Antibiofilm efficacy of green synthesized graphene oxide-silver nanocomposite using Lagerstroemia speciosa floral extract: A comparative study on inhibition of gram-positive and gram-negative biofilms

被引:66
|
作者
Kulshrestha, Shatavari [1 ]
Qayyurn, Shariq [1 ]
Khan, Asad U. [1 ]
机构
[1] Aligarh Muslim Univ, Interdisciplinary Biotechnol Unit, Aligarh 202002, Uttar Pradesh, India
关键词
Biofilm; Legistromia speciosa L; Graphene oxide-silver nanocomposite; Streptococcus mutans; Enterobacter cloacae; Quantitative RT-PCR; STREPTOCOCCUS-MUTANS BIOFILM; ANTIMICROBIAL ACTIVITY; BACTERIAL BIOFILMS; NANOPARTICLES; ANTIBACTERIAL; INFECTIONS; GOLD; BIOSYNTHESIS; SENSITIVITY; COMPOSITES;
D O I
10.1016/j.micpath.2016.12.022
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Biofilm architecture provides bacteria with enhanced antibiotic resistance, thus raising the need to search for alternative therapies that can inhibit the bacterial colonization. In the present study, we synthesized graphene oxide-silver nanocomposite (GO-Ag) by non-toxic and eco-friendly route using a floral extract of Legistromia speciosa (L) Pers. The gas chromatography-mass spectrometry (GC-MS) analysis of plant extract revealed the presence of compounds which can simultaneously act as reducing and capping agents. The sub-inhibitory concentrations of synthesized GO-Ag reduced the biofilm formation in both gram-negative (E. cloacae) and gram-positive (S. mutans) bacterial models. Growth curve assay, membrane integrity assay, scanning electron microscopy (SEM) and confocal scanning laser microscopy (CSLM) revealed different mechanisms of biofilm inhibition in E. cloacae and S. mutans. Moreover, quantitative RT-PCR (qRT-PCR) results suggested GO-Ag is acting on S. mutans biofilm formation cascade. Biofilm inhibitory concentrations GO-Ag were also found to be non-toxic against HEK-293 (human embryonic kidney cell line). The whole study highlights the therapeutic potential of GO-Ag to restrain the onset of biofilm formation in bacteria. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:167 / 177
页数:11
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