Insights into the CtrA regulon in development of stress resistance in obligatory intracellular pathogen Ehrlichia chaffeensis.
Insights into the CtrA regulon in development of stress resistance in obligatory intracellular pathogen Ehrlichia chaffeensis.
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DOI:
10.1111/j.1365-2958.2011.07885.x
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发表时间:
2011-12
影响因子:
3.6
通讯作者:
Rikihisa Y
中科院分区:
文献类型:
--
作者:
Cheng Z;Miura K;Popov VL;Kumagai Y;Rikihisa Y
Ehrlichia chaffeensis is an obligate intracellular bacterium that causes human monocytic ehrlichiosis. Ehrlichiae have a biphasic developmental cycle consisting of dense-cored cells (DCs) and reticulate cells (RCs). Isolated DCs are more stress resistant and infectious than RCs. Here, we report that a response regulator, CtrA was upregulated in human monocytes at the late growth stage when DCs develop. E. chaffeensis CtrA bound to the promoters of late-stage transcribed genes: ctrA, ompA (peptidoglycan-associated lipoprotein), bolA (stress-induced morphogen), and surE (stationary phase survival protein), which contain CtrA-binding motifs, and transactivated ompA, surE, and bolA promoter-lacZ fusions in Escherichia coli. OmpA was predominantly expressed in DCs. E. chaffeensis binding to and subsequent infection of monocytes were inhibited by anti-OmpA IgG. E. chaffeensis BolA bound to the promoters of genes encoding outer surface proteins TRP120 and ECH_1038, which were expressed in DCs, and transactivated trp120 and ECH_1038 promoter-lacZ fusions. E. chaffeensis bolA complemented a stress-sensitive E. coli bolA mutant. E. coli expressing E. chaffeensis surE exhibited increased resistance to osmotic stress. Our results suggest that E. chaffeensis CtrA plays a role in coordinating development of the stress resistance for passage from the present to the next host cells through its regulon.
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影响因子:
4.5
作者:
Dunning Hotopp JC;Lin M;Madupu R;Crabtree J;Angiuoli SV;Eisen JA;Seshadri R;Ren Q;Wu M;Utterback TR;Smith S;Lewis M;Khouri H;Zhang C;Niu H;Lin Q;Ohashi N;Zhi N;Nelson W;Brinkac LM;Dodson RJ;Rosovitz MJ;Sundaram J;Daugherty SC;Davidsen T;Durkin AS;Gwinn M;Haft DH;Selengut JD;Sullivan SA;Zafar N;Zhou L;Benahmed F;Forberger H;Halpin R;Mulligan S;Robinson J;White O;Rikihisa Y;Tettelin H
通讯作者:
Tettelin H
影响因子:
3.4
作者:
Cheng, Zhihui;Kumagai, Yumi;Rikihisa, Yasuko
通讯作者:
Rikihisa, Yasuko
影响因子:
2.1
作者:
Freire, Patrick;Vieira, Helena L. A.;Arraiano, Cecilia M.
通讯作者:
Arraiano, Cecilia M.
影响因子:
64.5
作者:
Domian, IJ;Quon, KC;Shapiro, L
通讯作者:
Shapiro, L
DOI:
10.1073/pnas.88.9.3937
发表时间:
1991-05-01
影响因子:
11.1
作者:
HACKSTADT, T;BAEHR, W;YING, Y
通讯作者:
YING, Y