2013
DOI: 10.1002/jcla.21627
|View full text |Cite
|
Sign up to set email alerts
|

A One-Step RT-PCR Array for Detection and Differentiation of Zoonotic Influenza Viruses H5N1, H9N2, and H1N1

Abstract: The high sensitivity, rapidity, reproducibility, and specificity of this zoonotic influenza viruses rRT-PCR array has been verified as being sufficient to detect the presence of multiple zoonotic influenza viruses in a single assay. The zoonotic influenza viruses RT-PCR array might provide rapid identification of emergent zoonotic influenza viruses strains during influenza outbreaks and disease surveillance initiatives.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2

Citation Types

0
2
0

Year Published

2014
2014
2024
2024

Publication Types

Select...
4
1

Relationship

0
5

Authors

Journals

citations
Cited by 5 publications
(2 citation statements)
references
References 39 publications
(67 reference statements)
0
2
0
Order By: Relevance
“…Currently emerging and re-emerging infectious diseases of zoonotic origin such as highly pathogenic avian influenza A pose a significant threat to human and animal health due to their elevated transmissibility [1,2]. Predicting the spread of these viruses is challenging because many of the drivers of disease are not easily identifiable.…”
Section: Introductionmentioning
confidence: 99%
“…Currently emerging and re-emerging infectious diseases of zoonotic origin such as highly pathogenic avian influenza A pose a significant threat to human and animal health due to their elevated transmissibility [1,2]. Predicting the spread of these viruses is challenging because many of the drivers of disease are not easily identifiable.…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, early and sensitive detection of the influenza A virus is important to control the outbreaks. To date, different methods have been developed for detecting influenza A viruses such as virus culture [4][5][6], loop-mediated isothermal amplification (LAMP) [7][8][9], polymerase chain reaction (PCR) methods [10][11][12], enzyme linked immunosorbent assay (ELISA) [13][14][15] and microarray technology [16][17][18]. However, they are labor intensive, have complex sample pretreatment, low sensitivity, high cost and require appropriate laboratory facilities and well-trained technicians.…”
Section: Introductionmentioning
confidence: 99%