2007
DOI: 10.3852/mycologia.99.6.797
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Identification and detection of Macrophomina phaseolina by using species-specific oligonucleotide primers and probe

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Cited by 69 publications
(66 citation statements)
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“…This was the first report of M. phaseolina from hemp, turnip, okra, mungbean, marigold and Sonchus in Iran. The speciesspecific primers designed by Babu et al (2007) amplified one 350 bp band in all isolates of Macrophomina, confirming that the isolates obtained belonged to the species M. phaseolina. No bands were present in the negative controls, confirming that the primers were specific to M. phaseolina.…”
Section: Resultsmentioning
confidence: 70%
See 1 more Smart Citation
“…This was the first report of M. phaseolina from hemp, turnip, okra, mungbean, marigold and Sonchus in Iran. The speciesspecific primers designed by Babu et al (2007) amplified one 350 bp band in all isolates of Macrophomina, confirming that the isolates obtained belonged to the species M. phaseolina. No bands were present in the negative controls, confirming that the primers were specific to M. phaseolina.…”
Section: Resultsmentioning
confidence: 70%
“…Isolates were identified to species using species-specific primers (MpKFI/MpKRI) according to Babu et al (2007). Controls included a no DNA negative control, DNA of isolates of Trichoderma harzianum, and Cytospora schusleri, Sclerotinia sclerotiorum.…”
Section: Open Accessmentioning
confidence: 99%
“…It was selected in a pathogenicity test conducted previously, in which no differences were observed among 22 isolates obtained from strawberry plants grown in San Pedro, Metropolitan region, Chile. To ensure a correct identification, the isolate Mp21.A was molecularly identified using the primers MpkF1 and MpkR1 [40]. For the greenhouse trial, the inoculum consisted in oat seeds infected with the plant pathogen.…”
Section: Inoculum Preparationmentioning
confidence: 99%
“…Little is known about the genetic complexity of M. phaseolina population in India or about the origin and spread of the pathogen i.e. whether it arose as a single lineage in one location or arose independently in several differentiation of M. phaseolina has been achieved using polymerase chain reaction (PCR) and hybridization based techniques [4][5][6][7][8]. The lack of strong correlation between genotype and geographical origin suggests a high level of diversity within and among the population of M. phaseolina analysis has many advantages as a means of characterizing genetic variability such as speed, low cost and minimal requirement for DNA.…”
Section: Introductionmentioning
confidence: 99%