Caspofungin enhances the potency of rifampin against Gram-negative bacteria

被引:0
作者
Li, Haotian [1 ,2 ]
Zhu, Xiaojing [1 ,2 ]
Zhang, Xing [1 ,2 ]
Dong, Changjiang [1 ,2 ]
机构
[1] Wuhan Univ, Sch Pharmaceut Sci, Wuhan, Peoples R China
[2] Wuhan Univ, Key Lab Combinatorial Biosynth & Drug Discovery, Minist Educ, Wuhan, Peoples R China
基金
中国国家自然科学基金;
关键词
antimicrobial resistance; Gram-negative bacteria; antibiotic adjuvant; bacterial envelope; PgaC; ANTIBIOTIC-RESISTANCE; MULTIDRUG-RESISTANT; ESCHERICHIA-COLI; PERMEABILITY; MECHANISM; BIOFILMS; ACTIVATION;
D O I
10.3389/fmicb.2024.1447485
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Introduction Developing antibiotic adjuvants is an effective strategy to combat antimicrobial resistance (AMR). The envelope of Gram-negative bacteria (GNB) is a barrier to prevent the entry of antibiotics, making it an attractive target for novel antibiotic and adjuvant development.Methods and Results In this study, we identified Caspofungin acetate (CAS) as an antibiotic adjuvant against GNB in the repurposing screen of 3,158 FDA-approved drugs. Checkerboard assays suggested that CAS could enhance the antimicrobial activity of rifampin or colistin against various GNB strains in vitro, Moreover, Galleria mellonella larvae infection model also indicated that CAS significantly potentiated the efficacy of rifampin against multidrug-resistant Escherichia coli 72 strain in vivo. Most importantly, resistance development assay showed that CAS was less susceptible to accelerating the resistance development of drug-sensitive strain E. coli MG1655. Functional studies and RNA-seq analysis confirmed that the mechanisms by which CAS enhanced the antimicrobial activities of antibiotics were involved in permeabilizing the bacterial cell envelope, disrupting proton motive force and inhibiting bacterial biofilm formation. Additionally, it has been found that PgaC is the CAS target and enzymatic assay has confirmed the inhibition activity.Discussion Our results illustrate the feasibility of CAS as an antibiotic adjuvant against GNB, which is an alternative strategy of anti-infection.
引用
收藏
页数:15
相关论文
共 66 条
  • [31] Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
    Love, Michael I.
    Huber, Wolfgang
    Anders, Simon
    [J]. GENOME BIOLOGY, 2014, 15 (12):
  • [32] Antibacterial mechanism of daptomycin antibiotic against Staphylococcus aureus based on a quantitative bacterial proteome analysis
    Ma, Wen
    Zhang, Dan
    Li, Guoshun
    Liu, Jingjing
    He, Gu
    Zhang, Peng
    Yang, Li
    Zhu, Hongxia
    Xu, Ningzhi
    Liang, Shufang
    [J]. JOURNAL OF PROTEOMICS, 2017, 150 : 242 - 251
  • [33] The Gram-negative permeability barrier: tipping the balance of the in and the out
    Maher, Claire
    Hassan, Karl A.
    [J]. MBIO, 2023, 14 (06):
  • [34] Bacterial Antibiotic Resistance: The Most Critical Pathogens
    Mancuso, Giuseppe
    Midiri, Angelina
    Gerace, Elisabetta
    Biondo, Carmelo
    [J]. PATHOGENS, 2021, 10 (10):
  • [36] Sensitization of KPC and NDM Klebsiella pneumoniae To Rifampicin by the Human Lactoferrin-Derived Peptide hLF1-11
    Morici, Paola
    Rizzato, Cosmeri
    Ghelardi, Emilia
    Rossolini, Gian Maria
    Lupetti, Antonella
    [J]. MICROBIOLOGY SPECTRUM, 2023, 11 (01):
  • [37] Morrison Vicki A, 2005, Expert Rev Anti Infect Ther, V3, P697, DOI 10.1586/14787210.3.5.697
  • [38] Development and transmission of antimicrobial resistance among Gram-negative bacteria in animals and their public health impact
    Mukerji, Shewli
    O'Dea, Mark
    Barton, Mary
    Kirkwood, Roy
    Lee, Terence
    Abraham, Sam
    [J]. ANTIMICROBIAL RESISTANCE, 2017, 61 (01): : 23 - 35
  • [39] Global burden of bacterial antimicrobial resistance in 2019: a systematic analysis
    Murray, Christopher J. L.
    Ikuta, Kevin Shunji
    Sharara, Fablina
    Swetschinski, Lucien
    Aguilar, Gisela Robles
    Gray, Authia
    Han, Chieh
    Bisignano, Catherine
    Rao, Puja
    Wool, Eve
    Johnson, Sarah C.
    Browne, Annie J.
    Chipeta, Michael Give
    Fell, Frederick
    Hackett, Sean
    Haines-Woodhouse, Georgina
    Hamadani, Bahar H. Kashef
    Kumaran, Emmanuelle A. P.
    McManigal, Barney
    Agarwal, Ramesh
    Akech, Samuel
    Albertson, Samuel
    Amuasi, John
    Andrews, Jason
    Aravkin, Aleskandr
    Ashley, Elizabeth
    Bailey, Freddie
    Baker, Stephen
    Basnyat, Buddha
    Bekker, Adrie
    Bender, Rose
    Bethou, Adhisivam
    Bielicki, Julia
    Boonkasidecha, Suppawat
    Bukosia, James
    Carvalheiro, Cristina
    Castaneda-Orjuela, Carlos
    Chansamouth, Vilada
    Chaurasia, Suman
    Chiurchiu, Sara
    Chowdhury, Fazle
    Cook, Aislinn J.
    Cooper, Ben
    Cressey, Tim R.
    Criollo-Mora, Elia
    Cunningham, Matthew
    Darboe, Saffiatou
    Day, Nicholas P. J.
    De Luca, Maia
    Dokova, Klara
    [J]. LANCET, 2022, 399 (10325) : 629 - 655
  • [40] Multiple ways to kill bacteria via inhibiting novel cell wall or membrane targets
    Naclerio, George A.
    Sintim, Herman O.
    [J]. FUTURE MEDICINAL CHEMISTRY, 2020, 12 (13) : 1253 - 1279