Biosynthesis of silver nanoparticle using Bacillus licheniformis culture-supernatant for combating pathogenic biofilms

被引:2
|
作者
Karley, Dugeshwar [1 ]
Shukla, Sudhir K. [2 ,3 ]
Rao, T. Subba [4 ]
机构
[1] Amity Univ Chhattisgarh, Amity Inst Biotechnol, Raipur 493225, India
[2] Bhabha Atom Res Ctr Facil, Water & Steam Chem Div, Biofouling & Biofilm Proc Sect, Kalpakkam 603102, India
[3] Homi Bhabha Natl Inst, Mumbai 400094, India
[4] Sai Univ, Sch Arts & Sci, Biol Sci, Chennai 603104, India
关键词
Biofilm control; Pseudomonas aeruginosa; Staphylococcus aureus; Bacillus licheniformis; Green synthesis; Biogenic silver nanoparticles; STAPHYLOCOCCUS-AUREUS BIOFILM; ANTIBIOFILM ACTIVITY; DAHB1;
D O I
10.1016/j.micpath.2024.106833
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Bacterial biofilms pose a significant threat to healthcare due to their recalcitrance to antibiotics and disinfectants. This study explores the anti-biofilm potential of Bacillus licheniformis cell-free culture supernatant (CFS) and its derived silver nanoparticles (bSNPs) against Staphylococcus aureus and Pseudomonas aeruginosa. . The CFS exhibited potent anti-biofilm activity against both bacterial species, even at low concentrations, while devoid of significant bactericidal effects, mitigating resistance risks. Characterization studies revealed the nonproteinaceous nature and thermal stability of the CFS's anti-biofilm agent, suggesting a robust and heat- resistant structure. Green synthesis of bSNPs from CFS resulted in nanoparticles with significant anti-biofilm properties, particularly against P. aeruginosa, , indicating differences in susceptibility between the bacterial species. Epifluorescence microscopy confirmed bSNPs' ability to inhibit and partially disrupt biofilm formation without inducing cellular lysis. The study highlights the potential of B. licheniformis CFS and bSNPs as promising biofilm control agents, offering insights into their mechanisms of action and broad-spectrum efficacy. Further research elucidating the underlying molecular mechanisms and identifying specific bioactive compounds is warranted for the translation of these findings into clinically relevant applications for combating biofilmassociated infections.
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页数:9
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