{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,4]],"date-time":"2026-05-04T19:32:43Z","timestamp":1777923163343,"version":"3.51.4"},"reference-count":21,"publisher":"SAGE Publications","issue":"9","license":[{"start":{"date-parts":[[2023,8,28]],"date-time":"2023-08-28T00:00:00Z","timestamp":1693180800000},"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":[[2023,9]]},"abstract":"<jats:p>\n                    To investigate the occurrence of oxazolidinone resistance genes, 18 florfenicol-resistant enterococci were isolated from 66 fecal samples collected from several cattle farms in central Italy. The PCR screening indicated that only a bovine florfenicol-resistant isolate,\n                    <jats:italic toggle=\"yes\">Enterococcus faecium<\/jats:italic>\n                    249031-C, was positive for the presence of\n                    <jats:italic toggle=\"yes\">optrA<\/jats:italic>\n                    and\n                    <jats:italic toggle=\"yes\">poxtA<\/jats:italic>\n                    genes. The strain was tested for its susceptibility to florfenicol, chloramphenicol, linezolid, tedizolid, tetracycline, erythromycin, and vancomycin. Whole Genome Sequencing analysis showed that\n                    <jats:italic toggle=\"yes\">E. faecium<\/jats:italic>\n                    249031-C, belonging to the ST22 lineage, harbored two plasmids: the\n                    <jats:italic toggle=\"yes\">optrA<\/jats:italic>\n                    -carrying p249031-S (179\u2009kb) and the\n                    <jats:italic toggle=\"yes\">poxtA<\/jats:italic>\n                    -carrying p1818-c (23\u2009kb). p249031-S, containing a new\n                    <jats:italic toggle=\"yes\">optrA<\/jats:italic>\n                    -carrying Tn\n                    <jats:italic toggle=\"yes\">7695<\/jats:italic>\n                    transposon, was closely related to the plasmid pF88_1 of\n                    <jats:italic toggle=\"yes\">E. faecium<\/jats:italic>\n                    F88, whereas p1818-c had already been detected in a human\n                    <jats:italic toggle=\"yes\">E. faecium<\/jats:italic>\n                    , both enterococci were from Switzerland. The linezolid resistance genes were cotransferred to the\n                    <jats:italic toggle=\"yes\">E. faecium<\/jats:italic>\n                    64\/3 recipient. Circular forms from both\n                    <jats:italic toggle=\"yes\">optrA<\/jats:italic>\n                    - and\n                    <jats:italic toggle=\"yes\">poxtA<\/jats:italic>\n                    -carrying genetic contexts were obtained. The occurrence of oxazolidinone resistance genes in a bovine\n                    <jats:italic toggle=\"yes\">E. faecium<\/jats:italic>\n                    isolate and their localization on conjugative and mobilizable plasmids pose a risk for public health.\n                  <\/jats:p>","DOI":"10.1089\/mdr.2023.0055","type":"journal-article","created":{"date-parts":[[2023,7,31]],"date-time":"2023-07-31T12:46:31Z","timestamp":1690807591000},"page":"438-442","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":4,"title":["An\n                    <i>Enterococcus faecium<\/i>\n                    Isolated from Bovine Feces in Italy Shares\n                    <i>optrA<\/i>\n                    - and\n                    <i>poxtA<\/i>\n                    -Carrying Plasmids with Enterococci from Switzerland"],"prefix":"10.1177","volume":"29","author":[{"given":"Marzia","family":"Cinthi","sequence":"first","affiliation":[{"name":"Department of Life and Environmental Sciences and Polytechnic University of Marche, Ancona, Italy."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sonia Nina","family":"Coccitto","sequence":"additional","affiliation":[{"name":"Department of Biomedical Sciences and Public Health, Polytechnic University of Marche, Ancona, Italy."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Serena","family":"Simoni","sequence":"additional","affiliation":[{"name":"Department of Life and Environmental Sciences and Polytechnic University of Marche, Ancona, Italy."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Carla","family":"Vignaroli","sequence":"additional","affiliation":[{"name":"Department of Life and Environmental Sciences and Polytechnic University of Marche, Ancona, Italy."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Andrea","family":"Brenciani","sequence":"additional","affiliation":[{"name":"Department of Biomedical Sciences and Public Health, Polytechnic University of Marche, Ancona, Italy."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Eleonora","family":"Giovanetti","sequence":"additional","affiliation":[{"name":"Department of Life and Environmental Sciences and Polytechnic University of Marche, Ancona, Italy."}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"179","published-online":{"date-parts":[[2023,8,28]]},"reference":[{"issue":"36","key":"e_1_3_5_2_2","doi-asserted-by":"crossref","first-page":"13339","DOI":"10.1073\/pnas.0804276105","article-title":"The oxazolidinone antibiotics perturb the ribosomal peptidyl-transferase center and effect tRNA positioning","volume":"105","author":"Wilson DN","year":"2008","unstructured":"Wilson DN, , Schluenzen F, , Harms JM, et al. The oxazolidinone antibiotics perturb the ribosomal peptidyl-transferase center and effect tRNA positioning. Proc Natl Acad Sci USA, 2008; 105(36):13339\u201313344; doi: 10.1073\/pnas.0804276105","journal-title":"Proc Natl Acad Sci USA"},{"issue":"10","key":"e_1_3_5_3_2","doi-asserted-by":"crossref","first-page":"2596","DOI":"10.1093\/jac\/dkac263","article-title":"Oxazolidinones: Mechanisms of resistance and mobile genetic elements involved","volume":"77","author":"Brenciani A","year":"2022","unstructured":"Brenciani A, , Morroni G, , Schwarz S, et al. Oxazolidinones: Mechanisms of resistance and mobile genetic elements involved. J Antimicrob Chemother, 2022; 77(10):2596\u20132621; doi: 10.1093\/jac\/dkac263","journal-title":"J Antimicrob Chemother"},{"issue":"3","key":"e_1_3_5_4_2","doi-asserted-by":"crossref","first-page":"598","DOI":"10.1093\/jac\/dkab456","article-title":"Occurrence of a plasmid cocarrying cfr(D) and poxtA2 linezolid resistance genes in Enterococcus faecalis and Enterococcus casseliflavus from porcine manure, Italy","volume":"77","author":"Cinthi M","year":"2022","unstructured":"Cinthi M, , Coccitto SN, , Fioriti S, et al. Occurrence of a plasmid cocarrying cfr(D) and poxtA2 linezolid resistance genes in Enterococcus faecalis and Enterococcus casseliflavus from porcine manure, Italy. J Antimicrob Chemother, 2022; 77(3):598\u2013603; doi: 10.1093\/jac\/dkab456","journal-title":"J Antimicrob Chemother"},{"issue":"2","key":"e_1_3_5_5_2","doi-asserted-by":"crossref","first-page":"331","DOI":"10.1093\/jac\/dkab408","article-title":"Linezolid-resistant Enterococcus gallinarum isolate of swine origin carrying cfr, optrA and poxtA genes","volume":"77","author":"Coccitto SN","year":"2022","unstructured":"Coccitto SN, , Cinthi M, , Fioriti S, et al. Linezolid-resistant Enterococcus gallinarum isolate of swine origin carrying cfr, optrA and poxtA genes. J Antimicrob Chemother, 2022; 77(2):331\u2013337; doi: 10.1093\/jac\/dkab408","journal-title":"J Antimicrob Chemother"},{"issue":"12","key":"e_1_3_5_6_2","doi-asserted-by":"crossref","first-page":"2021","DOI":"10.3390\/microorganisms8122021","article-title":"Detection of oxazolidinone resistance genes and characterization of genetic environments in enterococci of swine origin, Italy","volume":"8","author":"Fioriti S","year":"2020","unstructured":"Fioriti S, , Morroni G, , Coccitto SN, et al. Detection of oxazolidinone resistance genes and characterization of genetic environments in enterococci of swine origin, Italy. 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