2016
DOI: 10.1016/j.jviromet.2016.02.013
|View full text |Cite
|
Sign up to set email alerts
|

Multiplex real-time PCR for identification of canine parvovirus antigenic types

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
9
0

Year Published

2016
2016
2021
2021

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 18 publications
(9 citation statements)
references
References 20 publications
0
9
0
Order By: Relevance
“…Several assays have been reported for the detection or quantitation of CPV DNA [12][13][14][15][16][17][18], including PCR, nested PCR, iiPCR, RPA, LAMP-ELISA, LAMP-LFD, LAMP, polymerase spiral reaction, and SYBR Green based real-time PCR, but none of these assays enable differentiation CPV antigenic types and CPV-like viruses (MEV and FPV). Several other assays have been reported for the detection and differentiation of type 2-based vaccines and field strains of CPV [19] or typing of three antigenic types of CPV [20] or CPV and MEV [21] assay and MGB probe real-time RT-PCR, but none of these assays enables simultaneous detection and differentiation of four antigenic types of CPV.…”
Section: Introductionmentioning
confidence: 99%
“…Several assays have been reported for the detection or quantitation of CPV DNA [12][13][14][15][16][17][18], including PCR, nested PCR, iiPCR, RPA, LAMP-ELISA, LAMP-LFD, LAMP, polymerase spiral reaction, and SYBR Green based real-time PCR, but none of these assays enable differentiation CPV antigenic types and CPV-like viruses (MEV and FPV). Several other assays have been reported for the detection and differentiation of type 2-based vaccines and field strains of CPV [19] or typing of three antigenic types of CPV [20] or CPV and MEV [21] assay and MGB probe real-time RT-PCR, but none of these assays enables simultaneous detection and differentiation of four antigenic types of CPV.…”
Section: Introductionmentioning
confidence: 99%
“…DNA sequencing is the gold standard for identifying the CPV‐2 genotype, despite the fact that it is time‐consuming, costly and subject to artificial contamination. Other methods can be used to genotype CPV‐2, such as the MGB probe assay, multiplex real‐time PCR assay and the high‐resolution melting (HRM) curve method . However, multiplex real‐time PCR and HRM curve method require two to three primer pairs and take at least 4 hours .…”
Section: Discussionmentioning
confidence: 99%
“…Other methods can be used to genotype CPV‐2, such as the MGB probe assay, multiplex real‐time PCR assay and the high‐resolution melting (HRM) curve method . However, multiplex real‐time PCR and HRM curve method require two to three primer pairs and take at least 4 hours . In addition, due to the very short range of melting temperature (0.2‐0.6°C), using HRM analysis to differentiate between different genotypes of CPV‐2 has its limitation .…”
Section: Discussionmentioning
confidence: 99%
“…In India and Iran, the dominant types in recent outbreaks were CPV-2a and -2b [21,72,73] . In 2016, CPV-2c was detected in northern and central India [74,75] and Iran [73] .…”
Section: Prevalence Of Canine Parvovirus Type 2 Variantsmentioning
confidence: 99%