Sabino Yasmin Neves Vieira, de Araújo Katialaine Corrêa, de Assis Fábia Giovana do Val, Moreira Sofia Magalhães, Lopes Thaynara da Silva, Mendes Tiago Antônio de Oliveira, Huws Sharon Ann, Mantovani Hilário C
Departamento de Microbiologia, Universidade Federal de Viçosa, Viçosa, Brazil.
Departamento de Bioquímica e Biologia Molecular, Universidade Federal de Viçosa, Viçosa, Brazil.
Front Microbiol. 2020 Sep 11;11:576738. doi: 10.3389/fmicb.2020.576738. eCollection 2020.
Studies of rumen microbial ecology suggest that the capacity to produce antimicrobial peptides could be a useful trait in species competing for ecological niches in the ruminal ecosystem. However, little is known about the synthesis of lasso peptides by ruminal microorganisms. Here we analyzed the distribution and diversity of lasso peptide gene clusters in 425 bacterial genomes from the rumen ecosystem. Genome mining was performed using antiSMASH 5, BAGEL4, and a database of well-known precursor sequences. The genomic context of the biosynthetic clusters was investigated to identify putative genes and protein sequences from enzymes of the biosynthetic machinery were evaluated to identify conserved motifs. Metatranscriptome analysis evaluated the expression of the biosynthetic genes in the rumen microbiome. Several incomplete ( = 23) and complete ( = 11) putative lasso peptide clusters were detected in the genomes of ruminal bacteria. The complete gene clusters were exclusively found within the phylum , mainly (48%) in strains of the genus . The analysis of the genetic organization of complete putative lasso peptide clusters revealed the presence of co-occurring genes, including kinases (85%), transcriptional regulators (49%), and glycosyltransferases (36%). Moreover, a conserved pattern of cluster organization was detected between strains of the same genus/species. The maturation enzymes LasB, LasC, and LasD showed regions highly conserved, including the presence of a transglutaminase core in LasB, an asparagine synthetase domain in LasC, and an ABC-type transporter system in LasD. Phylogenetic trees of the essential biosynthetic proteins revealed that sequences split into monophyletic groups according to their shared single common ancestor. Metatranscriptome analyses indicated the expression of the lasso peptides biosynthetic genes within the active rumen microbiota. Overall, our screening allowed the discovery of novel biosynthetic gene clusters in the genomes of ruminal bacteria and revealed several strains with the genetic potential to synthesize lasso peptides, suggesting that the ruminal microbiota represents a potential source of these promising peptides.
瘤胃微生物生态学研究表明,产生抗菌肽的能力可能是瘤胃生态系统中竞争生态位的物种的一个有用特征。然而,关于瘤胃微生物合成套索肽的情况知之甚少。在这里,我们分析了瘤胃生态系统中425个细菌基因组中套索肽基因簇的分布和多样性。使用antiSMASH 5、BAGEL4和一个著名前体序列数据库进行基因组挖掘。研究了生物合成簇的基因组背景,以鉴定推定基因,并评估生物合成机制中酶的蛋白质序列以鉴定保守基序。宏转录组分析评估了瘤胃微生物群落中生物合成基因的表达。在瘤胃细菌基因组中检测到几个不完整(=23)和完整(=11)的推定套索肽簇。完整的基因簇仅在门内发现,主要(48%)在属的菌株中。对完整推定套索肽簇的遗传组织分析揭示了共现基因的存在,包括激酶(85%)、转录调节因子(49%)和糖基转移酶(36%)。此外,在同一属/种的菌株之间检测到簇组织的保守模式。成熟酶LasB、LasC和LasD显示出高度保守的区域,包括LasB中存在转谷氨酰胺酶核心、LasC中存在天冬酰胺合成酶结构域以及LasD中存在ABC型转运系统。必需生物合成蛋白的系统发育树表明,序列根据其共同的单一祖先分为单系类群。宏转录组分析表明套索肽生物合成基因在活跃的瘤胃微生物群中表达。总体而言,我们的筛选使得在瘤胃细菌基因组中发现了新的生物合成基因簇,并揭示了几种具有合成套索肽遗传潜力的菌株,这表明瘤胃微生物群是这些有前景的肽的潜在来源。