birth than in human preterm neonates who go on to develop BPD. The elevated AF cytokine levels despite negative AF culture results seen in our model also appears to replicate the clinical condition in Choriodecidual Infection Induces Fetal Lung Injury humans seen in up to 25% of preterm labor cases with elevated amniotic fluid IL-6 and a negative culture and/or PCR. Therefore, our model may reflect a common biological event of pro-inflammatory cytokine signaling induced by many different pathogens in the choriodecidual space and is not restricted specifically to GBS. A limitation of our study is the lack of lung morphometry, but the time course from infection to delivery was fairly short and differences may not yet have become apparent. Lung injury in this model was originally unexpected and the fetal lung was not preserved in such a way to accurately measure lung morphometry later. Another limitation, as well as study strength, is that our results reflect an early or limited choriodecidual infection. We may have interrupted pathways leading to further fetal lung injury, maturation, or possibly repair with further time in utero. The acute histologic changes seen in the GBS exposed animals lungs, including accumulation of inflammatory cells, interstitial wall tissue thickening, and fibrin exudation or hemorrhage, may be precursor findings that subsequently develop into the histopathologic findings of alveolar simplification and enlargement characteristic of the new BPD after 19770292 premature get CEM-101 infants are exposed to mechanical ventilation, hyperoxia, and/or sepsis. The risk for 17876302 developing BPD in 
association with histologic chorioamnionitis increases in infants who are exposed to mechanical ventilation postnatally. Since our model focused on early in utero time points, it is not known if the histopathologic findings in the GBS exposed animals would eventually develop BPD-like features if exposed to other postnatal insults associated with ventilation; however, our gene expression findings suggest this possibility. Therefore, future studies in our model are needed to determine if the fetal lung injury associated with elevated AF pro-inflammatory cytokines requires subsequent postnatal injury for BPD to develop. The timing, degree, and duration of exposures and events producing lung injury in utero and ex utero may influence the ultimate pulmonary phenotype of preterm infants at risk for BPD. Our sample size is also modest, which is typical of nonhuman primate studies and necessary for ethical reasons and conservation. Finally, not all the probe sets on the Affymetrix chip are annotated and some differentially regulated genes could not be identified. The microarray analysis reported in this study measured expression of thousands of genes in a limited number of biological replicates. A concern with this experimental design is a Type I or Type II error when assessing the statistical significance of expression changes of single genes. We minimized this concern with the following strategies. First, the samples that were used for microarray analysis were carefully phenotyped, i.e. lung injury was defined as an aggregate of histologic changes including accumulation of inflammatory cells, evidence of necrosis, inflammatory related tissue thickening, collapse or other injury such as fibrin exudation or hemorrhage. We also used a 1.5-fold expression change criteria in addition to a p-value cut-off to define differential gene expression. By using a combination
