The DNA from several clinical isolates of varicella-zoster virus (VZV) were compared with the DNA from the vaccine strain VZV using three restriction endonucleases: BamHI, BgII, and HpaI. When electrophoresed through an agarose gel, the vaccine DNA digestion pattern was significantly different from the digestion patterns of the wild-type DNAs. Variations in the digestion pattern of the separate clinical isolates were also observed.

Download full-text PDF

Source
http://dx.doi.org/10.1002/jmv.1890090110DOI Listing

Publication Analysis

Top Keywords

wild-type dnas
8
clinical isolates
8
digestion pattern
8
restriction endonuclease
4
endonuclease analysis
4
analysis varicella-zoster
4
varicella-zoster vaccine
4
vaccine virus
4
virus wild-type
4
dnas dna
4

Similar Publications

Ultrasensitive detection of cancer-associated nucleic acids and mutations by primer exchange reaction-based signal amplification and flow cytometry.

Biosens Bioelectron

January 2025

Laboratory of Experimental and Translational Oncology, Department of Oncology, Microbiology and Immunology, Faculty of Science and Medicine, University of Fribourg, Chemin Du Musée 18, PER17, 1700, Fribourg, Switzerland; NCCR Bio-inspired Materials, University of Fribourg, 1700, Fribourg, Switzerland. Electronic address:

The detection of cancer-associated nucleic acids and mutations through liquid biopsy has emerged as a highly promising non-invasive approach for early cancer detection and monitoring. In this study, we report the development of primer exchange reaction (PER) based signal amplification strategy that enables the rapid, sensitive and specific detection of nucleic acids bearing cancer specific single nucleotide mutations using flow cytometry. Using micrometer size beads as support for immobilizing oligonucleotides and programmable PER assembly for target oligonucleotide recognition and fluorescence signal amplification, we demonstrated the versatile detection of target nucleic acids including KRAS oligonucleotide, fragmented mRNAs, and miR-21.

View Article and Find Full Text PDF

Morphological Structure Identification, Comparative Mitochondrial Genomics and Population Genetic Analysis toward Exploring Interspecific Variations and Phylogenetic Implications of 'ZA' and Other Species.

Biomolecules

July 2024

Apple Technology Innovation Center of Shandong Province, Shandong Collaborative Innovation Center of Fruit & Vegetable Quality and Efficient Production, National Key Laboratory of Wheat Improvement, College of Horticultural Science and Engineering, Shandong Agricultural University, Taian 271018, China.

, a valuable germplasm resource in the genus , is indigenous to China and widely distributed. However, little is known about the lineage composition and genetic basis of 'ZA', a mutant type of . In this study, we compared the differences between 'ZA' and wild type from the perspective of morphology and ultrastructure and analyzed their chloroplast pigment content based on biochemical methods.

View Article and Find Full Text PDF
Article Synopsis
  • The study presents a one-step genome engineering method for making gene deletions and insertions in honey bee gut bacteria, which is simple and efficient.
  • This technique uses electroporation with plasmid DNA to integrate antibiotic resistance and fluorescent protein genes into bacterial chromosomes without needing additional recombination tools.
  • The approach shows promise for studying gene functions in various bee-associated microbes, aiding in the understanding of their role in bee health and interactions with their hosts.
View Article and Find Full Text PDF

We investigated the basic characteristics of a new murine cytomegalovirus (MCMV) vector platform. Using BAC technology, we engineered replication-competent recombinant MCMVs with deletions of up to 26% of the wild-type genome. To this end, we targeted five gene blocks (m01-m17, m106-m109, m129-m141, m144-m158, and m159-m170).

View Article and Find Full Text PDF
Article Synopsis
  • The infection affects about 50% of people globally, leading to chronic gastritis and gastric cancer, and resistance to antibiotics like clarithromycin complicates treatment efforts.
  • A new method called SHIELD was developed for simultaneously detecting the infection and clarithromycin resistance, utilizing RAA and CRISPR/Cas13a technology for enhanced accuracy.
  • SHIELD demonstrated high sensitivity and specificity, successfully diagnosing the infection and resistance mutations in saliva samples, suggesting its potential for rapid and large-scale clinical application.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!