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Klebsiella pneumoniae clinical isolates with features of both multidrug-resistance and hypervirulence have unexpectedly low virulence

Klebsiella pneumoniae has been classified into two types, classical K. pneumoniae (cKP) and hypervirulent K. pneumoniae (hvKP). cKP isolates are highly diverse and important causes of nosocomial infections; they include globally disseminated antibiotic-resistant clones. hvKP isolates are sensitive t...

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Autores principales: Kochan, Travis J., Nozick, Sophia H., Valdes, Aliki, Mitra, Sumitra D., Cheung, Bettina H., Lebrun-Corbin, Marine, Medernach, Rachel L., Vessely, Madeleine B., Mills, Jori O., Axline, Christopher M. R., Nelson, Julia A., VanGosen, Ethan M., Ward, Timothy J., Ozer, Egon A., van Duin, David, Chen, Liang, Kreiswirth, Barry N., Long, S. Wesley, Musser, James M., Bulman, Zackery P., Wunderink, Richard G., Hauser, Alan R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693551/
https://www.ncbi.nlm.nih.gov/pubmed/38042959
http://dx.doi.org/10.1038/s41467-023-43802-1
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author Kochan, Travis J.
Nozick, Sophia H.
Valdes, Aliki
Mitra, Sumitra D.
Cheung, Bettina H.
Lebrun-Corbin, Marine
Medernach, Rachel L.
Vessely, Madeleine B.
Mills, Jori O.
Axline, Christopher M. R.
Nelson, Julia A.
VanGosen, Ethan M.
Ward, Timothy J.
Ozer, Egon A.
van Duin, David
Chen, Liang
Kreiswirth, Barry N.
Long, S. Wesley
Musser, James M.
Bulman, Zackery P.
Wunderink, Richard G.
Hauser, Alan R.
author_facet Kochan, Travis J.
Nozick, Sophia H.
Valdes, Aliki
Mitra, Sumitra D.
Cheung, Bettina H.
Lebrun-Corbin, Marine
Medernach, Rachel L.
Vessely, Madeleine B.
Mills, Jori O.
Axline, Christopher M. R.
Nelson, Julia A.
VanGosen, Ethan M.
Ward, Timothy J.
Ozer, Egon A.
van Duin, David
Chen, Liang
Kreiswirth, Barry N.
Long, S. Wesley
Musser, James M.
Bulman, Zackery P.
Wunderink, Richard G.
Hauser, Alan R.
author_sort Kochan, Travis J.
collection PubMed
description Klebsiella pneumoniae has been classified into two types, classical K. pneumoniae (cKP) and hypervirulent K. pneumoniae (hvKP). cKP isolates are highly diverse and important causes of nosocomial infections; they include globally disseminated antibiotic-resistant clones. hvKP isolates are sensitive to most antibiotics but are highly virulent, causing community-acquired infections in healthy individuals. The virulence phenotype of hvKP is associated with pathogenicity loci responsible for siderophore and hypermucoid capsule production. Recently, convergent strains of K. pneumoniae, which possess features of both cKP and hvKP, have emerged and are cause of much concern. Here, we screen the genomes of 2,608 multidrug-resistant K. pneumoniae isolates from the United States and identify 47 convergent isolates. We perform phenotypic and genomic characterization of 12 representative isolates. These 12 convergent isolates contain a variety of antimicrobial resistance plasmids and virulence plasmids. Most convergent isolates contain aerobactin biosynthesis genes and produce more siderophores than cKP isolates but not more capsule. Unexpectedly, only 1 of the 12 tested convergent isolates has a level of virulence consistent with hvKP isolates in a murine pneumonia model. These findings suggest that additional studies should be performed to clarify whether convergent strains are indeed more virulent than cKP in mouse and human infections.
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spelling pubmed-106935512023-12-04 Klebsiella pneumoniae clinical isolates with features of both multidrug-resistance and hypervirulence have unexpectedly low virulence Kochan, Travis J. Nozick, Sophia H. Valdes, Aliki Mitra, Sumitra D. Cheung, Bettina H. Lebrun-Corbin, Marine Medernach, Rachel L. Vessely, Madeleine B. Mills, Jori O. Axline, Christopher M. R. Nelson, Julia A. VanGosen, Ethan M. Ward, Timothy J. Ozer, Egon A. van Duin, David Chen, Liang Kreiswirth, Barry N. Long, S. Wesley Musser, James M. Bulman, Zackery P. Wunderink, Richard G. Hauser, Alan R. Nat Commun Article Klebsiella pneumoniae has been classified into two types, classical K. pneumoniae (cKP) and hypervirulent K. pneumoniae (hvKP). cKP isolates are highly diverse and important causes of nosocomial infections; they include globally disseminated antibiotic-resistant clones. hvKP isolates are sensitive to most antibiotics but are highly virulent, causing community-acquired infections in healthy individuals. The virulence phenotype of hvKP is associated with pathogenicity loci responsible for siderophore and hypermucoid capsule production. Recently, convergent strains of K. pneumoniae, which possess features of both cKP and hvKP, have emerged and are cause of much concern. Here, we screen the genomes of 2,608 multidrug-resistant K. pneumoniae isolates from the United States and identify 47 convergent isolates. We perform phenotypic and genomic characterization of 12 representative isolates. These 12 convergent isolates contain a variety of antimicrobial resistance plasmids and virulence plasmids. Most convergent isolates contain aerobactin biosynthesis genes and produce more siderophores than cKP isolates but not more capsule. Unexpectedly, only 1 of the 12 tested convergent isolates has a level of virulence consistent with hvKP isolates in a murine pneumonia model. These findings suggest that additional studies should be performed to clarify whether convergent strains are indeed more virulent than cKP in mouse and human infections. Nature Publishing Group UK 2023-12-02 /pmc/articles/PMC10693551/ /pubmed/38042959 http://dx.doi.org/10.1038/s41467-023-43802-1 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kochan, Travis J.
Nozick, Sophia H.
Valdes, Aliki
Mitra, Sumitra D.
Cheung, Bettina H.
Lebrun-Corbin, Marine
Medernach, Rachel L.
Vessely, Madeleine B.
Mills, Jori O.
Axline, Christopher M. R.
Nelson, Julia A.
VanGosen, Ethan M.
Ward, Timothy J.
Ozer, Egon A.
van Duin, David
Chen, Liang
Kreiswirth, Barry N.
Long, S. Wesley
Musser, James M.
Bulman, Zackery P.
Wunderink, Richard G.
Hauser, Alan R.
Klebsiella pneumoniae clinical isolates with features of both multidrug-resistance and hypervirulence have unexpectedly low virulence
title Klebsiella pneumoniae clinical isolates with features of both multidrug-resistance and hypervirulence have unexpectedly low virulence
title_full Klebsiella pneumoniae clinical isolates with features of both multidrug-resistance and hypervirulence have unexpectedly low virulence
title_fullStr Klebsiella pneumoniae clinical isolates with features of both multidrug-resistance and hypervirulence have unexpectedly low virulence
title_full_unstemmed Klebsiella pneumoniae clinical isolates with features of both multidrug-resistance and hypervirulence have unexpectedly low virulence
title_short Klebsiella pneumoniae clinical isolates with features of both multidrug-resistance and hypervirulence have unexpectedly low virulence
title_sort klebsiella pneumoniae clinical isolates with features of both multidrug-resistance and hypervirulence have unexpectedly low virulence
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693551/
https://www.ncbi.nlm.nih.gov/pubmed/38042959
http://dx.doi.org/10.1038/s41467-023-43802-1
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