scholarly journals Reverse transcription-PCR using a Primer Set Targeting the 3D Region Detects Foot-and-Mouth Disease Virus with High Sensitivity

2018 ◽  
Author(s):  
Tatsuya Nishi ◽  
Toru Kanno ◽  
Nobuaki Shimada ◽  
Kazuki Morioka ◽  
Makoto Yamakawa ◽  
...  

AbstractBecause foot-and-mouth disease (FMD) has the potential to spread extensively, methods used for its diagnosis must be rapid and accurate. Therefore, reverse transcription-PCR (RT-PCR) plays an important diagnostic role. Here we designed the primer set FM8/9 to amplify 644 bases of the conserved 3D region of all seven serotypes of FMD virus (FMDV). We compared the performance of RT-PCR assays using FM8/9 with that using the primer set 1F/R targeting the 5’-UTR described in the manual of the World Organization for Animal Health. The detection limits of the RT-PCR assays were determined for 14 strains representing all serotypes. Compared with the sensitivities of the RT-PCR assay using 1F/R, those using FM8/9 were 101-to 104-fold higher for eight strains. To assess the validity of the methods for analyzing clinical samples, sera and saliva samples from pigs and cows infected with FMDV were collected daily and analyzed using the two PCR assays. The FM8/9 assay detected FMDV from all infected pigs and cows for longer times compared with the 1F/R assay, therefore revealing higher sensitivity for the clinical samples. Our results suggest that the FM8/9 RT-PCR assay is highly sensitive and is therefore suitable for the diagnosis of FMD.

2000 ◽  
Vol 38 (12) ◽  
pp. 4604-4613 ◽  
Author(s):  
Soren Alexandersen ◽  
Morag A. Forsyth ◽  
Scott M. Reid ◽  
Graham J. Belsham

A reverse transcription-PCR (RT-PCR)–enzyme-linked immunosorbent assay system that detects a relatively conserved region within the RNA genome of all seven serotypes of foot-and-mouth disease virus (FMDV) has been developed. The high specificity of the assay is achieved by including a rapid hybridization step with a biotin-labeled internal oligonucleotide. The assay is highly sensitive, fast, and easy to perform. A similar assay, based on a highly variable region of the FMDV genome and employing a single asymmetric RT-PCR and multiple hybridization oligonucleotides, was developed to demonstrate the method's ability to type FMDV. Based on our theoretical and practical knowledge of the methodology, we predict that similar assays are applicable to diagnosis and strain differentiation in any system amenable to PCR amplification.


2015 ◽  
Vol 54 (1) ◽  
pp. 216-219 ◽  
Author(s):  
Ji-Hyeon Hwang ◽  
Yong-Keol Shin ◽  
So-Yeon Park ◽  
Jeesoo Kim ◽  
Su-Mi Kim ◽  
...  

During an outbreak of foot-and-mouth disease (FMD), real-time reverse transcription-PCR (rRT-PCR) is the most commonly used diagnostic method to detect viral RNA. However, while this assay is often conducted during the outbreak period, there is an inevitable risk of carryover contamination. This study shows that the carryover contamination can be prevented by the use of target-specific restriction endonuclease in that assay.


Virus Genes ◽  
2022 ◽  
Author(s):  
Jitendra K. Biswal ◽  
Biswa Ranjan Jena ◽  
Syed Zeeshan Ali ◽  
Rajeev Ranjan ◽  
Jajati K. Mohapatra ◽  
...  

2016 ◽  
Vol 237 ◽  
pp. 114-120 ◽  
Author(s):  
Katarzyna Bachanek-Bankowska ◽  
Herieth R. Mero ◽  
Jemma Wadsworth ◽  
Valerie Mioulet ◽  
Raphael Sallu ◽  
...  

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