Rapid detection of Salmonella Typhi by loop-mediated isothermal amplification (LAMP) method
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Brazilian Journal of Microbiology |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822014000400032 |
Resumo: | An in-house loop-mediated isothermal amplification (LAMP) reaction was established and evaluated for sensitivity and specificity in detecting the presence of Salmonella Typhi (S. Typhi) isolates from Kelantan, Malaysia. Three sets of primers consisting of two outer and 4 inner were designed based on locus STBHUCCB_38510 of chaperone PapD of S. Typhi genes. The reaction was optimised using genomic DNA of S. Typhi ATCC7251 as the template. The products were visualised directly by colour changes of the reaction. Positive results were indicated by green fluorescence and negative by orange colour. The test was further evaluated for specificity, sensitivity and application on field samples. The results were compared with those obtained by gold standard culture method and Polymerase Chain Reaction (PCR). This method was highly specific and -10 times more sensitive in detecting S. Typhi compared to the optimised conventional polymerase chain reaction (PCR) method. |
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Brazilian Journal of Microbiology |
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Rapid detection of Salmonella Typhi by loop-mediated isothermal amplification (LAMP) methodloop-mediated isothermal amplification (LAMP)Salmonella TyphiAn in-house loop-mediated isothermal amplification (LAMP) reaction was established and evaluated for sensitivity and specificity in detecting the presence of Salmonella Typhi (S. Typhi) isolates from Kelantan, Malaysia. Three sets of primers consisting of two outer and 4 inner were designed based on locus STBHUCCB_38510 of chaperone PapD of S. Typhi genes. The reaction was optimised using genomic DNA of S. Typhi ATCC7251 as the template. The products were visualised directly by colour changes of the reaction. Positive results were indicated by green fluorescence and negative by orange colour. The test was further evaluated for specificity, sensitivity and application on field samples. The results were compared with those obtained by gold standard culture method and Polymerase Chain Reaction (PCR). This method was highly specific and -10 times more sensitive in detecting S. Typhi compared to the optimised conventional polymerase chain reaction (PCR) method.Sociedade Brasileira de Microbiologia2014-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822014000400032Brazilian Journal of Microbiology v.45 n.4 2014reponame:Brazilian Journal of Microbiologyinstname:Sociedade Brasileira de Microbiologia (SBM)instacron:SBM10.1590/S1517-83822014000400032info:eu-repo/semantics/openAccessAbdullah,J.Saffie,N.Sjasri,F.A.R.Husin,A.Abdul-Rahman,Z.Ismail,A.Aziah,I.Mohamed,M.eng2015-02-19T00:00:00Zoai:scielo:S1517-83822014000400032Revistahttps://www.scielo.br/j/bjm/ONGhttps://old.scielo.br/oai/scielo-oai.phpbjm@sbmicrobiologia.org.br||mbmartin@usp.br1678-44051517-8382opendoar:2015-02-19T00:00Brazilian Journal of Microbiology - Sociedade Brasileira de Microbiologia (SBM)false |
dc.title.none.fl_str_mv |
Rapid detection of Salmonella Typhi by loop-mediated isothermal amplification (LAMP) method |
title |
Rapid detection of Salmonella Typhi by loop-mediated isothermal amplification (LAMP) method |
spellingShingle |
Rapid detection of Salmonella Typhi by loop-mediated isothermal amplification (LAMP) method Abdullah,J. loop-mediated isothermal amplification (LAMP) Salmonella Typhi |
title_short |
Rapid detection of Salmonella Typhi by loop-mediated isothermal amplification (LAMP) method |
title_full |
Rapid detection of Salmonella Typhi by loop-mediated isothermal amplification (LAMP) method |
title_fullStr |
Rapid detection of Salmonella Typhi by loop-mediated isothermal amplification (LAMP) method |
title_full_unstemmed |
Rapid detection of Salmonella Typhi by loop-mediated isothermal amplification (LAMP) method |
title_sort |
Rapid detection of Salmonella Typhi by loop-mediated isothermal amplification (LAMP) method |
author |
Abdullah,J. |
author_facet |
Abdullah,J. Saffie,N. Sjasri,F.A.R. Husin,A. Abdul-Rahman,Z. Ismail,A. Aziah,I. Mohamed,M. |
author_role |
author |
author2 |
Saffie,N. Sjasri,F.A.R. Husin,A. Abdul-Rahman,Z. Ismail,A. Aziah,I. Mohamed,M. |
author2_role |
author author author author author author author |
dc.contributor.author.fl_str_mv |
Abdullah,J. Saffie,N. Sjasri,F.A.R. Husin,A. Abdul-Rahman,Z. Ismail,A. Aziah,I. Mohamed,M. |
dc.subject.por.fl_str_mv |
loop-mediated isothermal amplification (LAMP) Salmonella Typhi |
topic |
loop-mediated isothermal amplification (LAMP) Salmonella Typhi |
description |
An in-house loop-mediated isothermal amplification (LAMP) reaction was established and evaluated for sensitivity and specificity in detecting the presence of Salmonella Typhi (S. Typhi) isolates from Kelantan, Malaysia. Three sets of primers consisting of two outer and 4 inner were designed based on locus STBHUCCB_38510 of chaperone PapD of S. Typhi genes. The reaction was optimised using genomic DNA of S. Typhi ATCC7251 as the template. The products were visualised directly by colour changes of the reaction. Positive results were indicated by green fluorescence and negative by orange colour. The test was further evaluated for specificity, sensitivity and application on field samples. The results were compared with those obtained by gold standard culture method and Polymerase Chain Reaction (PCR). This method was highly specific and -10 times more sensitive in detecting S. Typhi compared to the optimised conventional polymerase chain reaction (PCR) method. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-12-01 |
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=S1517-83822014000400032 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1517-83822014000400032 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S1517-83822014000400032 |
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 Microbiologia |
publisher.none.fl_str_mv |
Sociedade Brasileira de Microbiologia |
dc.source.none.fl_str_mv |
Brazilian Journal of Microbiology v.45 n.4 2014 reponame:Brazilian Journal of Microbiology instname:Sociedade Brasileira de Microbiologia (SBM) instacron:SBM |
instname_str |
Sociedade Brasileira de Microbiologia (SBM) |
instacron_str |
SBM |
institution |
SBM |
reponame_str |
Brazilian Journal of Microbiology |
collection |
Brazilian Journal of Microbiology |
repository.name.fl_str_mv |
Brazilian Journal of Microbiology - Sociedade Brasileira de Microbiologia (SBM) |
repository.mail.fl_str_mv |
bjm@sbmicrobiologia.org.br||mbmartin@usp.br |
_version_ |
1752122206947639296 |