2019
DOI: 10.4025/actasciagron.v41i1.42708
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Improvement of the specific detection of <i>Xanthomonas phaseoli</i> pv. <i>manihotis</i> based on the <i>pthB</i> gene

Abstract: Modifications were made in the PCR conditions aiming to overcome the problem of non-amplification of the Xanthomonas phaseoli pv. manihotis (Xpm) fragment, using the primer pair XV / XK described in the literature. The objective of this study was to propose changes in the primers already described (XV / XK_MOD) and validate the use of these new primers in identifying Xpm. The validation procedure was carried out with the primer pair XV and XK_MOD, using different strains of Xpm, other plant pathogenic and endo… Show more

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Cited by 3 publications
(1 citation statement)
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“…Three PCR-based methods were reported for Xpm detection recently. The first method used an optimized version of a previous assay (Verdier et al, 1998) resulting in improved Xpm detection (Cerqueira-Melo et al, 2019). The second approach was based on a multiplexed nested PCR including a broadly conserved fragment of Xpm transcription activator-like (TAL) effector genes and a semispecific region of rpoB, resulting in a wider detection potential for Xpm strains (Bernal-Galeano et al, 2018).…”
Section: Diagnostic Toolsmentioning
confidence: 99%
“…Three PCR-based methods were reported for Xpm detection recently. The first method used an optimized version of a previous assay (Verdier et al, 1998) resulting in improved Xpm detection (Cerqueira-Melo et al, 2019). The second approach was based on a multiplexed nested PCR including a broadly conserved fragment of Xpm transcription activator-like (TAL) effector genes and a semispecific region of rpoB, resulting in a wider detection potential for Xpm strains (Bernal-Galeano et al, 2018).…”
Section: Diagnostic Toolsmentioning
confidence: 99%