秃鹫作为测试鸟类饮食专业化分子适应的模型

IF 1.6 2区 生物学 Q1 ORNITHOLOGY
Yanhong Chen , Ling Xiang , Pan Chen , Huabin Zhao
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引用次数: 0

摘要

秃鹫是现存脊椎动物中唯一的专性食腐动物。它们通过清除尸体在生态系统中提供宝贵的生态服务,从而防止其他食腐动物种群的增长和病原体的传播。此外,它们特殊的饮食使它们暴露于各种致命的病原体中,这使它们成为研究分子适应所需的潜在候选者,以生存这种极端特殊的食腐习惯。本文综述了新旧大陆秃鹫的形态特征和行为习性、起源和系统发育以及对食腐动物的分子适应。这两群秃鹫有着相似的外表,表明了趋同进化。秃鹫的感觉器官经历了不同程度的专业化;旧大陆的秃鹫依靠视觉,而新大陆的秃鹫依靠嗅觉和视觉。综合化石记录和分子数据表明,秃鹫是独立进化的,具有不同的系统发育位置。我们还探讨了它们在面部和肠道微生物群、胃酸分泌和免疫方面对清除的适应性。与面部微生物组相比,肠道微生物组的多样性较低,以梭菌属和梭菌属为主。噬菌体和以死亡细菌和原生动物为食的单一无脊椎动物Adineta vaga存在于肠道中,这表明可能存在另一种防御机制。一些参与胃酸分泌的基因(包括ATP4B、SLC26A7和SST)和免疫(包括BCL6、STING和TLRs)进行正选择,可能在消除侵袭性病原体和启动先天免疫应答中发挥重要作用。综上所述,本文综述了秃鹫的研究现状,并强调了秃鹫作为探索鸟类饮食专门化分子适应的模型。为研究秃鹫食腐的遗传机制提供了理论依据,并有助于秃鹫保护策略的制定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Vultures as a model for testing molecular adaptations of dietary specialization in birds

Vultures are the only obligate scavengers among extant vertebrates. They provide valuable ecological services in ecosystems through removing carcasses, thus preventing the growth of other scavenger populations and the spread of pathogens. Moreover, their specific diets expose them to various deadly pathogens, which makes them potential candidates for studying molecular adaptations required to survive this extremely specialized scavenging habit. In this review, we summarize the morphological characteristics and behavioral habits, origin and phylogeny, and molecular adaptations to scavenging in both Old and New World vultures. The two groups of vultures share a similar appearance, indicative of convergent evolution. Vultures have experienced different degrees of specialization in their sensory organs; Old World vultures depend on sight, while New World ones depend on both smell and sight. Combined fossil records and molecular data suggest that vultures evolved independently, with distinct phylogenetic positions. We also explored their adaptation to scavenging in facial and intestinal microbiomes, gastric acid secretion and immunity. Compared with the facial microbiome, the intestinal microbiome had a lower diversity, dominated by Fusobacteria and Clostridia. The phages and single invertebrate species Adineta vaga, which feeds on dead bacteria and protozoa, present in the gut suggest a possible alternative defense mechanism. Several genes involved in gastric acidic secretion (including ATP4B, SLC26A7 and SST) and immunity (including BCL6, STING, and TLRs) undergoing positive selection likely have essential roles in eliminating invasive pathogens and initiating an innate immune response. Taken together, this review presents the current research status of vultures and highlights the use of vultures as a model for exploring molecular adaptations of dietary specialization in birds. It also provides a theoretical basis for the study of the genetic mechanisms of vultures to scavenging, and contributes to the formulation of vulture conservation strategies.

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来源期刊
Avian Research
Avian Research ORNITHOLOGY-
CiteScore
2.90
自引率
16.70%
发文量
456
审稿时长
46 days
期刊介绍: Avian Research is an open access, peer-reviewed journal publishing high quality research and review articles on all aspects of ornithology from all over the world. It aims to report the latest and most significant progress in ornithology and to encourage exchange of ideas among international ornithologists. As an open access journal, Avian Research provides a unique opportunity to publish high quality contents that will be internationally accessible to any reader at no cost.
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