ArticlePloS one2012
High-resolution melting analysis as a powerful tool to discriminate and genotype Pseudomonas savastanoi pathovars and strains.
Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.
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Who cites it
18 citing papers in PubMed.
- Progress in Our Understanding of the Cross-Protection Mechanism of CTV-VT No-SY Isolates Against Homologous SY Isolates.Pathogens (Basel, Switzerland) · 2025Article
- Droplet Digital PCR for the Detection ofPlants (Basel, Switzerland) · 2025Article
- Article
- A Multiplex High-Resolution Melting (HRM) assay to differentiate Fusarium graminearum chemotypes.Scientific reports · 2024Article
- Review
- Identification and Characterisation ofPlants (Basel, Switzerland) · 2023Article
- Portuguese wild hop diversity assessment by fast SNP genotyping using high-resolution melting.Journal of applied genetics · 2022Article
- Optimization and development of high-resolution melting curve analysis (HRMA) assay for detection of New Delhi metallo-β-lactamase (NDM) producingAIMS microbiology · 2022Article
- Heterozygous Single-Nucleotide Polymorphism Genotypes at Heat Shock Protein 70 Gene Potentially Influence Thermo-Tolerance Among Four Zebu Breeds of Nigeria.Frontiers in genetics · 2021Article
- A MATE Transporter is Involved in Pathogenicity and IAA Homeostasis in the Hyperplastic Plant PathogenMicroorganisms · 2020Article
- Comparative genome analysis of the vineyard weed endophyte Pseudomonas viridiflava CDRTc14 showing selective herbicidal activity.Scientific reports · 2017Article
- A novel HRM assay for the simultaneous detection and differentiation of eight poxviruses of medical and veterinary importance.Scientific reports · 2017Article
- Molecular Identification of Broomrape Species from a Single Seed by High Resolution Melting Analysis.Frontiers in plant science · 2016Article
- Detection ofFrontiers in microbiology · 2016Article
- Development of a novel real-time PCR assay with high-resolution melt analysis to detect and differentiate OXA-48-Like β-lactamases in carbapenem-resistant Enterobacteriaceae.Antimicrobial agents and chemotherapy · 2015Article
- Trainable high resolution melt curve machine learning classifier for large-scale reliable genotyping of sequence variants.PloS one · 2014Article
- Article
- Real-time RT-PCR high-resolution melting curve analysis and multiplex RT-PCR to detect and differentiate grapevine leafroll-associated virus 3 variant groups I, II, III and VI.Virology journal · 2012Article
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3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Pseudomonas savastanoi is a serious pathogen of Olive, Oleander, Ash, and several other Oleaceae. Its epiphytic or endophytic presence in asymptomatic plants is crucial for the spread of Olive and Oleander knot disease, as already ascertained for P. savastanoi pv. savastanoi (Psv) on Olive and for pv. nerii (Psn) on Oleander, while no information is available for pv. fraxini (Psf) on Ash. Nothing is known yet about the distribution on the different host plants and the real host range of these pathovars in nature, although cross-infections were observed following artificial inoculations. A multiplex Real-Time PCR assay was recently developed to simultaneously and quantitatively discriminate in vitro and in planta these P. savastanoi pathovars, for routine culture confirmation and for epidemiological and diagnostical studies. Here an innovative High-Resolution Melting Analysis (HRMA)-based assay was set up to unequivocally discriminate Psv, Psn and Psf, according to several single nucleotide polymorphisms found in their Type Three Secretion System clusters. The genetic distances among 56 P. savastanoi strains belonging to these pathovars were also evaluated, confirming and refining data previously obtained by fAFLP. To our knowledge, this is the first time that HRMA is applied to a bacterial plant pathogen, and one of the few multiplex HRMA-based assays developed so far. This protocol provides a rapid, sensitive, specific tool to differentiate and detect Psv, Psn and Psf strains, also in vivo and against other related bacteria, with lower costs than conventional multiplex Real-Time PCR. Its application is particularly suitable for sanitary certification programs for P. savastanoi, aimed at avoiding the spreading of this phytopathogen through asymptomatic plants.
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