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Development of a Novel Primer-TaqMan Probe Set for Diagnosis and Quantification of Meloidogyne enterolobii in Soil Using qPCR and Droplet Digital PCR Assays.


ABSTRACT: Early detection of pathogens before the planting season is valuable to forecast disease occurrence. Therefore, rapid and reliable diagnostic approaches are urgently needed, especially for one of the most aggressive root knot nematodes, Meloidogyne enterolobii. In this study, we developed a novel primer-TaqMan probe set aimed at M. enterolobii. The primer-probe set was successfully applied in the identification and quantification of M. enterolobii via qPCR technology. It was also suitable for improved PCR technology, known as ddPCR analyses, and this work presents the first application of this technology for plant parasitic nematodes. Compared with qPCR, ddPCR exhibited better performance with regard to analytical sensitivity, which can provide a more accurate detection of M. enterolobii concealed in field soil. In addition, we generated standard curves to calculate the number of eggs in soil using the qPCR and ddPCR platforms. Hopefully, the results herein will be helpful for forecasting disease severity of M. enterolobii infection and adopting effective management strategies.

SUBMITTER: Chen Y 

PROVIDER: S-EPMC9569833 | biostudies-literature | 2022 Sep

REPOSITORIES: biostudies-literature

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Development of a Novel Primer-TaqMan Probe Set for Diagnosis and Quantification of <i>Meloidogyne enterolobii</i> in Soil Using qPCR and Droplet Digital PCR Assays.

Chen Yuan Y   Long Haibo H   Feng Tuizi T   Pei Yueling Y   Sun Yanfang Y   Zhang Xinchun X  

International journal of molecular sciences 20220923 19


Early detection of pathogens before the planting season is valuable to forecast disease occurrence. Therefore, rapid and reliable diagnostic approaches are urgently needed, especially for one of the most aggressive root knot nematodes, <i>Meloidogyne enterolobii</i>. In this study, we developed a novel primer-TaqMan probe set aimed at <i>M. enterolobii</i>. The primer-probe set was successfully applied in the identification and quantification of <i>M. enterolobii</i> via qPCR technology. It was  ...[more]

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