Superbug origins: high throughput culture, isolation and sequencing of environmental Acinetobacters

Acinetobacter baumannii (A. baumannii) is an opportunistic nosocomial pathogen [1] responsible for a larger number of deaths globally due to the rise of antibiotic resistance genes. Current methods of bacterial isolation, classification and characterisation are too slow and at times expensive, requi...

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Main Author: Tan, Ching Hai
Other Authors: Duan Hongwei
Format: Final Year Project
Language:English
Published: Nanyang Technological University 2023
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Online Access:https://hdl.handle.net/10356/166748
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Institution: Nanyang Technological University
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spelling sg-ntu-dr.10356-1667482023-07-06T08:42:33Z Superbug origins: high throughput culture, isolation and sequencing of environmental Acinetobacters Tan, Ching Hai Duan Hongwei Yap Peng Huat Eric School of Chemistry, Chemical Engineering and Biotechnology ericyap@ntu.edu.sg, hduan@ntu.edu.sg Engineering::Bioengineering Acinetobacter baumannii (A. baumannii) is an opportunistic nosocomial pathogen [1] responsible for a larger number of deaths globally due to the rise of antibiotic resistance genes. Current methods of bacterial isolation, classification and characterisation are too slow and at times expensive, requiring either large amounts of manpower or expensive machines and algorithms to carry out these processes, making them inaccessible in addition to generating large amounts of plastic waste. To address these issues, new methods and processes were formulated utilising an open-source liquid handler (Opentrons-2), custom grids designed and printed using reusable and sterilisable materials, serial dilution techniques, a custom-written protocol and a custom-developed image processing and segmentation program to maximise the number of environmental samples which could be processed simultaneously. To make the process more user-friendly, a user-interface was developed so they would not have to adjust the source code. Results showed that automating the bacterial culturing process on the OT-2 resulted in higher throughput than the traditional method of streaking as the increased time taken for liquid handler to plate the bacteria could be offset by the user’s ability to run multiple of such machines simultaneously. However, the image processing and segmentation program was unable to quantify the number of colonies in each well due to technical limitations which could be further corrected in future experiments. Given the relative success of these methods and processes, they could be adapted for other microbiological experiments such as antibiotic resistance testing or even other fields of biology such as cell-culturing. Bachelor of Engineering (Bioengineering) 2023-05-18T04:31:48Z 2023-05-18T04:31:48Z 2023 Final Year Project (FYP) Tan, C. H. (2023). Superbug origins: high throughput culture, isolation and sequencing of environmental Acinetobacters. Final Year Project (FYP), Nanyang Technological University, Singapore. https://hdl.handle.net/10356/166748 https://hdl.handle.net/10356/166748 en application/pdf Nanyang Technological University
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Engineering::Bioengineering
spellingShingle Engineering::Bioengineering
Tan, Ching Hai
Superbug origins: high throughput culture, isolation and sequencing of environmental Acinetobacters
description Acinetobacter baumannii (A. baumannii) is an opportunistic nosocomial pathogen [1] responsible for a larger number of deaths globally due to the rise of antibiotic resistance genes. Current methods of bacterial isolation, classification and characterisation are too slow and at times expensive, requiring either large amounts of manpower or expensive machines and algorithms to carry out these processes, making them inaccessible in addition to generating large amounts of plastic waste. To address these issues, new methods and processes were formulated utilising an open-source liquid handler (Opentrons-2), custom grids designed and printed using reusable and sterilisable materials, serial dilution techniques, a custom-written protocol and a custom-developed image processing and segmentation program to maximise the number of environmental samples which could be processed simultaneously. To make the process more user-friendly, a user-interface was developed so they would not have to adjust the source code. Results showed that automating the bacterial culturing process on the OT-2 resulted in higher throughput than the traditional method of streaking as the increased time taken for liquid handler to plate the bacteria could be offset by the user’s ability to run multiple of such machines simultaneously. However, the image processing and segmentation program was unable to quantify the number of colonies in each well due to technical limitations which could be further corrected in future experiments. Given the relative success of these methods and processes, they could be adapted for other microbiological experiments such as antibiotic resistance testing or even other fields of biology such as cell-culturing.
author2 Duan Hongwei
author_facet Duan Hongwei
Tan, Ching Hai
format Final Year Project
author Tan, Ching Hai
author_sort Tan, Ching Hai
title Superbug origins: high throughput culture, isolation and sequencing of environmental Acinetobacters
title_short Superbug origins: high throughput culture, isolation and sequencing of environmental Acinetobacters
title_full Superbug origins: high throughput culture, isolation and sequencing of environmental Acinetobacters
title_fullStr Superbug origins: high throughput culture, isolation and sequencing of environmental Acinetobacters
title_full_unstemmed Superbug origins: high throughput culture, isolation and sequencing of environmental Acinetobacters
title_sort superbug origins: high throughput culture, isolation and sequencing of environmental acinetobacters
publisher Nanyang Technological University
publishDate 2023
url https://hdl.handle.net/10356/166748
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