Infection with Burkholderia cepacia complex genomovars in patients with cystic fibrosis:: Virulent transmissible strains of genomovar III can replace Burkholderia multivorans

被引:171
作者
Mahenthiralingam, E
Vandamme, P
Campbell, ME
Henry, DA
Gravelle, AM
Wong, LTK
Davidson, AGF
Wilcox, PG
Nakielna, B
Speert, DP
机构
[1] Univ British Columbia, Dept Pediat, Vancouver, BC V6T 1W5, Canada
[2] British Columbia Childrens Hosp, British Columbias Res Inst Childrens & Womens Hlt, Vancouver, BC V6H 3V4, Canada
[3] State Univ Ghent, Fac Sci, Microbiol Lab, B-9000 Ghent, Belgium
[4] Univ British Columbia, Pulm Res Lab, Vancouver, BC, Canada
[5] Univ British Columbia, Div Resp Dis, Vancouver, BC V5Z 1M9, Canada
[6] St Pauls Hosp, Vancouver, BC V6Z 1Y6, Canada
关键词
D O I
10.1086/322684
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Infection with Burkholderia cepacia complex in patients with cystic fibrosis (CF) results in highly variable clinical outcomes. The purpose of this study was to determine if there are genomovar-specific disparities in transmission and disease severity. B. cepacia complex was recovered from 62 patients with CF on greater than or equal to1 occasions (genomovar III, 46 patients; genomovar II [B. multivorans], 19 patients; genomovar IV [B. stabilis], 1 patient; genomovar V [B. vietnamiensis], 1 patient; and an unclassified B. cepacia complex strain, 1 patient). Patient-to-patient spread was observed with B. cepacia genomovar III, but not with B. multivorans. Genomovar III strains replaced B. multivorans in 6 patients. Genomovar III strains were also associated with a poor clinical course and high mortality. Infection control practices should be designed with knowledge about B. cepacia complex genomovar status; patients infected with transmissible genomovar III strains should not be cohorted with patients infected with B. multivorans and other B. cepacia genomovars.
引用
收藏
页码:1469 / 1475
页数:7
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