Swiatek Lena-Sophie, Surmann Kristin, Eger Elias, Müller Justus U, Gesell Salazar Manuela, Heiden Stefan E, Werner Guido, Hübner Nils-Olaf, Bohnert Jürgen A, Becker Karsten, Völker Uwe, Schwabe Michael, Schaufler Katharina
Department of Epidemiology and Ecology of Antimicrobial Resistance, Helmholtz Institute for One Health, Helmholtz Centre for Infection Research HZI, Greifswald, Germany.
Department of Functional Genomics, Interfaculty Institute for Genetics and Functional Genomics, University Medicine Greifswald, Greifswald, Germany.
Front Microbiol. 2025 Aug 20;16:1657680. doi: 10.3389/fmicb.2025.1657680. eCollection 2025.
The (KP) species complex (KpSC) comprises KP as the predominant species, and six other taxa including two subspecies each of var (KV) and (KQ), all capable of causing clinical infections and often challenging to differentiate. Among these, KP is by far the most clinically significant, with the emergence of multidrug-resistant and hypervirulent strains leading to severe infections and limited treatment options, underscoring the need to understand the genomic features of KP.
This study compared globally disseminated KP lineages with less abundant KV strains in synthetic human urine (SHU) across multiple omics levels to identify characteristics differentiating these closely related species. Moreover, a large genomic dataset of over 6,000 publicly available genomes of KP, KV, and KQ was constructed for comparisons to other members of the KpSC.
Among eight clinical KP strains representing four different sequence types (STs), we identified 107 genes comprising the KP-specific core genome, while these genes were absent from two selected KV genomes. Transcriptome and proteome analyses in SHU revealed different regulatory patterns between KP and KV strains, with metabolic responses playing a pivotal role. A total of 193 genes specific to the investigated KP STs were identified, exhibiting differential expression at the transcriptomic and/or proteomic levels. Comparison to the genomic dataset highlighted genes adaptively regulated or uniquely present in KP genomes. For example, certain genes for citrate metabolism are uniquely upregulated in KP and a gene cluster for the cellobiose phosphotransferase system, previously linked to bacterial virulence and biofilm formation, was found exclusively in KP.
Our study underscores the metabolic flexibility of KP strains in response to specific environmental conditions, potentially contributing to opportunistic pathogenicity. We identified markers enriched in KP STs, providing a foundation for future investigations including their relevance for diagnostics.
肺炎克雷伯菌(KP)菌群(KpSC)以KP为主要菌种,还包括其他六个分类单元,其中肺炎克雷伯菌变种(KV)和肺炎克雷伯菌(KQ)各有两个亚种,所有这些菌种都能够引起临床感染,且常常难以鉴别。其中,KP是迄今为止临床上最重要的菌种,多重耐药和高毒力菌株的出现导致严重感染且治疗选择有限,这凸显了了解KP基因组特征的必要性。
本研究在多个组学水平上,将全球传播的KP谱系与合成人尿(SHU)中数量较少的KV菌株进行比较,以确定区分这些密切相关菌种的特征。此外,构建了一个包含超过6000个公开可用的KP、KV和KQ基因组的大型基因组数据集,用于与KpSC的其他成员进行比较。
在代表四种不同序列类型(STs)的八株临床KP菌株中,我们鉴定出107个基因构成KP特异性核心基因组,而在两个选定的KV基因组中不存在这些基因。在SHU中进行的转录组和蛋白质组分析揭示了KP和KV菌株之间不同的调控模式,代谢反应起关键作用。共鉴定出193个特定于所研究的KP STs的基因,它们在转录组和/或蛋白质组水平上表现出差异表达。与基因组数据集的比较突出了在KP基因组中适应性调控或独特存在的基因。例如,某些参与柠檬酸盐代谢的基因在KP中独特地上调,并且发现一个与细菌毒力和生物膜形成相关的纤维二糖磷酸转移酶系统基因簇仅存在于KP中。
我们的研究强调了KP菌株在应对特定环境条件时的代谢灵活性,这可能有助于其机会致病性。我们鉴定出在KP STs中富集的标志物,为未来的研究(包括它们与诊断的相关性)奠定了基础。