In Vitro Antibacterial Experiment of Fuzheng Jiedu Huayu Decoction Against Multidrug-Resistant Pseudomonas aeruginosa

被引:16
|
作者
Xu, Hongri [1 ]
Liu, Chang [2 ]
Li, Meng [3 ]
Wang, Chengxiang [2 ]
Liu, Guoxing [2 ]
Wang, Honghong [1 ]
Ma, Jie [4 ]
Li, Lei [2 ]
Chen, Meng [5 ]
Cheng, Miao [6 ]
Yao, Xingwei [7 ]
Lin, Ying [7 ]
Zhao, Shitong [6 ]
Wang, Yuting [6 ]
Wang, Mingzhe [8 ]
机构
[1] Beijing Univ Chinese Med BUCM, Affiliated Hosp 3, Emergency Dept, Beijing, Peoples R China
[2] BUCM Third Affiliated Hosp, Resp Dept, Beijing, Peoples R China
[3] ShaanXi Tradit Chinese Med TCM Hosp, Resp Dept, Xian, Peoples R China
[4] Beijing Hosp Integrated Tradit Chinese & Western, Resp Dept, Beijing, Peoples R China
[5] China Acad Inspect & Quarantine, Inst Ind & Consumer Prod Safety, Beijing, Peoples R China
[6] Dongzhimen Hosp Affiliated BUCM, Resp Dept, Beijing, Peoples R China
[7] Dongzhimen Hosp Affiliated BUCM, Clin Lab, Beijing, Peoples R China
[8] China Japan Friendship Hosp, Resp Dept, Beijing, Peoples R China
来源
FRONTIERS IN PHARMACOLOGY | 2020年 / 10卷
基金
中国国家自然科学基金; 高等学校博士学科点专项科研基金;
关键词
growth curve; Fuzheng Jiedu Huayu decoction; multidrug-resistant Pseudomonas aeruginosa; in vitro antibacterial; drug sensitivity test;
D O I
10.3389/fphar.2019.01682
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective Drawing a growth curve of multidrug-resistant Pseudomonas aeruginosa (MDR-PA) provides a foundation for susceptibility testing. By observing in vitro antibacterial activity and ultrastructure cthanges on MDR-PA of the effective components in the drug-containing serum of rats after the administration of Fuzheng Jiedu Huayu decoction (FJHD), we evaluated the inhibition and direct destruction effect of bacteria by TCM alone or combined with antibiotics. Methods The absorbance values of MDR-PA were determined at different detection time points, and a growth curve was drawn. After gavage with FJHD, drug-containing serum was collected from the rats. Using Imipenem/cilastatin sodium as the positive drug control, the in vitro antibacterial potency of FJHD and its drug-containing serum alone or in combination with antibiotics against MDR-PA was observed. The ultrastructural changes of MDR-PA treated by FJHD combined with antibiotics were observed by transmission electron microscopy. Results Growth of the experimental strain manifested a lag phase in the first 1-4 h, an exponential growth phase at 5-20 h, and a plateau phase after 20 h. The best detection time during the susceptibility test was 16-20 h. The minimum inhibitory concentration (MIC) value of the FJHD extract group was 0.2 g/mL. The MIC value of the pure Imipenem/cilastatin sodium group was 16 mu g/mL. The MIC values of Imipenem/cilastatin sodium + blank serum, 0.5-, 1-, and 2-fold drug-containing serum groups were all 16 mu g/mL. The MIC values of Imipenem/cilastatin sodium + 4- and 8-fold drug-containing serum groups were both 8 mu g/mL. By observation under a transmission electron microscope, Imipenem/cilastatin sodium + 0.5-, 1-, and 2-fold drug-containing serum groups showed bacterial structural damage. The degree of bacterial destruction was more obvious and the quantity of damaged bacteria was increased in the Imipenem/cilastatin sodium + 4- and 8-fold drug-containing serum groups. Conclusion Drawing the growth curve of the experimental strain had high application value for ensuring the accuracy of the drug sensitivity test results. TCM combined with antibiotics could enhance the antibacterial and direct destruction effect of bacteria in vitro, thereby inhibiting bacterial resistance to a certain extent.
引用
收藏
页数:11
相关论文
共 36 条
  • [21] Reducing the urine collection rate could prevent hospital-acquired horizontal transmission of multidrug-resistant Pseudomonas aeruginosa
    Hashimoto, Kenyu
    Gotoh, Kenji
    Masunaga, Kenji
    Iwahashi, Jun
    Sakamoto, Toru
    Miura, Miho
    Horita, Rie
    Sakai, Yoshiro
    Murotani, Kenta
    Watanabe, Hiroshi
    JOURNAL OF INFECTION AND CHEMOTHERAPY, 2022, 28 (06) : 786 - 790
  • [22] Post-cataract surgery cluster endophthalmitis due to multidrug-resistant Pseudomonas aeruginosa: A retrospective cohort study of six clusters
    Parchand, Swapnil M.
    Agrawal, Deepanshu
    Chatterjee, Samrat
    Gangwe, Anil
    Mishra, Mihir
    Agrawal, Deepshikha
    INDIAN JOURNAL OF OPHTHALMOLOGY, 2020, 68 (07) : 1424 - 1431
  • [23] Chemical Composition and Antibacterial Activity of Citrus Peels Essential Oils Against Multidrug-Resistant Bacteria: A Comparative Study
    Azghar, A.
    Dalli, M.
    Azizi, S.
    Benaissa, E. M.
    Ben Lahlou, Y.
    Elouennass, M.
    Maleb, A.
    JOURNAL OF HERBAL MEDICINE, 2023, 42
  • [24] In vitro efficacy of Colistin against multi-drug resistant Pseudomonas aeruginosa by minimum inhibitory concentration
    Gill, Maria Mushtaq
    Rao, Javaid Usman
    Kaleem, Fatima
    Hassan, Afreenish
    Khalid, Ali
    Anjum, Rabia
    PAKISTAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2013, 26 (01) : 7 - 10
  • [25] Lower neutrophil-to-lymphocyte ratio predicts high risk of multidrug-resistant Pseudomonas aeruginosa infection in patients with hospital-acquired pneumonia
    Zhou, Yu-Qi
    Feng, Ding-Yun
    Li, Wen-Juan
    Yang, Hai-Ling
    Wang, Zhao-Ni
    Zhang, Tian-Tuo
    Chen, Zhuang-Gui
    THERAPEUTICS AND CLINICAL RISK MANAGEMENT, 2018, 14 : 1863 - 1869
  • [26] Successful treatment of pneumonia caused by multidrug-resistant Pseudomonas aeruginosa after allogeneic hematopoietic stem cell transplantation with colistin and amikacin inhalation therapy
    Sato, Michiaki
    Honda, Akira
    Maki, Hiroaki
    Toyama, Kazuhiro
    Yamaguchi, Ryo
    Ikeda, Mahoko
    Moriya, Kyoji
    Kurokawa, Mineo
    JOURNAL OF INFECTION AND CHEMOTHERAPY, 2022, 28 (01) : 91 - 94
  • [27] Successful Colistin Treatment of Multidrug-Resistant Pseudomonas aeruginosa Infection Using a Rapid Method for Determination of Colistin in Plasma: Usefulness of Therapeutic Drug Monitoring
    Yamada, Takehiro
    Ishiguro, Nobuhisa
    Oku, Kenji
    Higuchi, Issei
    Nakagawa, Ikuma
    Noguchi, Atsushi
    Yasuda, Shinsuke
    Fukumoto, Tatsuya
    Iwasaki, Sumio
    Akizawa, Kouji
    Furugen, Ayako
    Yamaguchi, Hiroaki
    Iseki, Ken
    BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2015, 38 (09) : 1430 - 1433
  • [28] Role of miR-466 in mesenchymal stromal cell derived extracellular vesicles treating inoculation pneumonia caused by multidrug-resistant Pseudomonas aeruginosa
    Shi, Meng-meng
    Zhu, Ying-gang
    Yan, Jia-yang
    Rouby, Jean-Jacques
    Summah, Hanssa
    Monsel, Antoine
    Qu, Jie-ming
    CLINICAL AND TRANSLATIONAL MEDICINE, 2021, 11 (01):
  • [29] Antibacterial Activity of a Cationic Antimicrobial Peptide against Multidrug-Resistant Gram-Negative Clinical Isolates and Their Potential Molecular Targets
    Patricia Rivera-Sanchez, Sandra
    Astrid Agudelo-Gongora, Helen
    Onate-Garzon, Jose
    Janeth Florez-Elvira, Liliana
    Correa, Adriana
    Andrea Londono, Paola
    David Londono-Mosquera, Juan
    Aragon-Muriel, Alberto
    Polo-Ceron, Dorian
    Dario Ocampo-Ibanez, Ivan
    MOLECULES, 2020, 25 (21):
  • [30] Control of Multidrug-Resistant Pseudomonas aeruginosa in Allogeneic Hematopoietic Stem Cell Transplant Recipients by a Novel Bundle Including Remodeling of Sanitary and Water Supply Systems
    Kossow, Annelene
    Kampmeier, Stefanie
    Willems, Stefanie
    Berdel, Wolfgang E.
    Groll, Andreas H.
    Burckhardt, Birgit
    Rossig, Claudia
    Groth, Christoph
    Idelevich, Evgeny A.
    Kipp, Frank
    Mellmann, Alexander
    Stelljes, Matthias
    CLINICAL INFECTIOUS DISEASES, 2017, 65 (06) : 935 - 942