Details

Title

Sensitive and specific detection of Xanthomonas hortorum pv. pelargonii in geranium by real-time PCR

Journal title

Journal of Plant Protection Research

Yearbook

2016

Volume

vol. 56

Issue

No 3

Authors

Divisions of PAS

Nauki Biologiczne i Rolnicze

Publisher

Committee of Plant Protection PAS ; Institute of Plant Protection – National Research Institute

Date

2016

Identifier

DOI: 10.1515/jppr-2016-0039 ; ISSN 1427-4345 ; eISSN 1899-007X

Source

Journal of Plant Protection Research; 2016; vol. 56; No 3

References

Tuinier (1989), Use of serology to detectXanthomonas campestrispv pelargoniiin aqueous extracts of geranium plants, Plant Disease, 11, 875, doi.org/10.1094/PD-73-0875 ; Schaad (2002), Real - time polymerase chain reaction for one - hour on - site diagnosis of Pierces disease of grape in early season asymptomatic vines, Phytopathology, 721, doi.org/10.1094/PHYTO.2002.92.7.721 ; Anderson (1990), Development of a polyclonal antibody - based serodiagnostic assay for the detection ofXanthomonas campestrispv pelargoniiin geranium plants, Phytopathology, 357, doi.org/10.1094/Phyto-80-357 ; Nameth (1999), Bacterial blight of geranium : a history of diagnostic challenges, Plant Disease, 83, 204, doi.org/10.1094/PDIS.1999.83.3.204 ; Safaie Farahani (2014), Comparison of conventional , nested and real - time PCR for detection of the causal agent of ratoon stunt in Iran of, Journal Plant Pathology, 259. ; Cullen (2002), Detection ofColletotrichum coccodesfrom soil and potato tubers by conventional and quantitative real - time PCR, Plant Pathology, 51, 281, doi.org/10.1046/j.1365-3059.2002.00690.x ; Sulzinski (1996), Characteristics of a PCR - based assay forin plantadetection ofXanthomonas campestrispv pelargonii of, Journal Phytopathology, 144. ; Daughtrey (1993), Nursery - cultivatedGeraniumspp as a possible inoculum source forXanthomonas campestrispv pelargoniicausing bacterial blight disease of a green - housePelargoniumcrop, Phytopathology, 242. ; Hodge (1992), Diversity of four species ofXanthomonasas determined by cellular fatty acid analysis, Phytopathology, 1153. ; Lees (2002), Development of conventional and quantitative real - time PCR assays for the detection and identification ofRhizoctonia solaniAG - in potato and soil, Plant Pathology, 51, 293, doi.org/10.1046/j.1365-3059.2002.00712.x ; Weller (2002), Identification ofAgrobacteriumspp present withinBrassica napusseed by TaqMan PCR implications for GM screening procedures of, Archives Microbiology, 178. ; Weller (2000), Detection ofRalstonia solanacearumstrains with a quantitative multiplex real - time fluorogenic PCR Taq Man assay and, Applied Environmental Microbiology, 2853, doi.org/10.1128/AEM.66.7.2853-2858.2000 ; Faghihi (2014), Comparison of the efficiency of conventional PCR nested - PCR real - time PCR and loop - mediated isothermal amplification LAMP methods for detection of the causal agent of citrus huanglongbing in Iran of, Iranian Journal Plant Pathology, 237. ; Manulis (1994), Sensitive and specific detection ofXanthomonas campestrispv pelargoniiwith DNA primers and probes identified by random amplified polymorphic DNA analysis and, Applied Environmental Microbiology, 60, 4094. ; Sulzinski (1998), PCR - Based detection of artificial latent infections of geranium byXanthomonas campestrispv pelargonii of, Journal Phytopathology, 146.
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