Cyclic diguanylate (c‐di‐GMP) regulates Vibrio cholerae biofilm formation

Molecular Microbiology - Tập 53 Số 3 - Trang 857-869 - 2004
Anna D. Tischler1, Andrew Camilli1
1Department of Molecular Biology and Microbiology Tufts University School of Medicine, 136 Harrison Avenue, Boston MA 02111, USA

Tóm tắt

SummaryWhile studying virulence gene regulation in Vibrio cholerae during infection of the host small intestine, we identified VieA as a two‐component response regulator that contributes to activating expression of cholera toxin. Here we report that VieA represses transcription of Vibrio exopolysaccharide synthesis (vps) genes involved in biofilm formation by a mechanism independent of its phosphorelay and DNA‐binding activities. VieA controls the intracellular concentration of the cyclic nucleotide second messenger cyclic diguanylate (c‐di‐GMP) using an EAL domain that functions as a c‐di‐GMP phosphodiesterase. Two‐dimensional thin layer chromatography of nucleotide extracts confirmed that VieA reduces the concentration of c‐di‐GMP, opposing the action of  c‐di‐GMP synthetase proteins. Expression of unrelated V. cholerae c‐di‐GMP synthetase or phosphodiesterae proteins also modulated c‐di‐GMP concentration and vps gene expression. We propose that c‐di‐GMP synthetase and phosphodiesterase domain‐containing proteins contribute to regulating biofilm formation by controlling c‐di‐GMP concentration.

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Tài liệu tham khảo

10.1046/j.1365-2958.2003.03401.x

10.1128/IAI.68.12.6857-6864.2000

10.1099/13500872-145-5-1253

10.1111/j.1574-6968.2001.tb10880.x

10.1016/S0021-9258(18)34138-3

Boles B.R., 2003, Vibrio parahaemolyticus scrABC, a novel operon affecting swarming and capsular polysaccharide regulation, J Bacteriol, 184, 5946, 10.1128/JB.184.21.5946-5954.2002

10.1128/JB.185.4.1384-1390.2003

Callahan L.T., 1971, Biochemistry of Vibrio cholerae virulence. II. Skin permeability factor/cholera enterotoxin production in a chemically defined medium, Infect Immun, 4, 611, 10.1128/iai.4.5.611-618.1971

10.1111/j.1365-2958.1995.mmi_18040671.x

10.1021/bi0100236

D’Argenio D.A., 2002, Autolysis and autoaggregation in Pseudomonas aeruginosa colony morphology mutants, J Bacteriol, 184, 6481, 10.1128/JB.184.23.6481-6489.2002

10.1128/iai.59.12.4310-4317.1991

10.1038/416740a

10.1111/j.1574-6968.2001.tb10814.x

10.1128/jb.177.14.4121-4130.1995

10.1046/j.1365-2958.2003.03688.x

10.1016/S0022-2836(83)80284-8

10.1126/science.7618105

10.1128/9781555818364.ch11

10.1016/0092-8674(78)90046-6

10.1128/JB.180.9.2298-2305.1998

10.1016/S0092-8674(00)81551-2

10.1073/pnas.111581598

10.1046/j.1365-2958.2002.02857.x

Miller J.H., 1972, Experiments in Molecular Genetics.

10.1128/jb.170.6.2575-2583.1988

10.1002/1097-0134(20010201)42:2<210::AID-PROT80>3.0.CO;2-8

10.1016/S0378-1097(03)00657-8

10.1111/j.1574-6976.2002.tb00605.x

10.1046/j.1365-2958.2000.01822.x

10.1016/S0008-6215(00)90372-0

10.1038/325279a0

10.1016/S0021-9258(17)30606-3

10.1128/mr.55.1.35-58.1991

Sambrook J., 2001, Molecular Cloning: a Laboratory Manual.

10.1016/S1074-5521(02)00198-9

10.1128/JB.180.17.4416-4425.1998

10.1073/pnas.84.9.2833

10.1128/JB.184.15.4104-4113.2002

10.1046/j.1365-2958.1999.01624.x

10.1016/S0014-5793(97)01202-7

10.1073/pnas.96.7.4028

10.1128/JB.183.5.1716-1726.2001

10.1016/S1534-5807(03)00295-8

10.1073/pnas.052694299

10.1046/j.1365-2958.2001.02337.x