Composition and method for killing aspergillus fumigatus
A technology of Aspergillus fumigatus and bacterial strains, which is applied in the field of Aspergillus fumigatus biofilm and composition for killing Aspergillus fumigatus, and can solve the problems of Aspergillus fumigatus drug resistance and poor effect
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Embodiment 1
[0032] 1.1 Materials
[0033] 1.1.1 Antifungal drugs Chlorogenic acid (CRA, National Institute for Food and Drug Control, batch number 110753-201314), voriconazole (VRC, National Institute for Food and Drug Control, batch number 100862-200701). All were dissolved in 100% dimethyl sulfoxide, prepared into storage solutions with concentrations of 102400 μg / ml and 1280 μg / ml respectively, and stored at -20°C after aliquoting.
[0034]1.1.2 Strains From September 2012 to May 2013, 30 Aspergillus fumigatus strains were collected in the Bacteria Laboratory of the First Affiliated Hospital of Guangxi Medical University. The strain with the strongest biofilm formation ability was selected by the crystal violet method as the subject Test strains. The quality control strain was Candida parapsilosis ATCC22019, which was donated to the Bacteria Laboratory of the First Affiliated Hospital of Guangxi Medical University.
[0035] 1.1.3 Carrier Glass cell slides, 13 mm in diameter (Haimen S...
Embodiment 2
[0049] According to the implementation of embodiment 1, the result that draws, table 1 is that XTT reduces method and measures metabolic activity, the XTT% of each group
[0050] group Early Aspergillus fumigatus biofilm mature Aspergillus fumigatus biofilm VRC group 71.07 85.29 512μg / ml CRA group 99.97 98.02 1024μg / ml CRA group 99.12 98.68 512μg / ml CRA group + VRC 17.82 35.89 1024μg / ml CRA group + VRC 10.23 19.21
[0051] Fluorescent staining and observation of fluorescent dead and live bacteria stained with laser confocal microscope, whether it is early or mature chlorogenic acid intervention group compared with the blank group, there is no significant difference, the hyphae are also dense and all are vibrant green; There was no significant difference in the mycelial density between the voriconazole group and the blank group, and a small number of mycelia showed inactive red and yellow with poor vitality. When acting on the...
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