<abstract xmlns="http://www.w3.org/1999/xhtml">

<p>The stem and bulb nematode <italic>Ditylenchus dipsaci</italic> is a destructive nematode pest on many crops and is internationally quarantined in many countries, whereas <italic>Ditylenchus weischeri</italic>, only known to infect a weed plant (<italic>Cirsium arvense</italic>), is an unregulated nematode species with no known economic importance. In this study, we used comparative genomics to identify multiple gene regions and developed novel real-time PCR assays for the detection of <italic>D. dipsaci</italic> and <italic>D. weischeri</italic>. We sequenced the genomes of two mixed-stage nematode populations of <italic>D. dipsaci</italic> and two mixed-stage nematode populations of <italic>D. weischeri</italic>. The assembled genomes of <italic>D. dipsaci</italic> were 228.2 Mb and 239.5 Mb, and the genomes of <italic>D. weischeri</italic> were 177.0 Mb and 196.3 Mb. Depending on the species, 21,403–27,365 gene models were predicted. Using orthologous group analysis, single-copy and species-specific genes were identified. Primers and probes were designed targeting two species-specific genes in each species. The assays detected as low as 12 pg of DNA from the target species, or as few as five nematodes, with a C<sub>q</sub> of 31 cycles or less. Our study provides genome data for two additional <italic>D. dipsaci</italic> isolates and two <italic>D. weischeri</italic> isolates, and four new and validated molecular assays to be used for rapid detection and identification of the two species.</p></abstract>

The stem and bulb nematode Ditylenchus dipsaci is a destructive nematode pest on many crops and is internationally quarantined in many countries, whereas Ditylenchus weischeri, only known to infect a weed plant (Cirsium arvense), is an unregulated nematode species with no known economic importance. In this study, we used comparative genomics to identify multiple gene regions and developed novel real-time PCR assays for the detection of D. dipsaci and D. weischeri. We sequenced the genomes of two mixed-stage nematode populations of D. dipsaci and two mixed-stage nematode populations of D. weischeri. The assembled genomes of D. dipsaci were 228.2 Mb and 239.5 Mb, and the genomes of D. weischeri were 177.0 Mb and 196.3 Mb. Depending on the species, 21,403–27,365 gene models were predicted. Using orthologous group analysis, single-copy and species-specific genes were identified. Primers and probes were designed targeting two species-specific genes in each species. The assays detected as low as 12 pg of DNA from the target species, or as few as five nematodes, with a Cq of 31 cycles or less. Our study provides genome data for two additional D. dipsaci isolates and two D. weischeri isolates, and four new and validated molecular assays to be used for rapid detection and identification of the two species.

Genome Characterization and Development of Real-Time PCR Assays for <italic>Ditylenchus dipsaci</italic> and <italic>D. weischeri</italic>

Journal of Nematology

This work is licensed under the Creative Commons Attribution 4.0 International License.

Genome Characterization and Development of Real-Time PCR Assays for  and 

The stem and bulb nematode Ditylenchus dipsaci is a destructive nematode pest on many crops and is internationally quarantined in many countries, whereas...

Genome Characterization and Development of Real-Time PCR Assays for Ditylenchus dipsaci and D. weischeri

Article Category: Research Paper

Data publikacji: 01 lut 2023

Zakres stron: -

Otrzymano: 08 sie 2022

DOI: https://doi.org/10.2478/jofnem-2022-0058

Słowa kluczowe
detection, genomics, Illumina sequencing, Nanopore sequencing, real-time PCR, stem and bulb nematode

© 2022 Walter de Gruyter GmbH, Berlin/Boston

This work is licensed under the Creative Commons Attribution 4.0 International License.

Genome Characterization and Development of Real-Time PCR Assays for Ditylenchus dipsaci and D. weischeri

Article Category: Research Paper

Data publikacji: 01 lut 2023

Zakres stron: -

Otrzymano: 08 sie 2022

DOI: https://doi.org/10.2478/jofnem-2022-0058

Słowa kluczowedetection, genomics, Illumina sequencing, Nanopore sequencing, real-time PCR, stem and bulb nematode

© 2022 Walter de Gruyter GmbH, Berlin/Boston

This work is licensed under the Creative Commons Attribution 4.0 International License.

Słowa kluczowe
detection, genomics, Illumina sequencing, Nanopore sequencing, real-time PCR, stem and bulb nematode