Genetic Analysis Using an Isogenic Mating Pair of Aspergillus fumigatus Identifies Azole Resistance Genes and Lack of MAT Locus's Role in Virulence

被引:49
作者
Losada, Liliana [1 ]
Sugui, Janyce A. [2 ]
Eckhaus, Michael A. [3 ]
Chang, Yun C. [2 ]
Mounaud, Stephanie [1 ]
Figat, Abigail [2 ]
Joardar, Vinita [1 ]
Pakala, Suman B. [1 ]
Pakala, Suchitra [1 ]
Venepally, Pratap [1 ]
Fedorova, Natalie [4 ]
Nierman, William C. [1 ]
Kwon-Chung, Kyung J. [2 ]
机构
[1] J Craig Venter Inst, Rockville, MD USA
[2] NIAID, Mol Microbiol Sect, Lab Clin Infect Dis, NIH, Bethesda, MD 20892 USA
[3] NIH, Div Vet Resources, Off Res Serv, Bethesda, MD 20892 USA
[4] NCI, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
CRYPTOCOCCUS-NEOFORMANS; GALLERIA-MELLONELLA; AMPHOTERICIN-B; HISTOPLASMA-CAPSULATUM; CONGENIC STRAINS; IN-VITRO; PROTEIN; PATHOGEN; INVASIVENESS; VORICONAZOLE;
D O I
10.1371/journal.ppat.1004834
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Invasive aspergillosis (IA) due to Aspergillus fumigatus is a major cause of mortality in immunocompromised patients. The discovery of highly fertile strains of A. fumigatus opened the possibility to merge classical and contemporary genetics to address key questions about this pathogen. The merger involves sexual recombination, selection of desired traits, and genomics to identify any associated loci. We constructed a highly fertile isogenic pair of A. fumigatus strains with opposite mating types and used them to investigate whether mating type is associated with virulence and to find the genetic loci involved in azole resistance. The pair was made isogenic by 9 successive backcross cycles of the foundational strain AFB62 (MAT1-1) with a highly fertile (MAT1-2) progeny. Genome sequencing showed that the F-9 MAT1-2 progeny was essentially identical to the AFB62. The survival curves of animals infected with either strain in three different animal models showed no significant difference, suggesting that virulence in A. fumigatus was not associated with mating type. We then employed a relatively inexpensive, yet highly powerful strategy to identify genomic loci associated with azole resistance. We used traditional in vitro drug selection accompanied by classical sexual crosses of azole-sensitive with resistant isogenic strains. The offspring were plated under varying drug concentrations and pools of resulting colonies were analyzed by whole genome sequencing. We found that variants in 5 genes contributed to azole resistance, including mutations in erg11A (cyp51A), as well as multi-drug transporters, erg25, and in HMG-CoA reductase. The results demonstrated that with minimal investment into the sequencing of three pools from a cross of interest, the variation(s) that contribute any phenotype can be identified with nucleotide resolution. This approach can be applied to multiple areas of interest in A. fumigatus or other heterothallic pathogens, especially for virulence associated traits.
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页数:23
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