Mutations in the Second Alternative Oxidase Gene: A New Approach to Group Strains.

J Fungi (Basel)

Department of Biochemical Engineering, Faculty of Science and Technology, University of Debrecen, H-4032 Debrecen, Hungary.

Published: May 2023

AI Article Synopsis

  • Alternative oxidase serves as a key component in the mitochondrial electron transport chain of many fungi, particularly within the black aspergilli group.
  • Some isolates exhibit a second related gene, leading to genetic diversity among these fungi, which are known to cause serious infections in immunocompromised patients.
  • Analysis of various genome-sequenced strains has revealed five significant mutations affecting the alternative oxidase gene, highlighting the potential for rapid identification of different species based on these genetic variations.

Article Abstract

Alternative oxidase is a terminal oxidase in the branched mitochondrial electron transport chain of most fungi including (subgenus Circumdati, section Nigri). A second, paralogous gene () is extant in some isolates but also present in two divergent species of the subgenus Nidulantes- and -as well as in . Black aspergilli are cosmopolitan opportunistic fungi that can cause diverse mycoses and acute aspergillosis in immunocompromised individuals. Amongst the approximately 75 genome-sequenced strains, features considerable sequence variation. Five mutations were identified that rationally affect transcription or function or terminally modify the gene product. One mutant allele that occurs in CBS 513.88 and neotype strain CBS 554.65 involves a chromosomal deletion that removes exon 1 and intron 1 from . Another allele results from retrotransposon integration. Three other alleles result from point mutations: a missense mutation of the start codon, a frameshift, and a nonsense mutation. strain ATCC 1015 has a full-length gene. The complex can thus be subdivided into six taxa according to extant allele, which may facilitate rapid and accurate identification of individual species.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10219456PMC
http://dx.doi.org/10.3390/jof9050570DOI Listing

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