posted on 2015-09-21, 00:00authored byJiwang Chen, Gang Feng, Yang Song, Juliane B. Wardenburg, Simon Lin, Ichiro Inoshima, Michael Otto, Richard G. Wunderink
Background: Linezolid (LZD) is beneficial to patients with MRSA pneumonia, but whether and how LZD influences
global host lung immune responses at the mRNA level during MRSA-mediated pneumonia is still unknown.
Methods: A lethal mouse model of MRSA pneumonia mediated by USA300 was employed to study the influence of
LZD on survival, while the sublethal mouse model was used to examine the effect of LZD on bacterial clearance and
lung gene expression during MRSA pneumonia. LZD (100mg/kg/day, IP) was given to C57Bl6 mice for three days.
On Day 1 and Day 3 post infection, bronchoalveolar lavage fluid (BALF) protein concentration and levels of cytokines
including IL6, TNFα, IL1β, Interferon-γ and IL17 were measured. In the sublethal model, left lungs were used to
determine bacterial clearance and right lungs for whole-genome transcriptional profiling of lung immune responses.
Results: LZD therapy significantly improved survival and bacterial clearance. It also significantly decreased BALF
protein concentration and levels of cytokines including IL6, IL1β, Interferon-γ and IL17. No significant gene
expression changes in the mouse lungs were associated with LZD therapy.
Conclusion: LZD is beneficial to MRSA pneumonia, but it does not modulate host lung immune responses at the
transcriptional level.
Funding
This study was supported by Pfizer ASPIRE Award, Pfizer Investigator-Initiated Grant (WS1826185, to JC), the National Center for Advancing
Translational Sciences Grant (8UL1TR000150) and the NCI Cancer Center Support Grant (NCI CA060553 to GF and SL) and the Intramural Research
Program of the NIAID (to MO).