Investigations with real-time PCR assay on the transmissibility of pear decline phytoplasma (PDP) with dormant buds

被引:0
|
作者
Babini, A. R. [1 ]
Fiumi, E. [1 ]
Giunchedi, L. [1 ]
Pignatta, D. [1 ]
Pollini, C. Poggi [1 ]
Reggiani, N. [1 ]
机构
[1] Univ Bologna, DISTA, Bologna, Italy
关键词
Pyrus communis; diagnostic procedures; multiplex reaction; pome fruit trees phytoplasma; propagation material;
D O I
10.17660/ActaHortic.2008.781.72
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Pear decline (PD) is one of the most dangerous diseases of pear trees. A study was carried out to determine the possibility of transmitting the causal agent, pear decline phytoplasma (PDP), through grafting with dormant buds collected from naturally infected trees, due to winter degeneration of the sieve tubes of the above ground part of pear trees. A real-time PCR procedure for PDP detection was set up with a multiplex assay where host and pathogen DNA could be amplified simultaneously to distinguish between uninfected plant material and false negatives due to PCR inhibition. Real-time PCR assays were performed on 92 seedlings of Pyrus communis one year after grafting with dormant buds resulted PD-positive after PCR analysis, from cvs. Abate Fetel, Conference and William, grafted on P. communis rootstocks. Ten pear seedlings were also grafted with root samples from the above mentioned trees. No phytoplasmas were detected in the 92 grafted seedlings, on the contrary 6 plants on 10 tested positive after root grafting. The results suggested that in our conditions PDP is not transmissible with dormant buds to healthy trees.
引用
收藏
页码:495 / 497
页数:3
相关论文
共 50 条
  • [31] TaqMan real-time PCR versus four conventional PCR assays for detection of apple proliferation phytoplasma
    Baric, S.
    Kerschbamer, C.
    Dalla Via, J.
    PLANT MOLECULAR BIOLOGY REPORTER, 2006, 24 (02) : 169 - 184
  • [32] TaqMan real-time PCR versus four conventional PCR assays for detection of apple proliferation phytoplasma
    S. Baric
    C. Kerschbamer
    J. Dalla Via
    Plant Molecular Biology Reporter, 2006, 24
  • [33] Correction to: Differentiation of the Flavescence dorée phytoplasma genetic clusters by multiplex real-time PCR assay targeting the map gene
    Jelena Plavec
    Martina Seruga Music
    Journal of Plant Pathology, 2023, 105 : 417 - 417
  • [34] Development and Validation of a New TaqMan Real-Time PCR for Detection of 'Candidatus Phytoplasma pruni'
    Kogej, Zala
    Dermastia, Marina
    Mehle, Natasa
    PATHOGENS, 2020, 9 (08): : 1 - 13
  • [35] Real-time PCR technique-based detection of coconut root (wilt) phytoplasma
    Manimekalai, R.
    Nair, Smita
    Soumya, V. P.
    Roshna, O. M.
    Thomas, George V.
    CURRENT SCIENCE, 2011, 101 (09): : 1209 - 1213
  • [36] Characterization and optimization of a real-time PCR assay for SRY determination
    Mongia, Shella K.
    Procter, Melinda
    Mao, Rong
    AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2007, 128 (03) : 514 - 514
  • [37] A real-time PCR assay for the detection of Neisseria gonorrhoeae by LightCycler
    Whiley, DM
    LeCornec, GM
    Mackay, IM
    Siebert, DJ
    Sloots, TP
    DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2002, 42 (02) : 85 - 89
  • [38] Rapid identification of Leishmania complexes by a real-time PCR assay
    Wortmann, G
    Hochberg, L
    Houng, HH
    Sweeney, C
    Zapor, M
    Aronson, N
    Weina, P
    Ockenhouse, CF
    AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2005, 73 (06): : 999 - 1004
  • [39] A real-time PCR assay for quantification of canine adenoviral vectors
    Mercedes Segura, Maria
    Monfar, Merce
    Puig, Meritxell
    Mennechet, Franck
    Ibanes, Sandy
    Chillon, Miguel
    JOURNAL OF VIROLOGICAL METHODS, 2010, 163 (01) : 129 - 136
  • [40] SENSITIVE REAL-TIME PCR CHIMERISM ASSAY FOR HSCT MONITORING
    Smith, M. S.
    Cowden, S. M.
    Kleiboeker, S. B.
    BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2012, 18 (02) : S352 - S353