Berkow Elizabeth L, Lockhart Shawn R
Mycotic Diseases Branch, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Infect Drug Resist. 2017 Jul 31;10:237-245. doi: 10.2147/IDR.S118892. eCollection 2017.
and the emerging non- spp. have significant clinical relevance among many patient populations. Current treatment guidelines include fluconazole as a primary therapeutic option for the treatment of these infections, but it is only fungistatic against spp. and both inherent and acquired resistance to fluconazole have been reported. Such mechanisms of resistance include increased drug efflux, alteration or increase in the drug target, and development of compensatory pathways for producing the target sterol, ergosterol. While many mechanisms of resistance observed in are also found in the non- species, there are also important and unexpected differences between species. Furthermore, mechanisms of fluconazole resistance in emerging spp., including the global health threat , are largely unknown. In order to preserve the utility of one of our fundamental antifungal drugs, fluconazole, it is essential that we fully appreciate the manner by which spp. manifest resistance to it.
并且新兴的非 种在许多患者群体中具有重要的临床意义。当前的治疗指南将氟康唑作为治疗这些感染的主要治疗选择,但它仅对 种具有抑菌作用,并且已经报道了对氟康唑的固有耐药性和获得性耐药性。这种耐药机制包括药物外排增加、药物靶点改变或增加,以及产生靶标固醇麦角固醇的补偿途径的发展。虽然在 中观察到的许多耐药机制在非 种中也存在,但不同物种之间也存在重要且意想不到的差异。此外,新兴 种中氟康唑耐药的机制,包括全球健康威胁 ,在很大程度上尚不清楚。为了保留我们基本抗真菌药物之一氟康唑的效用,我们必须充分了解 种对其产生耐药性的方式。