首页> 外文期刊>Frontiers in Immunology >Interleukin-17A/F1 Deficiency Reduces Antimicrobial Gene Expression and Contributes to Microbiome Alterations in Intestines of Japanese medaka ( Oryzias latipes)
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Interleukin-17A/F1 Deficiency Reduces Antimicrobial Gene Expression and Contributes to Microbiome Alterations in Intestines of Japanese medaka ( Oryzias latipes)

机译:白细胞介素-17a / f1缺乏减少了抗微生物基因表达,有助于日本Medaka的肠道微生物组改变(<斜斜体> oryzias laidipes

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In mammals, interleukin (IL)-17A and F are hallmark inflammatory cytokines that play key roles in protection against infection and intestinal mucosal immunity. In the gastrointestinal tract (GI), the induction of antimicrobial peptide (AMP) production via Paneth cells is a fundamental role of IL-17A and F in maintaining homeostasis of the GI microbiome and health. Although mammalian IL-17A and F homologs (referred to as IL-17A/F1-3) have been identified in several fish species, their function in the intestine is poorly understood. Additionally, the fish intestine lacks Paneth cells, and its GI structure is very different from that of mammals. Therefore, the GI microbiome modulatory mechanism via IL-17A/F genes has not been fully elucidated. In this study, Japanese medaka ( Oryzias latipes ) were used as a teleost model, and IL-17A/F1-knockout (IL-17A/F1-KO) medaka were established using the CRISPR/Cas9 genome editing technique. Furthermore, two IL-17A/F1-deficient medaka strains were generated, including one strain containing a 7-bp deletion (-7) and another with an 11-bp addition (+11). After establishing F2 homozygous KO medaka, transcriptome analysis (RNA-seq) was conducted to elucidate IL-17A/F1-dependent gene induction in the intestine. Results of RNA-seq and real-time PCR (qPCR) demonstrated down-regulation of immune-related genes, including interleukin-1β ( IL-1 β), complement 1q subunit C ( C1qc ), transferrin a ( Tfa ), and G-type lysozyme ( LyzG ), in IL-17A/F1-KO medaka. Interestingly, protein and lipid digestive enzyme genes, including phospholipase A2, group IB ( pla2g1b ), and elastase-1-like ( CELA1 ), were also downregulated in the intestines of IL-17A/F1-KO medaka. Furthermore, to reveal the influence of these downregulated genes on the gut microbiome in IL-17A/F1-KO, 16S rRNA-based metagenomic sequencing analysis was conducted to analyze the microbiome constitution. Under a non-exposed state, the intestinal microbiome of IL-17A/F1-KO medaka differed at the phylum level from wild-type, with significantly higher levels of Verrucomicrobia and Planctomycetes. Additionally, at the operational taxonomic unit (OTU) level of the human and fish pathogens, the Enterobacteriaceae Plesiomonas shigelloides was the dominant species in IL-17A/F1-KO medaka. These findings suggest that IL-17A/F1 is involved in the maintenance of a healthy gut microbiome.
机译:在哺乳动物中,白细胞介素(IL)-17A和F是标志性炎症细胞因子,其在保护免受感染和肠粘膜抗扰度方面发挥关键作用。在胃肠道(GI)中,通过PANETH细胞诱导抗微生物肽(AMP)产生是IL-17A和F维持GI微生物组和健康的稳态的基本作用。虽然在几种鱼类中鉴定了哺乳动物IL-17A和F同源物(称为IL-17A / F1-3),但它们在肠中的功能较差地理解。另外,鱼肠缺乏群集细胞,其GI结构与哺乳动物的GI结构非常不同。因此,通过IL-17A / F基因的GI微生物组调节机制尚未得到完全阐明。在这项研究中,日本Medaka(Oryzias Lipipes)用作电源模型,使用CRISPR / CAS9基因组编辑技术建立了IL-17A / F1敲除(IL-17A / F1-KO)Medaka。此外,产生了两个IL-17A / F1缺陷的MedaKa菌株,包括含有7-BP缺失(-7)的一种菌株,另一种具有11-BP加法(+11)。在建立F2纯合KO medaka之后,进行转录组分析(RNA-SEQ)以阐明肠内的IL-17A / F1依赖性基因诱导。 RNA-SEQ和实时PCR(QPCR)的结果证明了免疫相关基因的下调,包括白细胞介素-1β(IL-1β),补体1Q亚基C(C1QC),转移素A(TFA)和G. -Type溶菌酶(Lyzg),IL-17A / F1-KO Medaka。有趣的是,蛋白质和脂质消化酶基因,包括磷脂酶A2,IB(PLA2G1B)和弹性蛋白酶-1状(CELA1)也在IL-17A / F1-KO MEDAKA的肠中下调。此外,为了揭示在IL-17A / F1-KO中的肠道微生物组上的这些下调基因的影响,进行了16S的基于RRNA的偏霉菌测序分析,分析了微生物组结构。在非暴露的状态下,IL-17A / F1-KO MEDAKA的肠道微生物组在野生型的场平均水平上不同,疣状病症和Planctomycetes显着较高。另外,在人类和鱼类病原体的运营分类单位(OTU)水平,肠杆菌菌Plesiomonashoides是IL-17A / F1-KO Medaka中的主要物种。这些发现表明IL-17A / F1参与了健康的肠道微生物组的维持。

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