Deletion of RD1 from Mycobacterium tuberculosis mimics bacille Calmette-Guerin attenuation

被引:440
|
作者
Lewis, KN
Liao, RL
Guinn, KM
Hickey, MJ
Smith, S
Behr, MA
Sherman, DR
机构
[1] Univ Washington, Dept Pathobiol, Seattle, WA 98195 USA
[2] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
[3] McGill Univ, Dept Microbiol & Immunol, Montreal, PQ, Canada
来源
JOURNAL OF INFECTIOUS DISEASES | 2003年 / 187卷 / 01期
关键词
D O I
10.1086/345862
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The tuberculosis (TB) vaccine bacille Calmette-Guerin (BCG) is a live attenuated organism, but the mutation responsible for its attenuation has never been defined. Recent genetic studies identified a single DNA region of difference, RD1, which is absent in all BCG strains and present in all Mycobacterium tuberculosis (MTB) strains. The 9 open-reading frames predicted within this 9.5-kb region are of unknown function, although they include the TB-specific immunodominant antigens ESAT-6 and CFP-10. In this study, RD1 was deleted from MTB strain H37Rv, and virulence of H37Rv: D RD1 was assessed after infections of the human macrophage-like cell line THP-1, human peripheral blood monocyte-derived macrophages, and C57BL/6 mice. In each of these systems, the H37Rv: D RD1 strain was strikingly less virulent than MTB and was very similar to BCG controls. Therefore, it was concluded that genes within or controlled by RD1 are essential for MTB virulence and that loss of RD1 was important in BCG attenuation.
引用
收藏
页码:117 / 123
页数:7
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