Development of a Mass-Producible Microfluidic Device for Single and Bulk Mycobacteria Investigations
Adrian J. T. Teo,
Jianhui Gu,
Alexander Govyadinov,
Pavel Kornilovitch,
Peiyun Wang,
Serene Goh,
Nguyen Truong Tung,
Zhen Peng,
Keith Koh,
King Ho Holden Li
Affiliations
Adrian J. T. Teo
School of Mechanical and Aerospace Engineering, Nanyang Technological University, Singapore 639798, Singapore
Jianhui Gu
HP Singapore Pte Ltd., 1A Depot Close, Singapore 109842, Singapore
Alexander Govyadinov
HP Pte Ltd., Corvallis, OR 97330, USA
Pavel Kornilovitch
HP Pte Ltd., Corvallis, OR 97330, USA
Peiyun Wang
HP Singapore Pte Ltd., 1A Depot Close, Singapore 109842, Singapore
Serene Goh
HP Singapore Pte Ltd., 1A Depot Close, Singapore 109842, Singapore
Nguyen Truong Tung
School of Chemistry, Chemical Engineering and Biotechnology, Nanyang Technological University, Singapore 639798, Singapore
Zhen Peng
School of Mechanical Engineering, State Key Laboratory of Intelligent Construction and Healthy Operation and Maintenance of Deep Underground Engineering, Sichuan University, Chengdu 610065, China
Keith Koh
School of Mechanical and Aerospace Engineering, Nanyang Technological University, Singapore 639798, Singapore
King Ho Holden Li
School of Mechanical and Aerospace Engineering, Nanyang Technological University, Singapore 639798, Singapore
We developed a mass-producible microfluidic device capable of long-term observations of single bacilli and bulk bacteria culture interactions for subsequent antimicrobial resistance (AMR) studies. The device provides high consistency across separate devices due to its standardized manufacturing process unlike conventional microfluidic devices. Mycobacteria bovis BCG and M. smegmatis are trapped within the microfluidic device using minimal equipment and capillary-based techniques, acting as a surrogate model for the highly pathogenic bacteria M. tuberculosis. Individual bacilli and bulk bacteria aggregates were observed across a span of ten growth cycles, revealing bacteria growth morphologies alike those in past research. We accordingly propose that this chip would be appropriate for observations of AMR trials involving M. tuberculosis.