{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,27]],"date-time":"2026-09-27T22:49:19Z","timestamp":1790549359461,"version":"4.1.0"},"reference-count":68,"publisher":"SAGE Publications","issue":"7","license":[{"start":{"date-parts":[[2020,7,1]],"date-time":"2020-07-01T00:00:00Z","timestamp":1593561600000},"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":[[2020,7,1]]},"abstract":"<jats:p>\n                    Integrons are prokaryotic genetic elements known to carry and exchange antibiotic resistance gene cassettes through a site-specific recombinase called integrase. In this work, 107\n                    <jats:italic toggle=\"yes\">Aeromonas<\/jats:italic>\n                    isolates from environmental origin, including fish, water, and sediments, were investigated for the presence of integrons. Using specific primers for Class 1, 2 and 3 integrases, only Class 1 and Class 2 integrons were detected. Detection of Class 2 integrases and their associated variable regions required two rounds of polymerase chain reaction (PCR). Sequencing of the\n                    <jats:italic toggle=\"yes\">intI<\/jats:italic>\n                    2 amplicons confirmed them as integrase-derived products. Class 1 integrons were detected in 26 out of 107 isolates. PCR amplification of the variable regions associated to these integrons revealed an outstanding homogeneity, 25 of them having variable regions with an identical\n                    <jats:italic toggle=\"yes\">dfr<\/jats:italic>\n                    A12-\n                    <jats:italic toggle=\"yes\">orf<\/jats:italic>\n                    F-\n                    <jats:italic toggle=\"yes\">aad<\/jats:italic>\n                    A2 cassette array and one integron carrying only the\n                    <jats:italic toggle=\"yes\">dfr<\/jats:italic>\n                    A16 cassette. To assess clone diversity, chromosomal DNA from isolates was subjected to enterobacterial repetitive intergenic consensus-PCR (ERIC-PCR), which discarded clonality in all instances. Class 2 integrons were surprisingly more prevalent than Class1 integrons, being detected in 60 out of 107 isolates. Forty-six of them showed a unique ERIC profile, while the remaining 14 strains displayed profiles that could be grouped in five different patterns. Cassette arrangements of all Class 2 variable regions were those described as the most prevalent (\n                    <jats:italic toggle=\"yes\">dfr<\/jats:italic>\n                    A1-\n                    <jats:italic toggle=\"yes\">sat<\/jats:italic>\n                    2-\n                    <jats:italic toggle=\"yes\">aad<\/jats:italic>\n                    A1). A rather startling result of this work is the sensitivity to trimethoprim, streptomycin, and streptothricin of most strains, despite the presence of the cognate resistance genes. To know the integron distribution in environmental\n                    <jats:italic toggle=\"yes\">Aeromonas<\/jats:italic>\n                    species, a phylogenetic reconstruction was done using\n                    <jats:italic toggle=\"yes\">rpo<\/jats:italic>\n                    D\/\n                    <jats:italic toggle=\"yes\">gyr<\/jats:italic>\n                    B or\n                    <jats:italic toggle=\"yes\">rpo<\/jats:italic>\n                    D\/\n                    <jats:italic toggle=\"yes\">gyr<\/jats:italic>\n                    A gene sequences. Isolates bearing these elements corresponded to\n                    <jats:italic toggle=\"yes\">Aeromonas hydrophila<\/jats:italic>\n                    ,\n                    <jats:italic toggle=\"yes\">Aeromonas veronii<\/jats:italic>\n                    ,\n                    <jats:italic toggle=\"yes\">Aeromonas salmonicida<\/jats:italic>\n                    ,\n                    <jats:italic toggle=\"yes\">Aeromonas dhakensis<\/jats:italic>\n                    ,\n                    <jats:italic toggle=\"yes\">Aeromonas sanarellii<\/jats:italic>\n                    ,\n                    <jats:italic toggle=\"yes\">Aeromonas taiwanensis<\/jats:italic>\n                    ,\n                    <jats:italic toggle=\"yes\">Aeromonas media<\/jats:italic>\n                    ,\n                    <jats:italic toggle=\"yes\">Aeromonas caviae<\/jats:italic>\n                    ,\n                    <jats:italic toggle=\"yes\">Aeromonas jandaei<\/jats:italic>\n                    , and\n                    <jats:italic toggle=\"yes\">Aeromonas<\/jats:italic>\n                    sp. This work revealed an unusual high incidence of Class 2 integrons and a low variability of cassette arrangements in environmental\n                    <jats:italic toggle=\"yes\">Aeromonas<\/jats:italic>\n                    species.\n                  <\/jats:p>","DOI":"10.1089\/mdr.2019.0250","type":"journal-article","created":{"date-parts":[[2020,1,28]],"date-time":"2020-01-28T16:31:55Z","timestamp":1580229115000},"page":"794-801","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":19,"title":["Low Cassette Variability in Class 2 and Class 1 Integrons of\n                    <i>Aeromonas<\/i>\n                    spp. Isolated from Environmental Samples"],"prefix":"10.1177","volume":"26","author":[{"given":"Jorge Erick","family":"Otero-Olarra","sequence":"first","affiliation":[{"name":"Department of Biochemistry, Escuela Nacional de Ciencias Biol\u00f3gicas del Instituto Polit\u00e9cnico Nacional, Mexico City, Mexico."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Everardo","family":"Curiel-Quesada","sequence":"additional","affiliation":[{"name":"Department of Biochemistry, Escuela Nacional de Ciencias Biol\u00f3gicas del Instituto Polit\u00e9cnico Nacional, Mexico City, Mexico."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jes\u00fas","family":"Baltazar-Cruz","sequence":"additional","affiliation":[{"name":"Department of Biochemistry, Escuela Nacional de Ciencias Biol\u00f3gicas del Instituto Polit\u00e9cnico Nacional, Mexico City, Mexico."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ma. Guadalupe","family":"Aguilera-Arreola","sequence":"additional","affiliation":[{"name":"Department of Microbiology, Escuela Nacional de Ciencias Biol\u00f3gicas del Instituto Polit\u00e9cnico Nacional, Mexico City, Mexico."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Abigail","family":"P\u00e9rez-Valdespino","sequence":"additional","affiliation":[{"name":"Department of Biochemistry, Escuela Nacional de Ciencias Biol\u00f3gicas del Instituto Polit\u00e9cnico Nacional, Mexico City, Mexico."}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"179","published-online":{"date-parts":[[2020,7,7]]},"reference":[{"key":"e_1_3_5_2_2","doi-asserted-by":"publisher","DOI":"10.1038\/nrmicro1462"},{"key":"e_1_3_5_3_2","first-page":"139","article-title":"The integron: adaptation on demand","volume":"3","author":"Escudero J.A.","year":"2015","unstructured":"Escudero J.A., , Loot C., , Nivina A., , and Mazel D.. 2015. The integron: adaptation on demand. 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