首页> 外文期刊>Frontiers in Microbiology >The Role of Complement in Cnidarian-Dinoflagellate Symbiosis and Immune Challenge in the Sea Anemone Aiptasia pallida
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The Role of Complement in Cnidarian-Dinoflagellate Symbiosis and Immune Challenge in the Sea Anemone Aiptasia pallida

机译:补充在海洋气藻糖中的CNIDARIAR-DINOFLAGLEATE和免疫攻击中的作用<斜体> AIPTASIA pallida

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The complement system is an innate immune pathway that in vertebrates, is responsible for initial recognition and ultimately phagocytosis and destruction of microbes. Several complement molecules including C3, Factor B, and mannose binding lectin associated serine proteases (MASP) have been characterized in invertebrates and while most studies have focused on their conserved role in defense against pathogens, little is known about their role in managing beneficial microbes. The purpose of this study was to (1) characterize complement pathway genes in the symbiotic sea anemone Aiptasia pallida , (2) investigate the evolution of complement genes in invertebrates, and (3) examine the potential dual role of complement genes Factor B and MASP in the onset and maintenance of cnidarian-dinoflagellate symbiosis and immune challenge using qPCR based studies. The results demonstrate that A. pallida has multiple Factor B genes (Ap_Bf-1, Ap_Bf-2a, and Ap_Bf-2b) and one MASP gene (Ap_MASP). Phylogenetic analysis indicates that the evolutionary history of complement genes is complex, and there have been many gene duplications or gene loss events, even within members of the same phylum. Gene expression analyses revealed a potential role for complement in both onset and maintenance of cnidarian-dinoflagellate symbiosis and immune challenge. Specifically, Ap_Bf-1 and Ap_MASP are significantly upregulated in the light at the onset of symbiosis and in response to challenge with the pathogen Serratia marcescens suggesting that they play a role in the initial recognition of both beneficial and harmful microbes. Ap_Bf-2b in contrast, was generally downregulated during the onset and maintenance of symbiosis and in response to challenge with S. marcescens . Therefore, the exact role of Ap_Bf-2b in response to microbes remains unclear, but the results suggest that the presence of microbes leads to repressed expression. Together, these results indicate functional divergence between Ap_Bf-1 and Ap_Bf-2b, and that Ap_Bf-1 and Ap_MASP may be functioning together in an ancestral hybrid of the lectin and alternative complement pathways. Overall, this study provides information on the role of the complement system in a basal metazoan and its role in host-microbe interactions.
机译:补体系统是一种在脊椎动物的先天免疫途径,负责初始识别和最终吞噬作用和微生物的破坏。包括C3,因子B和甘露糖结合凝集素相关的丝氨酸蛋白酶(MASP)的几种补体分子已经表征在无脊椎动物中,而大多数研究则重点关注其在防御病原体中的保守作用,而是关于它们在管理有益微生物中的作用。本研究的目的是(1)表征共同海洋海葵Aiptasia pallida中的补体途径基因,(2)调查亲脊椎动物中补体基因的演变,(3)检查补体基因因子B和MASP的潜在双重作用在基于QPCR的研究中,CNIDARIAR-DINOFLAGELATE共生和免疫攻击的发作和维持。结果表明,A.Pallida具有多个因子B基因(AP_BF-1,AP_BF-2A和AP_BF-2B)和一种麦克麻基因(AP_MASP)。系统发育分析表明,补体基因的进化史是复杂的,并且甚至在同一场系中的成员内已经存在许多基因重复或基因损失事件。基因表达分析揭示了Cnidarian-Dinoflagate共生和免疫攻击的起始和维持的潜在作用。具体而言,AP_BF-1和AP_MASP在共生发作的光明中显着上调,并且响应于病原体Serratia Marcescens的挑战表明它们在初始识别中发挥了有益和有害的微生物的作用。相比之下,AP_BF-2B通常在发作和维持共生期间和维持和攻击S. Marcescens的挑战期间。因此,AP_BF-2B响应微生物的确切作用仍然尚不清楚,但结果表明微生物的存在导致压抑的表达。这些结果在一起表示AP_BF-1和AP_BF-2B之间的功能性分歧,并且该AP_BF-1和AP_MASP可以在凝集素和替代补体途径的祖先杂种中运作。总体而言,本研究提供了有关补体系统在基础美唑烷中的作用及其在宿主微生物相互作用中的作用的信息。

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