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Transcriptional inhibitor of virulence factors in enteropathogenic Escherichia coli
被引:83
作者:
Gauthier, A
Robertson, ML
Lowden, M
Ibarra, JA
Puente, JL
Finlay, BB
[3
]
机构:
[1] Univ British Columbia, Dept Biochem, Vancouver, BC V6T 1Z3, Canada
[2] Univ British Columbia, Dept Microbiol, Vancouver, BC V6T 1Z3, Canada
[3] Univ British Columbia, Michael Smith Labs, Vancouver, BC V6T 1Z3, Canada
[4] Univ Nacl Autonoma Mexico, Dept Biol Mol, Inst Biotecnol, Cuernavaca 62210, Morelos, Mexico
关键词:
D O I:
10.1128/AAC.49.10.4101-4109.2005
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
The type III secretion system (ITSS) is a key virulence mechanism of many important gram-negative bacterial pathogens. The TTSS is conserved among different bacterial pathogens, and mutations and deletions to the system significantly decrease virulence, making the TTSS an important potential therapeutic target. We have developed a high-throughput assay to search for inhibitors of the TTSS. We screened a commercial library of 20,000 small molecules for their ability to inhibit type III secretion by enteropathogenic Escherichia coli (EPEC). After discarding compounds that had no effect on secretion, inhibited bacterial growth, and/or caused degradation of EPEC-secreted proteins, the search was focused on a class of compounds that, while not direct inhibitors of type III secretion, inhibit expression of TTSS-related genes and other genes involved in virulence. This class of compounds does not affect bacterial viability or motility, indicating that it is not significantly affecting the expression of essential genes and is specific to virulence-associated genes. Transcriptional fusion assays confirmed that virulence-associated promoters were more sensitive to inhibition by this class of compounds. Overall, we have identified a class of compounds that can be used as a tool to probe the mechanism(s) that regulates virulence gene expression in EPEC.
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页码:4101 / 4109
页数:9
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