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Screening the in vitro susceptibility of posaconazole in clinical isolates of Candida spp. and Aspergillus spp. and analyzing the sequence of ERG11 or CYP51A in non-wild-type isolates from China.

Authors :
Zhang, Hao
Tan, Jingwen
Kontoyiannis, Dimitrios P.
Zhou, Yabin
Liu, Weixia
Zhu, Pengfei
Shi, Xiuyan
Wan, Zhe
Li, Ruoyu
Liu, Wei
Source :
Diagnostic Microbiology & Infectious Disease. Oct2019, Vol. 95 Issue 2, p166-170. 5p.
Publication Year :
2019

Abstract

The present study was to determine the in vitro activity of posaconazole (POS) against 385 Candida and 268 Aspergillus clinical isolates from China. We found that POS was active against 85.5% Candida and 94.4% Aspergillus isolates. Non–wild-type (non-WT) phenotype was found in a subset of Candida albicans (15.4%), Candida tropicalis (11.9%), Aspergillus fumigatus (4.1%), and Aspergillus flavus (17.4%) isolates. Cross-resistance to POS and other triazoles was seen. Gene sequencing showed that 4 C. albicans , 1 C. tropicalis , and 9 A. fumigatus isolates with cross-resistance to POS and other triazoles had mutations in ERG11 or CYP51A. In conclusion, POS has potent in vitro activity against most of Candida and Aspergillus isolates from China. Non-WT phenotype and those with cross-resistance to POS and other triazoles exist, frequently driven by mutations of ERG11 in Candida spp. and CYP51A in Aspergillus spp. • The susceptibility to posaconazole in Candida spp. and Aspergillus spp. from China was determined for the first time. • Posaconazole was active against most of Candida and Aspergillus isolates in this study. • Non-WT phenotype for posaconazole and those with cross-resistance to posaconazole and other triazoles exist. • Cross-resistance may be caused by mutations of ERG11 in Candida spp. and CYP51A in Aspergillus spp. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
07328893
Volume :
95
Issue :
2
Database :
Academic Search Index
Journal :
Diagnostic Microbiology & Infectious Disease
Publication Type :
Academic Journal
Accession number :
138571872
Full Text :
https://doi.org/10.1016/j.diagmicrobio.2019.05.003