Institute for Glycomics, Griffith University, Gold Coast, Queensland 4222, Australia.
Department of Veterinary Medicine, University of Cambridge, Cambridge CB3 0ES, UK.
Nucleic Acids Res. 2018 Nov 30;46(21):11466-11476. doi: 10.1093/nar/gky913.
Streptococcus suis is a major pathogen of swine, responsible for a number of chronic and acute infections, and is also emerging as a major zoonotic pathogen, particularly in South-East Asia. Our study of a diverse population of S. suis shows that this organism contains both Type I and Type III phase-variable methyltransferases. In all previous examples, phase-variation of methyltransferases results in genome wide methylation differences, and results in differential regulation of multiple genes, a system known as the phasevarion (phase-variable regulon). We hypothesized that each variant in the Type I and Type III systems encoded a methyltransferase with a unique specificity, and could therefore control a distinct phasevarion, either by recombination-driven shuffling between different specificities (Type I) or by biphasic on-off switching via simple sequence repeats (Type III). Here, we present the identification of the target specificities for each Type III allelic variant from S. suis using single-molecule, real-time methylome analysis. We demonstrate phase-variation is occurring in both Type I and Type III methyltransferases, and show a distinct association between methyltransferase type and presence, and population clades. In addition, we show that the phase-variable Type I methyltransferase was likely acquired at the origin of a highly virulent zoonotic sub-population.
猪链球菌是猪的主要病原体,可引起多种慢性和急性感染,也是一种主要的人畜共患病病原体,特别是在东南亚。我们对多样化的猪链球菌种群进行的研究表明,该生物体既包含 I 型又包含 III 型可变性甲基转移酶。在所有先前的例子中,甲基转移酶的可变性变化导致全基因组甲基化差异,并导致多个基因的差异调控,这是一个称为相变异(phase-variable regulon)的系统。我们假设 I 型和 III 型系统中的每个变体都编码了一种具有独特特异性的甲基转移酶,因此可以通过不同特异性(I 型)之间的重组驱动改组或通过简单重复序列的双相开-关切换来控制不同的相变异(III 型)。在这里,我们使用单分子实时甲基组分析方法,鉴定了来自猪链球菌的每个 III 型等位变体的靶特异性。我们证明了 I 型和 III 型甲基转移酶都发生了可变性,并且甲基转移酶类型与存在以及群体分支之间存在明显的关联。此外,我们还表明,可变性的 I 型甲基转移酶可能是在高度毒力的人畜共患病亚群起源时获得的。