2010
DOI: 10.1016/j.jviromet.2009.08.024
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Human HepG2 cells support respiratory syncytial virus and human metapneumovirus replication

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Cited by 11 publications
(11 citation statements)
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“…For calibration purposes and as a quality control for each test, serial virus dilutions were run in parallel on each plate to ensure that the virus concentration in the inoculum was reciprocal to cell viability, as previously shown (17). As expected, the absorption rate increased with decreasing virus concentrations (Fig.…”
mentioning
confidence: 58%
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“…For calibration purposes and as a quality control for each test, serial virus dilutions were run in parallel on each plate to ensure that the virus concentration in the inoculum was reciprocal to cell viability, as previously shown (17). As expected, the absorption rate increased with decreasing virus concentrations (Fig.…”
mentioning
confidence: 58%
“…Serum samples from a total of 2,000 patient were randomly collected from the archives of the Institute of Virology of the University Hospital Bonn (which includes a large trauma center for the geographic area and a large obstetrics unit, resulting in many patients in the 20-to 50-year-old age range) and screened for neutralizing capacity, using the XTT-based neutralization test described previously (17).…”
mentioning
confidence: 99%
“…HMPV can be cultured in several cell lines, including tertiary monkey kidney cells (231), Vero cells (231), LLC-MK2-cells, BEAS-2B cells (226), A549 cells (14), and HepG2 cells (202). These cell culture models facilitate HMPV research; however, there are caveats related to the different envelopes the viruses acquire as they bud from the cells, and these different envelopes may modify immune responses and may interfere with some assays.…”
Section: Cell Culturementioning
confidence: 99%
“…6,14 Other cells (Hep2 and HepG2) can support the replication of some hMPV strains. 15,16 Its growth in cell culture is difficult and long and cytopathic effects (CPEs) are variable. The hMPV-induced CPE is characterized by a rounding of infected cells, subsequent detachment from cell culture matrix and occasionally the presence of small syncytia which do not usually appear before the second week of culture in LLC-MK2 cells.…”
Section: Diagnosismentioning
confidence: 99%