{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,30]],"date-time":"2026-07-30T18:22:00Z","timestamp":1785435720790,"version":"3.56.0"},"reference-count":34,"publisher":"American Society for Microbiology","issue":"6","license":[{"start":{"date-parts":[[2026,6,3]],"date-time":"2026-06-03T00:00:00Z","timestamp":1780444800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,6,3]],"date-time":"2026-06-03T00:00:00Z","timestamp":1780444800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"funder":[{"DOI":"10.13039\/501100003074","name":"Agencia Nacional de Promoci\u00f3n Cient\u00edfica y Tecnol\u00f3gica","doi-asserted-by":"publisher","award":["PICT-2018-03139"],"award-info":[{"award-number":["PICT-2018-03139"]}],"id":[{"id":"10.13039\/501100003074","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100003074","name":"Agencia Nacional de Promoci\u00f3n Cient\u00edfica y Tecnol\u00f3gica","doi-asserted-by":"publisher","award":["PICT-2021-0147"],"award-info":[{"award-number":["PICT-2021-0147"]}],"id":[{"id":"10.13039\/501100003074","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["Antimicrob Agents Chemother"],"published-print":{"date-parts":[[2026,6,3]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title\/>\n                    <jats:p>\n                      <jats:italic toggle=\"yes\">Pseudomonas aeruginosa<\/jats:italic>\n                      thrive to survive in harsh conditions imposed by the host. We have previously described two Zn\n                      <jats:sup>2+<\/jats:sup>\n                      -transporting members of the Cation Diffusion Facilitator family, YiiP and CzcD, inhibiting susceptibility to imipenem by decreasing the expression of the outer membrane porin OprD (A. Salusso and D. Raimunda, Front Cell Infect Microbiol 7:84, 2017,\n                      <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"https:\/\/doi.org\/10.3389\/fcimb.2017.00084\" xlink:type=\"simple\">https:\/\/doi.org\/10.3389\/fcimb.2017.00084<\/jats:ext-link>\n                      ). Here, we provide evidence that a protein encoded in\n                      <jats:italic toggle=\"yes\">yiiP<\/jats:italic>\n                      \u2019s operon, PA3962, is fundamental to the coupling of these processes. Immunodetection assay indicates that PA3962 locates in membranes. Supporting a role in\n                      <jats:italic toggle=\"yes\">oprD<\/jats:italic>\n                      regulation, a PA3962 insertional mutant has a significant increase of\n                      <jats:italic toggle=\"yes\">oprD<\/jats:italic>\n                      expression levels and imipenem sensitivity, which is suppressed by gene complementation but not in the presence of Zn\n                      <jats:sup>2+<\/jats:sup>\n                      , as opposed to the YiiP mutant. We identified two pairs of conserved acidic residues in a hydrophobic juxtamembrane domain. Metal binding specificity and stoichiometry were explored in wild-type and mutant versions of these. Zn\n                      <jats:sup>2+<\/jats:sup>\n                      appears as the cognate metal of PA3962, with residues D40, D47, and D65 required for its coordination. As the periplasmic Zn\n                      <jats:sup>2+<\/jats:sup>\n                      -sensor CzcS regulates\n                      <jats:italic toggle=\"yes\">oprD<\/jats:italic>\n                      expression, the interaction with it was analyzed\n                      <jats:italic toggle=\"yes\">in vitro<\/jats:italic>\n                      . Interaction was Zn\n                      <jats:sup>2+<\/jats:sup>\n                      -dependent, and mutations of D47A or D65A abolished it. We propose a role for PA3962, hereafter periplasmic metallochaperone of YiiP (PmcY), in the context of Zn\n                      <jats:sup>2+<\/jats:sup>\n                      signaling pathways in\n                      <jats:italic toggle=\"yes\">P. aeruginosa<\/jats:italic>\n                      . The relay YiiP\u2013PmcY supplies Zn\n                      <jats:sup>2+<\/jats:sup>\n                      and activates CzcS\/CzcR, down-regulating the transcription of the imipenem-permeable OprD. This mechanism would allow\n                      <jats:italic toggle=\"yes\">P. aeruginosa<\/jats:italic>\n                      to put a brake on unspecific mechanisms for micronutrient uptake, with potential xenobiotic entry, while the cytosolic Zn\n                      <jats:sup>2+<\/jats:sup>\n                      quota is still sufficient.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1128\/aac.00318-26","type":"journal-article","created":{"date-parts":[[2026,5,15]],"date-time":"2026-05-15T14:21:15Z","timestamp":1778854875000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":0,"title":["A periplasmic metallochaperone (PmcY) couples Zn\n                    <sup>2+<\/sup>\n                    transport to sensing in\n                    <i>Pseudomonas aeruginosa<\/i>"],"prefix":"10.1128","volume":"70","author":[{"ORCID":"https:\/\/orcid.org\/0009-0005-8467-0179","authenticated-orcid":false,"given":"Paula","family":"Mihelj","sequence":"first","affiliation":[{"id":[{"id":"https:\/\/ror.org\/04nh79216","id-type":"ROR","asserted-by":"publisher"}],"name":"Instituto de Investigaciones M\u00e9dicas Mercedes y Mart\u00edn Ferreyra, INIMEC-CONICET-Universidad Nacional de C\u00f3rdoba","place":["C\u00f3rdoba, Argentina"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tom\u00e1s","family":"Moreyra","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/04nh79216","id-type":"ROR","asserted-by":"publisher"}],"name":"Instituto de Investigaciones M\u00e9dicas Mercedes y Mart\u00edn Ferreyra, INIMEC-CONICET-Universidad Nacional de C\u00f3rdoba","place":["C\u00f3rdoba, 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Argentina"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4624-0822","authenticated-orcid":false,"given":"Teresita","family":"Padilla-Benavides","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/05h7xva58","id-type":"ROR","asserted-by":"publisher"}],"name":"Department of Molecular Biology and Biochemistry, Wesleyan University","place":["Middletown, USA"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-7392-1407","authenticated-orcid":true,"given":"Daniel","family":"Raimunda","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/04nh79216","id-type":"ROR","asserted-by":"publisher"}],"name":"Instituto de Investigaciones M\u00e9dicas Mercedes y Mart\u00edn Ferreyra, INIMEC-CONICET-Universidad Nacional de C\u00f3rdoba","place":["C\u00f3rdoba, 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