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DOI 10.1016/j.arcmed.2018.10.001

Медицинская библиотека · Archives of medical research · 2018

Varicella-Zoster Virus in Cerebrospinal Fluid at Relapses of Multiple Sclerosis is Infective in Vitro.

Hernández-González Olivia, Martínez-Palomo Adolfo, Sotelo Julio, Chávez-Munguía Bibiana, Ordoñez Graciela, Talamás-Lara Daniel, Pineda Benjamin, de Jesús Flores-Rivera José, Espinosa-Cantellano Martha

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

We have reported the presence of varicella-zoster virus (VZV) DNA and viral particles in the cerebrospinal fluid (CSF) of multiple sclerosis (MS) patients during exacerbation. It is not known whether these viruses are infective.

AIM: To determine whether the VZV found in CSF of MS patients in exacerbation phase are infective.

METHODS

VZV found in CSF of MS patients was quantified by qPCR. Vero E6 cell cultures were incubated with CSF of five MS cases positive for VZV DNA, containing herpes-like viral particles. Propagated virus harvested from these cultures were used to infect new VeroE6 cells. Localization of an immediate-early and a late structural VZV proteins was monitored by confocal microscopy after 72 h. CSF from five non-inflammatory neurological (NIN) patients were used as controls.

RESULTS

A cytopathic effect was found in cultured cells inoculated with CSF from MS patients. Both, structural VZV glycoprotein (gB) and immediate-early VZV protein (IE62) were detected in Vero E6 cultures inoculated with samples from all five MS cases. CSF from control patients produced no effect on Vero E6 cells.

CONCLUSION

When present in the CSF at relapses of MS, VZV is infective under in vitro conditions.

Для цитирования: Hernández-González Olivia, Martínez-Palomo Adolfo, Sotelo Julio, Chávez-Munguía Bibiana, Ordoñez Graciela, Talamás-Lara Daniel, Pineda Benjamin, de Jesús Flores-Rivera José, Espinosa-Cantellano Martha. Varicella-Zoster Virus in Cerebrospinal Fluid at Relapses of Multiple Sclerosis is Infective in Vitro.. Archives of medical research. 2018. DOI: 10.1016/j.arcmed.2018.10.001.

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