Development of a new probe for specific and sensitive detection of 'Candidatus Phytoplasma mali' in inoculated apple trees

被引:14
作者
Aldaghi, M.
Massart, S.
Roussel, S.
Jijakli, M. H.
机构
[1] Gembloux Agr Univ, Plant Pathol Unit, B-5030 Gembloux, Belgium
[2] Plant Pests & Dis Res Inst, Plant Dis Res Dept, Tehran, Iran
关键词
'Candidatus Phytoplasma mali'; detection; real-time PCR; sensitivity;
D O I
10.1111/j.1744-7348.2007.00171.x
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
A new TaqMan minor groove binding (MGB) probe and new PCR conditions were designed for quick, specific and sensitive detection of 'Candidatus Phytoplasma mali'. The new probe can distinguish a single mismatch between 'Ca. P. mali' and 'Candidatus Phytoplasma prunorum', this constituting an improvement over a previously published method. In our study, the relative position of the mismatch in the MGB probe influenced greatly the specificity of detection. Our new real-time PCR protocol was able to detect one plasmid copy in water and 100 copies in healthy plant DNA extracts. The sensitivity of this new real-time PCR method, three other real-time PCR protocols and a conventional PCR with fU5/rU3 primers was compared. Periwinkles and MM106 rootstocks were grafted with infected material and surveyed over time by symptom observation, conventional PCR and real-time PCR. Phytoplasma infection was detected by symptom observation in all periwinkles within 4 months and in 75% of the MM106 rootstocks by the end of 7 months. Conventional PCR detected phytoplasma infection in all periwinkles within 4 months and in all MM106 rootstocks within 7 months. Best results were obtained by our real-time PCR, which detected phytoplasma infection in all grafted plants within 3 months after inoculation.
引用
收藏
页码:251 / 258
页数:8
相关论文
共 25 条
  • [1] Aldaghi M., 2005, Communications in Agricultural and Applied Biological Sciences, V70, P253
  • [2] Detection of phormium yellow leaf phytoplasma in New Zealand flax (Phormium tenax) using nested PCRs
    Andersen, MT
    Beever, RE
    Gilman, AC
    Liefting, LW
    Balmori, E
    Beck, DL
    Sutherland, PW
    Bryan, GT
    Gardner, RC
    Forster, RLS
    [J]. PLANT PATHOLOGY, 1998, 47 (02) : 188 - 196
  • [3] A new approach to apple proliferation detection: a highly sensitive real-time PCR assay
    Baric, S
    Dalla Via, J
    [J]. JOURNAL OF MICROBIOLOGICAL METHODS, 2004, 57 (01) : 135 - 145
  • [4] Bianco P. A., 1993, Rivista di Patologia Vegetale, V3, P69
  • [5] *EPPO CABI, 1996, QUAR PESTS EUR, P959
  • [6] Cacopsylla costalis (Flor 1861), as a vector of apple proliferation in Trentino
    Frisinghelli, C
    Delaiti, L
    Grando, MS
    Forti, D
    Vindimian, ME
    [J]. JOURNAL OF PHYTOPATHOLOGY-PHYTOPATHOLOGISCHE ZEITSCHRIFT, 2000, 148 (7-8): : 425 - 431
  • [7] 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
    [J]. PROCEEDINGS OF THE XIXTH INTERNATIONAL SYMPOSIUM ON VIRUS AND VIRUS-LIKE DISEASES OF TEMPERATE FRUIT CROPS: FRUIT TREE DISEASES, 2004, (657): : 415 - 420
  • [8] Genetic variability of apple proliferation phytoplasmas as determined by PCR-RFLP and sequencing of a non-ribosomal fragment
    Jarausch, W
    Saillard, C
    Helliot, B
    Garnier, M
    Dosba, F
    [J]. MOLECULAR AND CELLULAR PROBES, 2000, 14 (01) : 17 - 24
  • [9] 3′-minor groove binder-DNA probes increase sequence specificity at PCR extension temperatures
    Kutyavin, IV
    Afonina, IA
    Mills, A
    Gorn, VV
    Lukhtanov, EA
    Belousov, ES
    Singer, MJ
    Walburger, DK
    Lokhov, SG
    Gall, AA
    Dempcy, R
    Reed, MW
    Meyer, RB
    Hedgpeth, J
    [J]. NUCLEIC ACIDS RESEARCH, 2000, 28 (02) : 655 - 661
  • [10] USE OF MYCOPLASMALIKE ORGANISM (MLO) GROUP-SPECIFIC OLIGONUCLEOTIDE PRIMERS FOR NESTED-PCR ASSAYS TO DETECT MIXED-MLO INFECTIONS IN A SINGLE HOST-PLANT
    LEE, IM
    GUNDERSEN, DE
    HAMMOND, RW
    DAVIS, RE
    [J]. PHYTOPATHOLOGY, 1994, 84 (06) : 559 - 566