Development and optimization of a group-specific loop-mediated isothermal amplification (LAMP) assay for the detection of patulin-producing Penicillium species

被引:21
作者
Frisch, Lisa M. [1 ]
Niessen, Ludwig [1 ]
机构
[1] Tech Univ Munich, Tech Microbiol, Gregor Mendel Str 4, D-85354 Freising Weihenstephan, Germany
关键词
LAMP; Mycotoxin; Patulin-producing Penicillium species; Isoepoxydon dehydrogenase; Diagnosis; Food; ISOEPOXYDON DEHYDROGENASE GENE; POLYPHASIC TAXONOMY; MYCOTOXIN PATULIN; DNA; FOOD; EXPANSUM; MOLDS; IDENTIFICATION; APPLE; ACID;
D O I
10.1016/j.ijfoodmicro.2019.03.010
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The mycotoxin patulin is a toxic fungal secondary metabolite occurring in food worldwide. Methods for rapid, simple and specific detection of patulin-producing fungi in food and feed are therefore urgently needed. In the current study, a loop-mediated isothermal amplification (LAMP) assay based on the isoepoxydon dehydrogenase (idh) gene of the patulin biosynthetic pathway was developed and optimized for the group-specific detection of patulin-producing Penicillium species. By testing purified DNA of 174 fungal strains representing 31 genera, the assay was demonstrated to be highly specific for the detection of patulin-producing species in Penicillium, Byssochlamys and Paecilomyces. The assay had a detection limit of 2.5 pg of purified genomic DNA of P. expansum per reaction. Moreover, the assay was demonstrated to detect patulin-producers when conidia were directly added to the master mix as template without any sample preparation. The applicability of the assay in food analyses was successfully tested on artificially contaminated grapes and apples requiring minimal sample preparation. A screening of grapes from the 2018 harvest from different locations in Germany revealed no presence of patulin-producers. The developed LAMP assay is a promising tool for rapid diagnosis in quality control applications in the food and beverage industry.
引用
收藏
页码:20 / 30
页数:11
相关论文
共 58 条
  • [51] Visual detection of isothermal nucleic acid amplification using pH-sensitive dyes
    Tanner, Nathan A.
    Zhang, Yinhua
    Evans, Thomas C., Jr.
    [J]. BIOTECHNIQUES, 2015, 58 (02) : 59 - 68
  • [52] Development of a real-time PCR assay for Penicillium expansum quantification and patulin estimation in apples
    Tannous, Joanna
    Atoui, Ali
    El Khoury, Andre
    Kantar, Sally
    Chdid, Nader
    Oswald, Isabelle P.
    Puel, Olivier
    Lteif, Roger
    [J]. FOOD MICROBIOLOGY, 2015, 50 : 28 - 37
  • [53] DNA module platform for developing colorimetric aptamer sensors
    Tomita, Yasuyuki
    Morita, Yuji
    Suga, Hiroaki
    Fujiwara, Daisuke
    [J]. BIOTECHNIQUES, 2016, 60 (06) : 285 - 292
  • [54] Enhancing melting curve analysis for the discrimination of loop-mediated isothermal amplification products from four pathogenic molds: Use of inorganic pyrophosphatase and its effect in reducing the variance in melting temperature values
    Tone, Kazuya
    Fujisaki, Ryuichi
    Yamazaki, Takashi
    Makimura, Koichi
    [J]. JOURNAL OF MICROBIOLOGICAL METHODS, 2017, 132 : 41 - 45
  • [55] Taxonomic revision of Aspergillus section Clavati based on molecular, morphological and physiological data
    Varga, J.
    Due, M.
    Frisvad, J. C.
    Samson, R. A.
    [J]. STUDIES IN MYCOLOGY, 2007, (59) : 89 - 106
  • [56] Vogt EI, 2017, J MICROB BIOTEC FOOD, V7, P265, DOI 10.15414/jmbfs.2017/18.7.3.265-270
  • [57] Patulin, a mycotoxin, has potent cytotoxic activity on actue lymphoblastic leukemia and induce apoptosis through intrinsic and extrinsic pathways
    Wang, Fengrong
    David, Ebeneier
    Lonial, Sagar
    Arellano, Martha
    Khoury, Hanna J.
    Langston, Amelia
    Lechowicz, Mary Jo
    Waller, Ned
    [J]. BLOOD, 2007, 110 (11) : 151B - 152B
  • [58] Screening and development of DNA aptamers as capture probes for colorimetric detection of patulin
    Wu, Shijia
    Duan, Nuo
    Zhang, Weixiao
    Zhao, Sen
    Wang, Zhouping
    [J]. ANALYTICAL BIOCHEMISTRY, 2016, 508 : 58 - 64