Abstract:
:Colistin remains one of the few antibiotics effective against multi-drug resistant (MDR) hospital pathogens, such as Klebsiella pneumoniae. Yet resistance to this last-line drug is rapidly increasing. Characterized mechanisms of colR in K. pneumoniae are largely due to chromosomal mutations in two-component regulators, although a plasmid-mediated colR mechanism has recently been uncovered. However, the effects of intrinsic colistin resistance are yet to be characterized on a whole-genome level. Here, we used a genomics-based approach to understand the mechanisms of adaptive colR acquisition in K. pneumoniae. In controlled directed-evolution experiments we observed two distinct paths to colistin resistance acquisition. Whole genome sequencing identified mutations in two colistin resistance genes: in the known colR regulator phoQ which became fixed in the population and resulted in a single amino acid change, and unstable minority variants in the recently described two-component sensor crrB. Through RNAseq and microscopy, we reveal the broad range of effects that colistin exposure has on the cell. This study is the first to use genomics to identify a population of minority variants with mutations in a colR gene in K. pneumoniae.
journal_name
Sci Repjournal_title
Scientific reportsauthors
Cain AK,Boinett CJ,Barquist L,Dordel J,Fookes M,Mayho M,Ellington MJ,Goulding D,Pickard D,Wick RR,Holt KE,Parkhill J,Thomson NRdoi
10.1038/s41598-018-28199-ysubject
Has Abstractpub_date
2018-06-29 00:00:00pages
9868issue
1issn
2045-2322pii
10.1038/s41598-018-28199-yjournal_volume
8pub_type
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