scholarly journals Identification of interspecific peach and Prunus sp. hybrids resistant to Plum pox virus infection

2010 ◽  
Vol 46 (No. 4) ◽  
pp. 139-144 ◽  
Author(s):  
J. Polák ◽  
I. Oukropec
Keyword(s):  
Virus Infection ◽  
Interspecific Hybrids ◽  
Prunus Persica ◽  
Relative Concentration ◽  
Plum Pox Virus ◽  
Rt Pcr ◽  
Sources Of Resistance ◽  
Peach Cultivar

Interspecific hybrids of Prunus persica, Barier, Fire, Cadaman, GF-677, and Prunus sp. hybrids and selections, MRS, NBS 540-73, and Pumiselect were evaluated for resistance to Plum pox virus. Hybrids were grafted onto trees of a peach cultivar artificially infected with PPV and evaluated for six years for resistance to the virus. The relative concentration of PPV protein was determined by semiquantitative ELISA in June every year. The presence of PPV in peach hybrids was confirmed by IC-RT-PCR in 2007–2008. The presence and intensity of PPV symptoms were evaluated monthly from May to September. The hybrid GF-677 (P. amygdalus × P. persica) was confirmed as highly resistant to PPV. Hybrids Cadaman (P. davidiana × P. persica) and Fire (P. amygdalus × P. persica) were characterized as resistant to PPV. Hybrids GF-677, Cadaman and Fire were selected as candidate sources of resistance to be crossed with peach cultivars susceptible to PPV.

scholarly journals First Report of Plum pox virus (Sharka Disease) in Prunus persica in the United States

Plant Disease ◽  
2000 ◽  
Vol 84 (2) ◽  
pp. 202-202 ◽  
Author(s):  
L. Levy ◽  
V. Damsteegt ◽  
R. Welliver
Keyword(s):  
Prunus Persica ◽  
Virus Disease ◽  
Sandwich Elisa ◽  
Pcr Amplification ◽  
The United States ◽  
Enzyme Linked Immunosorbent Assay ◽  
Plum Pox Virus ◽  
Rt Pcr ◽  
Peach Fruit ◽  
First Report

Plum pox (Sharka) is the most important virus disease of Prunus in Europe and the Mediterranean region and is caused by Plum pox potyvirus (PPV). In September 1999, PPV-like symptoms were observed in peach fruit culls in a packinghouse in Pennsylvania. All symptomatic fruit originated from a single block of peach (P. persica cv. Encore) in Adams County. Trees in the block exhibited ring pattern symptoms on their leaves. A potyvirus was detected in symptomatic fruit using the Poty-Group enzyme-linked immunosorbent assay (ELISA) test from Agdia (Elkhart, IN). Reactions for symptomatic peach fruit and leaves also were positive using triple-antibody sandwich ELISA with the PPV polyclonal antibody from Bioreba (Carrboro, NC) for coating, the Poty-Group monoclonal antibody (MAb; Agdia) as the intermediate antibody, and double-antibody sandwich ELISA with PPV detection kits from Sanofi (Sanofi Diagnostics Pasteur, Marnes-La-Coquette, France) and Agdia and the REAL PPV kit (Durviz, Valencia, Spain) containing universal (5B) and strain typing (4DG5 and AL) PPV MAbs (1). PPV also was identified by immunocapture-reverse transcription-polymerase chain reaction (IC-RT-PCR) amplification and subsequent sequencing of the 220-bp 3′ noncoding region (2) (>99% sequence homology to PPV) and by IC-RT-PCR amplification of a 243-bp product in the coat protein (CP) gene (1). The virus was identified as PPV strain D based on serological typing with strainspecific MAbs and on PCR-restriction fragment length polymorphism of the CP IC-RT-PCR product with Rsa1 and Alu1 (1). This is the first report of PPV in North America. References: (1) T. Candresse et al. Phytopathology 88:198, 1998. (2) L. Levy and A. Hadidi. EPPO Bull. 24:595, 1994.

scholarly journals Gene Expression Analysis of Induced Plum Pox Virus Resistance in Peach (Prunus Persica) by Almond (P. Dulcis) Grafting

2021 ◽  
Author(s):  
Manuel Rubio ◽  
Pedro Martínez-García ◽  
Nikbakht-Dehkordi Azam ◽  
Angela Prudencio ◽  
Eva Gómez ◽  
...  
Keyword(s):  
Gene Expression ◽  
Transcription Initiation ◽  
Prunus Persica ◽  
Initiation Factor ◽  
Induced Response ◽  
Plum Pox Virus ◽  
Sources Of Resistance ◽  
Transcription Initiation Factor ◽  
Pathogenesis Related ◽  
Related Proteins

Abstract No natural sources of resistance to Plum pox virus (PPV, sharka disease) have been identified in peach. However, previous studies have demonstrated that grafting ‘Garrigues’ almond onto ‘GF305’ peach seedlings heavily infected with PPV can progressively reduce disease symptoms and virus accumulation. Furthermore, grafting ‘Garrigues’ onto ‘GF305’ has completely prevented virus infection. This study aims to analyse the rewiring of gene expression associated with this resistance to PPV transmitted by grafting through phloem using RNA-Seq and RTqPCR analysis. A total of 18 candidate genes were differentially expressed after grafting ‘Garrigues’ almond onto healthy ‘GF305’ peach. Among the up-regulated genes, a HEN1 homolog stands out, which, together with the differential expression of RDR- and DCL2-homologs in some of the conditions assayed, suggests that the RNA silencing machinery is activated by PPV infection and can contribute to the resistance induced by ‘Garrigues’ almond. Glucan endo -1,3-Beta D-Glucosidase could be also relevant for the ‘Garrigues’-induced response, since its expression is much higher in ‘Garrigues’ than in ‘GF305’. We also discuss the potential relevance of the following in PPV infection and ‘Garrigues’-induced resistance: several pathogenesis-related proteins, No apical meristem proteins, the transcription initiation factor TFIIB, the Speckle-type POZ protein and a number of proteins involved in phytohormone signalling.

scholarly journals Evaluation of the Prunus interspecific progenies for resistance to Plum pox virus

2013 ◽  
Vol 49 (No. 2) ◽  
pp. 65-69 ◽  
Author(s):  
J. Salava ◽  
J. Polák ◽  
I. Oukropec
Keyword(s):  
Interspecific Hybrids ◽  
Agronomic Traits ◽  
Fruit Trees ◽  
Fruit Production ◽  
Stone Fruit ◽  
Plum Pox Virus ◽  
Prunus Amygdalus ◽  
Prunus Species ◽  
Sources Of Resistance ◽  
Resistance Transfer

Sharka disease caused by the infection with the Plum pox virus (PPV) in stone fruit trees is worldwide the most devastating for stone fruit production. Until now, good sources of resistance to PPV within the peach group have not been available. There are no commercial cultivars of peach that are resistant to PPV. Other Prunus species are known to show varying levels of resistance. Interspecific hybrids GF 677 (Prunus amygdalus × P. persica) and Cadaman (P. davidiana × P. persica) were revealed to be resistant to PPV. The resistance to a Dideron isolate of the descendants of Cresthaven × GF 677 and Cresthaven × Cadaman and their progenitors was evaluated after inoculation by chip-budding in a sealed screenhouse. Results demonstrate a certain level of resistance in both progenies of interspecific hybrids and indicate a potential for PPV resistance transfer to commercial peach cultivars but it will be necessary to perform backcrosses with peach cultivars of agricultural interest in order to return pomological and agronomic traits. For the definitive confirmation of resistance/susceptibility it will be necessary to wait until the adult stage of hybrids.

scholarly journals First Report of Prunus necrotic ringspot virus in Peach in Mexico

Plant Disease ◽  
2008 ◽  
Vol 92 (3) ◽  
pp. 482-482 ◽  
Author(s):  
R. De La Torre-Almaraz ◽  
J. V. Montoya-Piña ◽  
S. Alcacio-Rangel ◽  
G. Camarena-Gutiérrez ◽  
M. Salazar-Segura
Keyword(s):  
Prunus Persica ◽  
Rna Extraction ◽  
Ringspot Virus ◽  
Plum Pox Virus ◽  
Rt Pcr ◽  
First Report ◽  
Field Samples ◽  
Prunus Necrotic Ringspot Virus ◽  
San Martín ◽  
Das Elisa

Peach (Prunus persica (L.) Batsch) is one of the most important fruit crops in the temperate regions of Mexico. In 2006, during a survey conducted in commercial peach orchards in Puebla, Mexico for viral diseases, many trees were observed with foliar symptoms that included yellow mottle, ringspot, line patterns, and mosaic. Samples (flowers, young shoot tips, and leaves) were collected from 120 symptomatic trees in three locations (San Martin Texmelucan, Domingo Arenas, and Tepetzala). All samples were tested using double-antibody sandwich (DAS)-ELISA kits (Agdia, Inc., Elkhart, IN) for the presence of the following viruses: Apple mosaic virus, Plum pox virus, Prune dwarf virus, and Prunus necrotic ringspot virus (PNRSV). Sap extracts from young symptomatic leaves and shoots were used to mechanically inoculate Chenopodium quinoa, C. amaranticolor, Gomphrena globosa, Nicotiana tabacum cv. Xanthi, N. glutinosa, N. clevelandii, N. benthamiana, Datura stramonium, Capsicum annuum, and Solanum lycopersicum. Plants were kept in a greenhouse with approximate temperatures of 25 to 35°C, humidity of 70%, and 12 h of light. Sap extracts were also used for dsRNA extraction and analyses (2) and RNA extraction for use in reverse transcription (RT)-PCR with the Access RT-PCR system (Promega, Madison, WI) and primers that annealed to a conserved region in the PNRSV coat protein gene (1). The expected size amplicons of approximately 450 bp were generated from all field-collected samples. The PCR products from three geographically distinct PNRSV isolates (Domingo Arenas [Accession No. DQ979004], Tepetzala [Accession No. DQ979005], and San Martin Texmelucan [Accession No. EF456771]) were directly sequenced with a Genetic Analyzer 3100 (Applied Biosystems, Foster City, CA) and their nucleotide and deduced amino acids sequences were more than 93% identical to corresponding sequences of PNRSV available in the NCBI/GenBank database. PNRSV was the only virus detected by DAS-ELISA in flowers and young shoots from 60 of the symptomatic field samples tested from the three locations. DsRNA banding patterns were obtained from 40 field-collected symptomatic samples; all showed three bands of approximately 3.6, 2.5, and 1.8 kb, the expected sizes for RNAs 1, 2, and 3 of PNRSV, respectively. DsRNAs were not detected in asymptomatic plants. PNRSV transmission by mechanical inoculation induced mosaic symptoms in N. tabacum cv. Xanthi and necrotic local lesions in G. globosa. Although G. globosa is reported to be a systemic host of PNRSV and N. tabacum is not reported to be a host, symptomatic plants were positive for PNRSV in DAS-ELISA tests. It is possible that there was an additional virus not detected in our assays that was responsible for the unexpected reactions in the host range studies. To our knowledge, this is the first report of PNRSV in peach in Mexico. References: (1) D. J. MacKenzie et al. Plant Dis. 81:222, 1997. (2) R. A. Valverde et al. Plant Dis. 74:255,1990.

scholarly journals Resistance to Plum Pox Virus (Dideron Isolate RB3.30) in a Group of California Almonds and Transfer of Resistance to Peach

2004 ◽  
Vol 129 (4) ◽  
pp. 544-548 ◽  
Author(s):  
P. Martínez-Gómez ◽  
M. Rubio ◽  
F. Dicenta ◽  
T.M. Gradziel
Keyword(s):  
Prunus Persica ◽  
Prunus Avium ◽  
Sour Cherry ◽  
Prunus Armeniaca ◽  
Pcr Analysis ◽  
Plum Pox Virus ◽  
Rt Pcr ◽  
Resistance Transfer ◽  
High Level ◽  
Peach Rootstocks

Sharka [(plum pox virus (PPV)] mainly affects Prunus species, including apricot (Prunus armeniaca L.), peach (Prunus persica L.), plum (Prunus salicina Lindl., Prunus domestica L.), and, to a lesser degree, sweet (Prunus avium L.) and sour cherry (Prunus cerasus L.). Level of resistance to a Dideron isolate of PPV in seven California almond [P. dulcis (Miller) D.A. Webb], five processing peach cultivars, and two peach rootstocks was evaluated. In addition, almond and peach selections resulting from interspecific almond × peach hybridization and subsequent gene introgression were tested. Evaluations were conducted in controlled facilities after grafting the test genotypes onto inoculated GF305 peach rootstocks. Leaves were evaluated for PPV symptoms during three consecutive cycles of growth. ELISA-DASI and RT-PCR analysis were also employed to verify the presence or absence of PPV. Peach cultivars and rootstocks showed sharka symptoms and were ELISA-DASI or RT-PCR positive for some growth cycles, indicating their susceptibility to PPV. Almond cultivars and almond × peach hybrids did not show symptoms and were ELISA-DASI and RT-PCR negative, demonstrating resistance to PPV. Two (almond × peach) F2 selections as well as two of three backcrossed peach selections also showed a resistant behavior against the PPV-D isolate. Results demonstrate a high level of resistance in almond and indicate potential for PPV resistance transfer to commercial peach cultivars.

Oxidative stress induced by long-term plum pox virus infection in peach (Prunus persica)

2004 ◽  
Vol 122 (4) ◽  
pp. 486-495 ◽  
Author(s):  
Jose Antonio Hernandez ◽  
Manuel Rubio ◽  
Enrique Olmos ◽  
Alfonso Ros-Barcelo ◽  
Pedro Martinez-Gomez
Keyword(s):  
Oxidative Stress ◽  
Virus Infection ◽  
Prunus Persica ◽  
Plum Pox Virus

scholarly journals Gene Expression Analysis of Induced Plum pox virus (Sharka) Resistance in Peach (Prunus persica) by Almond (P. dulcis) Grafting

2021 ◽  
Vol 22 (7) ◽  
pp. 3585
Author(s):  
Manuel Rubio ◽  
Pedro J. Martínez-García ◽  
Azam Nikbakht-Dehkordi ◽  
Ángela S. Prudencio ◽  
Eva M. Gómez ◽  
...  
Keyword(s):  
Gene Expression ◽  
Transcription Initiation ◽  
Prunus Persica ◽  
Initiation Factor ◽  
Induced Response ◽  
Plum Pox Virus ◽  
Sources Of Resistance ◽  
Pathogenesis Related ◽  
Related Proteins ◽  
Sharka Resistance

No natural sources of resistance to Plum pox virus (PPV, sharka disease) have been identified in peach. However, previous studies have demonstrated that grafting a “Garrigues” almond scion onto “GF305” peach rootstock seedlings heavily infected with PPV can progressively reduce disease symptoms and virus accumulation. Furthermore, grafting a “Garrigues” scion onto the “GF305” rootstock has been shown to completely prevent virus infection. This study aims to analyse the rewiring of gene expression associated with this resistance to PPV transmitted by grafting through the phloem using RNA-Seq and RT-qPCR analysis. A total of 18 candidate genes were differentially expressed after grafting “Garrigues” almond onto healthy “GF305” peach. Among the up-regulated genes, a HEN1 homolog stands out, which, together with the differential expression of RDR- and DCL2-homologs, suggests that the RNA silencing machinery is activated by PPV infection and can contribute to the resistance induced by “Garrigues” almond. Glucan endo-1,3-beta D-glucosidase could be also relevant for the “Garrigues”-induced response, since its expression is much higher in “Garrigues” than in “GF305”. We also discuss the potential relevance of the following in PPV infection and “Garrigues”-induced resistance: several pathogenesis-related proteins; no apical meristem proteins; the transcription initiation factor, TFIIB; the speckle-type POZ protein; in addition to a number of proteins involved in phytohormone signalling.

scholarly journals First Report of Peach latent mosaic viroid in Peach Trees in Montenegro

Plant Disease ◽  
2012 ◽  
Vol 96 (1) ◽  
pp. 150-150 ◽  
Author(s):  
I. Mavric Pleško ◽  
M. Viršcek Marn ◽  
Z. Miladinovic ◽  
J. Zindovic
Keyword(s):  
Prunus Persica ◽  
Stone Fruit ◽  
Plum Pox Virus ◽  
Rt Pcr ◽  
First Report ◽  
Fruit Species ◽  
Hop Stunt Viroid ◽  
Viroid Infection ◽  
Fruit Samples ◽  
Peach Trees

Peach latent mosaic viroid (PLMVd) and Hop stunt viroid (HSVd) are known to infect stone fruit species worldwide. The viroid infection can be latent or induce a variety of disease symptoms. Stone fruit samples were collected in Montenegro for a Plum pox virus (PPV) survey in 2007. Thirteen samples infected with PPV, taken from 12-year-old peach trees (Prunus persica (L.) Batsch, cv. Elegant Lady) in the area of Cemovsko field, were tested for the presence of PLMVd and HSVd by reverse transcription (RT)-PCR. Mild or severe mosaic, chlorotic rings, and fruit deformations were observed on some trees. Total RNA was extracted from all samples with a RNeasy Plant Mini Kit (Qiagen, Chatsworth, CA) and RT-PCR was performed. Samples were tested for HSVd and PLMVd infection using primer pairs RF-43/RF-44 for PLMVd (1) and VP-19/VP-20 for HSVd (2). Amplification products of approximately 348 bp were obtained from nine samples with PLMVd primers. Amplification products from seven samples were successfully cloned into pGEM-T Easy Vector (Promega, Madison, WI) and used for transformation of Escherichia coli. At least four clones of each sample were sequenced. Obtained sequences were 337 and 338 nucleotides long and shared 90.3 to 100% identity. Consensus sequences of each sample were deposited in GenBank under Accession Nos. JF927892–JF927898. They showed 92.6 to 97.9% identity among each other, 94 to 98% identity with the PLMVd isolate G sequence (Accession No. EF591868) and 91.8 to 94.4% identity with PLMVd sequence M83545. HSVd was not detected in analyzed samples. PLMVd infections were found on peach trees in an area where approximately 40% of the peach production is located. Therefore, PLMVd infections can pose a threat to peach production in Montenegro. To our knowledge this is the first report of PLMVd infection of peach in Montenegro. References: (1) S. Ambrós et al. J. Virol. 72:7397, 1998. (2) S. A. Kofalvi et al. J. Gen. Virol. 78:3177, 1997.

scholarly journals Inheritance of resistance to Plum pox virus in the progeny of the apricot cv. ‘Harlayne’

2009 ◽  
Vol 57 (5) ◽  
pp. 243-250 ◽  
Author(s):  
Petra Pilařová ◽  
Boris Krška
Keyword(s):  
Prunus Persica ◽  
Natural Resistance ◽  
Plum Pox Virus ◽  
Inheritance Of Resistance ◽  
Sources Of Resistance ◽  
Growing Seasons ◽  
Ppv Resistance ◽  
Dominant Genes ◽  
Sharka Disease ◽  
Leaf Symptoms

Natural resistance toPlum pox virus(PPV), the agent of sharka disease, is one of the most important traits of interest to stone fruit breeders, although few sources of resistance have been identified. One of the few apricot cultivars which does show resistance, ‘Harlayne’, was chosen for a study of the genetics of PPV resistance. It was crossed with three different cultivars, two susceptible (‘Vestar’ and ‘Strepet’) and one immune (‘Orangered’). Four different lines (since there was one reciprocal combination) were established and the F1 crosses were subsequently inoculated with the PPV-M and PPV-D strains by grafting infected buds. A woody indicatorPrunus persica‘GF 305’ was then also top-grafted onto the plants of three of these F1 populations. The observations of leaf symptoms and accompanying ELISA tests were performed over three, or in one case five, growing seasons and then hybrids were classified accordingly, as either resistant or susceptible. The resistant : susceptible ratios were calculated and compared with expected theoretical ratios using the χ2-test. The ratios of resistant to susceptible plants in the progeny derived from the four apricot crosses are compatible with the hypothesis of three dominant genes being responsible for PPV resistance, with ‘Harlayne’ being heterozygous for all three genes. However, the possibility that resistance is controlled by just two dominant genes can not be ruled out just yet.

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