Experimental phage evolution results in expanded host ranges against antibiotic resistant Klebsiella pneumoniae isolates

Resistance to antibiotics is approaching crisis levels for organisms such as the ESKAPEE pathogens (includes Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, Enterobacter spp., and Escherichia coli) that often are acquired in hospitals. These organisms sometimes have acquired plasmids that confer resistance to most if not all beta-lactam antibiotics. We have been developing alternative means for dealing with antibiotic resistant microbes that cause infections in humans by developing viruses (bacteriophages) that attack and kill them. One of these pathogens, K. pneumoniae, has one of the highest propensities for antimicrobial resistance. We identified many phages that have lytic capacity against limited numbers of clinical isolates, and through experimental evolution over the course of 30 days, were able to vastly expand the host ranges of these phages to kill a broader range of clinical K. pneumoniae isolates including MDR (multi-drug resistant) and XDR (extensively-drug resistant) isolates. Most interestingly, they were capable of inhibiting growth of clinical isolates both on solid and in liquid medium over extended periods. That we were able to extend the host ranges of multiple naïve antibiotic resistant K. pneumoniae through experimental phage evolution suggests that such a technique may be applicable to other antibiotic-resistant organisms to help stem the tide of antibiotic resistance and offer further options for medical treatments.

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Publication Details

Journal
Nature Communications
Published
2025-11-19
DOI
https://doi.org/10.1038/s41467-025-66062-7
Citations
2
Primary Topic
Bacteriophages and microbial interactions
Type
article
Field-Weighted Citation Impact
3.43
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article

Experimental phage evolution results in expanded host ranges against antibiotic resistant Klebsiella pneumoniae isolates

Robert T. Schooley, Nicole Hitchcock, Pooja Ghatbale, Danielle Devequi Gomes Nunes et al.
2 citations
Nature Communications
Bacteriophages and microbial interactions
3.43
article

Experimental phage evolution results in expanded host ranges against antibiotic resistant Klebsiella pneumoniae isolates

Robert T. Schooley, Nicole Hitchcock, Pooja Ghatbale, Danielle Devequi Gomes Nunes, Maureen Bates, Andrew Sue, Chandrabali Ghose, Govind Prasad Sah, David T. Pride, Justin R. Meyer, Richard White, Ana G. Cobián-Güemes, Katrine Whiteson, Job Shiach, Andrew G. Garcia, Alisha N. Blanc, Jennifer Hensley, Jesse Leonard, Roberto Bardaró
article en
2 citations

Abstract

Resistance to antibiotics is approaching crisis levels for organisms such as the ESKAPEE pathogens (includes Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, Enterobacter spp., and Escherichia coli) that often are acquired in hospitals. These organisms sometimes have acquired plasmids that confer resistance to most if not all beta-lactam antibiotics. We have been developing alternative means for dealing with antibiotic resistant microbes that cause infections in humans by developing viruses (bacteriophages) that attack and kill them. One of these pathogens, K. pneumoniae, has one of the highest propensities for antimicrobial resistance. We identified many phages that have lytic capacity against limited numbers of clinical isolates, and through experimental evolution over the course of 30 days, were able to vastly expand the host ranges of these phages to kill a broader range of clinical K. pneumoniae isolates including MDR (multi-drug resistant) and XDR (extensively-drug resistant) isolates. Most interestingly, they were capable of inhibiting growth of clinical isolates both on solid and in liquid medium over extended periods. That we were able to extend the host ranges of multiple naïve antibiotic resistant K. pneumoniae through experimental phage evolution suggests that such a technique may be applicable to other antibiotic-resistant organisms to help stem the tide of antibiotic resistance and offer further options for medical treatments.

Nature CommunicationsVol. 16(1)
University of North Carolina at Charlotte (US), Serviço Nacional de Aprendizagem Industrial (BR), University of California, Irvine (US), University of California San Diego (US), Irvine University (US), Brooklyn Philharmonic (US)
Openalex Percentile: Top 7%
Bacteriophages and microbial interactions
3.43
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