Institute of Environmental Sciences (CML), Environmental Biology, Leiden University, Leiden, The Netherlands.
Institute of Biology Leiden (IBL), Animal Sciences, Leiden University, Leiden, The Netherlands.
Ecotoxicol Environ Saf. 2022 Jun 1;237:113522. doi: 10.1016/j.ecoenv.2022.113522. Epub 2022 Apr 19.
Many host-microbiota interactions depend on the recognition of microbial constituents by toll-like receptors of the host. The impacts of these interactions on host health can shape the hosts response to environmental pollutants such as nanomaterials. Here, we assess the role of toll-like receptor 2 (TLR2) signaling in the protective effects of colonizing microbiota against silver nanoparticle (nAg) toxicity to zebrafish larvae. Zebrafish larvae were exposed to nAg for two days, from 3 to 5 days post-fertilization. Using an il1ß-reporter line, we first characterized the accumulation and particle-specific inflammatory effects of nAg in the total body and intestinal tissues of the larvae. This showed that silver gradually accumulated in both the total body and intestinal tissues, yet specifically caused particle-specific inflammation on the skin of larvae. Subsequently, we assessed the effects of microbiota-dependent TLR2 signaling on nAg toxicity. This was done by comparing the sensitivity of loss-of-function zebrafish mutants for TLR2, and each of the TLR2-adaptor proteins MyD88 and TIRAP (Mal), under germ-free and microbially-colonized conditions. Irrespective of their genotype, microbially-colonized larvae were less sensitive to nAg than their germ-free siblings, supporting the previously identified protective effect of microbiota against nAg toxicity. Under germ-free conditions, tlr2, myd88 and tirap mutants were equally sensitive to nAg as their wildtype siblings. However, when colonized by microbiota, tlr2 and tirap mutants were more sensitive to nAg than their wildtype siblings. The sensitivity of microbially-colonized myd88 mutants did not differ significantly from that of wildtype siblings. These results indicate that the protective effect of colonizing microbiota against nAg-toxicity to zebrafish larvae involves TIRAP-dependent TLR2 signaling. Overall, this supports the conclusion that host-microbiota interactions affect nanomaterial toxicity to zebrafish larvae.
许多宿主-微生物相互作用依赖于宿主 Toll 样受体对微生物成分的识别。这些相互作用对宿主健康的影响可以塑造宿主对环境污染物(如纳米材料)的反应。在这里,我们评估了 Toll 样受体 2 (TLR2) 信号在定植菌群对斑马鱼幼虫银纳米颗粒 (nAg) 毒性的保护作用中的作用。斑马鱼幼虫在受精后 3 至 5 天进行了为期两天的 nAg 暴露。使用 il1ß 报告品系,我们首先描述了 nAg 在幼虫整体和肠道组织中的积累和颗粒特异性炎症效应。结果表明,银逐渐在整体和肠道组织中积累,但特异性地引起幼虫皮肤颗粒特异性炎症。随后,我们评估了 TLR2 依赖性微生物群信号对 nAg 毒性的影响。这是通过比较 TLR2 功能丧失斑马鱼突变体和 TLR2 衔接蛋白 MyD88 和 TIRAP (Mal) 的每个突变体在无菌和微生物定植条件下的敏感性来实现的。无论它们的基因型如何,微生物定植的幼虫对 nAg 的敏感性都低于无菌的同窝幼虫,这支持了先前确定的微生物群对 nAg 毒性的保护作用。在无菌条件下,tlr2、myd88 和 tirap 突变体对 nAg 的敏感性与野生型同窝幼虫相同。然而,当被微生物定植时,tlr2 和 tirap 突变体对 nAg 的敏感性高于野生型同窝幼虫。微生物定植 myd88 突变体的敏感性与野生型同窝幼虫没有显著差异。这些结果表明,定植菌群对斑马鱼幼虫 nAg 毒性的保护作用涉及 TIRAP 依赖性 TLR2 信号。总的来说,这支持了宿主-微生物相互作用影响纳米材料对斑马鱼幼虫毒性的结论。