Treatment of infection-induced vascular pathologies is protective against persistent rough morphotype Mycobacterium abscessus infection in zebrafish

被引:1
作者
Kam, Julia Y.
Wright, Kathryn
Britton, Warwick J. [1 ]
Oehlers, Stefan H. [2 ,3 ,4 ,5 ]
机构
[1] Univ Sydney, TB Res Program Centenary Inst, Camperdown, NSW 2050, Australia
[2] Royal Prince Alfred Hosp, Dept Clin Immunol, Camperdown, NSW 2050, Australia
[3] Univ Sydney, Sydney Inst Infect Dis, Camperdown, NSW 2050, Australia
[4] ASTAR Infect Dis Labs, ASTAR ID Labs, Agcy Sci, Technol & Res ASTAR, Singapore 138648, Singapore
[5] 8A Biomed Grove,05-13,Immunos, Singapore 138648, Singapore
基金
英国医学研究理事会;
关键词
Zebrafish; Mycobacteria; Angiogenesis; Vascular permeability; Platelet; SMOOTH; GROWTH;
D O I
10.1016/j.micpath.2022.105590
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mycobacterium abscessus infections are of increasing global prevalence and are often difficult to treat due to complex antibiotic resistance profiles. While there are similarities between the pathogenesis of M. abscessus and tuberculous mycobacteria, including granuloma formation and stromal remodelling, there are distinct molecular differences at the host-pathogen interface. Here we have used a zebrafish-M. abscessus model and host-directed therapies that were previously identified in the zebrafish-M. marinum model to identify potential host-directed therapies against M. abscessus infection. We find efficacy of anti-angiogenic and vascular normalizing therapies against rough M. abscessus infection, but no effect of anti-platelet drugs.
引用
收藏
页数:5
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