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Conference Paper: Multiplex Promoter Reporter Platform to Monitor Staphylococcus aureus Virulence Gene Expression

TitleMultiplex Promoter Reporter Platform to Monitor Staphylococcus aureus Virulence Gene Expression
Authors
Issue Date2016
Citation
2016 World Life Science Conference (WLSC2016), Beijing, China, 1-3 November 2016 How to Cite?
AbstractAs antibiotic resistance becomes phenomenal, alternative therapeutic strategies for bacterial infections such as anti-virulence treatments have been advocated. We have constructed a total of 20 gfp-luxABCDE dual-reporter plasmids with selected promoters from S. aureus virulence-associated genes. The plasmids were introduced into various S. aureus strains to establish a gfp-lux based multiplex promoter reporter platform for monitoring S. aureus virulence gene expressions in real time to identify factors or compounds that may perturb virulence of S. aureus. The gene expression profiles monitored by luminescence correlated well with qRT-PCR results and extrinsic factors including carbon dioxide and some antibiotics were shown to suppress or induce the expression of virulence factors in this platform. Using this platform, sub-inhibitory ampicillin was shown to be a potent inducer for the expression of many virulence factors in S. aureus. Bacterial adherence and invasion assays using mammalian cells were employed to measure S. aureus virulence induced by ampicillin. The platform was used for screening of natural extracts that perturb the virulence of S. aureus and usnic acid was identified to be a potent repressor for the expression of psm.
Persistent Identifierhttp://hdl.handle.net/10722/245582

 

DC FieldValueLanguage
dc.contributor.authorGao, P-
dc.contributor.authorWang, Y-
dc.contributor.authorVillanueva, I-
dc.contributor.authorHo, PL-
dc.contributor.authorDavies, J-
dc.contributor.authorKao, RYT-
dc.date.accessioned2017-09-18T02:13:14Z-
dc.date.available2017-09-18T02:13:14Z-
dc.date.issued2016-
dc.identifier.citation2016 World Life Science Conference (WLSC2016), Beijing, China, 1-3 November 2016-
dc.identifier.urihttp://hdl.handle.net/10722/245582-
dc.description.abstractAs antibiotic resistance becomes phenomenal, alternative therapeutic strategies for bacterial infections such as anti-virulence treatments have been advocated. We have constructed a total of 20 gfp-luxABCDE dual-reporter plasmids with selected promoters from S. aureus virulence-associated genes. The plasmids were introduced into various S. aureus strains to establish a gfp-lux based multiplex promoter reporter platform for monitoring S. aureus virulence gene expressions in real time to identify factors or compounds that may perturb virulence of S. aureus. The gene expression profiles monitored by luminescence correlated well with qRT-PCR results and extrinsic factors including carbon dioxide and some antibiotics were shown to suppress or induce the expression of virulence factors in this platform. Using this platform, sub-inhibitory ampicillin was shown to be a potent inducer for the expression of many virulence factors in S. aureus. Bacterial adherence and invasion assays using mammalian cells were employed to measure S. aureus virulence induced by ampicillin. The platform was used for screening of natural extracts that perturb the virulence of S. aureus and usnic acid was identified to be a potent repressor for the expression of psm.-
dc.languageeng-
dc.relation.ispartofWorld Life Science Conference, WLSC2016-
dc.titleMultiplex Promoter Reporter Platform to Monitor Staphylococcus aureus Virulence Gene Expression-
dc.typeConference_Paper-
dc.identifier.emailGao, P: gaopeng@hku.hk-
dc.identifier.emailHo, PL: plho@hku.hk-
dc.identifier.emailKao, RYT: rytkao@hkucc.hku.hk-
dc.identifier.authorityHo, PL=rp00406-
dc.identifier.authorityKao, RYT=rp00481-
dc.identifier.hkuros278390-

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