Unravelling the Evolutionary Dynamics of High-Risk Klebsiella pneumoniae ST147 Clones: Insights from Comparative Pangenome Analysis

被引:4
|
作者
Dey, Suchanda [1 ]
Gaur, Mahendra [1 ]
Sykes, Ellen M. E. [2 ]
Prusty, Monica [3 ]
Elangovan, Selvakumar [3 ]
Dixit, Sangita [1 ]
Pati, Sanghamitra [4 ]
Kumar, Ayush [2 ]
Subudhi, Enketeswara [1 ]
机构
[1] Siksha O Anusandhan Deemed Univ, Ctr Biotechnol, Sch Pharmaceut Sci, Bhubaneswar 751003, India
[2] Univ Manitoba, Dept Microbiol, Winnipeg, MB R3T2N2, Canada
[3] Kalinga Inst Ind Technol, Sch Biotechnol, Bhubaneswar 751024, India
[4] Reg Med Res Ctr, Bhubaneswar 751023, India
关键词
Klebsiella pneumoniae; high-risk clone; ST147; pangenome analysis; SNP; PHYLOGENETIC ANALYSIS; PAN-GENOME; SEQUENCE; ALIGNMENT; RESISTANT; TOOL;
D O I
10.3390/genes14051037
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: The high prevalence and rapid emergence of antibiotic resistance in high-risk Klebsiella pneumoniae (KP) ST147 clones is a global health concern and warrants molecular surveillance. Methods: A pangenome analysis was performed using publicly available ST147 complete genomes. The characteristics and evolutionary relationships among ST147 members were investigated through a Bayesian phylogenetic analysis. Results: The large number of accessory genes in the pangenome indicates genome plasticity and openness. Seventy-two antibiotic resistance genes were found to be linked with antibiotic inactivation, efflux, and target alteration. The exclusive detection of the bla(OXA-232) gene within the ColKp3 plasmid of KP_SDL79 suggests its acquisition through horizontal gene transfer. The association of seventy-six virulence genes with the acrAB efflux pump, T6SS system and type I secretion system describes its pathogenicity. The presence of Tn6170, a putative Tn7-like transposon in KP_SDL79 with an insertion at the flanking region of the tnsB gene, establishes its transmission ability. The Bayesian phylogenetic analysis estimates ST147's initial divergence in 1951 and the most recent common ancestor for the entire KP population in 1621. Conclusions: Present study highlights the genetic diversity and evolutionary dynamics of high-risk clones of K. pneumoniae. Further inter-clonal diversity studies will help us understand its outbreak more precisely and pave the way for therapeutic interventions.
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