Correction: Prunus persica 9, a new occupational allergen from peach tree pollen involved in rhinitis and asthma

2022 ◽  
Vol 79 (2) ◽  
pp. e2-e2
2019 ◽  
Vol 180 (3) ◽  
pp. 212-220 ◽  
Author(s):  
Laura Victorio Puche ◽  
Maria Luisa Somoza ◽  
José Damián López-Sánchez ◽  
María Garrido-Arandia ◽  
Araceli Díaz-Perales ◽  
...  

HortScience ◽  
2001 ◽  
Vol 36 (1) ◽  
pp. 101-103 ◽  
Author(s):  
T.G. Beckman ◽  
P.L. Pusey

Armillaria root rot is the second leading cause of peach tree mortality (after peach tree short life) in the southeastern United States. Currently, there are no commercially available rootstocks for peach with proven resistance to this pathogen in the United States. Since 1983, we have been screening rootstock candidates for resistance to Armillaria utilizing naturally infected field sites. Inoculation of peach [Prunus persica (L.) Batsch], plum (P. cerasifera J.F. Ehrh., P. munsoniana F.W. Wight & Hedr., P. salicina Lindl. or P. angustifolia Marsh.) × peach and plum × plum hybrid rootstocks with infected plant tissue (such as acorns, Quercus sp.) prior to planting has provided a significantly increased infection and mortality of candidate rootstock lines in comparison with sole reliance on natural inoculum on an infested site.


HortScience ◽  
1998 ◽  
Vol 33 (6) ◽  
pp. 1062-1065 ◽  
Author(s):  
T.G. Beckman ◽  
W.R. Okie ◽  
A.P. Nyczepir ◽  
P.L. Pusey ◽  
C.C. Reilly

Nearly 5000 seedling trees representing more than 100 peach [Prunus persica (L.) Batsch.] and plum (Prunus spp.) lines were planted at a 4 × 0.6-m spacing in Jan. 1983, on a site with a known history of peach tree short life (PTSL) and Armillaria root rot (ARR). Trees were arranged in a randomized complete-block with eight replicates of six trees each. Beginning in Spring 1984 and each year thereafter the cause of tree death was determined. At the end of 9 years, 50% of the trees had succumbed to PTSL and 35% had been killed by ARR apparently caused by Armillaria tabescens. Analysis of the data for trees killed by ARR showed a wide range in mortality, some peach lines appeared significantly more tolerant to ARR than others. Plum lines derived from native North American species also appeared to be a potential source of improved tolerance. We did not establish whether ARR tolerance is affected by PTSL.


Genes ◽  
2020 ◽  
Vol 11 (6) ◽  
pp. 611
Author(s):  
Duk Jun Yu ◽  
Sung Hoon Jun ◽  
Junhyung Park ◽  
Jung Hyun Kwon ◽  
Hee Jae Lee

We analyzed the transcriptomes in the shoots of five-year-old ‘Soomee’ peach trees (Prunus persica) during cold acclimation (CA), from early CA (end of October) to late CA (middle of January), and deacclimation (DA), from late CA to late DA (middle of March), to identify the genes involved in cold hardiness. Cold hardiness of the shoots increased from early to late CA, but decreased from late CA to late DA, as indicated by decreased and increased the median lethal temperature (LT50), respectively. Transcriptome analysis identified 17,208 assembled transcripts during all three stages. In total, 1891 and 3008 transcripts were differentially expressed with a |fold change| > 2 (p < 0.05) between early and late CA, and between late CA and late DA, respectively. Among them, 1522 and 2830, respectively, were functionally annotated with gene ontology (GO) terms having a greater proportion of differentially expressed genes (DEGs) associated with molecular function than biological process or cellular component categories. The biochemical pathways best represented both periods from early to late CA and from late CA to late DA were ‘metabolic pathway’ and ‘biosynthesis of secondary metabolites’. We validated these transcriptomic results by performing reverse transcription quantitative polymerase chain reaction on the selected DEGs showing significant fold changes. The relative expressions of the selected DEGs were closely related to the LT50 values of the peach tree shoots: ‘Soomee’ shoots exhibited higher relative expressions of the selected DEGs than shoots of the less cold-hardy ‘Odoroki’ peach trees. Irrespective of the cultivar, the relative expressions of the DEGs that were up- and then down-regulated during CA, from early to late CA, and DA, from late CA to late DA, were more closely correlated with cold hardiness than those of the DEGs that were down- and then up-regulated. Therefore, our results suggest that the significantly up- and then down-regulated DEGs are associated with cold hardiness in peach tree shoots. These DEGs, including early light-induced protein 1, chloroplastic, 14-kDa proline-rich protein DC2.15, glutamate dehydrogenase 2, and triacylglycerol lipase 2, could be candidate genes to determine cold hardiness.


2019 ◽  
Vol 143 (2) ◽  
pp. AB235
Author(s):  
Maria Luisa Somoza ◽  
Laura Victorio Puche ◽  
Natalia Blanca-Lopez ◽  
Elisa Haroun Diaz ◽  
Maria Garrido Arandia ◽  
...  

2020 ◽  
Vol 145 (2) ◽  
pp. AB72
Author(s):  
Laura Victorio Puche ◽  
Maria Somoza Alvarez ◽  
Jose Damian Lopez Sanchez ◽  
Maria Garrido-Arandia ◽  
Laura Martín-Pedraza ◽  
...  

2009 ◽  
Vol 134 (2) ◽  
pp. 236-243 ◽  
Author(s):  
Dongyan Hu ◽  
Ralph Scorza

Since the first report of the ‘A72’ semidwarf peach [Prunus persica (L.) Batsch] tree in 1975, no new information has become available on this genotype. We evaluated the growth habit and verified the inheritance of ‘A72’ in a population of 220 progeny derived from self-pollination. Detailed tree and branch measurements revealed a unique forked-branch (FBR) character of the ‘A72’ (Nn) phenotype. The progeny segregated into 1 NN:2 Nn:1 nn. NN trees were indistinguishable from standard peach trees, Nn were FBR, and nn were dwarf. Hybrids between ‘A72’ and columnar (brbr) peach trees confirmed that FBR is inherited as a monogenic trait that appears to express incomplete dominance. ‘A72’ (Nn) trees were later blooming than sibling NN trees. The relationship (linkage or pleiotropy) between the growth habit of ‘A72’ and late bloom is not known. The structure of ‘A72’ trees presents new opportunities to breeder/geneticists, physiologists, and horticulturists to further explore the plasticity of peach tree growth and architecture that can be achieved through breeding. Applications of the ‘A72’ growth habit for commercial fruit production and as an ornamental, particularly in the dwarf form (nn) and in combination with the columnar tree (brbr) form, present opportunities that await exploration.


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