TY - JOUR
T1 - Osteopontin impairs host defense during established gram-negative sepsis caused by Burkholderia pseudomallei(Melioidosis)
AU - van der Windt, Gerritje J.W.
AU - Wiersinga, W. Joost
AU - Wieland, Catharina W.
AU - Tjia, Ivo C.S.I.
AU - Day, Nicholas P.
AU - Peacock, Sharon J.
AU - Florquin, Sandrine
AU - van der Poll, Tom
PY - 2010/8
Y1 - 2010/8
N2 - Background: Melioidosis, caused by infection with Burkholderia (B.) pseudomallei, is a severe illness that is endemic in Southeast Asia. Osteopontin (OPN) is a phosphorylated glycoprotein that is involved in several immune responses including induction of T-helper 1 cytokines and recruitment of inflammatory cells. Methodology and Principal Findings:OPN levels were determined in plasma from 33 melioidosis patients and 31 healthy controls, and in wild-type (WT) mice intranasally infected with B. pseudomallei. OPN function was studied in experimental murine melioidosis using WT and OPN knockout (KO) mice. Plasma OPN levels were elevated in patients with severe melioidosis, even more so in patients who went on to die. In patients who recovered plasma OPN concentrations had decreased after treatment. In experimental melioidosis in mice plasma and pulmonary OPN levels were also increased. Whereas WT and OPN KO mice were indistinguishable during the first 24 hours after infection, after 72 hours OPN KO mice demonstrated reduced bacterial numbers in their lungs, diminished pulmonary tissue injury, especially due to less necrosis, and decreased neutrophil infiltration. Moreover, OPN KO mice displayed a delayed mortality as compared to WT mice. OPN deficiency did not influence the induction of proinflammatory cytokines. Conclusions: These data suggest that sustained production of OPN impairs host defense during established septic melioidosis.
AB - Background: Melioidosis, caused by infection with Burkholderia (B.) pseudomallei, is a severe illness that is endemic in Southeast Asia. Osteopontin (OPN) is a phosphorylated glycoprotein that is involved in several immune responses including induction of T-helper 1 cytokines and recruitment of inflammatory cells. Methodology and Principal Findings:OPN levels were determined in plasma from 33 melioidosis patients and 31 healthy controls, and in wild-type (WT) mice intranasally infected with B. pseudomallei. OPN function was studied in experimental murine melioidosis using WT and OPN knockout (KO) mice. Plasma OPN levels were elevated in patients with severe melioidosis, even more so in patients who went on to die. In patients who recovered plasma OPN concentrations had decreased after treatment. In experimental melioidosis in mice plasma and pulmonary OPN levels were also increased. Whereas WT and OPN KO mice were indistinguishable during the first 24 hours after infection, after 72 hours OPN KO mice demonstrated reduced bacterial numbers in their lungs, diminished pulmonary tissue injury, especially due to less necrosis, and decreased neutrophil infiltration. Moreover, OPN KO mice displayed a delayed mortality as compared to WT mice. OPN deficiency did not influence the induction of proinflammatory cytokines. Conclusions: These data suggest that sustained production of OPN impairs host defense during established septic melioidosis.
UR - http://www.scopus.com/inward/record.url?scp=78149272959&partnerID=8YFLogxK
U2 - 10.1371/journal.pntd.0000806
DO - 10.1371/journal.pntd.0000806
M3 - Article
C2 - 20824216
AN - SCOPUS:78149272959
SN - 1935-2727
VL - 4
JO - PLoS Neglected Tropical Diseases
JF - PLoS Neglected Tropical Diseases
IS - 8
M1 - e806
ER -