首页> 外文期刊>Journal of innate immunity >Thioester-Containing Protein-4 Regulates the Drosophila Immune Signaling and Function against the Pathogen Photorhabdus
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Thioester-Containing Protein-4 Regulates the Drosophila Immune Signaling and Function against the Pathogen Photorhabdus

机译:含硫酯的蛋白4调节果蝇免疫信号和功能对抗病原体Photorhabdus。

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Despite important progress in identifying the molecules that participate in the immune response of Drosophila melanogaster to microbial infections, the involvement of thioester-containing proteins (TEPs) in the antibacterial immunity of the fly is not fully clarified. Previous studies mostly focused on identifying the function of TEP2, TEP3 and TEP6 molecules in the D. melanogaster immune system. Here, we investigated the role of TEP4 in the regulation and function of D. melanogaster host defense against 2 virulent pathogens from the genus Photorhabdus , i.e. the insect pathogenic bacterium Photorhabdus luminescens and the emerging human pathogen P. asymbiotica . We demonstrate that Tep4 is strongly upregulated in adult flies following the injection of Photorhabdus bacteria. We also show that Tep4 loss-of-function mutants are resistant to P. luminescens but not to P. asymbiotica infection . In addition, we find that inactivation of Tep4 results in the upregulation of the Toll and Imd immune pathways, and the downregulation of the Jak/Stat and Jnk pathways upon Photorhabdus infection. We document that loss of Tep4 promotes melanization and phenoloxidase activity in the mutant flies infected with Photorhabdus . Together, these findings generate novel insights into the immune role of TEP4 as a regulator and effector of the D. melanogaster antibacterial immune response.
机译:尽管在鉴定参与果蝇对微生物感染的免疫反应的分子方面取得了重要进展,但尚不完全清楚含硫酯的蛋白质(TEP)与果蝇的抗菌免疫有关。先前的研究主要集中在鉴定黑腹果蝇免疫系统中TEP2,TEP3和TEP6分子的功能。在这里,我们调查了TEP4在D. melanogaster宿主防御中对来自Photorhabdus属的2种强力病原体(即昆虫致病性细菌Photorhabdus luminescens和新兴的人类病原体P.asymbiotica)的调节和功能的作用。我们证明,在注射Photorhabdus细菌后,成年果蝇中Tep4强烈上调。我们还显示,Tep4功能丧失的突变体对P. luminescens有抵抗力,但对P. asymbiotica感染没有抵抗力。此外,我们发现灭活Tep4导致Toll和Imd免疫途径的上调,以及Photorhabdus感染后Jak / Stat和Jnk途径的下调。我们证明,Tep4的缺失促进了感染Photorhabdus的突变苍蝇的黑色素化和酚氧化酶活性。总之,这些发现为TEP4作为D. melanogaster抗菌免疫反应的调节剂和效应物的免疫作用提供了新的见解。

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