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蠕虫抗菌肽。

Worms' Antimicrobial Peptides.

机构信息

Univ. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019 - UMR 8204 - CIIL - Center for Infection and Immunity of Lille, F-59000 Lille, France.

Univ. Lille, CNRS, UMR 8198 - Evo-Eco-Paleo, F-59000 Lille, France.

出版信息

Mar Drugs. 2019 Aug 29;17(9):512. doi: 10.3390/md17090512.

DOI:10.3390/md17090512
PMID:31470685
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6780910/
Abstract

Antimicrobial peptides (AMPs) are natural antibiotics produced by all living organisms. In metazoans, they act as host defense factors by eliminating microbial pathogens. But they also help to select the colonizing bacterial symbionts while coping with specific environmental challenges. Although many AMPs share common structural characteristics, for example having an overall size between 10-100 amino acids, a net positive charge, a γ-core motif, or a high content of cysteines, they greatly differ in coding sequences as a consequence of multiple parallel evolution in the face of pathogens. The majority of AMPs is specific of certain taxa or even typifying species. This is especially the case of annelids (ringed worms). Even in regions with extreme environmental conditions (polar, hydrothermal, abyssal, polluted, etc.), worms have colonized all habitats on Earth and dominated in biomass most of them while co-occurring with a large number and variety of bacteria. This review surveys the different structures and functions of AMPs that have been so far encountered in annelids and nematodes. It highlights the wide diversity of AMP primary structures and their originality that presumably mimics the highly diverse life styles and ecology of worms. From the unique system that represents marine annelids, we have studied the effect of abiotic pressures on the selection of AMPs and demonstrated the promising sources of antibiotics that they could constitute.

摘要

抗菌肽(AMPs)是所有生物体产生的天然抗生素。在后生动物中,它们通过消除微生物病原体作为宿主防御因子发挥作用。但它们也有助于在应对特定环境挑战的同时选择定植的细菌共生体。尽管许多 AMP 具有共同的结构特征,例如具有 10-100 个氨基酸之间的总体大小、净正电荷、γ-核心基序或高半胱氨酸含量,但由于面对病原体的多次平行进化,它们在编码序列上存在很大差异。大多数 AMP 是特定于某些分类群的,甚至是代表性物种的。环节动物(环节蠕虫)尤其如此。即使在环境条件极端的地区(极地、热液、深海、污染等),蠕虫也已经殖民了地球上的所有栖息地,并且在与大量和多种细菌共存的情况下,它们在生物量中占主导地位。本综述调查了迄今为止在环节动物和线虫中遇到的 AMP 的不同结构和功能。它强调了 AMP 一级结构的广泛多样性及其独特性,这可能模仿了蠕虫高度多样化的生活方式和生态。从代表海洋环节动物的独特系统出发,我们研究了非生物压力对 AMP 选择的影响,并证明了它们可能构成的有前途的抗生素来源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/021d/6780910/1dc774e81851/marinedrugs-17-00512-g014.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/021d/6780910/f977aea9c380/marinedrugs-17-00512-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/021d/6780910/2f969b4de3fd/marinedrugs-17-00512-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/021d/6780910/2533d4a35fc9/marinedrugs-17-00512-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/021d/6780910/ac51c985872d/marinedrugs-17-00512-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/021d/6780910/5f97c82f359e/marinedrugs-17-00512-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/021d/6780910/7736d4f2d7d5/marinedrugs-17-00512-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/021d/6780910/4b2d9d59e901/marinedrugs-17-00512-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/021d/6780910/1dc774e81851/marinedrugs-17-00512-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/021d/6780910/c6acf97efa6f/marinedrugs-17-00512-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/021d/6780910/5baee1ffa3bb/marinedrugs-17-00512-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/021d/6780910/c8f16c5de44f/marinedrugs-17-00512-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/021d/6780910/41538bad5417/marinedrugs-17-00512-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/021d/6780910/b22c195c2ecb/marinedrugs-17-00512-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/021d/6780910/a96fe142e76f/marinedrugs-17-00512-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/021d/6780910/f977aea9c380/marinedrugs-17-00512-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/021d/6780910/2f969b4de3fd/marinedrugs-17-00512-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/021d/6780910/2533d4a35fc9/marinedrugs-17-00512-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/021d/6780910/ac51c985872d/marinedrugs-17-00512-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/021d/6780910/5f97c82f359e/marinedrugs-17-00512-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/021d/6780910/7736d4f2d7d5/marinedrugs-17-00512-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/021d/6780910/4b2d9d59e901/marinedrugs-17-00512-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/021d/6780910/1dc774e81851/marinedrugs-17-00512-g014.jpg

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