The hop plant (Humulus lupulus) is an economically important perennial species of plant due to its role in beer production. While the majority of hop production occurs in central Washington State, local production in regions around the United States is gaining popularity due to local micro-breweries wanting to use locally grown hops in their production. In Florida, production has recently increased, and while most hop plants are grown from tissue culture, the development of a cost-effective diagnostic assay for hop viruses is critical to ensure planting material is clean. In this study, a tetraplex RT-dPCR assay was developed for the detection of four common hop viruses; Apple mosaic virus (ApMV), Hop mosaic virus (HMV), Hop latent virus (HLV) and American hop latent virus (AHLV). A synthetic control was generated with corresponding viral sequences inserted in tandem for optimization. Stem, petiole, and leaf tissue sampled from each of three different cultivars with different viral profiles were screened with the tetraplex RT-dPCR assay. Across all tissue types and cultivars, HLV had the highest titer level, followed by HMV and ApMV having the lowest levels. Additionally, there were significant levels of variation among tissue types across cultivars. These data highlight the utility of this assay for detecting viruses in hop tissue and provide a useful diagnostic tool for screening hop plants to confirm they are healthy. This assay will be utilized in vector studies but also integrated into diagnostic services.
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http://dx.doi.org/10.1094/PDIS-11-24-2351-RE | DOI Listing |
Plant Dis
March 2025
University of Florida, FLREC, 3205 College Ave., Davie, Davie, Florida, United States, 33314;
The hop plant (Humulus lupulus) is an economically important perennial species of plant due to its role in beer production. While the majority of hop production occurs in central Washington State, local production in regions around the United States is gaining popularity due to local micro-breweries wanting to use locally grown hops in their production. In Florida, production has recently increased, and while most hop plants are grown from tissue culture, the development of a cost-effective diagnostic assay for hop viruses is critical to ensure planting material is clean.
View Article and Find Full Text PDFMethods Mol Biol
February 2025
OncoRNALab, Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.
Induced pluripotent stem cells (iPSCs) have the potential to differentiate into any cell type, offering a valuable tool for research in developmental biology, regenerative medicine, and disease modeling. In this study, iPSCs were differentiated into cranial neural crest cells (CNCCs) over a 14-day period. RNA was extracted from these cells at day 0 (iPSCs), day 7, and day 14 to evaluate successful differentiation through the expression analysis of pluripotency and CNCC marker genes.
View Article and Find Full Text PDFInt J Mol Sci
December 2024
Institute of Physical Culture Sciences, University of Szczecin, 17C Narutowicza St., 70-240 Szczecin, Poland.
The transport of biological materials must protect samples from degradation and ensure courier safety. The main goal of this study was to evaluate the usefulness of a new type of container designed for the secured transport of biological material for storing samples for quantitative RNA analyses. This was achieved by analyzing changes in the expression of selected human leucocyte housekeeping genes (, , and ) using reverse transcription quantitative PCR (RT-qPCR) and digital PCR (RT-dPCR) techniques.
View Article and Find Full Text PDFClin Chem
March 2025
Biological Metrology, National Measurement Laboratory (NML), LGC, London, United Kingdom.
Background: Nucleic acid amplification tests (NAATs) assist in the diagnosis of numerous infectious diseases. They are typically sensitive and specific and can be quickly developed and adapted. Far more challenging is the development of standards to ensure NAATs are performing within specification; reference materials take time to develop and suitable reference measurement procedures (RMPs) have not been available.
View Article and Find Full Text PDFHeliyon
October 2024
Division of Research and Analysis, Food and Drug Administration, Ministry of Health and Welfare, Taipei, Taiwan.
Objectives: In response to the pandemic, the Taiwan Food and Drug Administration (TFDA) established an initial SARS-CoV-2 RNA national standard based on the original Wuhan strain. However, with the depletion of the first national standard and continued mutation of the virus, the establishment of new national standards was imminent.
Methods: Hence, new candidate national standards were established by heat-inactivation for 30 min for six representative strains of SARS-CoV-2, comprising the original strain and five variants with anticipated concentrations of 7.
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