Detection of Salmonella invA by isothermal and chimeric primer-initiated amplification of nucleic acids (ICAN) in Zambia

dc.contributor.authorYabe, John
dc.contributor.authorIsogai, Emiko
dc.contributor.authorMakungu, Chitwambi
dc.contributor.authorSinkala, Patson
dc.contributor.authorNambota, Andrew
dc.contributor.authorIsogai, Hiroshi
dc.contributor.authorFukushi, Hideto
dc.contributor.authorSilungwe, Manda
dc.contributor.authorMubita, Charles
dc.contributor.authorSyakalima, Michelo
dc.contributor.authorHang’ombe, Bernard Mudenda
dc.contributor.authorKozaki, Shunji
dc.contributor.authorYasuda, Jun
dc.date.accessioned2019-02-26T12:46:21Z
dc.date.available2019-02-26T12:46:21Z
dc.date.issued2005-09-13
dc.descriptionJournal articleen
dc.description.abstractThe isothermal and chimeric primer-initiated amplification of nucleic acids (ICAN) is a new isothermal DNA amplification method composed of exo Bca DNA polymerase, RNaseH and DNA–RNA chimeric primers. We detected invA of Salmonella from chicken carcasses, egg yolk and cattle fecal samples. Fifty-three of 59 isolates were invA-positive in ICAN-chromatostrip detection. The result was consistent with those obtained by standard PCR. Salmonella invA was detected in 12 of 14 carcass rinses by ICAN, while in 7 of 14 rinses by standard PCR. These results indicate that ICAN is an efficient, sensitive and simple system to detect invA of Salmonella species in developing countries such as Zambia.en
dc.identifier.urihttp://dspace.unza.zm/handle/123456789/5790
dc.language.isoenen
dc.publisherElsevieren
dc.subjectSalmonellaen
dc.subjectinvAen
dc.subjectICAN--PCR--Zambiaen
dc.titleDetection of Salmonella invA by isothermal and chimeric primer-initiated amplification of nucleic acids (ICAN) in Zambiaen
dc.typeArticleen
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