Production of exopolysaccharide by Burkholderia cenocepacia results in altered cell-surface interactions and altered bacterial clearance in mice

被引:67
作者
Conway, BAD
Chu, KK
Bylund, J
Altman, E
Speert, DP
机构
[1] Univ British Columbia, Dept Paediat, BC Res Inst Childrens & Womans Hlth, Vancouver, BC V5Z 4H4, Canada
[2] Univ British Columbia, Dept Pathol, BC Res Inst Childrens & Womans Hlth, Vancouver, BC V5Z 4H4, Canada
[3] Natl Res Council Canada, Inst Biol Sci, Ottawa, ON K1A 0R6, Canada
基金
加拿大健康研究院;
关键词
D O I
10.1086/423141
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Despite the characterization of some Burkholderia cepacia complex exopolysaccharides (EPSs), little is known about the role of EPSs in the pathogenicity of B. cepacia complex organisms. We describe 2 Burkholderia cenocepacia (genomovar III) isolates obtained from a patient with cystic fibrosis (CF): the nonmucoid isolate C8963 and the mucoid isolate C9343. Both isolates had identical random amplified polymorphic DNA patterns. C9343 produced a capsule composed of the EPSs PS-I and PS-II, as well as alpha-1,6-glucan. These isolates exhibited several phenotypic differences: C8963 synthesized octanoyl-homoserine lactone and produced biofilms, but C9343 did not; in a mouse model of pulmonary infection, C8963 was cleared more rapidly than was C9343; and C9343 interacted poorly with macrophages and neutrophils, compared with C8963, suggesting that the C9343 capsule interfered with cell-surface interactions. Overproduction of EPS by C9343 resulted in a mucoid appearance and interfered with cell-surface interactions and clearance in an animal model. This mucoid colonial appearance could enhance the persistence and virulence of this important CF-related pathogen.
引用
收藏
页码:957 / 966
页数:10
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