TY - JOUR
T1 - Proteome-wide antigen discovery of novel protective vaccine candidates against Staphylococcus aureus infection
AU - Rasmussen, Karina Juhl
AU - Mattsson, Andreas Holm
AU - Pilely, Katrine
AU - Asferg, Cecilie Antoinette
AU - Ciofu, Oana
AU - Vitved, Lars
AU - Koch, Claus
AU - Kemp, Michael
AU - Forfattergruppering (Peter Garred, Members)
A2 - Garred, Peter
N1 - Copyright © 2016 Elsevier Ltd. All rights reserved.
PY - 2016/8/31
Y1 - 2016/8/31
N2 - Methicillin-resistant Staphylococcus aureus (MRSA) is a rapidly growing problem, especially in hospitals where MRSA cause increased morbidity and mortality and a significant rise in health expenditures. As many strains of MRSA are resistant to other antimicrobials in addition to methicillin, there is an urgent need to institute non-antimicrobial measures, such as vaccination, against the spread of MRSA. With the aim of finding new protective antigens for vaccine development, this study used a proteome-wide in silico antigen prediction platform to screen the proteome of S. aureus strain MRSA252. Thirty-five different S. aureus proteins were identified, recombinantly expressed, and tested for protection in a lethal sepsis mouse model using S. aureus strain MRSA252 as the challenge organism. We found that 13 of the 35 recombinant peptides yielded significant protection and that 12 of these antigens were highly conserved across 70 completely sequenced S. aureus strains. Thus, this in silico platform was capable of identifying novel candidates for inclusion in future vaccines against MRSA.
AB - Methicillin-resistant Staphylococcus aureus (MRSA) is a rapidly growing problem, especially in hospitals where MRSA cause increased morbidity and mortality and a significant rise in health expenditures. As many strains of MRSA are resistant to other antimicrobials in addition to methicillin, there is an urgent need to institute non-antimicrobial measures, such as vaccination, against the spread of MRSA. With the aim of finding new protective antigens for vaccine development, this study used a proteome-wide in silico antigen prediction platform to screen the proteome of S. aureus strain MRSA252. Thirty-five different S. aureus proteins were identified, recombinantly expressed, and tested for protection in a lethal sepsis mouse model using S. aureus strain MRSA252 as the challenge organism. We found that 13 of the 35 recombinant peptides yielded significant protection and that 12 of these antigens were highly conserved across 70 completely sequenced S. aureus strains. Thus, this in silico platform was capable of identifying novel candidates for inclusion in future vaccines against MRSA.
KW - Journal Article
U2 - 10.1016/j.vaccine.2016.07.016
DO - 10.1016/j.vaccine.2016.07.016
M3 - Journal article
C2 - 27496278
SN - 0264-410X
VL - 34
SP - 4602
EP - 4609
JO - Vaccine
JF - Vaccine
IS - 38
ER -