Interkingdom interactions between Pseudomonas aeruginosa and Candida albicans affect clinical outcomes and antimicrobial responses

被引:21
作者
Kahl, Lisa J. [1 ]
Stremmel, Nina [1 ]
Esparza-Mora, M. Alejandra [1 ]
Wheatley, Rachel M. [2 ]
Maclean, R. Craig [2 ]
Ralser, Markus [1 ,3 ,4 ]
机构
[1] Charite Univ Med Berlin, Dept Biochem, Charitepl 1, D-10117 Berlin, Germany
[2] Univ Oxford, Dept Biol, Oxford OX1 3SZ, England
[3] Univ Oxford, Wellcome Ctr Human Genet, Nuffield Dept Med, Oxford OX3 7BN, England
[4] Max Planck Inst Mol Genet, D-14195 Berlin, Germany
基金
欧洲研究理事会;
关键词
VENTILATOR-ASSOCIATED PNEUMONIA; QUORUM-SENSING MOLECULE; GALLERIA-MELLONELLA; MODEL HOST; VIRULENCE; INFECTION; BACTERIAL; TOLERANCE; PHOSPHATE; SYSTEM;
D O I
10.1016/j.mib.2023.102368
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Infections that involve interkingdom microbial communities, such as those between bacteria and yeast pathogens, are difficult to treat, associated with worse patient outcomes, and may be a source of antimicrobial resistance. In this review, we address co-occurrence and co-infections of Candida albicans and Pseudomonas aeruginosa, two pathogens that occupy multiple infection niches in the human body, especially in immunocompromised patients. The interaction between the pathogen species influences microbe-host interactions, the effectiveness of antimicrobials and even infection outcomes, and may thus require adapted treatment strategies. However, the molecular details of bacteria-fungal interactions both inside and outside the infection sites, are insufficiently understanding the P. aeruginosa-C. albicans interaction network through integrated systems biology approaches will capture the highly dynamic and complex nature of these polymicrobial infections and lead to a more comprehensive understanding of clinical observations such as reshaped immune defences and low antimicrobial treatment efficacy.
引用
收藏
页数:13
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