| Literature DB >> 28235684 |
Michał M Bonar1, John C Tilton2.
Abstract
Detection of viruses by flow cytometry is complicated by their small size. Here, we characterized the ability of a standard (FACSAria II) and a sub-micron flow cytometer (A50 Micro) to resolve HIV-1 viruses. The A50 was superior at resolving small particles but did not reliably distinguish HIV-1, extracellular vesicles, and laser noise by light scatter properties alone. However, single fluorescent HIV-1 particles could readily be detected by both cytometers. Fluorescent particles were sorted and retained infectivity, permitting further exploration of the functional consequences of HIV-1 heterogeneity. Finally, flow cytometry had a limit of detection of 80 viruses/ml, nearly equal to PCR assays. These studies demonstrate the power of flow cytometry to detect and sort viral particles and provide a critical toolkit to validate methods to label wild-type HIV-1; quantitatively assess integrity and aggregation of viruses and virus-based therapeutics; and efficiently screen drugs inhibiting viral assembly and release.Entities:
Keywords: Extracellular vesicles; Flow cytometry; Flow virometry; HIV; Quantification; Virus sorting
Mesh:
Year: 2017 PMID: 28235684 PMCID: PMC5393045 DOI: 10.1016/j.virol.2017.02.016
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616