Outer Membrane Vesicles Derived from Klebsiella pneumoniae Are a Driving Force for Horizontal Gene Transfer.
Federica Dell'AnnunziataCarmela Dell'AversanaNunzianna DotiGiuliana DonadioFabrizio Dal PiazViviana IzzoAnna De FilippisMarilena GaldieroLucia AltucciGiovanni BocciaMassimiliano GaldieroVeronica FollieroGianluigi FranciPublished in: International journal of molecular sciences (2021)
Gram-negative bacteria release Outer Membrane Vesicles (OMVs) into the extracellular environment. Recent studies recognized these vesicles as vectors to horizontal gene transfer; however, the parameters that mediate OMVs transfer within bacterial communities remain unclear. The present study highlights for the first time the transfer of plasmids containing resistance genes via OMVs derived from Klebsiella pneumoniae (K. pneumoniae). This mechanism confers DNA protection, it is plasmid copy number dependent with a ratio of 3.6 times among high copy number plasmid (pGR) versus low copy number plasmid (PRM), and the transformation efficiency was 3.6 times greater. Therefore, the DNA amount in the vesicular lumen and the efficacy of horizontal gene transfer was strictly dependent on the identity of the plasmid. Moreover, the role of K. pneumoniae-OMVs in interspecies transfer was described. The transfer ability was not related to the phylogenetic characteristics between the donor and the recipient species. K. pneumoniae-OMVs transferred plasmid to Escherichia coli, Salmonella enterica, Pseudomonas aeruginosa and Burkholderia cepacia. These findings address the pivotal role of K. pneumoniae-OMVs as vectors for antimicrobial resistance genes spread, contributing to the development of antibiotic resistance in the microbial communities.
Keyphrases
- copy number
- escherichia coli
- klebsiella pneumoniae
- genome wide
- mitochondrial dna
- dna methylation
- antimicrobial resistance
- pseudomonas aeruginosa
- crispr cas
- biofilm formation
- multidrug resistant
- electron transfer
- genome wide identification
- single molecule
- cystic fibrosis
- cell free
- staphylococcus aureus
- gene expression
- transcription factor
- respiratory tract
- acinetobacter baumannii
- drug resistant