TY - JOUR
T1 - Diagnostic techniques for rapid detection of Vibrio species
AU - Loo, Ke-Yan
AU - Law, Jodi Woan-Fei
AU - Tan, Loh Teng-Hern
AU - Pusparajah, Priyia
AU - Letchumanan, Vengadesh
AU - Lee, Learn-Han
N1 - Funding Information:
This work is supported by the Jeffrey Cheah School of Medicine and Health Sciences (JCSMHS) Strategic Grant 2021 (Grant Code: STG-000051), and SEED Funding from Jeffrey Cheah School of Medicine and Health Sciences (JCSMHS) 2020.The authors would like to acknowledge Prof. Dr. Shajahan Yasin from Jeffrey Cheah School of Medicine and Health Sciences, Monash University Malaysia.
Funding Information:
This work is supported by the Jeffrey Cheah School of Medicine and Health Sciences (JCSMHS) Strategic Grant 2021 (Grant Code: STG-000051 ), and SEED Funding from Jeffrey Cheah School of Medicine and Health Sciences (JCSMHS) 2020.
Publisher Copyright:
© 2022 The Authors
PY - 2022/12/15
Y1 - 2022/12/15
N2 - Background: Vibrio sp. has caused several foodborne outbreaks of gastroenteritis around the world. Given the mounting evidence that Vibrio sp. poses a significant public health threat, and that initiating effective treatment for Vibrio infection requires rapid identification of the causative organism, there is a need for reliable, cost-effective point of care diagnostic testing. Conventional detection techniques that are the current gold standard in detecting Vibrio sp., are typically resource-intensive, laborious, and time-consuming. These limitations greatly hinder their efficiency in under-developed countries, which are usually the regions most affected by Vibrio infections. Thus, the development of rapid, reliable point of care detection methods is crucial to overcome the limitations of conventional methods. Aim of the review: This review aims to summarize and give insights into the array of diagnostic techniques for rapid detection of Vibrio sp. Key scientific concepts of review: This review focuses on different rapid methods to detect Vibrio sp., including polymerase chain reactions, loop-mediated isothermal amplification, enzyme-linked immunosorbent assays, microarrays, lateral flow immunoassays, aptasensors, spot dye-based sensors and CRISPR/Cas-PCR systems. The rapid detection methods were found to have high specificity and sensitivity in detecting various species within the genus Vibrio. However, each detection method has its own advantages and limitations, thus continuous effort is needed to improve on what is currently available and develop techniques with high sensitivity, specificity, affordability with minimal effort to obtain consistent and accurate diagnoses.
AB - Background: Vibrio sp. has caused several foodborne outbreaks of gastroenteritis around the world. Given the mounting evidence that Vibrio sp. poses a significant public health threat, and that initiating effective treatment for Vibrio infection requires rapid identification of the causative organism, there is a need for reliable, cost-effective point of care diagnostic testing. Conventional detection techniques that are the current gold standard in detecting Vibrio sp., are typically resource-intensive, laborious, and time-consuming. These limitations greatly hinder their efficiency in under-developed countries, which are usually the regions most affected by Vibrio infections. Thus, the development of rapid, reliable point of care detection methods is crucial to overcome the limitations of conventional methods. Aim of the review: This review aims to summarize and give insights into the array of diagnostic techniques for rapid detection of Vibrio sp. Key scientific concepts of review: This review focuses on different rapid methods to detect Vibrio sp., including polymerase chain reactions, loop-mediated isothermal amplification, enzyme-linked immunosorbent assays, microarrays, lateral flow immunoassays, aptasensors, spot dye-based sensors and CRISPR/Cas-PCR systems. The rapid detection methods were found to have high specificity and sensitivity in detecting various species within the genus Vibrio. However, each detection method has its own advantages and limitations, thus continuous effort is needed to improve on what is currently available and develop techniques with high sensitivity, specificity, affordability with minimal effort to obtain consistent and accurate diagnoses.
KW - Aptasensors
KW - CRISPR/Cas-PCR systems
KW - Enzyme-linked immunosorbent assays
KW - Lateral flow immunoassays
KW - Loop-mediated isothermal amplification
KW - Polymerase chain reactions
UR - https://www.scopus.com/pages/publications/85135421201
U2 - 10.1016/j.aquaculture.2022.738628
DO - 10.1016/j.aquaculture.2022.738628
M3 - Review Article
AN - SCOPUS:85135421201
SN - 0044-8486
VL - 561
JO - Aquaculture
JF - Aquaculture
M1 - 738628
ER -