{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,18]],"date-time":"2026-07-18T20:04:59Z","timestamp":1784405099645,"version":"3.55.0"},"reference-count":50,"publisher":"American Society for Microbiology","issue":"3","license":[{"start":{"date-parts":[[2020,2,24]],"date-time":"2020-02-24T00:00:00Z","timestamp":1582502400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.asm.org\/non-commercial-tdm-license"}],"content-domain":{"domain":["journals.asm.org"],"crossmark-restriction":true},"short-container-title":["J Clin Microbiol"],"published-print":{"date-parts":[[2020,2,24]]},"abstract":"<jats:p>We reevaluated 20 cases of blastomycosis diagnosed in South Africa between 1967 and 2014, with<jats:named-content content-type=\"genus-species\">Blastomyces dermatitidis<\/jats:named-content>considered to be the etiological agent, in light of newly described species and the use of more advanced technologies. In addition to histopathological and\/or culture-based methods, all 20 isolates were phenotypically and genotypically characterized, including multilocus typing of five genes and whole-genome sequencing.<\/jats:p>","DOI":"10.1128\/jcm.01661-19","type":"journal-article","created":{"date-parts":[[2020,1,3]],"date-time":"2020-01-03T12:58:31Z","timestamp":1578056311000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":56,"title":["Human Blastomycosis in South Africa Caused by<i>Blastomyces percursus<\/i>and<i>Blastomyces emzantsi<\/i>sp. nov., 1967 to 2014"],"prefix":"10.1128","volume":"58","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-6117-4309","authenticated-orcid":false,"given":"Tsidiso G.","family":"Maphanga","sequence":"first","affiliation":[{"name":"National Institute for Communicable Diseases, National Health Laboratory Service, Johannesburg, South Africa"},{"name":"University of the Free State, Bloemfontein, 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