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Azole-Resistance Development; How the Lifecycle Defines the Potential for Adaptation

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Journal J Fungi (Basel)
Date 2021 Aug 26
PMID 34436138
Citations 10
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Abstract

In order to successfully infect or colonize human hosts or survive changing environments, needs to adapt through genetic changes or phenotypic plasticity. The genomic changes are based on the capacity of the fungus to produce genetic variation, followed by selection of the genotypes that are most fit to the new environment. Much scientific work has focused on the metabolic plasticity, biofilm formation or the particular genetic changes themselves leading to adaptation, such as antifungal resistance in the host. Recent scientific work has shown advances made in understanding the natural relevance of parasex and how both the asexual and sexual reproduction can lead to tandem repeat elongation in the target gene of the azoles: the 51A gene. In this review, we will explain how the fungus can generate genetic variation that can lead to adaptation. We will discuss recent advances that have been made in the understanding of the lifecycle of to explain the differences observed in speed and type of mutations that are generated under different environments and how this can facilitate adaptation, such as azole-resistance selection.

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References
1.
Stevens D, Moss R, Hernandez C, Clemons K, Martinez M . Effect of Media Modified To Mimic Cystic Fibrosis Sputum on the Susceptibility of Aspergillus fumigatus, and the Frequency of Resistance at One Center. Antimicrob Agents Chemother. 2016; 60(4):2180-4. PMC: 4808157. DOI: 10.1128/AAC.02649-15. View

2.
Sugui J, Losada L, Wang W, Varga J, Ngamskulrungroj P, Abu-Asab M . Identification and characterization of an Aspergillus fumigatus "supermater" pair. mBio. 2011; 2(6). PMC: 3225970. DOI: 10.1128/mBio.00234-11. View

3.
Debets F, Swart K, Hoekstra R, Bos C . Genetic maps of eight linkage groups of Aspergillus niger based on mitotic mapping. Curr Genet. 1993; 23(1):47-53. DOI: 10.1007/BF00336749. View

4.
Pegues D, Lasker B, McNeil M, Hamm P, Lundal J, Kubak B . Cluster of cases of invasive aspergillosis in a transplant intensive care unit: evidence of person-to-person airborne transmission. Clin Infect Dis. 2001; 34(3):412-6. DOI: 10.1086/338025. View

5.
Hagiwara D, Arai T, Takahashi H, Kusuya Y, Watanabe A, Kamei K . Non-cyp51A Azole-Resistant Aspergillus fumigatus Isolates with Mutation in HMG-CoA Reductase. Emerg Infect Dis. 2018; 24(10):1889-1897. PMC: 6154143. DOI: 10.3201/eid2410.180730. View