scholarly journals A quantitative RT-PCR assay for rapid detection of Eurasian-lineage H10 subtype influenza A virus

2016 ◽  
Vol 31 (5) ◽  
pp. 444-447 ◽  
Author(s):  
Hailiang Sun ◽  
Jian-Li Xue ◽  
Elizabeth Bailey ◽  
Yifei Xu ◽  
Guoliang Hu ◽  
...  
PLoS ONE ◽  
2021 ◽  
Vol 16 (2) ◽  
pp. e0246690
Author(s):  
Gustavo Lopez Moreno ◽  
Jayaveeramuthu Nirmala ◽  
Christa Goodell ◽  
Marie Culhane ◽  
Montserrat Torremorell

Influenza A virus (IAV) is one of the most important respiratory viruses affecting pig health and vaccination is the most common strategy to control influenza infections. In this field study we assessed the onset and duration of shedding of a live attenuated influenza virus (LAIV) vaccine, its ability to transmit to non-vaccinated pigs and whether the LAIV could be aerosolized and detected in the environment. Thirty-three litters (n = 33) of a farm using the LAIV vaccine were selected for the study, a subset of them (n = 12) were left unvaccinated and a subset of piglets (n = 3) in vaccinated litters were also left unvaccinated to serve as sentinels. Selected piglets from the litters were sampled multiple days post vaccination (DPV) by collecting nasal swabs and blood, and were tested using a LAIV vaccine specific RT-PCR assay and hemagglutination inhibition assay against the LAIV strains respectively. Environmental specimens consisting of air and surface wipes were also collected. One hundred percent (21/21) of the vaccinated litters tested LAIV positive 1 DPV and until 6 DPV. In contrast, only five (5/33) of the thirty-three non-vaccinated pigs tested positive during the course of the study. Viable LAIV was confirmed in vaccinated pigs by cell culture and whole genome sequencing. In addition, low levels of LAIV RNA (RT-PCR Ct values ranging between 33 and 38) were detected in all air specimens collected on the day of vaccination and until 6 DPV (3/10). Pigs had maternally derived antibodies reactive against the LAIV strains which may have influenced the degree of shedding observed. Under the conditions of this study, shedding of the LAIV from vaccinated pigs was limited in time, resulted in minimal transmission to non-vaccinated pigs and was detected in low levels in aerosols collected in the vaccinated rooms likely influenced by the presence of maternally derived antibodies against the LAIV strains.


The Analyst ◽  
2011 ◽  
Vol 136 (10) ◽  
pp. 2064 ◽  
Author(s):  
Keiichiro Yamanaka ◽  
Masato Saito ◽  
Kenji Kondoh ◽  
Mohammad Mosharraf Hossain ◽  
Ritsuko Koketsu ◽  
...  

2009 ◽  
Vol 58 (3) ◽  
pp. 365-370 ◽  
Author(s):  
B. Ghebremedhin ◽  
I. Engelmann ◽  
W. König ◽  
B. König

Nowadays, influenza antigen detection test kits are used most frequently to detect influenza A or B virus to establish the diagnosis of influenza rapidly and initiate appropriate therapy. This study was conducted to evaluate the performance of the actim Influenza A&B test (Medix Biochemica). Overall, 473 respiratory specimens were analysed in the actim Influenza A&B test and the results were compared with those from an RT-PCR assay; 461 of these samples originated from paediatric patients aged 7 weeks to 6.5 years either with influenza-related symptoms or from the intensive care unit, and 12 samples originated from adults with underlying lung or haematological diseases. Diagnosis of influenza A or B virus could be established using the actim Influenza A&B test (9/473 samples for influenza A virus and 6/473 for influenza B virus). RT-PCR revealed 23 patients with influenza virus (13/473 for influenza A virus and 10/473 for influenza B virus). The sensitivity and specificity of the actim Influenza A&B test were 65 and 100 % compared with the RT-PCR assay. However, 32 external quality assessment samples containing seven different strains of influenza A subtypes H1N1 and H3N2 and the avian H5N1 were detected correctly by the actim Influenza A&B test. No cross-reactivity to a range of bacterial, fungal and other viral pathogens was observed. In conclusion, the actim Influenza A&B test is reliable for positive results due to its high specificity. Nevertheless, negative results from this test need to be confirmed by a more sensitive assay because of the low sensitivity observed with diagnostic samples.


2013 ◽  
Vol 188 (1-2) ◽  
pp. 73-75 ◽  
Author(s):  
Ikuyo Takayama ◽  
Mina Nakauchi ◽  
Seiichiro Fujisaki ◽  
Takato Odagiri ◽  
Masato Tashiro ◽  
...  

2006 ◽  
Vol 6 (1) ◽  
Author(s):  
Lisa FP Ng ◽  
Ian Barr ◽  
Tung Nguyen ◽  
Suriani Mohd Noor ◽  
Rosemary Sok-Pin Tan ◽  
...  

2017 ◽  
Vol 35 ◽  
pp. 57-63
Author(s):  
Andrey Komissarov ◽  
Artem Fadeev ◽  
Anna Kosheleva ◽  
Kseniya Sintsova ◽  
Mikhail Grudinin
Keyword(s):  
Rt Pcr ◽  

2021 ◽  
pp. 104063872199481
Author(s):  
Yixin Xiao ◽  
Fan Yang ◽  
Fumin Liu ◽  
Hangping Yao ◽  
Nanping Wu ◽  
...  

The H2 subtypes of avian influenza A viruses (avian IAVs) have been circulating in poultry, and they have the potential to infect humans. Therefore, establishing a method to quickly detect this subtype is pivotal. We developed a TaqMan minor groove binder real-time RT-PCR assay that involved probes and primers based on conserved sequences of the matrix and hemagglutinin genes. The detection limit of this assay was as low as one 50% egg infectious dose (EID50)/mL per reaction. This assay is specific, sensitive, and rapid for detecting avian IAV H2 subtypes.


2015 ◽  
Vol 14 (4) ◽  
pp. 17496-17504 ◽  
Author(s):  
C.Y. Mu ◽  
A.Y. Wang ◽  
C. Chen ◽  
L. Zhao ◽  
Z. Li
Keyword(s):  
Rt Pcr ◽  

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