{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,3]],"date-time":"2026-09-03T15:21:14Z","timestamp":1788448874596,"version":"build-2803163510"},"reference-count":41,"publisher":"Public Library of Science (PLoS)","issue":"8","license":[{"start":{"date-parts":[[2025,8,1]],"date-time":"2025-08-01T00:00:00Z","timestamp":1754006400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"name":"Department of Agriculture, Land Reform and Rural Development","award":["OVI012403000074"],"award-info":[{"award-number":["OVI012403000074"]}]},{"DOI":"10.13039\/501100005274","name":"North West University","doi-asserted-by":"crossref","award":["OVI012403000074"],"award-info":[{"award-number":["OVI012403000074"]}],"id":[{"id":"10.13039\/501100005274","id-type":"DOI","asserted-by":"crossref"}]}],"content-domain":{"domain":["www.plosone.org"],"crossmark-restriction":false},"short-container-title":["PLoS One"],"abstract":"<jats:p>\n                    Salmonellosis remains one of the most frequently reported foodborne diseases globally, with the highest burden in low-resource areas. The millions of deaths caused by Nontyphoidal\n                    <jats:italic>\n                      <jats:italic>Salmonella<\/jats:italic>\n                    <\/jats:italic>\n                    (NTS) infections emphasize the urgent need for timely, detailed, and evidence-based interventions to effectively manage and monitor NTS burdens. This study retrospectively analyzed 1,028 NTS isolates from animals, the environment, and food products in South Africa, collected between 1960 and 2023. Among the 102 serotypes identified,\n                    <jats:italic>\n                      <jats:italic>S<\/jats:italic>\n                    <\/jats:italic>\n                    . Heidelberg, isolated only between 2000\u22122009 and 2020\u22122023, accounted for 94.3% of isolations during the latter period, suggesting a recent shift in\n                    <jats:italic>\n                      <jats:italic>Salmonella<\/jats:italic>\n                    <\/jats:italic>\n                    epidemiology in the region. The highest resistance rates were observed for cefoxitin (65.7%), cephalothin (62.8%), and tetracycline (59.8%), with a significant increase in resistance to several antibiotics, including ceftriaxone and aztreonam, from 2010\u22122023. Genetic analysis revealed that\n                    <jats:italic>\n                      <jats:italic>S<\/jats:italic>\n                    <\/jats:italic>\n                    . Gallinarium had the highest prevalence of antibiotic resistance genes, such as\n                    <jats:italic>\n                      <jats:italic>tetA<\/jats:italic>\n                    <\/jats:italic>\n                    (71.4%),\n                    <jats:italic>\n                      <jats:italic>qnrA<\/jats:italic>\n                    <\/jats:italic>\n                    (64.3%),\n                    <jats:italic>\n                      <jats:italic>cat<\/jats:italic>\n                    <\/jats:italic>\n                    1 (64.3%),\n                    <jats:italic>\n                      <jats:italic>bla<\/jats:italic>\n                    <\/jats:italic>\n                    <jats:sub>\n                      <jats:italic>PSE<\/jats:italic>\n                    <\/jats:sub>\n                    (57.1%), and both\n                    <jats:italic>\n                      <jats:italic>bla<\/jats:italic>\n                    <\/jats:italic>\n                    <jats:sub>\n                      <jats:italic>CMY-2<\/jats:italic>\n                    <\/jats:sub>\n                    and\n                    <jats:italic>\n                      <jats:italic>qnrB<\/jats:italic>\n                    <\/jats:italic>\n                    at 50%. The\n                    <jats:italic>\n                      <jats:italic>bla<\/jats:italic>\n                    <\/jats:italic>\n                    <jats:sub>\n                      <jats:italic>PSE<\/jats:italic>\n                    <\/jats:sub>\n                    and\n                    <jats:italic>\n                      <jats:italic>bla<\/jats:italic>\n                    <\/jats:italic>\n                    <jats:sub>\n                      <jats:italic>SHV<\/jats:italic>\n                    <\/jats:sub>\n                    genes were strongly associated with ceftriaxone resistance in\n                    <jats:italic>\n                      <jats:italic>S<\/jats:italic>\n                    <\/jats:italic>\n                    . Dublin isolates, while\n                    <jats:italic>\n                      <jats:italic>bla<\/jats:italic>\n                    <\/jats:italic>\n                    <jats:sub>\n                      <jats:italic>PSE<\/jats:italic>\n                    <\/jats:sub>\n                    and\n                    <jats:italic>\n                      <jats:italic>qnrS<\/jats:italic>\n                    <\/jats:italic>\n                    were linked to chloramphenicol resistance in\n                    <jats:italic>\n                      <jats:italic>S<\/jats:italic>\n                    <\/jats:italic>\n                    . Enteritidis and\n                    <jats:italic>\n                      <jats:italic>S<\/jats:italic>\n                    <\/jats:italic>\n                    . Dublin isolates. Additionally, 87% of the virulence genes screened were present in over 50% of the serotypes, indicating increased adaptability and potential shifts in disease dynamics. The rise in antimicrobial resistance, driven by antimicrobial misuse, horizontal gene transfer, and biofilm formation, could alter serotype dynamics and changing disease epidemiology. This trend underscores the urgent need for effective antimicrobial stewardship and surveillance to combat the spread of antibiotic resistance in\n                    <jats:italic>\n                      <jats:italic>Salmonella<\/jats:italic>\n                    <\/jats:italic>\n                    populations.\n                  <\/jats:p>","DOI":"10.1371\/journal.pone.0329061","type":"journal-article","created":{"date-parts":[[2025,8,1]],"date-time":"2025-08-01T17:54:58Z","timestamp":1754070898000},"page":"e0329061","update-policy":"https:\/\/doi.org\/10.1371\/journal.pone.corrections_policy","source":"Crossref","is-referenced-by-count":7,"title":["Monitoring, surveillance, antimicrobial resistance and genetic diversity analysis of non-typhoidal Salmonella in South Africa from 1960\u20132023 from animal and animal products"],"prefix":"10.1371","volume":"20","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-1495-357X","authenticated-orcid":true,"given":"Itumeleng","family":"Matle","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Davies Mubika","family":"Pfukenyi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-7426-9366","authenticated-orcid":true,"given":"Nozipho","family":"Maphori","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nkagiseng","family":"Moatshe","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Thabo","family":"Nkabinde","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0008-8474-2824","authenticated-orcid":true,"given":"Annah","family":"Motaung","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tracy","family":"Schmidt","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-9212-1066","authenticated-orcid":true,"given":"Emmanuel","family":"Seakamela","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mulunda","family":"Mwanza","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lubanza","family":"Ngoma","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mohamed","family":"Sirdar","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Khanyisile R.","family":"Mbatha","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kudakwashe","family":"Magwedere","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"340","published-online":{"date-parts":[[2025,8,1]]},"reference":[{"issue":"23","key":"pone.0329061.ref001","doi-asserted-by":"crossref","first-page":"3666","DOI":"10.3390\/ani13233666","article-title":"Salmonella and Salmonellosis: an update on public health implications and control strategies","volume":"13","author":"\u00c1 Gal\u00e1n-Rela\u00f1o","year":"2023","journal-title":"Animals (Basel)"},{"key":"pone.0329061.ref002","first-page":"1","volume-title":"Antigenic formulae of the Salmonella serovars","author":"P Grimont","year":"2007","edition":"9"},{"key":"pone.0329061.ref003","doi-asserted-by":"crossref","first-page":"1133241","DOI":"10.3389\/fmicb.2023.1133241","article-title":"Comprehensive profiling of serotypes, 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