2003
DOI: 10.1016/s0732-8893(03)00063-4
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Cloning and sequencing an unknown gene of Tropheryma whipplei and development of two LightCycler® PCR assays

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Cited by 18 publications
(5 citation statements)
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“…In this study, only the 16S and 23S rDNA sequences of the Tropheryma variant were determined. BLAST analysis of 16S rDNA primers described in literature for detection of T. whipplei [12,13] indicates that not all of them will detect the new variant. For example, primer W3AF [14] has a mismatch at its 3 0 end which might interfere with PCR amplification.…”
Section: Discussionmentioning
confidence: 99%
“…In this study, only the 16S and 23S rDNA sequences of the Tropheryma variant were determined. BLAST analysis of 16S rDNA primers described in literature for detection of T. whipplei [12,13] indicates that not all of them will detect the new variant. For example, primer W3AF [14] has a mismatch at its 3 0 end which might interfere with PCR amplification.…”
Section: Discussionmentioning
confidence: 99%
“…Thus, qPCR is used to quantify DNA o cDNA, determining gene or transcript numbers present within different samples [25,26,27]. qPCR offers advantages such as speed in the result, the reduced risk of contamination and the ease in handling technology [28,29]. This PCR uses fluorescence detection systems which are generally of two types: intercalating agents and labeled probes with fluorophores.…”
Section: Real Time Pcrmentioning
confidence: 99%
“…The PCR technique described by Meibach et al . in 2003 was used [11]. Having diagnosed Tropheryma whipplei right heart endocarditis, we switched the antibiotic regimen to ceftriaxone 2 g once daily.…”
Section: Case Presentationmentioning
confidence: 99%