

Volume 4, Issue 6(Suppl)
J Infect Dis Ther
ISSN: 2332-0877 JIDT, an open access journal
Page 42
Notes:
Influenza 2016
September 12-13, 2016
conferenceseries
.com
Influenza
September 12-13, 2016 Berlin, Germany
2
nd
International Conference on
Kallikrein-related peptidase 5 contributes to H3N2 influenza virus infection in human lungs
Melia Magnen
1, 2
, Fabien Gueugnon
1, 2
, Antoine Guillon
1, 2
, Thomas Baranek
1, 2
, Agnes Petit-Courty
1, 2
, Alison A Humbles
3
, Mustapha Si-Tahar
1, 2
and
Yves Courty
1, 2
1
Institut National de la Santé et de la Recherche Médicale, France
2
Université François Rabelais, France
3
MedImmune, USA
T
he cleavage of the influenza A virus hemagglutinin (HA) by host serine-proteases is essential for viral infectivity. Several serine
proteases of the kallikrein-related peptidase (KLK) family are produced and secreted by the airways and we investigated whether
KLK1, 5 and 14 were involved in seasonal IAV infection. Expression of KLK1, 5 and 14 was assessed at the protein levels, in human
tracheal aspirates from flu patients in intensive care unit, using ELISA. Primary human bronchial epithelial cells (hBEC) cultured at
the Air-liquid interface were infected with IAV and the expression of KLKs was analyzed by RT-qPCR and flow cytometry. We also
investigated in vitro if KLK1, 5 and 14 were able to cleave HA precursors. Finally, inactivated virions (mouse adapted A/Scotland20/74,
H3N2) were treated with KLKs and the infectiveness was determined in MDCK cells and in mice. Flu infection selectively increased
expression of KLK5 in hBEC and its secretion in the human airways. KLK1, 5 and 14 were able to cleave in vitro HA precursor from
several subtypes of influenza viruses. Furthermore, only the KLK5 treatment of H3N2 virions promoted IAV infection in MDCK
cells. In mice, the treated virus led to severe infection with KLK5 treatment and to moderate one with KLK14 treatment. KLK1 virus
treatment did not result in infection. Expression and secretion of KLK5 is specifically induced in airways upon flu. This induction
likely contributes to the propagation of the virus in favoring its multi-cycle replication through activation of the HA precursor.
Biography
Melia Magnen is currently pursuing her PhD at the CEPR, Tours, France, working under Dr. Yves Courty, Centre d’Étude des Pathologies Respiratoires (INSERM U1100).
Her research interest mainly focuses on influenza and other respiratory viruses.
melia.magnen@univ-tours.frMelia Magnen et al., J Infect Dis Ther 2016, 4:6(Suppl)
http://dx.doi.org/10.4172/2332-0877.C1.014