scholarly journals Comparison of a Multiplex Real-Time PCR Assay with a Multiplex Luminex Assay for Influenza Virus Detection

2013 ◽  
Vol 51 (4) ◽  
pp. 1124-1129 ◽  
Author(s):  
S. B. Munro ◽  
J. Kuypers ◽  
K. R. Jerome
2020 ◽  
Vol 16 (1) ◽  
Author(s):  
Xiyu Zhang ◽  
Ming Yao ◽  
Zhihui Tang ◽  
Daning Xu ◽  
Yan Luo ◽  
...  

Abstract Background Pathogens including duck-origin avian influenza virus (AIV), duck-origin Newcastle disease virus (NDV) and duck Tembusu virus (DTMUV) posed great harm to ducks and caused great economic losses to the duck industry. In this study, we aim to develop a triplex real-time polymerase chain reaction (PCR) assay to detect these three viruses as early as possible in the suspicious duck flocks. Results The detection limit of the triplex real-time PCR for AIV, NDV, and DTMUV was 1 × 101 copies/μL, which was at least 10 times higher than the conventional PCR. In addition, the triplex assay was highly specific, and won’t cross-react with other duck pathogens. Besides, the intra-day relative standard deviation and inter-day relative standard deviation were lower than 4.44% for these viruses at three different concentrations. Finally, a total of 120 clinical samples were evaluated by the triplex real-time PCR, the conventional PCR and virus isolation, and the positive rates for these three methods were 20.83, 21.67, 19.17%, respectively. Taking virus isolation as the gold standard, the diagnostic specificity and positive predictive value of the three viruses were all above 85%, while the diagnostic sensitivity and negative predictive value of the three viruses were all 100%. Conclusion The developed triplex real-time PCR is fast, specific and sensitive, and is feasible and effective for the simultaneous detection of AIV, NDV, and DTMUV in ducks.


2010 ◽  
Vol 16 (4) ◽  
pp. 317-321 ◽  
Author(s):  
M. Bouscambert Duchamp ◽  
J.S. Casalegno ◽  
Y. Gillet ◽  
E. Frobert ◽  
E. Bernard ◽  
...  

2011 ◽  
Vol 93 (2) ◽  
pp. 797-805 ◽  
Author(s):  
Naixing Zhang ◽  
Shisong Fang ◽  
Ting Wang ◽  
Jianxiong Li ◽  
Xiaowen Cheng ◽  
...  

2021 ◽  
Vol 11 (4) ◽  
pp. 290-296
Author(s):  
Man Jin Kim ◽  
Hyunwoong Park ◽  
You La Jeon ◽  
Ho Seob Shin ◽  
Sung Im Cho ◽  
...  

2013 ◽  
Vol 60 (3) ◽  
Author(s):  
Dawid Nidzworski ◽  
Edyta Wasilewska ◽  
Krzysztof Smietanka ◽  
Bogusław Szewczyk ◽  
Zenon Minta

Newcastle disease virus (NDV), member of the Paramyxoviridae family and avian influenza virus (AIV), member of the Orthomyxoviridae family, are two main avian pathogens causing serious economic problems in poultry health. Both are enveloped, single-stranded, negative-sense RNA viruses and cause similar symptoms, ranging from sub-clinical infections to severe diseases, including decrease in egg production, acute respiratory syndrome, and high mortality. Similar symptoms hinder the differentiation of infection with the two viruses by standard veterinary procedures like clinical examination or necropsy. To overcome this problem, we have developed a new duplex real-time PCR assay for the detection and differentiation of these two viruses. Eighteen NDV strains, fourteen AIV strains, and twelve other (negative control) strains viruses were isolated from allantoic fluids of specific pathogen-free (SPF), embryonated eggs. Four-weeks-old SPF chickens were co-infected with both viruses (NDV - LaSota and AIV - H7N1). Swabs from cloaca and trachea were collected and examined. The results obtained in this study show that by using duplex real-time PCR, it was possible to detect and distinguish both viruses within less than three hours and with high sensitivity, even in case a bird was co-infected. Additionally, the results show the applicability of the real-time PCR assay in laboratory practice for the identification and differentiation of Newcastle disease and influenza A viruses in birds.


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