Mientrung Institute for Scientific Research, Vietnam National Museum of Nature, Vietnam Academy of Science and Technology (VAST), 321 Huynh Thuc Khang, Hue City 531600, Vietnam.
Laboratory of Microbiology, Wageningen University & Research, Stippeneng 4, 6708 WE Wageningen, The Netherlands.
Mar Drugs. 2022 Dec 29;21(1):29. doi: 10.3390/md21010029.
Recent reviews have reinforced sponge-associated bacteria as a valuable source of structurally diverse secondary metabolites with potent biological properties, which makes these microbial communities promising sources of new drug candidates. However, the overall diversity of secondary metabolite biosynthetic potential present in bacteria is difficult to access due to the fact that the majority of bacteria are not readily cultured in the laboratory. Thus, use of cultivation-independent approaches may allow accessing "silent" and "cryptic" secondary metabolite biosynthetic gene clusters present in bacteria that cannot yet be cultured. In the present study, we investigated the diversity of secondary metabolite biosynthetic gene clusters (BGCs) in metagenomes of bacterial communities associated with three sponge species: , , and sp. The results reveal that the three metagenomes contain a high number of predicted BGCs, ranging from 282 to 463 BGCs per metagenome. The types of BGCs were diverse and represented 12 different cluster types. Clusters predicted to encode fatty acid synthases and polyketide synthases (PKS) were the most dominant BGC types, followed by clusters encoding synthesis of terpenes and bacteriocins. Based on BGC sequence similarity analysis, 363 gene cluster families (GCFs) were identified. Interestingly, no GCFs were assigned to pathways responsible for the production of known compounds, implying that the clusters detected might be responsible for production of several novel compounds. The KS gene sequences from PKS clusters were used to predict the taxonomic origin of the clusters involved. The KS sequences were related to 12 bacterial phyla with , , and as the most predominant. At the genus level, the KSs were most related to those found in the genera , , , and . Phylogenetic analysis of KS sequences resulted in detection of two known 'sponge-specific' BGCs, i.e., and as well as a new 'sponge-specific' cluster related to fatty acid synthesis in the phylum Poribacteria and composed only by KS sequences of the three sponge-associated bacterial communities assessed here.
最近的评论强调了海绵相关细菌是具有潜在生物活性的结构多样的次生代谢产物的有价值来源,这使得这些微生物群落成为新药物候选物的有前途的来源。然而,由于大多数细菌在实验室中不易培养,因此很难获得存在于细菌中的次生代谢产物生物合成潜力的整体多样性。因此,使用非培养方法可能可以访问目前无法培养的细菌中存在的“沉默”和“隐藏”次生代谢产物生物合成基因簇。在本研究中,我们调查了与三种海绵物种(,和)相关的细菌群落的宏基因组中次生代谢产物生物合成基因簇(BGCs)的多样性。结果表明,这三个宏基因组包含大量预测的 BGCs,每个宏基因组的 BGC 数量范围为 282 至 463 个。BGC 的类型多种多样,代表了 12 种不同的簇类型。预测编码脂肪酸合酶和聚酮合酶(PKS)的簇是最主要的 BGC 类型,其次是编码萜类和细菌素合成的簇。基于 BGC 序列相似性分析,鉴定出 363 个基因簇家族(GCFs)。有趣的是,没有 GCF 被分配到负责产生已知化合物的途径,这意味着检测到的簇可能负责产生几种新化合物。从 PKS 簇的 KS 基因序列预测了参与的簇的分类学起源。KS 序列与 12 个细菌门有关,其中门和门最为突出。在属水平上,KSs 与属,属,属和属中发现的最相关。KS 序列的系统发育分析导致检测到两个已知的“海绵特异性” BGC,即和以及与门 Poribacteria 中的脂肪酸合成有关的新的“海绵特异性”簇,仅由这里评估的三个海绵相关细菌群落的 KS 序列组成。