scholarly journals Evaluation of a Field-Deployable Insulated Isothermal Polymerase Chain Reaction Nucleic Acid Analyzer for Influenza A Virus Detection at Swine Exhibitions

2019 ◽  
Vol 19 (3) ◽  
pp. 212-216
Author(s):  
Sarah E. Lauterbach ◽  
Sarah N. Nelson ◽  
Jacqueline M. Nolting ◽  
Jessie D. Trujillo ◽  
Jürgen A. Richt ◽  
...  
Genome ◽  
1999 ◽  
Vol 42 (4) ◽  
pp. 592-604 ◽  
Author(s):  
Rudra P Singh

Potato is the fourth most important food crop in the world and it forms the diet of a billion consumers in developing countries, where potato production is increasing rapidly. However, potato virus diseases in developing countries are one of the major causes of lower yields. Their control requires the development of appropriate virus-detection and seed-production technologies for the region. Recent progress in developing nucleic acid based virus detection methods are reviewed. Refinements of the protocols applicable to the laboratories located in seed producing areas are discussed. Nucleic acid spot hybridization (NASH) and reverse transcription polymerase chain reaction (RT-PCR) methods are described for the detection of viruses and viroids in dormant seed tubers and insect vectors. Although the potato crop is susceptible to over 25 virus and viroid diseases, only universally economically important viruses have been dealt with here. The progress of pathogen-derived resistance for the control of potato virus diseases is elaborated, and the results of field tests indicate their feasibility in virus control.Key words: dot-blot, spot-hybridization, reverse transcription, polymerase chain reaction, transgenic plants.


2004 ◽  
Vol 17 (4) ◽  
pp. 588-593 ◽  
Author(s):  
Sunchai Payungporn ◽  
Piraya Phakdeewirot ◽  
Salin Chutinimitkul ◽  
Apiradee Theamboonlers ◽  
Juthatip Keawcharoen ◽  
...  

Author(s):  
Abdulazeez A. Anjorin ◽  
Olumuyiwa B. Salu ◽  
Robert K. Obi ◽  
Bamidele O. Oke ◽  
Akeeb O. Oyefolu ◽  
...  

Introduction: Early detection of emerging influenza virus variant is a key factor in the WHO influenza Global strategies for prevention and control. Rapid, accurate, inexpensive and portable detection systems are needed for influenza virus diagnosis and surveillance. Such a detection system should easily identify all the subtypes of influenza virus. Degenerate primers and probes designed from evolutionally conserved regions for known influenza A viruses present the best way to identify unknown subtypes of influenza A virus by polymerase chain reaction PCR and array techniques. The isothermal reactions, Nucleic Acid Sequencing Based Amplification (NASBA) and Loop-mediated isothermal Amplification (LAMP) possess great potential for influenza A virus detection especially in developing countries. However, multiplex real-time (rT) or quantitative (q) polymerase chain reaction (qPCR) remains a rapid, accurate and timesaving technique used for influenza virus detection. Aim: This manuscript explained the principles of nucleic acid amplification techniques commonly used in developing countries. Methods: Literature search was done in NCBI PUBMED, PUBMED Central and Google Scholar using words and phrases including “Influenzamolecular diagnosis, NAAT”, Molecular techniques/ methods, PCR, qPCR, NASBA, LAMP, and DNA microarray. Results: The underlining principles and basic processes involved in the application of nucleic acid amplification techniques for the detection and epidemiological surveillance of influenza virus were identified and grouped under PCR (RT-PCR and qRT-PCR) and Non-PCR (LCR, pyrosequencing, NASBA, LAMP and DNA microarray) amplifications. Conclusion: It is hoped that by understanding the techniques and basic principles of Nucleic acid amplifications, less expensive, and more convenient protocols for influenza virus detection and surveillance can be developed Keywords: Influenza, NAAT, Molecular, PCR, qPCR, Viral diagnosis.


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