{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,23]],"date-time":"2026-09-23T06:10:54Z","timestamp":1790143854439,"version":"4.0.1"},"reference-count":52,"publisher":"Frontiers Media SA","license":[{"start":{"date-parts":[[2026,9,23]],"date-time":"2026-09-23T00:00:00Z","timestamp":1790121600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["frontiersin.org"],"crossmark-restriction":true},"short-container-title":["Front. Microbiol."],"abstract":"<jats:sec>\n                    <jats:title>Introduction<\/jats:title>\n                    <jats:p>\n                      <jats:italic>Aeromonas<\/jats:italic>\n                      spp. are increasingly recognized opportunistic pathogens of humans, yet integrated genomic and phenotypic data from clinical, extra-intestinal isolates remain limited. We characterized 74 non-duplicate\n                      <jats:italic>Aeromonas<\/jats:italic>\n                      isolates recovered from extra-intestinal clinical specimens at a tertiary hospital in Ningbo, China, between 2020 and 2025, combining whole-genome sequencing (WGS)-based taxonomy, antimicrobial susceptibility testing, and resistome and putative virulence factor (VF) prediction.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>Species were identified by average nucleotide identity (ANI) analysis and sequence types (STs) by multilocus sequence typing (MLST). Susceptibility to 11 agents was interpreted according to the Clinical and Laboratory Standards Institute (CLSI) guideline M45. Resistance genes were predicted against the Comprehensive Antibiotic Resistance Database (CARD) and VFs against the Virulence Factors of Pathogenic Bacteria database (VFDB); genotype\u2013phenotype concordance was quantified with Cohen\u2019s \u03ba, and VF profiles were analyzed by principal coordinates analysis and permutational multivariate analysis of variance (PERMANOVA).<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Six species were identified, dominated by\n                      <jats:italic>Aeromonas caviae<\/jats:italic>\n                      (32.4%),\n                      <jats:italic>Aeromonas veronii<\/jats:italic>\n                      (25.7%) and\n                      <jats:italic>Aeromonas dhakensis<\/jats:italic>\n                      (24.3%). Bile was the leading source of isolation (51.4%), and species were significantly associated with isolation site (Fisher\u2019s exact test,\n                      <jats:italic>p<\/jats:italic>\n                      \u202f&amp;lt;\u202f0.001). The population was genetically diverse (71 STs, 39 novel). Resistance was highest to piperacillin\/tazobactam (29.7%), whereas only one isolate was resistant to amikacin. Eighty-five resistance genes were detected, with a ubiquitous intrinsic \u03b2-lactamase background (\n                      <jats:italic>OXA-12-like<\/jats:italic>\n                      ,\n                      <jats:italic>cphA\/imiH<\/jats:italic>\n                      and\n                      <jats:italic>MOX-type<\/jats:italic>\n                      genes in 63.5, 58.1 and 41.9% of isolates, respectively) and the acquired carbapenemase gene\n                      <jats:italic>\n                        bla\n                        <jats:sub>NDM-1<\/jats:sub>\n                      <\/jats:italic>\n                      in three isolates. Genotype\u2013phenotype agreement was substantial for trimethoprim\/sulfamethoxazole (\u03ba\u202f=\u202f0.773\u20130.856) and fluoroquinolones (\n                      <jats:italic>\u03ba<\/jats:italic>\n                      \u202f=\u202f0.706) but poor for \u03b2-lactams. Fifty-six VFs were detected, comprising a conserved 26-VF core virulome and accessory determinants structured by species (PERMANOVA\n                      <jats:italic>R<\/jats:italic>\n                      <jats:sup>2<\/jats:sup>\n                      \u202f=\u202f0.797,\n                      <jats:italic>p<\/jats:italic>\n                      \u202f=\u202f0.001).\n                      <jats:italic>A. dhakensis<\/jats:italic>\n                      and\n                      <jats:italic>A. hydrophila<\/jats:italic>\n                      carried the heaviest VF loads and were enriched for aerolysin, ExoA, MARTX\/RtxA and T6SS, whereas\n                      <jats:italic>A. caviae<\/jats:italic>\n                      lacked aerolysin and had the sparsest virulome.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Discussion<\/jats:title>\n                    <jats:p>\n                      Species identity was the dominant correlate of clinical distribution and virulence potential, supporting genome-based species identification as the basis for risk assessment of clinical\n                      <jats:italic>Aeromonas<\/jats:italic>\n                      isolates.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.3389\/fmicb.2026.1952096","type":"journal-article","created":{"date-parts":[[2026,9,23]],"date-time":"2026-09-23T05:50:30Z","timestamp":1790142630000},"update-policy":"https:\/\/doi.org\/10.3389\/crossmark-policy","source":"Crossref","is-referenced-by-count":0,"title":["Species distribution, antimicrobial resistance, and putative virulence factor profiles of Aeromonas isolates from extra-intestinal clinical specimens: a whole-genome sequencing study"],"prefix":"10.3389","volume":"17","author":[{"given":"Qifeng","family":"Jiang","sequence":"first","affiliation":[{"name":"Department of Clinical Laboratory, The First Affiliated Hospital of Ningbo University","place":["Ningbo, Zhejiang, China"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xingbei","family":"Weng","sequence":"additional","affiliation":[{"name":"Department of Clinical Laboratory, The First Affiliated Hospital of Ningbo University","place":["Ningbo, Zhejiang, China"]}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"1965","published-online":{"date-parts":[[2026,9,23]]},"reference":[{"key":"ref1","doi-asserted-by":"publisher","first-page":"7712","DOI":"10.1038\/s41598-023-34887-1","article-title":"Whole spectrum of Aeromonas hydrophila virulence determinants and the identification of novel SNPs using comparative pathogenomics","volume":"13","author":"Abdella","year":"2023","journal-title":"Sci. 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