Mechanism of butyl alcohol extract of Baitouweng Decoction (BAEB) on Candida albicans biofilms based on pH signal pathway.
10.19540/j.cnki.cjcmm.20181012.001
- Author:
Yun-Xia WANG
1
;
Ke-Long MA
1
;
Yan WANG
1
;
Da-Qiang WU
1
;
Jing SHAO
1
;
Tian-Ming WANG
1
;
Chang-Zhong WANG
2
Author Information
1. Institute of Integrated Traditional Chinese and Western Medicine,Anhui University of Traditional Chinese Medicine Hefei 230012,China Institute of Integrated Traditional Chinese and Western Medicine,Anhui Academy of Traditional Chinese Medicine Hefei 230012,China.
2. Institute of Integrated Traditional Chinese and Western Medicine,Anhui University of Traditional Chinese Medicine Hefei 230012,China Institute of Integrated Traditional Chinese and Western Medicine,Anhui Academy of Traditional Chinese Medicine Hefei 230012,China Key Laboratory of Chinese Medicinal Formula of Anhui Province Hefei 230012,China.
- Publication Type:Journal Article
- Keywords:
Candida albicans biofilms;
PHR1 gene;
RIM101 gene;
butyl alcohol extract of Baitouweng Decoction(BAEB);
pH signaling pathway
- MeSH:
1-Butanol;
Biofilms;
drug effects;
Candida albicans;
drug effects;
Drugs, Chinese Herbal;
pharmacology;
Fungal Proteins;
Gene Expression Regulation, Fungal;
Hydrogen-Ion Concentration;
Plant Extracts;
pharmacology;
Signal Transduction
- From:
China Journal of Chinese Materia Medica
2019;44(2):350-356
- CountryChina
- Language:Chinese
-
Abstract:
This study aimed to investigate the effect of butyl alcohol extract of Baitouweng Decoction( BAEB) on Candida albicans biofilms based on pH signal pathway. The morphology of biofilms of the pH mutants was observed by scanning electron microscope. The biofilm thickness of the pH mutants was measured by CLSM. The biofilm activity of the pH mutants was analyzed by microplate reader.The biofilm damage of the pH mutants was detected by flow cytometry. The expression of pH mutant biofilm-related genes was detected by qRT-PCR. The results showed that the deletion of PHR1 gene resulted in the defect of biofilm,but there were more substrates for PHR1 complementation. BAEB had no significant effect on the two strains. RIM101 gene deletion or complementation did not cause significant structural damage,but after BAEB treatment,the biofilms of both strains were significantly inhibited. For the biofilm thickness,PHR1 deletion or complementation caused the thickness to decrease,after BAEB treatment,the thickness of the two strains did not change significantly. However,RIM101 gene deletion or complementation had little effect on the thickness,and the thickness of the two strains became thinner after adding BAEB. For biofilm activity,PHR1 deletion or complementation and RIM101 deletion resulted in decreased activity,RIM101 complementation did not change significantly; BAEB significantly inhibited biofilm activity of PHR1 deletion,PHR1 complemetation,RIM101 deletion and RIM101 complemetation strains. For the biofilm damage,PHR1 gene deletion or complementation,RIM101 gene deletion or complementation all showed different degrees of damage; after adding BAEB,the damage rate of PHR1 deletion or complementation was not significantly different,but the damage rate of RIM101 deletion or complementation was significantly increased. Except to the up-regulation of HSP90 gene expression,ALS3,SUN41,HWP1,UME6 and PGA10 genes of PHR1 deletion,PHR1 complementation,RIM101 deletion,and RIM101 complementation strains showed a downward expression trend. In a word,this study showed that mutations in PHR1 and RIM101 genes in the pH signaling pathway could enhance the sensitivity of the strains to the antifungal drug BAEB,thus inhibiting the biofilm formation and related genes expression in C. albicans.
