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We evaluated sulbactam-durlobactam activity against 94 isolates from Brazil. Durlobactam markedly reduced sulbactam MICs, restoring susceptibility in all CRAb. They belonged to seven STs, mainly ST730 and ST79. Despite genetic and phenotypic diversity, including distinct carbapenemase genes (particularly\n                      <jats:italic toggle=\"yes\">bla<\/jats:italic>\n                      <jats:sub>OXA-23-like<\/jats:sub>\n                      ) and the presence of PBP3 mutations, activity remained consistent. These findings support sulbactam-durlobactam as an effective option against CRAb in this high-endemic setting.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1128\/aac.00109-26","type":"journal-article","created":{"date-parts":[[2026,6,12]],"date-time":"2026-06-12T13:33:34Z","timestamp":1781271214000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":0,"title":["Consistent\n                    <i>in vitro<\/i>\n                    activity of sulbactam-durlobactam against genetically diverse carbapenem-resistant\n                    <i>Acinetobacter baumannii<\/i>\n                    in a high-endemic Brazilian setting"],"prefix":"10.1128","volume":"70","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-2819-0769","authenticated-orcid":true,"given":"Gabriela da 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