Polar infection of Echovirus-30 causes differential barrier affection and gene regulation at the Blood-Cerebrospinal fluid barrier

Echovirus-30 (E-30) is responsible for the extensive global outbreaks of meningitis in children. To gain access to the central nervous system, E-30 first has to cross the epithelial blood-cerebrospinal fluid barrier. Several meningitis causing bacteria preferentially infect human choroid plexus papi...

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Hauptverfasser: Wiatr, Marie (VerfasserIn) , Figueiredo, Ricardo (VerfasserIn) , Stump-Guthier, Carolin (VerfasserIn) , Winter, Peter (VerfasserIn) , Ishikawa, Hiroshi (VerfasserIn) , Adams, Ortwin (VerfasserIn) , Schwerk, Christian (VerfasserIn) , Schroten, Horst (VerfasserIn) , Rudolph, Henriette (VerfasserIn) , Tenenbaum, Tobias (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 29 August 2020
In: International journal of molecular sciences
Year: 2020, Jahrgang: 21, Heft: 17, Pages: 1-22
ISSN:1422-0067
DOI:10.3390/ijms21176268
Online-Zugang:Verlag, kostenfrei, Volltext: https://doi.org/10.3390/ijms21176268
Verlag, kostenfrei, Volltext: https://www.mdpi.com/1422-0067/21/17/6268
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Verfasserangaben:Marie Wiatr, Ricardo Figueiredo, Carolin Stump-Guthier, Peter Winter, Hiroshi Ishikawa, Ortwin Adams, Christian Schwerk, Horst Schroten, Henriette Rudolph and Tobias Tenenbaum

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520 |a Echovirus-30 (E-30) is responsible for the extensive global outbreaks of meningitis in children. To gain access to the central nervous system, E-30 first has to cross the epithelial blood-cerebrospinal fluid barrier. Several meningitis causing bacteria preferentially infect human choroid plexus papilloma (HIBCPP) cells in a polar fashion from the basolateral cell side. Here, we investigated the polar infection of HIBCPP cells with E-30. Both apical and basolateral infections caused a significant decrease in the transepithelial electrical resistance of HIBCPP cells. However, to reach the same impact on the barrier properties, the multiplicity of infection of the apical side had to be higher than that of the basolateral infection. Furthermore, the number of infected cells at respective time-points after basolateral infection was significantly higher compared to apical infection. Cytotoxic effects of E-30 on HIBCPP cells during basolateral infection were observed following prolonged infection and appeared more drastically compared to the apical infection. Gene expression profiles determined by massive analysis of cDNA ends revealed distinct regulation of specific genes depending on the side of HIBCPP cells’ infection. Altogether, our data highlights the polar effects of E-30 infection in a human in vitro model of the blood-cerebrospinal fluid barrier leading to central nervous system inflammation. 
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