ArticleVirology journal2010
A simple and rapid method for detection of Goose Parvovirus in the field by loop-mediated isothermal amplification.
Article in Virology journal, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.
What it found
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
16 citing papers in PubMed, 40 citations in OpenAlex.
- Rapid on-site differentiation of two invasive whitefly cryptic species using LAMP.Scientific reports · 2025Article
- Rapid and visual detection of an isolated and identified goose parvovirus (GPV) strain by a loop-mediated isothermal amplification assay.Veterinary research forum : an international quarterly journal · 2023Article
- Development and Evaluation of NanoPCR for the Detection of Goose Parvovirus.Veterinary sciences · 2022Article
- Elimination of Carryover Contamination in Real-Time Reverse Transcriptase Loop-Mediated Isothermal Amplification for Rapid Detection of the SARS-CoV-2 Virus in Point-of-Care Testing.Frontiers in cellular and infection microbiology · 2022Article
- Elaboration of Triplex PCR for Detection of Selected Viral Infections in Waterfowl.Journal of veterinary research · 2019Article
- A Sensitive, Specific and Simple Loop Mediated Isothermal Amplification Method for Rapid Detection ofFrontiers in microbiology · 2019Article
- Development of Colloidal Gold-Based Immunochromatographic Assay for Rapid Detection of Goose Parvovirus.Frontiers in microbiology · 2018Article
- Development of a Quantitative Loop-Mediated Isothermal Amplification Assay for the Rapid Detection of Novel Goose Parvovirus.Frontiers in microbiology · 2017Article
- One-Pot Reverse Transcriptional Loop-Mediated Isothermal Amplification (RT-LAMP) for Detecting MERS-CoV.Frontiers in microbiology · 2016Article
- Rapid detection of Mycoplasma synoviae by loop-mediated isothermal amplification.Archives of microbiology · 2015Article
- Reverse transcription loop-mediated isothermal amplification for rapid detection of the newly emerged poultry Flavivirus.Folia microbiologica · 2013Article
- Development and evaluation of a loop-mediated isothermal amplification assay for the rapid detection of porcine cytomegalovirus under field conditions.Virology journal · 2012Article
- Development and evaluation of loop-mediated isothermal amplification assay for rapid and sensitive detection of canine parvovirus DNA directly in faecal specimens.Letters in applied microbiology · 2012Article
- Loop-mediated isothermal amplification for the detection of goose circovirus.Virology journal · 2012Article
- Quantitative analysis of waterfowl parvoviruses in geese and Muscovy ducks by real-time polymerase chain reaction: correlation between age, clinical symptoms and DNA copy number of waterfowl parvoviruses.BMC veterinary research · 2012Article
- Rapid detection of sacbrood virus (SBV) by one-step reverse transcription loop-mediated isothermal amplification assay.Virology journal · 2012Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors at 4 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundGoose parvovirus (GPV) is a Dependovirus associated with latent infection and mortality in geese. Currently, in a worldwide scale, GPV severely affects geese production. The objective of this study is to develop a loop-mediated isothermal amplification (LAMP) method for the sensitive, rapid, and inexpensive detection of GPV in the field.
resultsA set of six specific primers was designed by targeting the GPV VP3 DNA. With Bst DNA polymerase large fragment, the target DNA could be amplified at 65 degrees C as early as 20 min of incubation in a simple water bath. A positive reaction was identified through the detection of the LAMP product by color change visible to the naked eye. The detection limit of the assay was 28 copies/microl of plasmid pVP3, and with equal sensitivity and specificity to fluorescent quantitative real-time PCR (FQ-PCR).
conclusionsThe high sensitivity, specificity, and simplicity, as well as the high throughput, make this method suitable for specific detection of GPV infection in both field conditions and laboratory settings. The utilization of complicated equipment and conduct of technical training on the GPV LAMP were not necessary.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.