Comparative analysis of neuroinvasion by Japanese encephalitis virulent and vaccine viral strains in an in vitro model of human blood-brain barrier

被引:4
作者
Khou, Cecile [1 ,5 ]
Diaz-Salinas, Marco Aurelio [1 ,6 ]
da Costa, Anaelle [2 ,7 ]
Prehaud, Christophe [2 ]
Jeannin, Patricia [3 ]
Afonso, Philippe V. [3 ]
Vignuzzi, Marco [4 ]
Lafon, Monique [2 ]
Pardigon, Nathalie [1 ]
机构
[1] Inst Pasteur, Unite Rech & Expertise Environm & Risques Infect, Grp Arbovirus, Paris, France
[2] Inst Pasteur, Unite Neuroimmunol Virale, Paris, France
[3] Inst Pasteur, CNRS UMR 3569, Unite Epidemiol & Physiopathol Virus Oncogenes, Paris, France
[4] Inst Pasteur, Unite Populat Virales & Pathogenese, Paris, France
[5] Direct Gen Armement, Vert Le Petit, France
[6] Univ Massachusetts, Sch Med, Dept Microbiol & Physiol Syst, Worcester, MA USA
[7] Theranexus, Fontenay Aux Roses, France
关键词
VIRUS; INFECTION; SA14-14-2; FLAVIVIRUSES; EXPRESSION;
D O I
10.1371/journal.pone.0252595
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Japanese encephalitis virus (JEV) is the major cause of viral encephalitis in South East Asia. It has been suggested that, as a consequence of the inflammatory process during JEV infection, there is disruption of the blood-brain barrier (BBB) tight junctions that in turn allows the virus access to the central nervous system (CNS). However, what happens at early times of JEV contact with the BBB is poorly understood. In the present work, we evaluated the ability of both a virulent and a vaccine strain of JEV (JEV RP9 and SA14-14-2, respectively) to cross an in vitro human BBB model. Using this system, we demonstrated that both JEV RP9 and SA14-14-2 are able to cross the BBB without disrupting it at early times post viral addition. Furthermore, we find that almost 10 times more RP9 infectious particles than SA14-14 cross the model BBB, indicating this BBB model discriminates between the virulent RP9 and the vaccine SA14-14-2 strains of JEV. Beyond contributing to the understanding of early events in JEV neuroinvasion, we demonstrate this in vitro BBB model can be used as a system to study the viral determinants of JEV neuroinvasiveness and the molecular mechanisms by which this flavivirus crosses the BBB during early times of neuroinvasion.
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页数:16
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