{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,30]],"date-time":"2026-07-30T12:59:24Z","timestamp":1785416364826,"version":"3.56.0"},"reference-count":24,"publisher":"American Society for Microbiology","issue":"7","license":[{"start":{"date-parts":[[2026,7,8]],"date-time":"2026-07-08T00:00:00Z","timestamp":1783468800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,7,8]],"date-time":"2026-07-08T00:00:00Z","timestamp":1783468800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"funder":[{"DOI":"10.13039\/501100003977","name":"Israel Science Foundation","doi-asserted-by":"publisher","award":["2973\/24"],"award-info":[{"award-number":["2973\/24"]}],"id":[{"id":"10.13039\/501100003977","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["mBio"],"published-print":{"date-parts":[[2026,7,8]]},"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                      is a prominent pathogen causing life-threatening bloodstream infections. Although biofilm formation and resistance to human serum are well-recognized virulence traits, their interrelatedness during\n                      <jats:italic toggle=\"yes\">K. pneumoniae<\/jats:italic>\n                      bloodstream infections remains unclear. Here, we hypothesize that biofilm production is related to\n                      <jats:italic toggle=\"yes\">K. pneumoniae<\/jats:italic>\n                      \u2019s ability to thrive in human serum and, therefore, may predict the strains\u2019 ability for serum survival. We analyzed 57 clinical, genetically diverse classical\n                      <jats:italic toggle=\"yes\">K. pneumoniae<\/jats:italic>\n                      strains and characterized their survival and biofilm-producing ability in human serum. Serum survival patterns revealed three serum resistance categories\u2014Low, Mid, and High. In addition, the biofilm biomass produced by the strains correlated with their serum resistance level (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      &lt; 0.001), and 3D biofilm visualization using confocal microscopy further confirmed that biofilm extracellular polysaccharide substances and biomass patterns were consistent with the serum resistance categories. Moreover, we revealed a direct correlation between the level of biofilm formation and the strain\u2019s serum survival level (\n                      <jats:italic toggle=\"yes\">R<\/jats:italic>\n                      <jats:sup>2<\/jats:sup>\n                      = 0.696), a prerequisite for systemic\n                      <jats:italic toggle=\"yes\">K. pneumoniae<\/jats:italic>\n                      dissemination. As biofilm formation in serum reflects both survival and biofilm-forming ability, we assessed biofilm formation in defined modified basal medium (BM2), to rule out serum-mediated killing, and discovered a strong and significant association between the serum resistance category and BM2 biofilm biomass (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      &lt; 0.0001). By applying regression models, we discovered that biofilm formation serves as a significant predictor for bacterial survival in serum. Overall, our findings establish biofilm production in\n                      <jats:italic toggle=\"yes\">K. pneumoniae<\/jats:italic>\n                      as a biomarker of serum survival and may open a new avenue for predicting bloodstream infection risk in clinical settings.\n                    <\/jats:p>\n                    <jats:sec>\n                      <jats:title>IMPORTANCE<\/jats:title>\n                      <jats:p>\n                        Bloodstream infections caused by\n                        <jats:italic toggle=\"yes\">Klebsiella pneumoniae<\/jats:italic>\n                        are devastating life-threatening infections worldwide. Understanding the survival strategies of\n                        <jats:italic toggle=\"yes\">K. pneumoniae<\/jats:italic>\n                        in the bloodstream is critical for elucidating key aspects of bacterial pathogenicity and developing new diagnostic and therapeutic modalities. Although serum survival is a recognized virulence trait necessary to thrive in the bloodstream, the relationship between serum resistance and biofilm formation, a multicellular organization that may protect bacteria from bloodstream stressors, remains poorly understood. In this article, we demonstrate biofilm production in human serum by clinical classical\n                        <jats:italic toggle=\"yes\">K. pneumoniae<\/jats:italic>\n                        strains for the first time and discovered a direct correlation between the level of biofilm biomass formation and the degree of serum survival in human serum and in defined modified basal medium. These findings offer insights into the importance of biofilm production in\n                        <jats:italic toggle=\"yes\">K. pneumoniae<\/jats:italic>\n                        serum resistance and may be used to develop future therapeutic strategies targeting bloodstream infections.\n                      <\/jats:p>\n                    <\/jats:sec>\n                  <\/jats:sec>","DOI":"10.1128\/mbio.00752-26","type":"journal-article","created":{"date-parts":[[2026,6,3]],"date-time":"2026-06-03T13:01:07Z","timestamp":1780491667000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":0,"title":["<i>Klebsiella pneumoniae<\/i>\n                    biofilm formation predicts its survival in human serum"],"prefix":"10.1128","volume":"17","author":[{"given":"Hadas","family":"Fulman-Levy","sequence":"first","affiliation":[{"id":[{"id":"https:\/\/ror.org\/03nz8qe97","id-type":"ROR","asserted-by":"publisher"}],"name":"The Department of Molecular Biology, The Faculty of Natural Sciences, Ariel University","place":["Ariel, Israel"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Liat A.","family":"Sinberger","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/03nz8qe97","id-type":"ROR","asserted-by":"publisher"}],"name":"The Department of Molecular Biology, The Faculty of Natural Sciences, Ariel University","place":["Ariel, Israel"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Polina","family":"Geva","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/03nz8qe97","id-type":"ROR","asserted-by":"publisher"}],"name":"The Department of Molecular Biology, The Faculty of Natural Sciences, Ariel University","place":["Ariel, Israel"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jonathan","family":"Lellouche","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/03nz8qe97","id-type":"ROR","asserted-by":"publisher"}],"name":"The Adelson School of Medicine, Ariel University","place":["Ariel, Israel"]},{"id":[{"id":"https:\/\/ror.org\/044wvm991","id-type":"ROR","asserted-by":"publisher"}],"name":"Clinical Laboratories Department, Sanz Medical Center, Laniado Hospital","place":["Netanya, Israel"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4916-110X","authenticated-orcid":true,"given":"Shiri","family":"Navon-Venezia","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/03nz8qe97","id-type":"ROR","asserted-by":"publisher"}],"name":"The Department of Molecular Biology, The Faculty of Natural Sciences, Ariel University","place":["Ariel, Israel"]},{"id":[{"id":"https:\/\/ror.org\/03nz8qe97","id-type":"ROR","asserted-by":"publisher"}],"name":"The Adelson School of Medicine, Ariel University","place":["Ariel, Israel"]}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"235","reference":[{"key":"e_1_3_5_2_2","unstructured":"Institute for Health Metrics and Evaluation. 2025. 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