2018
DOI: 10.1007/s10658-018-01633-7
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Rapid diagnosis of Ditylenchus destructor by loop-mediated isothermal amplification assay based on 28S rRNA sequences

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Cited by 11 publications
(9 citation statements)
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“…The amplification of ITS1-5.8S-ITS2 of the ribosomal DNA produced a fragment of almost 1000 bp. Nowadays, the molecular diagnostic of D. destructor is primarily based on the specific sequences of some conserved regions by the conventional PCR, and the most commonly used regions are small subunits and internal transcribed spacer (ITS) of ribosomal RNA [2].…”
Section: Tablementioning
confidence: 99%
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“…The amplification of ITS1-5.8S-ITS2 of the ribosomal DNA produced a fragment of almost 1000 bp. Nowadays, the molecular diagnostic of D. destructor is primarily based on the specific sequences of some conserved regions by the conventional PCR, and the most commonly used regions are small subunits and internal transcribed spacer (ITS) of ribosomal RNA [2].…”
Section: Tablementioning
confidence: 99%
“…ITS1 differed in length from 315 to 473 bp, 5.8S measured ca 154bp and ITS2 was 207 bp. The identified distinction in length in the ITS1 was affected by the insertion of 57 to 188 bp in the entire length in some D. destructor [2]. A mentioned primer set can be used for specific identification of D. destructor.…”
Section: Plant Protectionmentioning
confidence: 99%
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“…[2] Ditylenchus destructor is an important plant pathogenic nematode in agricultural production and is listed as a quarantine pest by many countries and regions. [3] Currently, plant-parasitic nematodes are major pests responsible for global agricultural losses amounting to an estimated $157 billion annually. [4] The widespread using of synthetic pesticides has resulted in the development of insecticide-resistant populations and harmful effects on human health and the environment.…”
Section: Introductionmentioning
confidence: 99%