Metabolic adaptation of Mycobacterium avium subsp. paratuberculosis to the gut environment.
Metabolic adaptation of Mycobacterium avium subsp. paratuberculosis to the gut environment.
复制标题
鸟分枝杆菌副结核亚种对肠道环境的代谢适应
DOI:
10.1099/mic.0.062737-0
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发表时间:
2013
期刊:
影响因子:
1.5
通讯作者:
Goethe R
中科院分区:
文献类型:
--
作者:
Weigoldt M;Meens J;Bange FC;Pich A;Gerlach GF;Goethe R
Knowledge on the proteome level about the adaptation of pathogenic mycobacteria to the environment in their natural hosts is limited.Mycobacterium aviumsubsp.paratuberculosis(MAP) causes Johne’s disease, a chronic and incurable granulomatous enteritis of ruminants, and has been suggested to be a putative aetiological agent of Crohn’s disease in humans. Using a comprehensive LC-MS-MS and 2D difference gel electrophoresis (DIGE) approach, we compared the protein profiles of clinical strains of MAP prepared from the gastrointestinal tract of diseased cows with the protein profiles of the same strains after they were grownin vitro. LC-MS-MS analyses revealed that the principal enzymes for the central carbon metabolic pathways, including glycolysis, gluconeogenesis, the tricaboxylic acid cycle and the pentose phosphate pathway, were present under both conditions. Moreover, a broad spectrum of enzymes for β-oxidation of lipids, nine of which have been shown to be necessary for mycobacterial growth on cholesterol, were detectedin vivoandin vitro. Using 2D-DIGE we found increased levels of several key enzymes that indicated adaptation of MAP to the host. Among these, FadE5, FadE25 and AdhB indicated that cholesterol is used as a carbon source in the bovine intestinal mucosa; the respiratory enzymes AtpA, NuoG and SdhA suggested increased respiration during infection. Furthermore higher levels of the pentose phosphate pathway enzymes Gnd2, Zwf and Tal as well as of KatG, SodA and GroEL indicated a vigorous stress response of MAPin vivo. In conclusion, our results provide novel insights into the metabolic adaptation of a pathogenic mycobacterium in its natural host.
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影响因子:
14
作者:
Boeer, Ulrike;Lohrenz, Andrea;Wilhelmi, Mathias
通讯作者:
Wilhelmi, Mathias
影响因子:
--
作者:
T. Jaeger
通讯作者:
T. Jaeger
影响因子:
2.2
作者:
Granger, K;Moore, RJ;Tizard, MLV
通讯作者:
Tizard, MLV
影响因子:
2.4
作者:
BUERGELT, CD;HALL, C;DUNCAN, JR
通讯作者:
DUNCAN, JR
影响因子:
30.3
作者:
Russell DG;VanderVen BC;Lee W;Abramovitch RB;Kim MJ;Homolka S;Niemann S;Rohde KH
通讯作者:
Rohde KH