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Real-time monitoring of mono- and dual-species biofilm formation and eradication using microfluidic platform.
Tran, Van Nam; Khan, Fazlurrahman; Han, Won; Luluil, Maknuna; Truong, Van Gia; Yun, Hyo Geun; Choi, Sungyoung; Kim, Young-Mog; Shin, Joong Ho; Kang, Hyun Wook.
Afiliação
  • Tran VN; Industry 4.0 Convergence Bionics Engineering and Marine-Integrated Biomedical Technology Center, Pukyong National University, Busan, 48513, South Korea.
  • Khan F; Research Center for Marine Integrated Bionics Technology, Pukyong National University, Busan, 48513, South Korea.
  • Han W; Department of Biomedical Engineering, Pukyong National University, Busan, 48513, South Korea.
  • Luluil M; Industry 4.0 Convergence Bionics Engineering and Marine-Integrated Biomedical Technology Center, Pukyong National University, Busan, 48513, South Korea.
  • Truong VG; Industry 4.0 Convergence Bionics Engineering and Marine-Integrated Biomedical Technology Center, Pukyong National University, Busan, 48513, South Korea.
  • Yun HG; Department of Electronic Engineering, Hanyang University, Seoul, 04763, South Korea.
  • Choi S; Department of Electronic Engineering, Hanyang University, Seoul, 04763, South Korea.
  • Kim YM; Department of Biomedical Engineering, Hanyang University, Seoul, 04763, South Korea.
  • Shin JH; Research Center for Marine Integrated Bionics Technology, Pukyong National University, Busan, 48513, South Korea.
  • Kang HW; Department of Food Science and Technology, Pukyong National University, Busan, 48513, South Korea.
Sci Rep ; 12(1): 9678, 2022 06 11.
Article em En | MEDLINE | ID: mdl-35690659
ABSTRACT
In a human host, bacterial Staphylococcus aureus and fungal Candida albicans pathogens form a mixed biofilm that causes severe mortality and morbidity. However, research on the formation and eradication of mixed biofilms under dynamic conditions is lacking. Thus, this study employed a microfluidic technique to analyze the real-time formation of mono- and dual-species (S. aureus and C. albicans) biofilms and noninvasive optical treatment of the established mature biofilm using 405-nm laser light. A herringbone mixer thoroughly mixed both bacterial and fungal cells in the growth media before being injected into the observation channels on the microfluidic chip. At a flow rate of 1.0 µL/min of growth media for 24 h, the bacterial biofilm coverage was up to 15% higher than that of the fungal biofilm (50% for bacteria vs. 35% for fungus). On the other hand, the dual-species biofilm yielded the highest coverage of ~ 96.5% because of the collective interaction between S. aureus and C. albicans. The number of cell proliferation events in S. aureus was higher than that of C. albicans for 12 h, which indicates that the S. aureus biofilm was developed faster than C. albicans. The novel in situ test platform showed a significant bactericidal effect (80%) of the 405-nm laser light at 1080 J/cm2 towards the established S. aureus biofilm, whereas the same treatment removed approximately 69% of the mixed cells in the dual-species biofilm. This study revealed that the developed microfluidic platform could be utilized to monitor the formation of dual-species biofilms in real-time and laser-induced antimicrobial effects on dual-species biofilms.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Staphylococcus aureus / Microfluídica Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Staphylococcus aureus / Microfluídica Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article