Rapid and selective detection of macrocyclic trichothecene producing Stachybotrys chartarum strains by loop-mediated isothermal amplification (LAMP)

被引:8
作者
Koeck, Johannes [1 ]
Gottschalk, Christoph [1 ]
Ulrich, Sebastian [2 ]
Schwaiger, Karin [3 ]
Gareis, Manfred [1 ]
Niessen, Ludwig [4 ]
机构
[1] Ludwig Maximilians Univ Munchen, Fac Vet Med, Schoenleutnerstr 8, D-85764 Oberschleissheim, Germany
[2] Ludwig Maximilians Univ Munchen, Fac Vet Med, Inst Infect Dis & Zoonoses, Vet Str 13, D-80539 Munich, Germany
[3] Univ Vet Med, Inst Food Safety Food Technol & Vet Publ Hlth, Unit Food Hyg & Technol, Vet Pl 1, A-1210 Vienna, Austria
[4] Tech Univ Munich, TUM Sch Life Sci, Gregor Mendel Str 4, D-85354 Freising Weihenstephan, Germany
关键词
Stachybotryotoxicosis; Sick building syndrome; Indoor air quality; Water damage; Diagnostic test kit; sat14; gene; ACUTE PULMONARY HEMORRHAGE; REAL-TIME DETECTION; PURE CULTURES; FUSARIUM SPP; FUNGI; DNA; MYCOTOXINS; INFANTS; IDENTIFICATION; EXTRACTION;
D O I
10.1007/s00216-021-03436-y
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Cytotoxic macrocyclic trichothecenes such as satratoxins are produced by chemotype S strains of Stachybotrys chartarum. Diseases such as stachybotryotoxicosis in animals and the sick building syndrome as a multifactorial disease complex in humans have been associated with this mold and its toxins. Less toxic non-chemotype S strains of S. chartarum are morphologically indistinguishable from chemotype S strains, which results in uncertainties in hazard characterization of isolates. To selectively identify macrocyclic trichothecene producing S. chartarum isolates, a set of sat14 gene-specific primers was designed and applied in a loop-mediated isothermal amplification (LAMP) assay using neutral red for visual signal detection. The assay was highly specific for S. chartarum strains of the macrocyclic trichothecene producing chemotype and showed no cross-reaction with non-macrocyclic trichothecene producing S. chartarum strains or 152 strains of 131 other fungal species. The assay's detection limit was 0.635 pg/rxn (picogram per reaction) with a reaction time of 60 min. Its high specificity and sensitivity as well as the cost-saving properties make the new assay an interesting and powerful diagnostic tool for easy and rapid testing.
引用
收藏
页码:4801 / 4813
页数:13
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