Sheikh Aadil, Scano Colin, Xu Julia, Ojo Tolulope, Conforti Jessica M, Haberman Kayla L, King Bryan, Martinez Alysia S, Pujol Michelle, Watkins Juli, Lotter James, Lin Emily L, Zechmann Bernd, Sevcik Amanda, Sayes Christie, Gallagher Elyssia S, Lang Steven P, Mell Joshua, Ehrlich Garth D, Taube Joseph H, Greathouse K Leigh
Department of Biology, Baylor University, Waco, USA.
Department of Chemistry & Biochemistry, Baylor University, Waco, USA.
bioRxiv. 2025 Jun 27:2025.06.25.661399. doi: 10.1101/2025.06.25.661399.
Alterations to the community structure and function of the microbiome are associated with changes to host physiology, including immune responses. However, the contribution of microbe-derived RNAs carried by outer membrane vesicles (OMVs) to host immune responses remain unclear. This study investigated the role of OMVs and OMV-associated small RNA (sRNA) species from pathogenic and commensal (ETBF and NTBF respectively) in eliciting different immune responses from intestinal epithelial cells. To distinguish the differences in the sRNA profiles of the two strains and their OMVs, RNA-seq, qRT-PCR, and northern blotting were conducted to identify enrichment of discrete sRNA species in OMVs, which were also differentially expressed between the two strains. Specifically, both coding and non-coding RNAs were enriched in OMVs from NTBF and ETBF, with BF9343_RS22680 and BF9343_RS17870 being significantly enriched in ETBF OMVs compared to NTBF. To understand the effects of OMVs on pattern recognition receptors, reporter cells of Toll-like receptor (TLR) activation were treated with OMVs, demonstrating activation of TLRs 2, 3, and 7. Treatment of Caco-2 and HT29-MTX cells with OMVs demonstrated increased expression of IL-8. Surprisingly, we discovered that degradation of RNase-accessible RNAs within ETBF OMVs, but not NTBF OMVs, resulted in vesicles with enhanced capacity to stimulate IL-8 expression, indicating that these extravesicular RNAs exert an immunosuppressive effect. This suggests a dual role for OMV-associated RNAs in modulating host immune responses, with implications for both bacterial pathogenesis and therapeutic applications.
微生物群落结构和功能的改变与宿主生理变化相关,包括免疫反应。然而,外膜囊泡(OMV)携带的微生物衍生RNA对宿主免疫反应的贡献仍不清楚。本研究调查了来自致病性和共生性(分别为ETBF和NTBF)的OMV及其相关小RNA(sRNA)在引发肠上皮细胞不同免疫反应中的作用。为了区分两种菌株及其OMV的sRNA谱差异,进行了RNA测序、qRT-PCR和Northern印迹分析,以鉴定OMV中离散sRNA种类的富集情况,这两种菌株之间也存在差异表达。具体而言,编码和非编码RNA在NTBF和ETBF的OMV中均有富集,与NTBF相比,BF9343_RS22680和BF9343_RS17870在ETBF的OMV中显著富集。为了了解OMV对模式识别受体的影响,用OMV处理Toll样受体(TLR)激活的报告细胞,结果显示TLR 2、3和7被激活。用OMV处理Caco-2和HT29-MTX细胞后,IL-8的表达增加。令人惊讶的是,我们发现ETBF的OMV内可被核糖核酸酶作用的RNA降解,但NTBF的OMV则不然,这导致囊泡刺激IL-8表达的能力增强,表明这些囊泡外RNA发挥了免疫抑制作用。这表明OMV相关RNA在调节宿主免疫反应中具有双重作用,对细菌发病机制和治疗应用都有影响。