{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,30]],"date-time":"2026-07-30T14:18:23Z","timestamp":1785421103520,"version":"3.56.0"},"reference-count":43,"publisher":"American Society for Microbiology","issue":"6","license":[{"start":{"date-parts":[[2025,6,11]],"date-time":"2025-06-11T00:00:00Z","timestamp":1749600000000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2025,6,11]],"date-time":"2025-06-11T00:00:00Z","timestamp":1749600000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"funder":[{"DOI":"10.13039\/501100001711","name":"Schweizerischer Nationalfonds zur F\u00f6rderung der Wissenschaftlichen Forschung","doi-asserted-by":"publisher","award":["192514"],"award-info":[{"award-number":["192514"]}],"id":[{"id":"10.13039\/501100001711","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["J Clin Microbiol"],"published-print":{"date-parts":[[2025,6,11]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title\/>\n                    <jats:p>\n                      <jats:italic toggle=\"yes\">Klebsiella oxytoca<\/jats:italic>\n                      complex (\n                      <jats:italic toggle=\"yes\">Ko<\/jats:italic>\n                      C) are important nosocomial pathogens that can be reservoirs of transmissible extended-spectrum \u03b2-lactamase (ESBL) genes. Therefore, it is essential for clinical microbiology laboratories to distinguish between\n                      <jats:italic toggle=\"yes\">Ko<\/jats:italic>\n                      C producing ESBLs (ESBL-\n                      <jats:italic toggle=\"yes\">Ko<\/jats:italic>\n                      C) and those hyperproducing the natural OXY-type \u03b2-lactamases (hOXY-\n                      <jats:italic toggle=\"yes\">Ko<\/jats:italic>\n                      C). We investigated the abilities of VITEK 2 with and without using the Advanced Expert System (AES) to detect ESBL producers among 44 well-characterized\n                      <jats:italic toggle=\"yes\">Ko<\/jats:italic>\n                      C strains (including 11 ESBL-\n                      <jats:italic toggle=\"yes\">Ko<\/jats:italic>\n                      C and 21 hOXY-\n                      <jats:italic toggle=\"yes\">Ko<\/jats:italic>\n                      C). VITEK 2\/AES showed 100% sensitivity (Se) and 64.7% specificity (Sp), whereas the VITEK 2 coupled by the Clinical Laboratory Standards Institute (CLSI) ESBL confirmatory tests (ESBL-CTs; i.e., disk-combination tests) showed 100% Se and 97.5% Sp to detect ESBL-\n                      <jats:italic toggle=\"yes\">Ko<\/jats:italic>\n                      C. We also analyzed\n                      <jats:italic toggle=\"yes\">Ko<\/jats:italic>\n                      C-specific screening cutoffs for ceftriaxone (CRO), cefpodoxime (CPD), ceftazidime (CAZ), cefotaxime (CTX), and aztreonam (ATM) to negate unnecessary ESBL-CTs. As a result, we propose the following screening cutoffs (minimum inhibitory concentration [MIC] and inhibition zone diameter): CRO, &gt;4 \u00b5g\/mL and \u226416 mm; CPD, &gt;4 \u00b5g\/mL and \u226410 mm; CAZ, &gt;1 \u00b5g\/mL and \u226422 mm (European Committee on Antimicrobial Susceptibility Testing [EUCAST] disk)\/\u226430 mm (CLSI disk); CTX, &gt;4 \u00b5g\/mL and \u226412 mm (EUCAST disk)\/\u226422 mm (CLSI disk); ATM, &gt;1 \u00b5g\/mL and \u226428 mm. Notably, all suggested cutoffs could assure 100% Se and high Sp\/positive predictive values for our 44\n                      <jats:italic toggle=\"yes\">Ko<\/jats:italic>\n                      C strains. In conclusion, the AES performed poorly, while VITEK 2 with the CLSI ESBL-CTs yielded a reliable methodology to distinguish ESBL-\n                      <jats:italic toggle=\"yes\">Ko<\/jats:italic>\n                      C from hOXY-\n                      <jats:italic toggle=\"yes\">Ko<\/jats:italic>\n                      C. This study also proposed revised screening cutoffs for detecting ESBL-\n                      <jats:italic toggle=\"yes\">Ko<\/jats:italic>\n                      C and reducing the unnecessary use of ESBL-CTs.\n                    <\/jats:p>\n                    <jats:sec>\n                      <jats:title>IMPORTANCE<\/jats:title>\n                      <jats:p>\n                        Species within the\n                        <jats:italic toggle=\"yes\">Klebsiella oxytoca<\/jats:italic>\n                        complex (\n                        <jats:italic toggle=\"yes\">Ko<\/jats:italic>\n                        C) are emerging clinical pathogens of increasing concern. These bacteria can acquire plasmid-mediated ESBL genes, seriously complicating antibiotic treatment and overall management of infected patients. Differentiating ESBL-producing from non-ESBL-producing\n                        <jats:italic toggle=\"yes\">Ko<\/jats:italic>\n                        C isolates is therefore crucial. However, this task presents significant challenges for clinical laboratories. In this work, we showed that the automated VITEK 2 system equipped with its AES fails to differentiate the two groups of\n                        <jats:italic toggle=\"yes\">Ko<\/jats:italic>\n                        C isolates. In contrast, VITEK 2 alone followed by the ESBL screen and phenotypic confirmatory tests provides accurate differentiation. Since this latter approach increases the diagnostic workload, we also proposed new screening cutoffs for key cephalosporins that may reduce the current high number of unnecessary confirmatory tests.\n                      <\/jats:p>\n                    <\/jats:sec>\n                  <\/jats:sec>","DOI":"10.1128\/jcm.00128-25","type":"journal-article","created":{"date-parts":[[2025,5,9]],"date-time":"2025-05-09T09:07:19Z","timestamp":1746781639000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":1,"title":["Detection of ESBL-producing\n                    <i>Klebsiella oxytoca<\/i>\n                    complex with VITEK 2 system and screening cutoffs for implementing confirmatory tests"],"prefix":"10.1128","volume":"63","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-1846-9857","authenticated-orcid":false,"given":"Edgar I.","family":"Campos-Madueno","sequence":"first","affiliation":[{"id":[{"id":"https:\/\/ror.org\/02k7v4d05","id-type":"ROR","asserted-by":"publisher"}],"name":"Institute for Infectious Diseases (IFIK), University of Bern","place":["Bern, Switzerland"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Gisele","family":"Peirano","sequence":"additional","affiliation":[{"name":"Division of Microbiology, Alberta Precision Laboratories","place":["Calgary, Canada"]},{"id":[{"id":"https:\/\/ror.org\/03yjb2x39","id-type":"ROR","asserted-by":"publisher"}],"name":"Pathology and Laboratory Medicine, University of Calgary","place":["Calgary, Canada"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Claudia","family":"Aldeia","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/02k7v4d05","id-type":"ROR","asserted-by":"publisher"}],"name":"Institute for Infectious Diseases (IFIK), University of Bern","place":["Bern, Switzerland"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Maria V.","family":"Elzi","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/02k7v4d05","id-type":"ROR","asserted-by":"publisher"}],"name":"Institute for Infectious Diseases (IFIK), University of Bern","place":["Bern, Switzerland"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Claudine","family":"Kocher","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/02k7v4d05","id-type":"ROR","asserted-by":"publisher"}],"name":"Institute for Infectious Diseases (IFIK), University of Bern","place":["Bern, Switzerland"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-5160-5286","authenticated-orcid":true,"given":"Laurent","family":"Poirel","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/022fs9h90","id-type":"ROR","asserted-by":"publisher"}],"name":"Medical and Molecular Microbiology, Department of Medicine, University of Fribourg","place":["Fribourg, Switzerland"]},{"name":"National Reference Center for Emerging Antibiotic Resistance (NARA)","place":["Fribourg, Switzerland"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-1343-1622","authenticated-orcid":true,"given":"Patrice","family":"Nordmann","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/022fs9h90","id-type":"ROR","asserted-by":"publisher"}],"name":"Medical and Molecular Microbiology, Department of Medicine, University of Fribourg","place":["Fribourg, Switzerland"]},{"name":"National Reference Center for Emerging Antibiotic Resistance (NARA)","place":["Fribourg, Switzerland"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-5722-9445","authenticated-orcid":true,"given":"Vincent","family":"Perreten","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/02k7v4d05","id-type":"ROR","asserted-by":"publisher"}],"name":"Institute of Veterinary Bacteriology, University of Bern","place":["Bern, Switzerland"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Johann D. 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