作者: S. Timothy Motley , Brian J. Morrow , Xuejun Liu , Ingrid L. Dodge , Antonella Vitiello
DOI: 10.1111/J.1462-5822.2004.00407.X
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摘要: Summary A fundamental goal in the study of infections is to understand dynamic interplay between host and pathogen; however, direct vivo interrogation this disease process via transcriptional profiling has been lacking. Here we describe development application novel bacterial RNA amplification technology simultaneously identify key elements both pathogen responses a murine infection model. On side, found induction an unusual pattern stress response genes, host-induced metal ion limitation, failure achieve stationary phase vivo. mammalian observed surprising several genes encoding acute proteins including hepcidin, haptoglobin, complement C3 metallothionein 1 at site infection, as well other mediators innate immunity. Thus, our results reveal host–pathogen cross-talk not predicted by previous vitro analyses provide framework eavesdrop on broad array interactions As described here, comprehensive examination during critical discovery approaches for intervention current models.