Literature DB >> 24361981

Methods in virus diagnostics: from ELISA to next generation sequencing.

Neil Boonham1, Jan Kreuze2, Stephan Winter3, René van der Vlugt4, Jan Bergervoet4, Jenny Tomlinson1, Rick Mumford5.   

Abstract

Despite the seemingly continuous development of newer and ever more elaborate methods for detecting and identifying viruses, very few of these new methods get adopted for routine use in testing laboratories, often despite the many and varied claimed advantages they possess. To understand why the rate of uptake of new technologies is so low, requires a strong understanding of what makes a good routine diagnostic tool to begin. This can be done by looking at the two most successfully established plant virus detection methods: enzyme-linked immunosorbant assay (ELISA) and more recently introduced real-time polymerase chain reaction (PCR). By examining the characteristics of this pair of technologies, it becomes clear that they share many benefits, such as an industry standard format and high levels of repeatability and reproducibility. These combine to make methods that are accessible to testing labs, which are easy to establish and robust in their use, even with new and inexperienced users. Hence, to ensure the establishment of new techniques it is necessary to not only provide benefits not found with ELISA or real-time PCR, but also to provide a platform that is easy to establish and use. In plant virus diagnostics, recent developments can be clustered into three core areas: (1) techniques that can be performed in the field or resource poor locations (e.g., loop-mediated isothermal amplification LAMP); (2) multiplex methods that are able to detect many viruses in a single test (e.g., Luminex bead arrays); and (3) methods suited to virus discovery (e.g., next generation sequencing, NGS). Field based methods are not new, with Lateral Flow Devices (LFDs) for the detection being available for a number of years now. However, the widespread uptake of this technology remains poor. LAMP does offer significant advantages over LFDs, in terms of sensitivity and generic application, but still faces challenges in terms of establishment. It is likely that the main barrier to the uptake of field-based technologies is behavioural influences, rather than specific concerns about the performance of the technologies themselves. To overcome this, a new relationship will need to develop between centralised testing laboratories offering services and those requiring tests; a relationship which is currently in its infancy. Looking further into the future, virus discovery and multiplex methods seem to converge as NGS becomes ever cheaper, easier to perform and can provide high levels of multiplexing without the use of virus specific reagents. So ultimately the key challenge from a routine testing lab perspective will not be one of investment in platforms-which could even be outsourced to commercial sequencing services-but one of having the skills and expertise to analyse the large datasets generated and their subsequent interpretation. In conclusion, only time will tell which of the next-generation of methods currently in development will become the routine diagnostics of the future. This will be determined through a combination of factors. And while the technology itself will have to offer performance advantages over existing methods in order to supplant them, it is likely to be human factors e.g., the behaviours of end users, laboratories and policy makers, the availability of appropriate expertise, that ultimately determine which ones become established. Hence factors cannot be ignored and early engagement with diagnostic stakeholders is essential. Crown
Copyright © 2013. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Field testing; LAMP assays; Molecular diagnostics; Multiplex, Luminex; Next generation sequencing; Real-time PCR

Mesh:

Year:  2013        PMID: 24361981     DOI: 10.1016/j.virusres.2013.12.007

Source DB:  PubMed          Journal:  Virus Res        ISSN: 0168-1702            Impact factor:   3.303


  79 in total

Review 1.  Next-generation sequencing in clinical virology: Discovery of new viruses.

Authors:  Sibnarayan Datta; Raghvendra Budhauliya; Bidisha Das; Soumya Chatterjee; Vijay Veer
Journal:  World J Virol       Date:  2015-08-12

2.  Identification of HIV Mutation as Diagnostic Biomarker through Next Generation Sequencing.

Authors:  Wen Hui Shaw; Qianqian Lin; Zikry Zhiwei Bin Roslee Muhammad; Jia Jun Lee; Wei Xin Khong; Oon Tek Ng; Eng Lee Tan; Peng Li
Journal:  J Clin Diagn Res       Date:  2016-07-01

3.  Enhancement of PCR Detection Limit by Single-Tube Restriction Endonuclease-PCR (RE-PCR).

Authors:  Sibnarayan Datta; Raghvendra Budhauliya; Soumya Chatterjee; Vijay Veer; Runu Chakravarty
Journal:  Mol Diagn Ther       Date:  2016-06       Impact factor: 4.074

4.  Rapid and Sensitive Detection of Lymphocystis Disease Virus Genotype VII by Loop-Mediated Isothermal Amplification.

Authors:  Estefanía J Valverde; Irene Cano; Dolores Castro; Richard K Paley; Juan J Borrego
Journal:  Food Environ Virol       Date:  2016-10-05       Impact factor: 2.778

5.  Post-COVID-19 Action: Guarding Africa's Crops against Viral Epidemics Requires Research Capacity Building That Unifies a Trio of Transdisciplinary Interventions.

Authors:  Francis O Wamonje
Journal:  Viruses       Date:  2020-11-09       Impact factor: 5.048

Review 6.  Virological and Immunological Outcomes of Coinfections.

Authors:  Naveen Kumar; Shalini Sharma; Sanjay Barua; Bhupendra N Tripathi; Barry T Rouse
Journal:  Clin Microbiol Rev       Date:  2018-07-05       Impact factor: 26.132

7.  On-Site Molecular Detection of Soil-Borne Phytopathogens Using a Portable Real-Time PCR System.

Authors:  Joseph B DeShields; Rachel A Bomberger; James W Woodhall; David L Wheeler; Natalia Moroz; Dennis A Johnson; Kiwamu Tanaka
Journal:  J Vis Exp       Date:  2018-02-23       Impact factor: 1.355

8.  Multiplexed Isothermal Amplification Based Diagnostic Platform to Detect Zika, Chikungunya, and Dengue 1.

Authors:  Ozlem Yaren; Barry W Alto; Kevin M Bradley; Patricia Moussatche; Lyudmyla Glushakova; Steven A Benner
Journal:  J Vis Exp       Date:  2018-03-13       Impact factor: 1.355

9.  Pigeonpea sterility mosaic virus: a legume-infecting Emaravirus from South Asia.

Authors:  Basavaprabhu L Patil; P Lava Kumar
Journal:  Mol Plant Pathol       Date:  2015-04-23       Impact factor: 5.663

10.  Development of an RT-PCR assay to detect genetically divergent wheat streak mosaic virus isolates for plant quarantine inspections in South Korea.

Authors:  Junghwa Lee; Keumhee Lee; Jaeyong Chun; Seungmo Lim
Journal:  Virusdisease       Date:  2021-03-17
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.