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Mitogenome Announcement

Complete mitochondrial genome sequence of Afla-Guard®, commercially available non-toxigenic Aspergillus flavus

ORCID Icon, ORCID Icon, , &
Pages 3572-3574 | Received 20 Apr 2020, Accepted 26 Apr 2020, Published online: 21 Oct 2020

Abstract

Afla-Guard® is a commercial non-toxigenic Aspergillus flavus strain used to decrease aflatoxin contamination level in field. Its mitochondrial genome was sequenced, showing that its length is 29,208 bp with typical configuration of Aspergillus mitochondrial genome. 17 SNPs and 27 INDELs were identified by comparing with previous A. flavus mitochondrial genome. Phylogenetic trees present that A. flavus of Afla-Guard® was clustered with the previous A. flavus mitochondrial genome.

Afla-Guard® is a commercial product to decrease aflatoxin contamination level for improving quality of corns and peanuts (Wu et al. Citation2008; Durham et al. Citation2010; Dorner and Lamb Citation2006). This product contains Aspergillus flavus without aflatoxin gene cluster usually found in A. flavus (Abdel-Hadi et al. Citation2012). It can be used to understand phylogenetic position of nontoxic A. flavus. In addition, two mitochondrial genomes of A. flavus present that two genomes show different phylogenetic positions (data not shown), requiring additional mitochondrial genomes of A. flavus for clarifying this problem.

DNA of Afla-Guard® purchased from Syngenta was extracted using the optimized protocol (Lee et al. Citation2017). It was originally isolated from peanut seed at the USDA National Peanut Research Laboratory (Georgia, USA) in 1991 (NRRL 21882 in Agricultural Research Service Culture Collection). Raw data generated by HiSeq2500 and de novo assembly was conducted by Velvet 1.2.10 (Zerbino and Birney Citation2008). Gap filling was done by SOAPGapCloser 1.12 (Zhao et al. Citation2011) after confirming each base using BWA 0.7.17 and SAMtools 1.9 (Li et al. Citation2009; Li Citation2013). Geneious R11 11.0.5 (Biomatters Ltd, Auckland, New Zealand) was used to annotate its mitogenome by comparing with those of A. flavus (JQ355000; Joardar et al. Citation2012).

The length of Afla-Guard® A. flavus mitogenome (GenBank accession is MT335777) is 29,208 bp, which is 3 bp longer than that of previously reported A. flavus (JQ355000). It is the 8th shortest mitogenome among 23 available Aspergillus mitogenomes (Park et al., in preparation). Numbers of PCGs, tRNAs, and rRNAs are 17, 27, and 2, respectively a typical configuration of Aspergillus mitogenomes.

Seventeen SNPs and 27 INDELs were identified as intraspecific variation on two A. flavus mitochondrial genomes. Two non-synonymous SNPs (nsSNPs) were identified in NAD1, two nsSNPs and three INDELs were found in hypothetical protein, and one nsSNP was in NAD4. Two synonymous SNPs (sSNPs) were found in COX1 and another two sSNPs were in NAD5. The remaining SNPs and INDELs were in intergenic space. Numbers of intraspecific variations are relatively large in comparison to those of Aspergillus oryzae, Aspergillus terrus, and Penicillium digitatum (Park et al., in preparation).

Sequence alignments of ten conserved genes from twelve Aspergillus and one Penicillium mitogenomes (Juhász et al. Citation2008; Futagami et al. Citation2011; Sun et al. Citation2011; Joardar et al. Citation2012; Zhao et al. Citation2012; Park, Kwon, Huang, et al. Citation2019; Park, Kwon, Zhu, Mageswari, Heo, Han, et al. Citation2019; Park, Kwon, Zhu, Mageswari, Heo, Kim, et al. Citation2019) including that of Afla-Guard® and one Podospora mitochondrial genome (Cummings et al. Citation1990) as an outgroup were calculated by MAFFT 7.450 (Katoh and Standley Citation2013) and concatenated. The neighbour-joining (10,000 bootstrap repeats) and maximum-likelihood (1,000 bootstrap repeats) phylogenetic trees were constructed using MEGA X (Kumar et al. Citation2018). Phylogenetic trees showed that two A. flavus mitochondrial genomes were clustered in one clade together with A. oryzae (). In addition, another A. flavus mitochondrial genome (NC_026920) was clustered with A. nidulans (), addressing its species identification.

Figure 1. Maximum-likelihood (bootstrap repeat is 1000) and neighbour-joining (bootstrap repeat is 10,000) phylogenetic trees of twelve Aspergillus, one Penicillium mitochondrial genome, and Podospora mitochondrial genome as an outgroup: Aspergillus flavus (MT335777 in this study, JQ355000, and NC_026920), Aspergillus oryzae (NC_018100), Aspergillus parasiticus (NC_041445), Aspergillus fischeri (JQ354995), Aspergillus fumigatus (NC_017016), Aspergillus pseudoglaucus (NC_041427), Aspergillus niger (NC_007445), Aspergillus kawachii (AP012272), Aspergillus luchuensis (NC_040166), Aspergillus nidulans (NC_017896), Penicillium digitatum (NC_015080), and Podospora anserina (NC_001329). Phylogenetic tree was drawn based on maximum-likelihood phylogenetic tree. The numbers above or below branches indicate bootstrap support values of maximum likihood and neighbour-joining phylogenetic trees, respectively.

Figure 1. Maximum-likelihood (bootstrap repeat is 1000) and neighbour-joining (bootstrap repeat is 10,000) phylogenetic trees of twelve Aspergillus, one Penicillium mitochondrial genome, and Podospora mitochondrial genome as an outgroup: Aspergillus flavus (MT335777 in this study, JQ355000, and NC_026920), Aspergillus oryzae (NC_018100), Aspergillus parasiticus (NC_041445), Aspergillus fischeri (JQ354995), Aspergillus fumigatus (NC_017016), Aspergillus pseudoglaucus (NC_041427), Aspergillus niger (NC_007445), Aspergillus kawachii (AP012272), Aspergillus luchuensis (NC_040166), Aspergillus nidulans (NC_017896), Penicillium digitatum (NC_015080), and Podospora anserina (NC_001329). Phylogenetic tree was drawn based on maximum-likelihood phylogenetic tree. The numbers above or below branches indicate bootstrap support values of maximum likihood and neighbour-joining phylogenetic trees, respectively.

Disclosure statement

The authors declare that they have no competing interests.

Data availability statement

The sequence can be accessed via accession number MT335777 in NCBI GenBank. https://www.ncbi.nlm.nih.gov/genbank/.

Additional information

Funding

This research was supported by a grant [20162MDF007-3] from Ministry of Food and Drug Safety (2020), and the National Research Foundation of Korea (NRF) grants funded by the Korea government to JHK [2017R1D1A3B03031326] and to KHH [2017R1D1A3B06035312].

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