{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T08:21:17Z","timestamp":1787732477675,"version":"build-2784847793"},"reference-count":26,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2026,8,23]],"date-time":"2026-08-23T00:00:00Z","timestamp":1787443200000},"content-version":"vor","delay-in-days":22,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,8,1]],"date-time":"2026-08-01T00:00:00Z","timestamp":1785542400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["MicrobiologyOpen"],"published-print":{"date-parts":[[2026,8]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>\n                      Antimicrobial\u2010resistant\n                      <jats:italic>Klebsiella pneumoniae<\/jats:italic>\n                      is a major clinical threat in Pakistan and the wider South Asian region, where genomic surveillance remains limited. We analyzed 122 publicly available human clinical\n                      <jats:italic>K. pneumoniae<\/jats:italic>\n                      whole\u2010genome sequencing datasets from Pakistan to define lineage structure, antimicrobial\u2010resistance determinants, virulence\u2010associated loci, surface\u2010antigen profiles, plasmid replicons, and genomic relatedness.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      Reads were extracted, quality\u2010filtered and assembled de novo, and assembly quality was assessed. Assemblies were characterized using Kleborate and ABRicate with the PlasmidFinder database. Trimmed reads were mapped to the\n                      <jats:italic>K. pneumoniae<\/jats:italic>\n                      MGH 78578 reference genome, and high\u2010confidence biallelic SNPs (QUAL\u2009\u2265\u200930; per\u2010isolate depth \u2265\u200910) were used to calculate pairwise genomic distances.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      The cohort contained 23 sequence types and was dominated by ST15 (41\/122, 33.61%), followed by ST48 (17\/122, 13.93%), ST336 (11\/122, 9.02%), ST711 (7\/122, 5.74%), and ST3805 (7\/122, 5.74%). Acquired resistance profiling detected 48 distinct antimicrobial\u2010resistance genes.\n                      <jats:italic>bla<\/jats:italic>\n                      <jats:sub>CTX\u2010M\u201015<\/jats:sub>\n                      was present in 121 isolates (99.18%),\n                      <jats:italic>bla<\/jats:italic>\n                      <jats:sub>VEB\u20105<\/jats:sub>\n                      in 45 (36.89%), and\n                      <jats:italic>bla<\/jats:italic>\n                      <jats:sub>NDM\u20101<\/jats:sub>\n                      in 16 (13.11%).\n                      <jats:italic>bla<\/jats:italic>\n                      <jats:sub>NDM\u20101<\/jats:sub>\n                      \u2010positive isolates occurred in four principal ST\/capsule\/O\u2010locus backgrounds. Yersiniabactin and aerobactin loci were detected in 48 (39.34%) and 43 (35.25%) isolates, respectively; 43 isolates had a Kleborate virulence score \u2265\u20093, whereas colibactin and\n                      <jats:italic>rmpADC<\/jats:italic>\n                      were not detected. IncFIB(K)_1_Kpn3 was the most frequent plasmid replicon marker (101\/122, 82.79%). Analysis of 169,220 high\u2010confidence biallelic SNP sites yielded 7381 pairwise comparisons, with a median distance of 30,224 SNPs and no pairs differing by \u2264\u200910 SNPs.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      The cohort showed broad genomic diversity, near\u2010universal\n                      <jats:italic>bla<\/jats:italic>\n                      <jats:sub>CTX\u2010M\u201015<\/jats:sub>\n                      carriage, lineage\u2010structured\n                      <jats:italic>bla<\/jats:italic>\n                      <jats:sub>NDM\u20101<\/jats:sub>\n                      backgrounds, frequent siderophore\u2010associated virulence loci, and distinct plasmid\u2010replicon profiles. The findings support multiple co\u2010circulating multidrug\u2010resistant genomic backgrounds rather than a single clonal expansion and provide a reference point for genomic surveillance in Pakistan.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1002\/mbo3.70381","type":"journal-article","created":{"date-parts":[[2026,8,24]],"date-time":"2026-08-24T05:19:05Z","timestamp":1787548745000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Genomic Epidemiology of Multidrug\u2010Resistant Clinical\n                    <i>Klebsiella pneumoniae<\/i>\n                    From Pakistan"],"prefix":"10.1002","volume":"15","author":[{"given":"Hakeem","family":"Zada","sequence":"first","affiliation":[{"name":"Department of Microbiology Kohat University of Science and Technology Kohat 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