Identification of Potential Anti-Infectives against Staphylococcus aureus Using a Caenorhabditis elegans Infection Model

被引:1
|
作者
Kong, Cin [1 ]
Abd Rahman, Noorsaadah [2 ]
Nathan, Sheila [1 ]
机构
[1] Univ Kebangsaan Malaysia, Fac Sci & Technol, Sch Biosci & Biotechnol, Ukm Bangi 43600, Selangor, Malaysia
[2] Univ Malaya, Fac Sci, Dept Chem, Kuala Lumpur 50603, Malaysia
来源
2014 UKM FST POSTGRADUATE COLLOQUIUM: PROCEEDINGS OF THE UNIVERSITI KEBANGSAAN MALAYSIA, FACULTY OF SCIENCE AND TECHNOLOGY 2014 POSTGRADUATE COLLOQUIUM | 2014年 / 1614卷
关键词
Anti-infectives; Staphylococcus aureus; Caenorhabditis elegans; HOST;
D O I
10.1063/1.4895251
中图分类号
O59 [应用物理学];
学科分类号
摘要
The alarming increase of antibiotic-resistant Staphylococcus aureus and a delay in antibiotics development point to the need for novel therapeutic approaches to combat infection. To discover novel anti-infective agents, we screened a number of synthetic compounds comprising mainly of chalcone derivatives to explore their potential in promoting the survival of the nematode Caenorhabditis elegans upon infection by S. aureus. Screening of seven chalcone derivatives using both agar-and liquid-based assays revealed three positive hits that significantly prolonged the survival of S. aureus-infected nematodes. All the hits did not interfere with bacterial growth in vitro, proposing that the three compounds identified most probably act through mechanisms distinct from conventional antibiotics that target bacterial replication.
引用
收藏
页码:513 / 516
页数:4
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