scholarly journals Enhancement of Hepatitis B Virus Infection by Noninfectious Subviral Particles

1998 ◽  
Vol 72 (2) ◽  
pp. 1462-1468 ◽  
Author(s):  
Michael Bruns ◽  
Stefan Miska ◽  
Sylvie Chassot ◽  
Hans Will

ABSTRACT The biological function of the huge excess of subviral particles over virions in hepatitis B virus infections is unknown. Using the duck hepatitis B virus as a model, we unexpectedly found that subviral particles strongly enhance intracellular viral replication and gene expression. This effect is dependent on the multiplicity of infection, the ratio of virions over subviral particles, and the time point of addition of subviral particles. Most importantly, we show that the pre-S protein of the subviral particles triggers enhancement and requires the presence of the binding regions for putative cell-encoded virus receptor proteins. These data suggest that enhancement is due either to the recently described transactivation function of the pre-S protein or to signalling pathways which become activated upon binding of subviral particles to cellular receptors. The findings are of clinical importance, since they imply that infectivity of sera containing hepadnaviruses depends not only on the amount of infectious virions but also decisively on the number of particles devoid of nucleic acids. A similarly dramatic enhancing effect of noninfectious particles in other virus infections is well conceivable.

1992 ◽  
Vol 66 (3) ◽  
pp. 1377-1388 ◽  
Author(s):  
A R Jilbert ◽  
T T Wu ◽  
J M England ◽  
P M Hall ◽  
N Z Carp ◽  
...  

2020 ◽  
Vol 101 ◽  
pp. 328-329
Author(s):  
A. Lawal ◽  
A. Alhaji Abubakar ◽  
S. Muawiyya ◽  
Babale ◽  
A. Abayomi. Olorukooba ◽  
...  

2017 ◽  
Vol 84 (5) ◽  
pp. 525-530 ◽  
Author(s):  
Marco Sebastiani ◽  
Fabiola Atzeni ◽  
Laura Milazzo ◽  
Luca Quartuccio ◽  
Carlo Scirè ◽  
...  

Virology ◽  
1993 ◽  
Vol 192 (1) ◽  
pp. 217-223 ◽  
Author(s):  
Sylvie Chassot ◽  
Véronique Lambert ◽  
Alan Kay ◽  
Catherine Godinot ◽  
Bernard Roux ◽  
...  

PLoS ONE ◽  
2013 ◽  
Vol 8 (11) ◽  
pp. e80346 ◽  
Author(s):  
Alexandra Ducancelle ◽  
Pierre Abgueguen ◽  
Jacques Birguel ◽  
Wael Mansour ◽  
Adeline Pivert ◽  
...  

PEDIATRICS ◽  
1985 ◽  
Vol 75 (2) ◽  
pp. 362-364
Author(s):  

Infants born to mothers who are hepatitis B surface antigen (HBsAg) positive are frequently infected with hepatitis B virus (HBV). Many of these newborns will become chronic carriers of HBV and will subsequently develop chronic liver disease. Recent studies have demonstrated that perinatal transmission can be prevented by immunization of the newborn. Recommendations for the management of infants at risk are presented. PERINATAL TRANSMISSION OF HBV INFECTIONS Perinatal infection of infants by mothers who are HBsAg positive is most likely to occur if mothers are also hepatitis Be antigen positive. About 90% of infants whose mothers are positive for both markers will become infected and most will become permanent carriers.1 Infants whose mothers are HBeAg negative or who have antibody to HBeAg are at lesser risk, but can still be infected.2 Infected infants usually will not become HBsAg positive until several weeks after birth. Although clinical jaundice or acute hepatitis are rare in infected infants, elevations in transaminase levels are frequent.3 It is estimated that about one in four infants who become chronic carriers following perinatal infection will develop cirrhosis or hepatocellular carcinoma later in life. As they are persistent carriers, later in life they may transmit infection to other family members, to sexual contacts, or to others by transfusions or inoculation of their blood. Infection of female infants may eventually result in transmission of HBV to their own infants. Indeed, transmission from mother to infant is a major method of perpetuation of this virus in hyperendemic areas, eg, the Far East.


1979 ◽  
Vol 140 (6) ◽  
pp. 972-974 ◽  
Author(s):  
F. Hardt ◽  
J. Aldershvile ◽  
O. Dietrichson ◽  
E. Juhl ◽  
J. O. Nielsen ◽  
...  

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