VirBR, a transcription regulator, promotes IncX3 plasmid transmission, and persistence of bla NDM-5 in zoonotic bacteria.
Tengfei MaNing XieYuan GaoJiani FuChun E TanQiu E YangShaolin WangZhangqi ShenQuanjiang JiJulian ParkhillCongming WuWang YangTimothy R WalshJianzhong ShenPublished in: Nature communications (2024)
IncX3 plasmids carrying the New Delhi metallo-β-lactamase-encoding gene, bla NDM-5 , are rapidly spreading globally in both humans and animals. Given that carbapenems are listed on the WHO AWaRe watch group and are prohibited for use in animals, the drivers for the successful dissemination of Carbapenem-Resistant Enterobacterales (CRE) carrying bla NDM-5 -IncX3 plasmids still remain unknown. We observe that E. coli carrying bla NDM-5 -IncX3 can persist in chicken intestines either under the administration of amoxicillin, one of the largest veterinary β-lactams used in livestock, or without any antibiotic pressure. We therefore characterise the bla NDM-5 -IncX3 plasmid and identify a transcription regulator, VirBR, that binds to the promoter of the regulator gene actX enhancing the transcription of Type IV secretion systems (T4SS); thereby, promoting conjugation of IncX3 plasmids, increasing pili adhesion capacity and enhancing the colonisation of bla NDM-5 -IncX3 transconjugants in animal digestive tracts. Our mechanistic and in-vivo studies identify VirBR as a major factor in the successful spread of bla NDM-5 -IncX3 across one-health AMR sectors. Furthermore, VirBR enhances the plasmid conjugation and T4SS expression by the presence of copper and zinc ions, thereby having profound ramifications on the use of universal animal feeds.
Keyphrases
- klebsiella pneumoniae
- escherichia coli
- transcription factor
- multidrug resistant
- biofilm formation
- healthcare
- public health
- crispr cas
- dna methylation
- genome wide
- copy number
- mental health
- poor prognosis
- gene expression
- risk assessment
- quantum dots
- pseudomonas aeruginosa
- cystic fibrosis
- autism spectrum disorder
- staphylococcus aureus
- genome wide identification
- long non coding rna
- human health
- oxide nanoparticles
- binding protein
- genome wide analysis