{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,19]],"date-time":"2026-02-19T22:29:07Z","timestamp":1771540147492,"version":"3.50.1"},"reference-count":30,"publisher":"Canadian Science Publishing","issue":"11","license":[{"start":{"date-parts":[[2015,11,1]],"date-time":"2015-11-01T00:00:00Z","timestamp":1446336000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.nrcresearchpress.com\/page\/about\/CorporateTextAndDataMining"}],"content-domain":{"domain":["cdnsciencepub.com"],"crossmark-restriction":false},"short-container-title":["Can. J. Microbiol."],"published-print":{"date-parts":[[2015,11]]},"abstract":"<jats:p> In recent years, the search for drugs to treat systemic and opportunistic mycoses has attracted great interest from the scientific community. This study evaluated the in vitro inhibitory effect of the antituberculosis drugs isoniazid and ethionamide alone and combined with itraconazole and fluconazole against biofilms of Cryptococcus neoformans and Cryptococcus gattii. Antimicrobials were tested at defined concentrations after susceptibility assays with Cryptococcus planktonic cells. In addition, we investigated the synergistic interaction of antituberculosis drugs and azole derivatives against Cryptococcus planktonic cells, as well as the influence of isoniazid and ethionamide on ergosterol content and cell membrane permeability. Isoniazid and ethionamide inhibited both biofilm formation and viability of mature biofilms. Combinations formed by antituberculosis drugs and azoles proved synergic against both planktonic and sessile cells, showing an ability to reduce Cryptococcus biofilms by approximately 50%. Furthermore, isoniazid and ethionamide reduced the content of ergosterol in Cryptococcus spp. planktonic cells and destabilized or permeabilized the fungal cell membrane, leading to leakage of macromolecules. Owing to the paucity of drugs able to inhibit Cryptococcus biofilms, we believe that the results presented here might be of interest in the designing of new antifungal compounds. <\/jats:p>","DOI":"10.1139\/cjm-2015-0230","type":"journal-article","created":{"date-parts":[[2015,8,6]],"date-time":"2015-08-06T21:35:35Z","timestamp":1438896935000},"page":"827-836","update-policy":"https:\/\/doi.org\/10.1139\/csp-crossmark-policy","source":"Crossref","is-referenced-by-count":6,"title":["Inhibitory activity of isoniazid and ethionamide against <i>Cryptococcus<\/i> biofilms"],"prefix":"10.1139","volume":"61","author":[{"given":"Rossana de Aguiar","family":"Cordeiro","sequence":"first","affiliation":[{"name":"Postgraduate Program in Medical Microbiology, Federal University of Cear\u00e1, Fortaleza, Cear\u00e1, Brazil."},{"name":"Postgraduate Program in Medical Sciences, Federal University of Cear\u00e1, Fortaleza, Cear\u00e1, 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