Chiu Karen K, Bashir Shah Tauseef, Abdel-Hamid Ahmed M, Clark Lindsay V, Laws Mary J, Cann Isaac, Nowak Romana A, Flaws Jodi A
Division of Nutritional Sciences, College of Agricultural, Consumer and Environmental Sciences, University of Illinois, Urbana, IL 61801, USA.
Department of Comparative Biosciences, College of Veterinary Medicine, University of Illinois, Urbana, IL 61802, USA.
Toxics. 2022 Feb 6;10(2):75. doi: 10.3390/toxics10020075.
Di-isononyl phthalate (DiNP) is a plasticizer used to impart flexibility or stability in a variety of products including polyvinyl chloride, cable coatings, artificial leather, and footwear. Previous studies have examined the impact of DiNP on gut integrity and the colonic immune microenvironment, but this study further expands the research by examining whether DiNP exposure alters the colonic microbiota and various immune markers. Previous studies have also revealed that environmental microbes degrade various phthalates, but no studies have examined whether anaerobic gut bacteria can degrade DiNP. Thus, this study tested the hypothesis that DiNP exposure alters the gut microbiota and immune-related factors, and that anaerobic bacteria in the gut can utilize DiNP as the sole carbon source. To test this hypothesis, adult female mice were orally dosed with corn oil or various doses of DiNP for 10-14 consecutive days. After the treatment period, mice were euthanized during diestrus. Colonic contents were collected for full-length 16S rRNA gene sequencing to identify the bacteria in the colon contents. Sanger sequencing of the 16S rRNA gene was used to identify bacteria that were able to grow in minimal media with DiNP as the sole carbon source. Colon tissues were collected for immunohistochemistry of immune(-related) factors. An environmentally relevant dose of DiNP (200 µg/kg) significantly increased a taxon and decreased compared to the control. Collectively, minimal changes in the colonic microbiota were observed as indicated by non-significant beta-diversities between DiNP treatments and control. Furthermore, three strains of anaerobic bacteria derived from the colon were identified to use DiNP as the sole carbon source. Interestingly, DiNP exposure did not alter protein levels of interleukin-6, tumor necrosis factor alpha, claudin-1, and mucin-1 compared to the control. Collectively, these findings show that DiNP exposure alters the gut microbiota and that the gut contains DiNP-degrading microbes.
邻苯二甲酸二异壬酯(DiNP)是一种增塑剂,用于赋予包括聚氯乙烯、电缆涂层、人造皮革和鞋类在内的各种产品柔韧性或稳定性。以往的研究探讨了DiNP对肠道完整性和结肠免疫微环境的影响,但本研究通过研究DiNP暴露是否会改变结肠微生物群和各种免疫标志物,进一步拓展了该研究。以往的研究还表明,环境微生物会降解各种邻苯二甲酸盐,但尚无研究探讨肠道厌氧菌是否能降解DiNP。因此,本研究检验了以下假设:DiNP暴露会改变肠道微生物群和免疫相关因子,且肠道中的厌氧菌可将DiNP用作唯一碳源。为验证这一假设,成年雌性小鼠连续10 - 14天经口给予玉米油或不同剂量的DiNP。治疗期结束后,在间情期对小鼠实施安乐死。收集结肠内容物用于全长16S rRNA基因测序,以鉴定结肠内容物中的细菌。利用16S rRNA基因的桑格测序法鉴定能够在以DiNP作为唯一碳源的基本培养基中生长的细菌。收集结肠组织用于免疫(相关)因子的免疫组织化学检测。与对照组相比,环境相关剂量的DiNP(200 µg/kg)显著增加了一个分类群并减少了另一个分类群。总体而言,DiNP处理组与对照组之间的β-多样性无显著差异,表明结肠微生物群的变化极小。此外,鉴定出三株源自结肠的厌氧菌可将DiNP用作唯一碳源。有趣的是,与对照组相比,DiNP暴露并未改变白细胞介素-6、肿瘤坏死因子α、闭合蛋白-1和粘蛋白-1的蛋白质水平。总体而言,这些发现表明DiNP暴露会改变肠道微生物群,且肠道中含有可降解DiNP的微生物。