Back Catherine R, Stennett Henry L, Williams Sam E, Wang Luoyi, Ojeda Gomez Jorge, Abdulle Omar M, Duffy Thomas, Neal Christopher, Mantell Judith, Jepson Mark A, Hendry Katharine R, Powell David, Stach James E M, Essex-Lopresti Angela E, Willis Christine L, Curnow Paul, Race Paul R
School of Biochemistry, University of Bristol, University Walk, Bristol BS8 1TD, UK.
School of Chemistry, University of Bristol, Cantock's Close, Bristol BS8 1TS, UK.
Mar Drugs. 2021 Feb 11;19(2):105. doi: 10.3390/md19020105.
To tackle the growing problem of antibiotic resistance, it is essential to identify new bioactive compounds that are effective against resistant microbes and safe to use. Natural products and their derivatives are, and will continue to be, an important source of these molecules. Sea sponges harbour a diverse microbiome that co-exists with the sponge, and these bacterial communities produce a rich array of bioactive metabolites for protection and resource competition. For these reasons, the sponge microbiota constitutes a potential source of clinically relevant natural products. To date, efforts in bioprospecting for these compounds have focused predominantly on sponge specimens isolated from shallow water, with much still to be learned about samples from the deep sea. Here we report the isolation of a new strain, designated 28ISP2-46, recovered from the microbiome of a mid-Atlantic deep-sea sponge. Whole-genome sequencing reveals the capacity of this bacterium to produce a diverse array of natural products, including kosinostatin and isoquinocycline B, which exhibit both antibiotic and antitumour properties. Both compounds were isolated from 28ISP2-46 fermentation broths and were found to be effective against a plethora of multidrug-resistant clinical isolates. This study suggests that the marine production of isoquinocyclines may be more widespread than previously supposed and demonstrates the value of targeting the deep-sea sponge microbiome as a source of novel microbial life with exploitable biosynthetic potential.
为应对日益严重的抗生素耐药性问题,识别对耐药微生物有效且使用安全的新型生物活性化合物至关重要。天然产物及其衍生物一直是并将继续是这些分子的重要来源。海绵动物拥有与海绵共生的多样微生物群落,这些细菌群落产生一系列丰富的生物活性代谢产物用于保护自身和资源竞争。基于这些原因,海绵微生物群构成了临床相关天然产物的潜在来源。迄今为止,对这些化合物的生物勘探工作主要集中在从浅海分离的海绵标本上,对于深海样本仍有许多有待了解之处。在此,我们报告从大西洋中部深海海绵的微生物群中分离出一种新菌株,命名为28ISP2 - 46。全基因组测序揭示了这种细菌产生多种天然产物的能力,包括具有抗生素和抗肿瘤特性的科斯他汀和异喹啉环素B。这两种化合物均从28ISP2 - 46发酵液中分离得到,并被发现对大量多重耐药临床分离株有效。这项研究表明,海洋中异喹啉环素的产生可能比之前认为的更为普遍,并证明了将深海海绵微生物群作为具有可开发生物合成潜力的新型微生物来源进行靶向研究的价值。