27T00:00:00Zoai:scielo:S0085-56262006000300014Revistahttp://www.rbentomologia.com/https://old.scielo.br/oai/scielo-oai.php||sbe@ufpr.br1806-96650085-5626opendoar:2006-10-27T00:00Revista brasileira de entomologia (Online) - Sociedade Brasileira De Entomologia (SBE)false
dc.title.none.fl_str_mv PCR-RAPD and PCR-RFLP polymorphisms detected in Anopheles cruzii (Diptera, Culicidae)
title PCR-RAPD and PCR-RFLP polymorphisms detected in Anopheles cruzii (Diptera, Culicidae)
spellingShingle PCR-RAPD and PCR-RFLP polymorphisms detected in Anopheles cruzii (Diptera, Culicidae)
Calado,Daniéla
Anophelinae
genetic variability
ITS2
molecular markers
title_short PCR-RAPD and PCR-RFLP polymorphisms detected in Anopheles cruzii (Diptera, Culicidae)
title_full PCR-RAPD and PCR-RFLP polymorphisms detected in Anopheles cruzii (Diptera, Culicidae)
title_fullStr PCR-RAPD and PCR-RFLP polymorphisms detected in Anopheles cruzii (Diptera, Culicidae)
title_full_unstemmed PCR-RAPD and PCR-RFLP polymorphisms detected in Anopheles cruzii (Diptera, Culicidae)
title_sort PCR-RAPD and PCR-RFLP polymorphisms detected in Anopheles cruzii (Diptera, Culicidae)
author Calado,Daniéla
author_facet Calado,Daniéla
Navarro-Silva,Mario Antonio
Sallum,Maria Anice Mureb
author_role author
author2 Navarro-Silva,Mario Antonio
Sallum,Maria Anice Mureb
author2_role author
author
dc.contributor.author.fl_str_mv Calado,Daniéla
Navarro-Silva,Mario Antonio
Sallum,Maria Anice Mureb
dc.subject.por.fl_str_mv Anophelinae
genetic variability
ITS2
molecular markers
topic Anophelinae
genetic variability
ITS2
molecular markers
description The aim of the present study was to examine genetic variability in populations of An. cruzii by employing PCR-RAPD and PCR-RFLP markers. All analyses were carried out using individuals of the F1 generation of wild caught females obtained in Santa Catarina State (Florianópolis and São Francisco do Sul), Paraná State (Morretes, Paranaguá and Guaratuba) and São Paulo State (Cananéia). In the PCR-RAPD experiments, seven primers were used for comparisons within and among populations. The restriction profile of the ITS2 including a fragment of both 5.8S and 28S regions of the rDNA was obtained with the enzymes BstUI, HaeIII, TaqI, HhaI, Sau96I, HinfI, HincII and NruI. The PCR-RAPD method detected a large number of polymorphic bands. Genetic distance among populations of An. cruzii varied from 0,0214 to 0,0673, suggesting that all individuals used in the analyses belong to a single species. The number of migrants per generation (Nm) was 4.3, showing the existence of gene flow among populations. The restriction profile of the ITS2, 5.8S and 28S gene regions was similar in all An. cruzii samples, whereas the results obtained by using HhaI and NruI are indicative that the individuals analyzed have nucleotide sequences distinct from those of An. cruzii samples from Peruíbe and Juquiazinho deposited in GenBank.
publishDate 2006
dc.date.none.fl_str_mv 2006-09-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0085-56262006000300014
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0085-56262006000300014
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0085-56262006000300014
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira De Entomologia
publisher.none.fl_str_mv Sociedade Brasileira De Entomologia
dc.source.none.fl_str_mv Revista Brasileira de Entomologia v.50 n.3 2006
reponame:Revista brasileira de entomologia (Online)
instname:Sociedade Brasileira De Entomologia (SBE)
instacron:SBE
instname_str Sociedade Brasileira De Entomologia (SBE)
instacron_str SBE
institution SBE
reponame_str Revista brasileira de entomologia (Online)
collection Revista brasileira de entomologia (Online)
repository.name.fl_str_mv Revista brasileira de entomologia (Online) - Sociedade Brasileira De Entomologia (SBE)
repository.mail.fl_str_mv ||sbe@ufpr.br
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