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Expression of Borrelia burgdorferi OspC and DbpA is controlled by a RpoN-RpoS regulatory pathway
被引:283
作者:

Hübner, A
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机构: Univ Texas, SW Med Ctr, Dept Microbiol, Dallas, TX 75390 USA

Yang, XF
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机构: Univ Texas, SW Med Ctr, Dept Microbiol, Dallas, TX 75390 USA

Nolen, DM
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机构: Univ Texas, SW Med Ctr, Dept Microbiol, Dallas, TX 75390 USA

Popova, TG
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机构: Univ Texas, SW Med Ctr, Dept Microbiol, Dallas, TX 75390 USA

Cabello, FC
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机构: Univ Texas, SW Med Ctr, Dept Microbiol, Dallas, TX 75390 USA

Norgard, MV
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Univ Texas, SW Med Ctr, Dept Microbiol, Dallas, TX 75390 USA Univ Texas, SW Med Ctr, Dept Microbiol, Dallas, TX 75390 USA
机构:
[1] Univ Texas, SW Med Ctr, Dept Microbiol, Dallas, TX 75390 USA
[2] New York Med Coll, Dept Microbiol & Immunol, Valhalla, NY 10595 USA
来源:
关键词:
D O I:
10.1073/pnas.231442498
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
RpoS and RpoN are two alternative sigma factors typically associated with general stress responses in bacteria. To date, there has been no experimental evidence that RpoS and RpoN can directly control the expression of one another. Herein, using a combined strategy of gene disruption and genetic complementation targeting rpoN and rpoS in Borrelia burgdorferi strain 297, we describe a regulatory network for B. burgdorferi. In this network, RpoN controls the expression of RpoS, which, in turn, governs the expression of two important membrane lipoproteins, outer surface protein C and decorin-binding protein A, and likely other proteins of B. burgdorferi. Our findings provide a foundation for elucidating further key regulatory networks that potentially impact many aspects of B. burgdorferi's parasitic strategy, host range, and virulence expression.
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页码:12724 / 12729
页数:6
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