Nguyen Thao Thi, Lee Hyun-Hee, Park Inmyoung, Seo Young-Su
Department of Microbiology, Pusan National University, Busan 46241, Korea.
Department of Asian Food and Culinary Arts, Youngsan University, Busan 48015, Korea.
Plant Pathol J. 2018 Feb;34(1):11-22. doi: 10.5423/PPJ.FT.11.2017.0231. Epub 2018 Feb 1.
Type VI secretion system (T6SS) has been discovered in a variety of gram-negative bacteria as a versatile weapon to stimulate the killing of eukaryotic cells or prokaryotic competitors. Type VI secretion effectors (T6SEs) are well known as key virulence factors for important pathogenic bacteria. In many species, T6SS has evolved as the most complicated secretion pathway with distinguished types to translocate diverse T6SEs, suggesting their essential roles in this genus. Here we attempted to detect and characterize T6SSs and potential T6SEs in target genomes of plant-associated and environmental species based on computational analyses. In total, 66 potential functional T6SS clusters were found in 30 target bacterial genomes, of which 33% possess three or four clusters. The core proteins in each cluster were specified and phylogenetic trees of three components (i.e., TssC, TssD, TssL) were constructed to elucidate the relationship among the identified T6SS clusters. Next, we identified 322 potential T6SEs in the target genomes based on homology searches and explored the important domains conserved in effector candidates. In addition, using the screening approach based on the profile hidden Markov model (pHMM) of T6SEs that possess markers for type VI effectors (MIX motif) (MIX T6SEs), 57 revealed proteins that were not included in training datasets were recognized as novel MIX T6SE candidates from the species. This approach could be useful to identify potential T6SEs from other bacterial genomes.
VI型分泌系统(T6SS)已在多种革兰氏阴性细菌中被发现,它是一种多功能武器,可用于刺激真核细胞或原核竞争者的杀伤。VI型分泌效应蛋白(T6SEs)是重要病原菌的关键毒力因子,广为人知。在许多物种中,T6SS已进化为最复杂的分泌途径,具有不同类型以转运多种T6SEs,这表明它们在该属中具有重要作用。在这里,我们试图基于计算分析在植物相关和环境物种的目标基因组中检测和表征T6SSs及潜在的T6SEs。总共在30个目标细菌基因组中发现了66个潜在的功能性T6SS簇,其中33%拥有三个或四个簇。确定了每个簇中的核心蛋白,并构建了三个组分(即TssC、TssD、TssL)的系统发育树,以阐明已鉴定的T6SS簇之间的关系。接下来,我们基于同源性搜索在目标基因组中鉴定了322个潜在的T6SEs,并探索了效应蛋白候选物中保守的重要结构域。此外,使用基于具有VI型效应蛋白标记(MIX基序)的T6SEs的轮廓隐马尔可夫模型(pHMM)的筛选方法(MIX T6SEs),从该物种中识别出57个未包含在训练数据集中的揭示蛋白作为新的MIX T6SE候选物。这种方法可能有助于从其他细菌基因组中鉴定潜在的T6SEs。