{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,5]],"date-time":"2026-03-05T14:27:26Z","timestamp":1772720846176,"version":"3.50.1"},"reference-count":126,"publisher":"Akademiai Kiado Zrt.","issue":"1","content-domain":{"domain":["akjournals.com"],"crossmark-restriction":true},"short-container-title":["AMICR"],"published-print":{"date-parts":[[2026,3,5]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>\n                    The emergence of carbapenem-resistant\n                    <jats:italic>Klebsiella pneumoniae<\/jats:italic>\n                    (CRKP) poses a significant challenge globally. This study reports on a ceftazidime-avibactam resistant KPC-35 producing\n                    <jats:italic>K. pneumoniae<\/jats:italic>\n                    strain from a patient with cerebral hemorrhage undergoing ceftazidime-avibactam (CZA) treatment. In this study, three\n                    <jats:italic>K. pneumoniae<\/jats:italic>\n                    strains were isolated from blood samples of a patient after intracerebral hemorrhage. Broth microdilution, checkerboard assays, and time-kill assays were employed to evaluate antimicrobial susceptibility and combination regimens. Whole-genome sequencing (WGS) was used to investigate the genetic characteristics of the three\n                    <jats:italic>K. pneumoniae<\/jats:italic>\n                    strains. The results showed that,\n                    <jats:italic>K. pneumoniae<\/jats:italic>\n                    KP29870 strain belonged to ST15, it was KPC-35 positive and exhibited a 16-fold higher minimum inhibitory concentration (MIC) of CZA (32 vs 1\u20132\u2009mg L\n                    <jats:sup>\u22121<\/jats:sup>\n                    ) but significantly lower MICs of imipenem (2 vs \u2265 16\u2009mg L\n                    <jats:sup>\u22121<\/jats:sup>\n                    ) and meropenem (1 vs \u2265 16\u2009mg L\n                    <jats:sup>\u22121<\/jats:sup>\n                    ), compared to the other two\u2009\n                    <jats:italic>K. pneumoniae<\/jats:italic>\n                    strains, that harboured KPC-2. CZA resistant\n                    <jats:italic>K. pneumoniae<\/jats:italic>\n                    remained highly susceptible to aztreonam-avibactam (MIC 0.03\/4\u2009mg L\n                    <jats:sup>\u22121<\/jats:sup>\n                    ). The single base mutation (T503C) resulted in the substitution of leucine with proline at Ambler amino acid position 169 (L169P), corresponding to an evolution from\n                    <jats:italic>bla<\/jats:italic>\n                    <jats:sub>KPC-2<\/jats:sub>\n                    to\n                    <jats:italic>bla<\/jats:italic>\n                    <jats:sub>KPC-35<\/jats:sub>\n                    . Checkerboard and time-kill assays demonstrated synergistic antibacterial effects for CZA combined with imipenem, meropenem, or with aztreonam against KPC-35 positive\n                    <jats:italic>K. pneumoniae<\/jats:italic>\n                    . This is the first report in China of a\n                    <jats:italic>K. pneumoniae<\/jats:italic>\n                    ST15 strain harboring\n                    <jats:italic>bla<\/jats:italic>\n                    <jats:sub>KPC-35<\/jats:sub>\n                    emerging from a\n                    <jats:italic>bla<\/jats:italic>\n                    <jats:sub>KPC-2<\/jats:sub>\n                    -positive ancestor during CZA treatment. The new \u03b2-lactamase inhibitor combination such as aztreonam-avibactam monotherapy or CZA combined with carbapenems or with aztreonam represents promising treatment strategies against such KPC mutants. We recommend prompt susceptibility testing and KPC genotyping if resistance emergence is suspected during CZA therapy.\n                  <\/jats:p>","DOI":"10.1556\/030.2026.02845","type":"journal-article","created":{"date-parts":[[2026,1,14]],"date-time":"2026-01-14T11:05:38Z","timestamp":1768388738000},"page":"45-53","update-policy":"https:\/\/doi.org\/10.1556\/policypage.crossmark.crossref.2","source":"Crossref","is-referenced-by-count":0,"title":["Characterization of ceftazidime-avibactam resistant blaKPC-35-harbouring Klebsiella pneumoniae ST15 from bloodstream infection"],"prefix":"10.1556","volume":"73","author":[{"given":"Yihui","family":"Gong","sequence":"first","affiliation":[{"name":"Jinling Clinical Medical College, Nanjing Medical University, Nanjing, 210002, Jiangsu, China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lingfei","family":"Wang","sequence":"additional","affiliation":[{"name":"Department of Clinical Pharmacy, Jinling Hospital, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, 210002, Guangdong, China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Qiao","family":"Wang","sequence":"additional","affiliation":[{"name":"Jinling Clinical Medical College, Nanjing Medical University, Nanjing, 210002, Jiangsu, China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Huijie","family":"Yue","sequence":"additional","affiliation":[{"name":"Department of Clinical Pharmacy, Jinling Hospital, Affiliated Hospital of Medical School, State Key Laboratory of Analytical Chemistry for Life Science, Nanjing University, Nanjing, 210002, Jiangsu, China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ying","family":"Wang","sequence":"additional","affiliation":[{"name":"Clinical Laboratory, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, 210002, Jiangsu, China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tao","family":"Li","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, School of Medicine, Jinling Hospital, Nanjing University, Nanjing, 210002, Jiangsu, China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-6675-4452","authenticated-orcid":true,"given":"Guohua","family":"Zhou","sequence":"additional","affiliation":[{"name":"Jinling Clinical Medical College, Nanjing Medical University, Nanjing, 210002, Jiangsu, China"},{"name":"Department of Clinical Pharmacy, Jinling Hospital, Affiliated Hospital of Medical School, State Key Laboratory of Analytical Chemistry for Life Science, Nanjing University, Nanjing, 210002, Jiangsu, China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-5600-4508","authenticated-orcid":true,"given":"Xuejiao","family":"Liu","sequence":"additional","affiliation":[{"name":"Department of Clinical Pharmacy, Jinling Hospital, Affiliated Hospital of Medical School, State Key Laboratory of Analytical Chemistry for Life Science, Nanjing University, Nanjing, 210002, Jiangsu, China"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"425","reference":[{"issue":"9","key":"B1","series-title":"Lancet Infect Dis","doi-asserted-by":"publisher","first-page":"1033","DOI":"10.1016\/S1473-3099(25)00118-5","article-title":"The WHO bacterial priority pathogens list 2024: a prioritisation study to guide research, development, and public health strategies against antimicrobial resistance","volume":"25","author":"Sati H","year":"2025","unstructured":"Sati H, Carrara E, Savoldi A, Hansen P, Garlasco J, Campagnaro E, et al. 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