National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD 20894, USA.
Environ Microbiol. 2012 Nov;14(11):2870-90. doi: 10.1111/j.1462-2920.2012.02841.x. Epub 2012 Aug 13.
Three classes of low-G+C Gram-positive bacteria (Firmicutes), Bacilli, Clostridia and Negativicutes, include numerous members that are capable of producing heat-resistant endospores. Spore-forming firmicutes include many environmentally important organisms, such as insect pathogens and cellulose-degrading industrial strains, as well as human pathogens responsible for such diseases as anthrax, botulism, gas gangrene and tetanus. In the best-studied model organism Bacillus subtilis, sporulation involves over 500 genes, many of which are conserved among other bacilli and clostridia. This work aimed to define the genomic requirements for sporulation through an analysis of the presence of sporulation genes in various firmicutes, including those with smaller genomes than B. subtilis. Cultivable spore-formers were found to have genomes larger than 2300 kb and encompass over 2150 protein-coding genes of which 60 are orthologues of genes that are apparently essential for sporulation in B. subtilis. Clostridial spore-formers lack, among others, spoIIB, sda, spoVID and safA genes and have non-orthologous displacements of spoIIQ and spoIVFA, suggesting substantial differences between bacilli and clostridia in the engulfment and spore coat formation steps. Many B. subtilis sporulation genes, particularly those encoding small acid-soluble spore proteins and spore coat proteins, were found only in the family Bacillaceae, or even in a subset of Bacillus spp. Phylogenetic profiles of sporulation genes, compiled in this work, confirm the presence of a common sporulation gene core, but also illuminate the diversity of the sporulation processes within various lineages. These profiles should help further experimental studies of uncharacterized widespread sporulation genes, which would ultimately allow delineation of the minimal set(s) of sporulation-specific genes in Bacilli and Clostridia.
三类低 G+C 革兰氏阳性菌(厚壁菌门),芽孢杆菌、梭菌和阴性菌,包括许多能够产生耐热芽孢的成员。产芽孢的厚壁菌门包括许多环境重要的生物,如昆虫病原体和纤维素降解的工业菌株,以及炭疽、肉毒中毒、气性坏疽和破伤风等疾病的人类病原体。在研究最充分的模式生物枯草芽孢杆菌中,孢子形成涉及超过 500 个基因,其中许多基因在其他芽孢杆菌和梭菌中保守。这项工作旨在通过分析各种厚壁菌门中孢子形成基因的存在来定义孢子形成的基因组要求,包括那些基因组小于枯草芽孢杆菌的厚壁菌门。可培养的孢子形成体的基因组大于 2300kb,包含超过 2150 个编码蛋白的基因,其中 60 个是与枯草芽孢杆菌中显然对孢子形成必不可少的基因的同源物。梭菌孢子形成体缺乏 spoIIB、sda、spoVID 和 safA 等基因,并且 spoIIQ 和 spoIVFA 的非同源置换,表明芽孢杆菌和梭菌在吞噬和孢子壳形成步骤中存在显著差异。许多枯草芽孢杆菌孢子形成基因,特别是编码小酸溶性孢子蛋白和孢子壳蛋白的基因,仅存在于芽孢杆菌科,甚至存在于芽孢杆菌属的一个亚群中。本文中汇编的孢子形成基因的系统发育谱证实了共同的孢子形成基因核心的存在,但也阐明了各种谱系中孢子形成过程的多样性。这些图谱应该有助于进一步研究尚未表征的广泛存在的孢子形成基因,这最终将允许在芽孢杆菌和梭菌中划定孢子形成特异性基因的最小集合。