{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,30]],"date-time":"2026-07-30T16:52:40Z","timestamp":1785430360866,"version":"3.56.0"},"reference-count":18,"publisher":"American Society for Microbiology","issue":"4","license":[{"start":{"date-parts":[[2026,4,7]],"date-time":"2026-04-07T00:00:00Z","timestamp":1775520000000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,4,7]],"date-time":"2026-04-07T00:00:00Z","timestamp":1775520000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"funder":[{"name":"The First Affiliated Hospital of Nanchang University","award":["YFYPY202413"],"award-info":[{"award-number":["YFYPY202413"]}]},{"DOI":"10.13039\/501100009102","name":"Education Department of Jiangxi Province","doi-asserted-by":"publisher","award":["GJJ2400132"],"award-info":[{"award-number":["GJJ2400132"]}],"id":[{"id":"10.13039\/501100009102","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["Microbiol Spectr"],"published-print":{"date-parts":[[2026,4,7]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title\/>\n                    <jats:p>\n                      <jats:italic toggle=\"yes\">Klebsiella quasipneumoniae<\/jats:italic>\n                      has emerged as a multidrug-resistant (MDR) pathogen of growing clinical concern, driven by its capacity to acquire mobile genetic elements encoding carbapenemases and novel resistance determinants. This study aimed to characterize the genomic architecture, resistance profile, and phenotypic impact of plasmids in a clinical\n                      <jats:italic toggle=\"yes\">K. quasipneumoniae<\/jats:italic>\n                      strain co-producing\n                      <jats:italic toggle=\"yes\">bla<\/jats:italic>\n                      <jats:sub>NDM-1<\/jats:sub>\n                      and the tigecycline efflux pump gene cluster\n                      <jats:italic toggle=\"yes\">tmexCD2-toprJ2<\/jats:italic>\n                      . Whole-genome sequencing and plasmid reconstruction were performed for strain KP10883 (KL159\/ST1929). Antimicrobial susceptibility testing, plasmid curing, biofilm quantification, serum resistance assays, human lung epithelial cell infection assays, and\n                      <jats:italic toggle=\"yes\">Galleria mellonella<\/jats:italic>\n                      infection models were used to evaluate the functional consequences of plasmid carriage. KP10883 harbored two functionally distinct plasmids: pKP10883-1, an IncU conjugative plasmid carrying\n                      <jats:italic toggle=\"yes\">bla<\/jats:italic>\n                      <jats:sub>NDM-1<\/jats:sub>\n                      and\n                      <jats:italic toggle=\"yes\">tmexCD2-toprJ2<\/jats:italic>\n                      , conferring broad-spectrum antibiotic resistance, and pKP10883-2, a nonconjugative IncFIB\/IncFII plasmid encoding stability and adaptation modules without classical resistance genes. Curing of pKP10883-1 resulted in complete loss of resistance to \u03b2-lactams, carbapenems, and tigecycline, confirming plasmid-mediated resistance. Paradoxically, plasmid loss led to increased biofilm formation, enhanced serum resistance, greater epithelial cell adhesion and cytotoxicity, and higher virulence in\n                      <jats:italic toggle=\"yes\">G. mellonella<\/jats:italic>\n                      , indicating suppression of chromosomal virulence by plasmid-borne regulatory elements. This study reveals a plasmid-mediated trade-off between antimicrobial resistance and virulence in\n                      <jats:italic toggle=\"yes\">K. quasipneumoniae<\/jats:italic>\n                      . The functional complementarity of pKP10883-1 and pKP10883-2 supports their stable coexistence and reflects a broader adaptive strategy balancing drug resistance with pathogenic potential. These findings underscore the importance of considering the regulatory impact of MDR plasmids on host virulence in developing strategies against emerging MDR pathogens.\n                    <\/jats:p>\n                    <jats:sec>\n                      <jats:title>IMPORTANCE<\/jats:title>\n                      <jats:p>\n                        The emergence of multidrug-resistant (MDR)\n                        <jats:italic toggle=\"yes\">Klebsiella quasipneumoniae<\/jats:italic>\n                        poses an escalating threat to clinical treatment and infection control. This study provides the first comprehensive genomic and functional characterization of a clinical\n                        <jats:italic toggle=\"yes\">K. quasipneumoniae<\/jats:italic>\n                        strain co-harboring\n                        <jats:italic toggle=\"yes\">bla<\/jats:italic>\n                        <jats:sub>NDM-1<\/jats:sub>\n                        and the tigecycline efflux pump cluster\n                        <jats:italic toggle=\"yes\">tmexCD2-toprJ2<\/jats:italic>\n                        . By integrating genomic, phenotypic, and virulence analyses, we reveal a paradoxical trade-off in which plasmid acquisition confers extensive antibiotic resistance while suppressing host virulence. These findings uncover a novel plasmid-mediated regulatory mechanism balancing bacterial survival and pathogenicity. Understanding this interplay between resistance and virulence expands the current knowledge of MDR plasmid biology and provides valuable insights into how resistance evolution may reshape bacterial pathogenic potential\u2014information critical for surveillance, therapeutic development, and containment of emerging high-risk\n                        <jats:italic toggle=\"yes\">Klebsiella<\/jats:italic>\n                        lineages.\n                      <\/jats:p>\n                    <\/jats:sec>\n                  <\/jats:sec>","DOI":"10.1128\/spectrum.02401-25","type":"journal-article","created":{"date-parts":[[2026,3,17]],"date-time":"2026-03-17T13:00:21Z","timestamp":1773752421000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":0,"title":["Genomic and functional characterization of a\n                    <i>bla<\/i>\n                    <sub>NDM-1<\/sub>\n                    and\n                    <i>tmexCD2-toprJ2<\/i>\n                    co-producing\n                    <i>Klebsiella quasipneumoniae<\/i>\n                    (KL159\/ST1929) reveals plasmid-mediated suppression of virulence"],"prefix":"10.1128","volume":"14","author":[{"given":"Feng","family":"Nie","sequence":"first","affiliation":[{"id":[{"id":"https:\/\/ror.org\/05gbwr869","id-type":"ROR","asserted-by":"publisher"}],"name":"Jiangxi Provincial Key Laboratory of Respiratory Diseases, Jiangxi Institute of Respiratory Diseases, The Department of Respiratory and Critical Care Medicine, Jiangxi Clinical Research Center for Respiratory Diseases, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University","place":["Nanchang, China"]},{"id":[{"id":"https:\/\/ror.org\/042v6xz23","id-type":"ROR","asserted-by":"publisher"}],"name":"China-Japan Friendship Jiangxi Hospital, National Regional Center for Respiratory Medicine","place":["Nanchang, 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