Literature DB >> 26190467

A Rapid Field-Deployable Reverse Transcription-Insulated Isothermal Polymerase Chain Reaction Assay for Sensitive and Specific Detection of Bluetongue Virus.

A Ambagala1, S Pahari1, M Fisher1, P-Y A Lee2, J Pasick3, E N Ostlund4, D J Johnson4, O Lung1.   

Abstract

Bluetongue is a non-contagious, haemorrhagic, Culicoides-borne disease of ruminants. The causative agent, bluetongue virus (BTV), is a member of the Orbivirus genus of the Reoviridae family. So far, 26 BTV serotypes have been identified worldwide. The global distribution of bluetongue has been expanding, and rapid detection of BTV, preferably in the field, is critical for timely implementation of animal movement restrictions and vector control measures. To date, many laboratory-based, molecular assays for detection of BTV have been developed. These methods require the samples to be shipped to a central laboratory with sophisticated instruments and highly skilled technicians to perform the assays, conduct analyses and interpret the results. Here, we report the development and evaluation of a rapid, portable, user-friendly, pan-BTV reverse transcription-insulated isothermal polymerase chain reaction (RT-iiPCR) assay that can potentially be used in low-resource field conditions. The total length of the assay was <60 min, and at the end of the assay, the results were automatically displayed as '+' or '-' without the need for data interpretation. The RT-iiPCR assay detected 36 BTV isolates and two in vitro transcribed RNA samples representing all 26 BTV serotypes. The assay did not cross-react with other animal viruses tested, including two closely related orbiviruses. The analytical sensitivity of the assay was as low as nine copies of in vitro transcribed double-stranded BTV RNA. Analysis of BTV-infected whole blood samples showed that the BTV RT-iiPCR assay was as sensitive as real-time RT-PCR. The assay can potentially be used for rapid screening of animals for BTV in routine diagnostics and for monitoring bluetongue outbreaks both in ruminants and in Culicoides vectors in the field and in the laboratory. © Her Majesty the Queen in Right of Canada (2015). Reproduced with the permission of the Minister of Health of Canadian Food Inspection Agency.

Entities:  

Keywords:  bluetongue virus; detection; field-deployable; portable; reverse transcription-insulated isothermal polymerase chain reaction

Mesh:

Substances:

Year:  2015        PMID: 26190467     DOI: 10.1111/tbed.12388

Source DB:  PubMed          Journal:  Transbound Emerg Dis        ISSN: 1865-1674            Impact factor:   5.005


  13 in total

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2.  Potential Point-of-Care Testing for Dengue Virus in the Field.

Authors:  Wei-Kung Wang; Duane J Gubler
Journal:  J Clin Microbiol       Date:  2018-04-25       Impact factor: 5.948

3.  Validation of the Pockit Dengue Virus Reagent Set for Rapid Detection of Dengue Virus in Human Serum on a Field-Deployable PCR System.

Authors:  Jih-Jin Tsai; Li-Teh Liu; Ping-Chang Lin; Ching-Yi Tsai; Pin-Hsing Chou; Yun-Long Tsai; Hsiao-Fen Grace Chang; Pei-Yu Alison Lee
Journal:  J Clin Microbiol       Date:  2018-04-25       Impact factor: 5.948

4.  A Pan-Dengue Virus Reverse Transcription-Insulated Isothermal PCR Assay Intended for Point-of-Need Diagnosis of Dengue Virus Infection by Use of the POCKIT Nucleic Acid Analyzer.

Authors:  Yun Young Go; R P V Jayanthe Rajapakse; Senanayake A M Kularatne; Pei-Yu Alison Lee; Keun Bon Ku; Sangwoo Nam; Pin-Hsing Chou; Yun-Long Tsai; Yu-Lun Liu; Hsiao-Fen Grace Chang; Hwa-Tang Thomas Wang; Udeni B R Balasuriya
Journal:  J Clin Microbiol       Date:  2016-03-30       Impact factor: 5.948

5.  Rapid and sensitive insulated isothermal PCR for point-of-need feline leukaemia virus detection.

Authors:  Rebecca P Wilkes; Eman Anis; Dawn Dunbar; Pei-Yu A Lee; Yun-Long Tsai; Fu-Chun Lee; Hsiao-Fen G Chang; Hwa-Tang T Wang; Elizabeth M Graham
Journal:  J Feline Med Surg       Date:  2017-06-07       Impact factor: 2.015

6.  Evaluation of a field-deployable reverse transcription-insulated isothermal PCR for rapid and sensitive on-site detection of Zika virus.

Authors:  Mariano Carossino; Yanqiu Li; Pei-Yu A Lee; Chuan-Fu Tsai; Pin-Hsing Chou; Dennis Williams; Ashley Skillman; R Frank Cook; Grayson Brown; Hsiao-Fen G Chang; Hwa-Tang T Wang; Udeni B R Balasuriya
Journal:  BMC Infect Dis       Date:  2017-12-19       Impact factor: 3.090

7.  Evaluation and Clinical Validation of Two Field-Deployable Reverse Transcription-Insulated Isothermal PCR Assays for the Detection of the Middle East Respiratory Syndrome-Coronavirus.

Authors:  Yun Young Go; Yeon-Sook Kim; Shinhye Cheon; Sangwoo Nam; Keun Bon Ku; Meehyein Kim; Nam Hyuk Cho; Hyun Park; Pei-Yu Alison Lee; Yu-Chun Lin; Yun-Long Tsai; Hwa-Tang Thomas Wang; Udeni B R Balasuriya
Journal:  J Mol Diagn       Date:  2017-08-12       Impact factor: 5.568

8.  A field-deployable insulated isothermal RT-PCR assay for identification of influenza A (H7N9) shows good performance in the laboratory.

Authors:  Ken Inui; Tung Nguyen; Hsin-Jou Tseng; ChuanFu Mark Tsai; Yun-Long Tsai; Simon Chung; Pawin Padungtod; Huachen Zhu; Yi Guan; Wantanee Kalpravidh; Filip Claes
Journal:  Influenza Other Respir Viruses       Date:  2019-09-05       Impact factor: 4.380

9.  Rapid and sensitive detection of Mycoplasma synoviae by an insulated isothermal polymerase chain reaction-based assay on a field-deployable device.

Authors:  Hung-Chih Kuo; Dan-Yuan Lo; Chiou-Lin Chen; Yun-Long Tsai; Jia-Fong Ping; Chien-Hsien Lee; Pei-Yu Alison Lee; Hsiao-Fen Grace Chang
Journal:  Poult Sci       Date:  2016-07-07       Impact factor: 3.352

10.  Rapid Diagnosis of Babesia gibsoni by Point-of-Need Testing by Insulated Isothermal PCR in Dogs at High Risk of Infection.

Authors:  K L Cooke; P Frenzer; S J Tucker; P C Crawford; S K Kirk; J K Levy
Journal:  J Vet Intern Med       Date:  2018-01       Impact factor: 3.333

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