ArticlePLoS genetics2025
Genomic profiling and experimental validation of type VI secretion system-associated proteins in Klebsiella.
Article in PLoS genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
What it found
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Who cites it
5 citing papers in PubMed.
- The type VI secretion system of Acinetobacter: mechanisms, biology and therapeutic potential.Communications biology · 2026Review
- Piecing together the puzzle: current knowledge and open questions about the Klebsiella pneumoniae type VI secretion system (T6SS).Memorias do Instituto Oswaldo Cruz · 2026Review
- Type VI secretion system completeness shapes evolutionary trade-offs in theFrontiers in microbiology · 2026Article
- The Type VI secretion system in enteric pathogen colonization: molecular mechanisms, ecological dynamics, and therapeutic potential.Frontiers in microbiology · 2026Review
- Etiological and Pathological Investigation of Bacterial Pneumonia in Forest Musk Deer (Veterinary medicine international · 2026Article
Corrections and comments
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Authors and funding
12 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Klebsiella is widely distributed in nature and recognized for its dual role as a human commensal and an opportunistic pathogen capable of causing severe infections. Among its key virulence mechanisms, the Type VI Secretion System (T6SS) plays a critical role in microbial competition, interspecies interactions, and environmental adaptation. In this study, we investigated a representative set of high-quality Klebsiella genomes and identified two major T6SS loci (T6SSkleb1 and T6SSkleb2), which exhibit distinct structural features and are predominantly found within the Klebsiella pneumoniae species complex (KpSC). Comparative genomics further revealed the diverse distribution of effector and immunity proteins and their correlation with T6SS loci. Based on this distributional bias, we developed a novel computational approach to identify protein families significantly associated with T6SS. These T6SS-associated gene clusters were implicated in mediating adhesion to host cell surfaces during urinary tract infections, as well as in metabolism and immune defense. Moreover, we identified three putative orphan effectors harboring DUF3258, DUF3751, and Sel1 domains. Overexpression of these proteins in Escherichia coli resulted in cytotoxic effects, supporting their potential as T6SS effectors. These findings establish a comprehensive framework for T6SS analysis, aiming to expand and enrich our understanding of the diversity, evolutionary trajectory, and functional implications of T6SS in Klebsiella.
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Registered trials
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