Kuryłek Aleksandra, Gawor Jan, Żuchniewicz Karolina, Gromadka Robert, Kern-Zdanowicz Izabela
Laboratory of Bacterial Drug Resistance, Institute of Biochemistry and Biophysics Polish Academy of Sciences, ul. Pawinskiego 5a, 02-106, Warsaw, Poland.
DNA Sequencing and Synthesis Facility, Institute of Biochemistry and Biophysics Polish Academy of Sciences, Warsaw, Poland.
Sci Rep. 2025 Sep 25;15(1):32863. doi: 10.1038/s41598-025-18002-0.
Streptococcus anginosus, part of the Streptococcus anginosus group (SAG), is a human commensal increasingly recognized as an opportunistic pathogen responsible for abscesses formation and infections, also invasive ones. Despite its growing clinical importance, the genetic determinants of its pathogenicity remain poorly understood. This study aimed to identify essential genes in S. anginosus 980/01, a bloodstream isolate, under nutrient-rich laboratory conditions using a transposon mutagenesis combined with Transposon-Directed Insertion Site Sequencing (TraDIS). A mutant library was generated using the ISS1 transposon delivered via the thermosensitive plasmid pGh9:ISS1. Following transposition, insertions were mapped using Illumina sequencing and subsequently analyzed. Essential genes were identified based on the absence of insertions and statistical filtering. The library exhibited 98% genome saturation with over 130,000 unique insertion sites. Among 1825 genes, 348 (19.1%) were essential, 1446 non-essential, and 30 non-conclusive. Comparative analyses were performed with S. pyogenes MGAS5005 and S. agalactiae A909. Similarly to the latter, essential genes were enriched in functions related to translation, transcription, and cell wall biosynthesis. However, 40 genes uniquely essential to S. anginosus 980/01 were identified, suggesting unique survival strategies in S. anginosus. This study presents the first genome-wide identification of essential genes for S. anginosus 980/01, highlighting conserved and unique essential genes. These findings provide a basis for understanding its physiology and key genetic determinants of bacterial viability, and may help to uncover the pathogenic potential of S. anginosus in future studies.
咽峡炎链球菌是咽峡炎链球菌群(SAG)的一部分,是一种人体共生菌,越来越多地被认为是导致脓肿形成和感染(包括侵袭性感染)的机会致病菌。尽管其临床重要性日益增加,但其致病性的遗传决定因素仍知之甚少。本研究旨在利用转座子诱变结合转座子定向插入位点测序(TraDIS),在营养丰富的实验室条件下,鉴定血流分离株咽峡炎链球菌980/01中的必需基因。使用通过温度敏感质粒pGh9:ISS1传递的ISS1转座子生成了一个突变体文库。转座后,使用Illumina测序对插入位点进行定位,随后进行分析。根据插入位点的缺失和统计筛选来鉴定必需基因。该文库显示基因组饱和度为98%,有超过130000个独特的插入位点。在1825个基因中,348个(19.1%)是必需基因,1446个是非必需基因,30个不确定。对化脓性链球菌MGAS5005和无乳链球菌A909进行了比较分析。与后者相似,必需基因在与翻译、转录和细胞壁生物合成相关的功能中富集。然而,鉴定出了40个对咽峡炎链球菌980/01独特必需的基因,表明咽峡炎链球菌有独特的生存策略。本研究首次对咽峡炎链球菌980/01进行了全基因组范围的必需基因鉴定,突出了保守和独特的必需基因。这些发现为理解其生理学和细菌生存能力的关键遗传决定因素提供了基础,并可能有助于在未来的研究中揭示咽峡炎链球菌的致病潜力。