M;
pneumoniae;
Platycodin center dot D;
P1;
P30;
Animal models;
PCR;
D O I:
10.1016/j.etap.2017.01.001
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
Platycodin D is one of the most important monomers of the Qinbaiqingfei pellet (Qjnbai), which has already been approved as the first effective new Traditional Chinese Medicine used to fight against Mycoplasma pneumoniae (M. pneumoniae) in clinic in China. In previous studies, pharmacodynamics experiment has proved that Platycodin D has anti-M. pneumoniae effect and the minimum inhibitory concentration (MIC) is 16m mu g/ml. This paper further clarified that the mechanism underlying the anti M. pneumoniae effect of Platycodin D might be due to M. pneumoniae adhesion proteins P1 and P30. P1 and P30 expression levels in M. pneumoniae strain, M. pneumoniae-infected BALB/c mice, and M. pneumoniae-infected A549 cells were determined by reverse transcription PCR. Platycodin D strongly inhibited P1 and P30 expression in M. pneumonia and high dosage of Platycodin D exhibited a greater effect on reducing P1 and P30 expression than low dose Platycodin D. Platycodin D prevented M. pneumoniae infection through inhibiting the expression of adhesion proteins, which might be one of the mechanisms for the anti-M. pneumoniae properties of Qinbai. These results provide a foundation to further explore the mechanisms of action of Qinbai in future studies. (C) 2017 Elsevier B.V. All rights reserved.
机构:
Univ Georgia, Dept Microbiol, Riverbend Res Labs S 019, Athens, GA 30602 USAUniv Georgia, Dept Microbiol, Riverbend Res Labs S 019, Athens, GA 30602 USA
Chang, How-Yi
Jordan, Jarrat L.
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h-index: 0
机构:
Univ Georgia, Dept Microbiol, Riverbend Res Labs S 019, Athens, GA 30602 USAUniv Georgia, Dept Microbiol, Riverbend Res Labs S 019, Athens, GA 30602 USA
Jordan, Jarrat L.
Krause, Duncan C.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Georgia, Dept Microbiol, Riverbend Res Labs S 019, Athens, GA 30602 USAUniv Georgia, Dept Microbiol, Riverbend Res Labs S 019, Athens, GA 30602 USA