{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,30]],"date-time":"2026-07-30T10:32:37Z","timestamp":1785407557360,"version":"3.56.0"},"reference-count":53,"publisher":"American Society for Microbiology","issue":"9","license":[{"start":{"date-parts":[[2025,9,2]],"date-time":"2025-09-02T00:00:00Z","timestamp":1756771200000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2025,9,2]],"date-time":"2025-09-02T00:00:00Z","timestamp":1756771200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"funder":[{"name":"Bundesministerium f\u00fcr Forschung, Technologie und Raumfahrt","award":["13GW0424"],"award-info":[{"award-number":["13GW0424"]}]},{"name":"Bundesministerium f\u00fcr Forschung, Technologie und Raumfahrt","award":["01KI2410"],"award-info":[{"award-number":["01KI2410"]}]}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["Microbiol Spectr"],"published-print":{"date-parts":[[2025,9,2]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title\/>\n                    <jats:p>\n                      <jats:italic toggle=\"yes\">Klebsiella pneumoniae<\/jats:italic>\n                      , an important opportunistic pathogen, is traditionally classified into classic and hypervirulent pathotypes. Convergent strains combining antimicrobial resistance (AMR) and hypervirulence have emerged globally, posing a significant health challenge. In this study, we investigated potential in-host evolution and morphotypic variation among consecutive\n                      <jats:italic toggle=\"yes\">K. pneumoniae<\/jats:italic>\n                      ST147 isolates from a single patient. As described in a previous study, the isolates displayed distinct morphotypes\u2014small white, normal white, gray, and gray\/dry (g\/d) colonies. In this study, we now present new genomic and phenotypic analyses, which suggest the acquisition of AMR and virulence genes through plasmid gain. The early isolates carried fewer plasmids, resulting in low resistance and virulence, while later isolates acquired a hybrid IncFIB-IncHI1B plasmid encoding different resistance and aerobactin genes, significantly increasing their geno- and phenotypic AMR and virulence potential. Chromosomal integration of this plasmid in one isolate stabilized the acquired traits. Disruptions in the K locus, mediated by insertion sequences, were linked to the gray and g\/d morphotypes, impairing capsule biosynthesis. Uronic acid assays confirmed reduced capsule production in these isolates. In contrast, small colony variants showed significant transcriptomic changes, including upregulation of capsule biosynthesis, iron uptake pathways, and AMR genes, suggesting persistence through altered metabolism. Our findings suggest in-host microevolution of\n                      <jats:italic toggle=\"yes\">K. pneumoniae<\/jats:italic>\n                      ST147 from a classic to a convergent pathotype and highlight the genomic and transcriptomic adaptations underlying morphotypic diversity, providing new insights into the pathogen\u2019s adaptability and persistence in certain environments.\n                    <\/jats:p>\n                    <jats:sec>\n                      <jats:title>IMPORTANCE<\/jats:title>\n                      <jats:p>\n                        <jats:italic toggle=\"yes\">Klebsiella pneumoniae<\/jats:italic>\n                        is an important bacterial pathogen that can cause severe infections, particularly in healthcare settings. Traditionally, strains are classified as either drug-resistant or highly virulent, but recent strains combining both features have led to hard-to-treat infections. In this study, we investigated the potential in-host evolution of\n                        <jats:italic toggle=\"yes\">K. pneumoniae<\/jats:italic>\n                        ST147 isolates from a single patient, revealing key genomic and phenotypic changes driving their adaptability. Over time, isolates acquired additional plasmids carrying antimicrobial resistance and virulence genes, including a hybrid plasmid integrated into the bacterial chromosome, stabilizing its beneficial traits. In addition, morphotypic diversity emerged, linked to genomic disruptions in capsule biosynthesis genes (K locus). While capsule-deficient morphotypes displayed structural changes, small colony variants exhibited transcriptomic adaptations to persist under stress. This work underscores the dynamic evolutionary capacity of\n                        <jats:italic toggle=\"yes\">K. pneumoniae<\/jats:italic>\n                        adapting within the host, providing critical insights into its persistence, resilience, and the challenges posed by emerging convergent strains in clinical settings.\n                      <\/jats:p>\n                    <\/jats:sec>\n                  <\/jats:sec>","DOI":"10.1128\/spectrum.00170-25","type":"journal-article","created":{"date-parts":[[2025,7,18]],"date-time":"2025-07-18T13:00:39Z","timestamp":1752843639000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":6,"title":["Potential in-host evolution of\n                    <i>Klebsiella pneumoniae<\/i>\n                    ST147: convergence and the role of capsular alterations in morphotype diversity"],"prefix":"10.1128","volume":"13","author":[{"ORCID":"https:\/\/orcid.org\/0009-0000-9172-8774","authenticated-orcid":true,"given":"Katharina","family":"Sydow","sequence":"first","affiliation":[{"id":[{"id":"https:\/\/ror.org\/03d0p2685","id-type":"ROR","asserted-by":"publisher"}],"name":"Department of Epidemiology and Ecology of Antimicrobial Resistance, Helmholtz Institute for One Health, Helmholtz Center for Infection Research HZI","place":["Greifswald, Germany"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ey\u00fcp","family":"Do\u011fan","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/025vngs54","id-type":"ROR","asserted-by":"publisher"}],"name":"Friedrich Loeffler-Institute of Medical Microbiology, University Medicine Greifswald","place":["Greifswald, 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