A Quantitative Real-Time PCR Assay for Early Detection and Quantification of Ramularia mali, an Emerging Pathogen of Apple Causing Dry Lenticel Rot

被引:5
|
作者
Prencipe, Simona [1 ]
Valente, Silvia [1 ,2 ]
Nari, Luca [3 ]
Spadaro, Davide [1 ,2 ]
机构
[1] Univ Torino, Dept Agr Forestry & Food Sci DiSAFA, I-10095 Turin, Italy
[2] Univ Turin, Ctr Competence Innovat, Agroenvironm SectAGROINNOVA, I-10095 Turin, Italy
[3] Fdn Ric Innovaz & Sviluppo Tecnol Agr Piemontese, AGRION, I-12030 Manta, Cuneo, Italy
关键词
apple; dry lenticel rot; qPCR; Ramularia mali;
D O I
10.1094/PDIS-07-22-1586-RE
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ramularia mali is an emerging pathogen of apple (Malus domestica) causing dry lenticel rot. No preventive measures have been adopted due to the lack of knowledge about the life cycle and epidemiology of this pathogen. In a preliminary survey to identify the agents of dry lenticel rot of apple, R. mali was constantly associated with the disease. Using isolates from this survey, a SYBR Green quantitative PCR (qPCR) assay was developed, using calmodulin as target gene, for the detection and quantification of R. mali in apple fruit. The qPCR assay was validated in terms of specificity, sensitivity, repeatability, and reproducibility following the international European and Mediterranean Plant Protection Organization standard PM 7/98. The primers amplified a region of 237 bp specific to R. mali. The specificity was validated with 20 fungal species commonly found on apple, and 36 strains of R. mali and closely related species of the R. eucalypti species complex. Positive amplifications were obtained only with DNA of R. mali and no cross-reaction was detected with the other fungal species. Sensitivity was assessed with serial dilutions of target DNA and the limit of detection was 100 fg. No influence of host DNA was observed when target DNA was diluted on the DNA of Ambrosia and Golden Delicious apple. The assay permitted to detect and quantify R. mali in symptomatic and asymptomatic fruit. The presence of R. mali on asymptomatic Ambrosia and Golden Delicious apple fruit was demonstrated, and the presence of the pathogen was reported for the first time on Jeromine, Gala, Opal, and Story Inored fruit. This assay could be useful in clarifying the life cycle of this pathogen in order to build up an effective disease management strategy. Furthermore, the early detection of the pathogen on asymptomatic apple fruit could be used to forecast the development of dry lenticel rot, supporting the packinghouse operators in deciding the storage length of apple lots.
引用
收藏
页码:1399 / 1407
页数:9
相关论文
共 50 条
  • [1] Direct quantitative real-time PCR assay for detection of the emerging pathogen Neonectria neomacrospora
    Nielsen, Knud N.
    Thomsen, Iben M.
    Hansen, Ole K.
    FOREST PATHOLOGY, 2019, 49 (03)
  • [2] Development of a quantitative real-time PCR assay for the detection of Phytophthora austrocedrae, an emerging pathogen in Britain
    Mulholland, V.
    Schlenzig, A.
    MacAskill, G. A.
    Green, S.
    FOREST PATHOLOGY, 2013, 43 (06) : 513 - 517
  • [3] Real-time PCR assay for the early detection and relative quantification of the Rubus idaeus pathogen Aculeastrum americanum
    Varela, Ana Rita
    Oliveira, Melissa Y.
    Luz, Francisco
    Trindade, Caendida Sofia
    Silva, Maria Jose
    Valdiviesso, Teresa
    de Oliveira, Pedro Bras
    Nobrega, Filomena
    PHYSIOLOGICAL AND MOLECULAR PLANT PATHOLOGY, 2025, 136
  • [4] Establishment of a quantitative real-time PCR assay for the quantification of apple proliferation phytoplasmas in plants and insects
    Jarausch, W
    Peccerella, T
    Schwind, N
    Jarausch, B
    Krczal, G
    PROCEEDINGS OF THE XIXTH INTERNATIONAL SYMPOSIUM ON VIRUS AND VIRUS-LIKE DISEASES OF TEMPERATE FRUIT CROPS: FRUIT TREE DISEASES, 2004, (657): : 415 - 420
  • [5] A quantitative real-time PCR assay for the detection of Ramularia collo-cygni from barley (Hordeum vulgare)
    Taylor, J. M. G.
    Paterson, L. J.
    Havis, N. D.
    LETTERS IN APPLIED MICROBIOLOGY, 2010, 50 (05) : 493 - 499
  • [6] Real-time PCR assay for quantitative mismatch detection
    Shively, L
    Chang, L
    LeBron, JM
    Liu, Q
    Riggs, AD
    Singer-Sam, J
    BIOTECHNIQUES, 2003, 34 (03) : 498 - +
  • [7] Development of a Real-Time PCR Assay for the Early Detection of the Eucalyptus Pathogen Quambalaria eucalypti
    Faedda, Roberto
    Silva, Gabriela B.
    FORESTS, 2024, 15 (02):
  • [8] A real-time PCR assay for detection and quantification of Lactococcus garvieae
    Jung, M. Y.
    Chang, Y-H.
    Kim, W.
    JOURNAL OF APPLIED MICROBIOLOGY, 2010, 108 (05) : 1694 - 1701
  • [9] Detection and quantification of Phialophora gregata in soybean and soil samples with a quantitative, real-time PCR assay
    Malvick, D. K.
    Impullitti, A. E.
    PLANT DISEASE, 2007, 91 (06) : 736 - 742
  • [10] Quantitative real-time PCR assay for detection of Ehrlichia chaffeensis
    Loftis, AD
    Massung, RF
    Levin, ML
    JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (08) : 3870 - 3872