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生物活性筛选和基因组分析揭示深海鱼微生物组分离物是新型抗菌药物的来源。

Bioactivity Screening and Genomic Analysis Reveals Deep-Sea Fish Microbiome Isolates as Sources of Novel Antimicrobials.

机构信息

Department of Microbiology, University College Cork, T12 K8AF Cork, Ireland.

APC Microbiome Ireland, T12 K8AF Cork, Ireland.

出版信息

Mar Drugs. 2023 Aug 7;21(8):444. doi: 10.3390/md21080444.

DOI:10.3390/md21080444
PMID:37623725
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10456417/
Abstract

With the increase in antimicrobial resistance and the subsequent demand for novel therapeutics, the deep-sea fish microbiome can be a relatively untapped source of antimicrobials, including bacteriocins. Previously, bacterial isolates were recovered from the gut of deep-sea fish sampled from the Atlantic Ocean.In this study, we used in vitro methods to screen a subset of these isolates for antimicrobial activity, and subsequently mined genomic DNA from isolates of interest for bacteriocin and other antimicrobial metabolite genes. We observed antimicrobial activity against foodborne pathogens, including , , and . In total, 147 candidate biosynthetic gene clusters were identified in the genomic sequences, including 35 bacteriocin/RiPP-like clusters. Other bioactive metabolite genes detected included non-ribosomal peptide synthases (NRPS), polyketide synthases (PKS; Types 1 and 3), beta-lactones and terpenes. Moreover, four unique bacteriocin gene clusters were annotated and shown to encode novel peptides: a class IIc bacteriocin, two class IId bacteriocins and a class I lanthipeptide (LanM subgroup). Our dual in vitro and in silico approach allowed for a more comprehensive understanding of the bacteriocinogenic potential of these deep-sea isolates and an insight into the antimicrobial molecules that they may produce.

摘要

随着抗菌药物耐药性的增加以及对新型治疗方法的需求,深海鱼类微生物组可以成为抗菌药物(包括细菌素)的相对未开发来源。此前,从大西洋采集的深海鱼类肠道中分离出了细菌分离株。在这项研究中,我们使用体外方法筛选了这些分离株中的一部分,以检测其抗菌活性,然后从感兴趣的分离株中提取基因组 DNA,以寻找细菌素和其他抗菌代谢产物基因。我们观察到这些分离株对食源性病原体具有抗菌活性,包括 、 、 和 。在基因组序列中总共鉴定出 147 个候选生物合成基因簇,其中包括 35 个细菌素/RiPP 样簇。检测到的其他生物活性代谢产物基因包括非核糖体肽合成酶(NRPS)、聚酮合酶(PKS;类型 1 和 3)、β-内酰胺和萜类化合物。此外,还注释了四个独特的细菌素基因簇,并证明它们编码新型肽:一种 IIc 类细菌素、两种 IId 类细菌素和一种 I 类兰尼肽(LanM 亚群)。我们的体外和计算机结合的方法使我们更全面地了解了这些深海分离株的细菌素生成潜力,并深入了解了它们可能产生的抗菌分子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cea5/10456417/dd4e1b222b73/marinedrugs-21-00444-g011.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cea5/10456417/dd4e1b222b73/marinedrugs-21-00444-g011.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cea5/10456417/fd73f121ccde/marinedrugs-21-00444-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cea5/10456417/e73a8722b86d/marinedrugs-21-00444-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cea5/10456417/70987f6185b1/marinedrugs-21-00444-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cea5/10456417/a29bd3b2b8a0/marinedrugs-21-00444-g008.jpg
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