Nature Communications (Jul 2024)

Characterization of a Salmonella enterica serovar Typhimurium lineage with rough colony morphology and multidrug resistance

  • Ying Xiang,
  • Kunpeng Zhu,
  • Kaiyuan Min,
  • Yaowen Zhang,
  • Jiangfeng Liu,
  • Kangkang Liu,
  • Yiran Han,
  • Xinge Li,
  • Xinying Du,
  • Xin Wang,
  • Ying Huang,
  • Xinping Li,
  • Yuqian Peng,
  • Chaojie Yang,
  • Hongbo Liu,
  • HONGBO Liu,
  • Xiaoying Li,
  • Hui Wang,
  • Chao Wang,
  • Qi Wang,
  • Huiqun Jia,
  • Mingjuan Yang,
  • Ligui Wang,
  • Yarong Wu,
  • Yujun Cui,
  • Fei Chen,
  • Haiyan Yang,
  • Stephen Baker,
  • Xuebin Xu,
  • Juntao Yang,
  • Hongbin Song,
  • Shaofu Qiu

DOI
https://doi.org/10.1038/s41467-024-50331-y
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 15

Abstract

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Abstract Salmonella enterica serovar Typhimurium (S. Typhimurium) is a major cause of salmonellosis, and the emergence of multidrug-resistant pathovariants has become a growing concern. Here, we investigate a distinct rough colony variant exhibiting a strong biofilm-forming ability isolated in China. Whole-genome sequencing on 2,212 Chinese isolates and 1,739 publicly available genomes reveals the population structure and evolutionary history of the rough colony variants. Characterized by macro, red, dry, and rough (mrdar) colonies, these variants demonstrate enhanced biofilm formation at 28 °C and 37 °C compared to typical rdar colonies. The mrdar variants exhibit extensive multidrug resistance, with significantly higher resistance to at least five classes of antimicrobial agents compared to non-mrdar variants. This resistance is primarily conferred by an IncHI2 plasmid harboring 19 antimicrobial resistance genes. Phylogenomic analysis divides the global collections into six lineages. The majority of mrdar variants belong to sublineage L6.5, which originated from Chinese smooth colony strains and possibly emerged circa 1977. Among the mrdar variants, upregulation of the csgDEFG operons is observed, probably due to a distinct point mutation (−44G > T) in the csgD gene promoter. Pangenome and genome-wide association analyses identify 87 specific accessory genes and 72 distinct single nucleotide polymorphisms associated with the mrdar morphotype.