Background Ventilator-associated pneumonia (VAP) is a fatal intensive care infection. VAP caused by methicillin-resistant Staphylococcus aureus (MRSA) can be exacerbated by Prevotella intermedia culture supernatant ( P. int. sup.). Solithromycin (SOL), a fourth-generation macrolide, inhibits bacterial protein synthesis and modulates immunity; however, its effects on exacerbation of MRSA-VAP by P. int . sup. remain unclear. This study examined whether SOL inhibits bacterial protein synthesis by binding to the 50S ribosomal subunits in P. int . sup. and subsequently reduces the worsening of MRSA-VAP caused by P. int. sup. Methods BALB/cCrSlc mice received MRSA and P. int. sup. with or without sub-minimum inhibitory concentrations of SOL ( P. int . sup. (SOL)) or clarithromycin (CAM; P. int. sup. (CAM)). Outcomes included survival rates, lung MRSA burden, and transcriptomics (reverse transcription polymerase chain reaction, bulk RNA sequencing RNA-seq). In vitro , bone marrow-derived alveolar macrophage-like cells (AMLCs) from C57BL/6J mice were infected with MRSA ± SOL; bactericidal activity and mRNA expression were measured. Results P. int . sup. increased mortality, bacterial load, and neutrophilic infiltration; however, P. int . sup. (SOL) significantly improved survival rate (100%, n = 8, ****P 0.0001), reduced MRSA burden ( n = 10–11, **P 0.01), and enhanced macrophage recruitment ( n = 7–8, ****P 0.001). P. int. sup. downregulated Ccr2 expression ( n = 7–8, ***P 0.001). RNA-seq analysis revealed P. int . sup. (SOL) upregulated macrophage phagocytosis and bactericidal pathways. SOL-pretreated AMLCs infected with MRSA exhibited reduced bacterial burden ( n = 8, *P 0.05 vs control, **P 0.01 vs CAM-pretreated AMLCs) and upregulated Tnf-α expression ( n = 7–8, *P 0.05 vs control). Conclusion SOL protects by activating alveolar macrophages and promoting TNF-related responses, suggesting a novel immunomodulatory role for SOL in host defense against exacerbation of MRSA-VAP by P. int. sup.
Fukushima et al. (Mon,) studied this question.