Human Emerging and Re‐emerging Infections 2015
DOI: 10.1002/9781118644843.ch8
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Pathogenesis of West Nile Virus in Humans

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“…Moreover, the only virus detected by RT-PCR following a single passage of this population in Vero cells was the smaller KTG➔MGV virus (Figure 4B), suggesting that the GLuc sequence, like the TAT(1-67) sequence, was unstable. This instability was further confirmed by the observation that a single passage of the day 4 p0 virus, which had produced only small plaques, yielded a virus stock of mixed small- and large-plaque phenotypes [26] and RT-PCR products of variable lengths (Figure 4B). …”
Section: Resultsmentioning
confidence: 80%
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“…Moreover, the only virus detected by RT-PCR following a single passage of this population in Vero cells was the smaller KTG➔MGV virus (Figure 4B), suggesting that the GLuc sequence, like the TAT(1-67) sequence, was unstable. This instability was further confirmed by the observation that a single passage of the day 4 p0 virus, which had produced only small plaques, yielded a virus stock of mixed small- and large-plaque phenotypes [26] and RT-PCR products of variable lengths (Figure 4B). …”
Section: Resultsmentioning
confidence: 80%
“…Vero cells were electroporated with in vitro- transcribed WNV-NY/TAT RNA. Although no cytopathic effects (CPE) were observed, a relatively high titer viral stock (p0) (2.5 × 10 6 plaque-forming units (pfu)/mL), with a plaque phenotype indistinguishable from that of wild-type WNV-NY [26], was recovered at 7 days post-electroporation. Passage of this viral stock in Vero cells generated a 4.9 × 10 7 pfu/mL (p1) stock.…”
Section: Resultsmentioning
confidence: 99%
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