{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,21]],"date-time":"2026-08-21T12:45:23Z","timestamp":1787316323290,"version":"build-2736575974"},"reference-count":54,"publisher":"American Society for Microbiology","issue":"8","license":[{"start":{"date-parts":[[2025,8,5]],"date-time":"2025-08-05T00:00:00Z","timestamp":1754352000000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2025,8,5]],"date-time":"2025-08-05T00:00:00Z","timestamp":1754352000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["Microbiol Spectr"],"published-print":{"date-parts":[[2025,8,5]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title\/>\n                    <jats:p>\n                      In view of insufficient data on the epidemiology and genomics of\n                      <jats:italic toggle=\"yes\">bla<\/jats:italic>\n                      <jats:sub>KPC-2<\/jats:sub>\n                      producing\n                      <jats:italic toggle=\"yes\">Klebsiella pneumoniae<\/jats:italic>\n                      subsp.\n                      <jats:italic toggle=\"yes\">pneumoniae<\/jats:italic>\n                      (KPC-2\n                      <jats:italic toggle=\"yes\">Kpn<\/jats:italic>\n                      ) from India, this study, first of its kind, was conducted to characterize blood-borne KPC-2\n                      <jats:italic toggle=\"yes\">Kpn<\/jats:italic>\n                      isolates according to their resistome, plasmid types, and genotypes. This study included 45 blood-borne KPC-2\n                      <jats:italic toggle=\"yes\">Kpn<\/jats:italic>\n                      isolates from ICU-admitted sepsis patients in Kolkata from 2015 to 2024. These isolates were tested for antibiotic susceptibility against \u226510 antimicrobial classes. Antimicrobial resistance gene profiles, genetic environment of\n                      <jats:italic toggle=\"yes\">bla<\/jats:italic>\n                      <jats:sub>KPC-2<\/jats:sub>\n                      , plasmid types, MLST genotypes, and virulence genes were determined by whole-genome shotgun sequencing (WGS). The transmissibility of\n                      <jats:italic toggle=\"yes\">bla<\/jats:italic>\n                      <jats:sub>KPC-2<\/jats:sub>\n                      genes was evaluated by conjugation experiment. Pulsed-field gel electrophoresis (PFGE) was conducted to confirm their clonality. SNP-based phylogenomic analysis was performed to compare the study isolates with global KPC-2\n                      <jats:italic toggle=\"yes\">Kpn<\/jats:italic>\n                      isolates. All 45 (100%) KPC-2\n                      <jats:italic toggle=\"yes\">Kpn<\/jats:italic>\n                      isolates showed resistance to 21 antimicrobials. In addition, 55.55% and 33.33% isolates were resistant to colistin and ceftazidime-avibactam, respectively. Presence of triple carbapenemase (\n                      <jats:italic toggle=\"yes\">bla<\/jats:italic>\n                      <jats:sub>KPC-2<\/jats:sub>\n                      ,\n                      <jats:italic toggle=\"yes\">bla<\/jats:italic>\n                      <jats:sub>NDM-1\/5<\/jats:sub>\n                      and\n                      <jats:italic toggle=\"yes\">bla<\/jats:italic>\n                      <jats:sub>OXA-181\/232<\/jats:sub>\n                      ) was observed in six isolates.\n                      <jats:italic toggle=\"yes\">bla<\/jats:italic>\n                      <jats:sub>KPC-2<\/jats:sub>\n                      transferable by IncFII\/IncFII(pBK30683)\/ColRNAI conjugative plasmids. WGS identified two distinct genetic environments of\n                      <jats:italic toggle=\"yes\">bla<\/jats:italic>\n                      <jats:sub>KPC-2<\/jats:sub>\n                      among the isolates based on presence or absence of Tn\n                      <jats:italic toggle=\"yes\">4401<\/jats:italic>\n                      . PFGE identified 45 pulsotypes with a 39.3% similarity coefficient, indicating a variety of infection sources. Of the 16 MLST genotypes found in circulation, ST15 was predominant and ST7485 was novel. Hypervirulent genetic markers (\n                      <jats:italic toggle=\"yes\">iucA<\/jats:italic>\n                      ,\n                      <jats:italic toggle=\"yes\">iutA<\/jats:italic>\n                      , and\n                      <jats:italic toggle=\"yes\">rmpA2<\/jats:italic>\n                      ) were identified in four isolates. Hospital infection control and surveillance programs should be strengthened to detect and combat\n                      <jats:italic toggle=\"yes\">K. pneumoniae<\/jats:italic>\n                      co-harboring\n                      <jats:italic toggle=\"yes\">bla<\/jats:italic>\n                      <jats:sub>KPC-2<\/jats:sub>\n                      and\/or\n                      <jats:italic toggle=\"yes\">bla<\/jats:italic>\n                      <jats:sub>NDM<\/jats:sub>\n                      and\/or\n                      <jats:italic toggle=\"yes\">bla<\/jats:italic>\n                      <jats:sub>OXA-48-like<\/jats:sub>\n                      carbapenemase.\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                        (\n                        <jats:italic toggle=\"yes\">Kpn<\/jats:italic>\n                        ) is the primary etiology of ICU-related bloodstream infections in India. Multi-drug resistance, including resistance to carbapenems and colistin, along with myriad virulence factors, makes this bacterium really troublesome with respect to effective treatment. In India,\n                        <jats:italic toggle=\"yes\">bla<\/jats:italic>\n                        <jats:sub>NDM<\/jats:sub>\n                        and\n                        <jats:italic toggle=\"yes\">bla<\/jats:italic>\n                        <jats:sub>OXA-48-like<\/jats:sub>\n                        carbapenemases are the most prevalent types with only sporadic reports of\n                        <jats:italic toggle=\"yes\">bla<\/jats:italic>\n                        <jats:sub>KPC<\/jats:sub>\n                        in\n                        <jats:italic toggle=\"yes\">Kpn<\/jats:italic>\n                        . This study focuses on the emergence of\n                        <jats:italic toggle=\"yes\">bla<\/jats:italic>\n                        <jats:sub>KPC-2<\/jats:sub>\n                        in\n                        <jats:italic toggle=\"yes\">Kpn<\/jats:italic>\n                        along with other carbapenemases in Kolkata, India. This study is also the first of its kind to describe the presence of triple carbapenemase (\n                        <jats:italic toggle=\"yes\">bla<\/jats:italic>\n                        <jats:sub>KPC-2<\/jats:sub>\n                        ,\n                        <jats:italic toggle=\"yes\">bla<\/jats:italic>\n                        <jats:sub>NDM-1\/5<\/jats:sub>\n                        and\n                        <jats:italic toggle=\"yes\">bla<\/jats:italic>\n                        <jats:sub>OXA-181\/232<\/jats:sub>\n                        ) and concurrent resistance to carbapenems, colistin, and ceftazidime-avibactam antimicrobials in\n                        <jats:italic toggle=\"yes\">Kpn.<\/jats:italic>\n                        In addition, this study also highlights the diverse genotypes (sequence types) identified in KPC-2\n                        <jats:italic toggle=\"yes\">Kpn,<\/jats:italic>\n                        including the novel ST7485 identified in this study. Routine monitoring of antimicrobial resistance genes in\n                        <jats:italic toggle=\"yes\">Kpn<\/jats:italic>\n                        should be encouraged to identify the emerging resistome, which will aid in determining the most effective treatment.\n                      <\/jats:p>\n                    <\/jats:sec>\n                  <\/jats:sec>","DOI":"10.1128\/spectrum.00126-25","type":"journal-article","created":{"date-parts":[[2025,6,12]],"date-time":"2025-06-12T08:27:18Z","timestamp":1749716838000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":7,"title":["Antimicrobial resistance and phylogenetic lineages of KPC-2-producing blood-borne\n                    <i>Klebsiella pneumoniae<\/i>\n                    subsp.\n                    <i>pneumoniae<\/i>\n                    from Kolkata, India during 2015\u20132024: Emergence of\n                    <i>Klebsiella pneumoniae<\/i>\n          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