{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T15:48:43Z","timestamp":1787759323194,"version":"build-2784847793"},"reference-count":28,"publisher":"SAGE Publications","issue":"4","license":[{"start":{"date-parts":[[2026,2,12]],"date-time":"2026-02-12T00:00:00Z","timestamp":1770854400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Microbial Drug Resistance"],"published-print":{"date-parts":[[2026,4,1]]},"abstract":"<jats:sec>\n                    <jats:title>Background:<\/jats:title>\n                    <jats:p>There are limited oral treatment options available for resistant Gram-negative bacterial (GNB) infections. Minocycline, a second-generation tetracycline antibiotic, offers good bioavailability and broad-spectrum coverage that may be an option for GNB infections.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods:<\/jats:title>\n                    <jats:p>\n                      We conducted a retrospective review of minocycline susceptibility testing performed on GNB isolates at the Mayo Clinic reference lab between 2013 and 2022. Minocycline susceptibility was evaluated with a focus on difficult-to-treat organisms and relevant anatomic source. Organisms included resistant isolates of\n                      <jats:italic toggle=\"yes\">Escherichia coli<\/jats:italic>\n                      and\n                      <jats:italic toggle=\"yes\">Klebsiella pneumoniae<\/jats:italic>\n                      ; high-risk ampC-derepressors, including\n                      <jats:italic toggle=\"yes\">Citrobacter freundii, Enterobacter cloacae,<\/jats:italic>\n                      and\n                      <jats:italic toggle=\"yes\">K. aerogenes;<\/jats:italic>\n                      and clinically challenging non-Enterobacterales,\n                      <jats:italic toggle=\"yes\">Acinetobacter species, Achromobacter species,<\/jats:italic>\n                      and\n                      <jats:italic toggle=\"yes\">Stenotrophomonas maltophilia<\/jats:italic>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results:<\/jats:title>\n                    <jats:p>\n                      Of 217,206 GNB isolates, 18,148 Enterobacterales (EB) and 8,190 non-\n                      <jats:italic toggle=\"yes\">Enterobacter<\/jats:italic>\n                      isolates were tested for minocycline susceptibility. Of these, 80% of all EB and 92% of non-EB isolates were susceptible. Among\n                      <jats:italic toggle=\"yes\">E. coli<\/jats:italic>\n                      isolates with ceftriaxone, ciprofloxacin, meropenem, or multidrug resistance, minocycline susceptibility was 78%, 76%, 70%, and 70.9%, respectively. Among the\n                      <jats:italic toggle=\"yes\">K. pneumoniae<\/jats:italic>\n                      isolates with ceftriaxone, ciprofloxacin, meropenem, or multidrug resistance, minocycline susceptibility was 46%, 38%, 37%, and 39.3%, respectively. 85% of\n                      <jats:italic toggle=\"yes\">C. freundii<\/jats:italic>\n                      , 81% of\n                      <jats:italic toggle=\"yes\">E. cloacae,<\/jats:italic>\n                      and 85% of\n                      <jats:italic toggle=\"yes\">K. aerogenes<\/jats:italic>\n                      isolates were susceptible to Minocycline. 83.5% of\n                      <jats:italic toggle=\"yes\">Achromobacter<\/jats:italic>\n                      species isolates, 66% of\n                      <jats:italic toggle=\"yes\">Acinetobacter<\/jats:italic>\n                      species isolates, and 99.1% of\n                      <jats:italic toggle=\"yes\">S. maltophilia<\/jats:italic>\n                      isolates were susceptible.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions:<\/jats:title>\n                    <jats:p>\n                      Our study reports the largest collection of minocycline susceptibility findings in GNB. Minocycline showed\n                      <jats:italic toggle=\"yes\">in vitro<\/jats:italic>\n                      activity against many difficult-to-treat GNB isolates, including ceftriaxone- and multidrug-resistant\n                      <jats:italic toggle=\"yes\">E. coli<\/jats:italic>\n                      and some\n                      <jats:italic toggle=\"yes\">K. pneumoniae<\/jats:italic>\n                      isolates, common Amp-C-producing species, and non-fermenting GNB, including\n                      <jats:italic toggle=\"yes\">Stenotrophomonas<\/jats:italic>\n                      ,\n                      <jats:italic toggle=\"yes\">Acinetobacter<\/jats:italic>\n                      , and\n                      <jats:italic toggle=\"yes\">Achromobacter<\/jats:italic>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1177\/10766294261424485","type":"journal-article","created":{"date-parts":[[2026,3,31]],"date-time":"2026-03-31T13:45:56Z","timestamp":1774964756000},"page":"128-134","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":1,"title":["Show Me the \u201cMino:\u201d\n                    <i>In Vitro<\/i>\n                    Efficacy of Minocycline on Clinical Gram-Negative Bacterial Isolates"],"prefix":"10.1177","volume":"32","author":[{"given":"Patrick D.","family":"Crowley","sequence":"first","affiliation":[{"name":"Division of Public Health, Infectious Diseases, and Occupational Medicine, Mayo Clinic, Rochester, Minnesota, USA."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nischal","family":"Ranganath","sequence":"additional","affiliation":[{"name":"Division of Public Health, Infectious Diseases, and Occupational Medicine, Mayo Clinic, Rochester, Minnesota, USA."},{"name":"Division of Hospital Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Portia","family":"Mira","sequence":"additional","affiliation":[{"name":"Division of Clinical Microbiology, Mayo Clinic, Rochester, Minnesota, USA."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nicholas","family":"Streck","sequence":"additional","affiliation":[{"name":"Division of Clinical Microbiology, Mayo Clinic, Rochester, Minnesota, USA."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Douglas W.","family":"Challener","sequence":"additional","affiliation":[{"name":"Division of Public Health, Infectious Diseases, and Occupational Medicine, Mayo Clinic, Rochester, Minnesota, USA."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Christina G.","family":"Rivera","sequence":"additional","affiliation":[{"name":"Department of Pharmacy, Mayo Clinic, Rochester, Minnesota, USA."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Omar","family":"Abu Saleh","sequence":"additional","affiliation":[{"name":"Division of Public Health, Infectious Diseases, and Occupational Medicine, Mayo Clinic, Rochester, Minnesota, USA."}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"179","published-online":{"date-parts":[[2026,2,12]]},"reference":[{"key":"e_1_3_2_2_2","first-page":"2669","volume-title":"Mandell, Douglas, and Bennett\u2019s Principles and Practice of Infectious Diseases","author":"Nelson GE","year":"2020","unstructured":"Nelson GE, , Greene, , Matthew H. 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