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Mitogenome Announcement

The complete mitochondrial genome of Alphitobius diaperinus Panzer, 1797 (Coleoptera: Tenebrionidae)

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Pages 2291-2293 | Received 18 Apr 2020, Accepted 16 May 2020, Published online: 02 Jun 2020

Abstract

Alphitobius diaperinus Panzer, 1797 is a major pest in poultry production and easily observed in poultry litter. We have determined mitochondrial genome of A. diaperinus collected in Chungcheongbuk-do, Republic of Korea. The circular mitogenome of A. diaperinus is 15,511 bp long which is longer than that of Z. atratus but shorter than that of T. obscurus. It includes 13 protein-coding genes, two ribosomal RNA genes, and 22 transfer RNAs. The base composition was AT-biased (72.4%). Phylogenetic tree displays that tribe Alphitobiini is clustered with tribes Helopini and Diaperini with enough supportive values of three phylogenetic trees.

The darkling beetle, Alphitobius diaperinus Panzer, 1797 (Coleoptera: Tenebrionidae), is a significant pest in poultry worldwide. Though these beetles are small, their importance as a poultry pest is enormous. It is also considered a primary structural pest in the poultry industry, causing extensive damage to broiler housing, which has led to increased heating and repair costs for poultry producers (Axtell and Arends Citation1990).

To understand its genetic background, we completed mitogenome of A. diaperinus, as the first mitochondrial genome in tribe Alphitobiini, collected in Daeso-myeon, Eumseong-gun, Chungcheongbuk-do, Republic of Korea (36°96′77″N, 127°51′61″E; the specimen and its DNA were deposited at the Sunchon National University, Korea; Accession number: 190925HK004). DNA was extracted using DNeasy Blood &Tissue Kit (QIAGEN, Hilden, Germany). Raw sequences from Illumina HiSeqX (Macrogen, Korea) were filtered by Trimmomatic 0.33 (Bolger et al. Citation2014) and de novo assembled using Velvet 1.2.10 (Zerbino and Birney Citation2008), SOAPGapCloser 1.12 (Zhao et al. Citation2011), BWA 0.7.17 (Li Citation2013), and SAMtools 1.9 (Li et al. Citation2009). Geneious R11 11.1.5 (Biomatters Ltd, Auckland, New Zealand) was used to annotate based on several mitogenomes including Zophobas atratus (NC_041101; Bai et al. Citation2019), Tenebrio obscurus (NC_037196; Bai et al. Citation2018), and Tenebrio molitor (NC_024633; Li-Na and Cheng-Ye Citation2014).

Alphitobius diaperinus mitogenome (GenBank accession is MT165524) is 15,511 bp long, which is longer than that of Z. atratus (15,494 bp) but shorter than those of T. obscurus (15,771 bp) and T. molitor (15,785 bp). It contains 13 protein-coding genes (PCGs), 37 tRNAs, and two rRNAs. The base composition was AT-biased (72.4%) and gene order was identical to 23 available Tenebrionidae mitogenomes.

We inferred the phylogenetic relationship of 24 Tenebrionidae mitogenomes, including A. diaperinus mitogenome. Complete mitochondrial genomes were aligned by MAFFT 7.450 (Katoh and Standley Citation2013) after rearranging sequences including utilizing reverse complement sequences and moving unaligned sequences to the end of mitogenomes. Multiple sequence alignment was used for constructing bootstrapped neighbor-joining, maximum-likelihood, and Bayesian inference phylogenetic trees with MEGA X (Kumar et al. Citation2018) and Mr. Bayes (Huelsenbeck and Ronquist Citation2001), respectively. Phylogenetic tree displays that tribe Alphitobiini is clustered with tribes Helopini and Diaperini with enough supportive values of three phylogenetic trees (). Some of higher clades not supported by three phylogenetic trees (see bold supportive values in ) indicate that the phylogenetic relationship of species in Tenebrioninae should be investigated more with additional mitochondrial genomes which will be available in near future. In addition, three mitochondrial genomes of Tribolium castaneum display high supportive values of three phylogenetic trees, which is similar to those of Laodelphax striatellus (Park, Jung, et al. Citation2019; Seo et al. Citation2019) and Stegobium paniceum (Park et al., Citationunder review); while it is different from those of Nilaparvata lugens (Choi et al. Citation2019; Park, Kwon, et al. Citation2019; Choi et al., Citationunder review).

Figure 1. Bayesian inference (1,000,000 generations), maximum-likelihood (1000 bootstrap repeats), and neighbor-joining (10,000 bootstrap repeats) phylogenetic trees of 24 Tenebrionidae mitochondrial genomes: Alphitobius diaperinus (MT165524), Amarygmini sp. (MH789725; Partial mitochondrial genome; MH836607, and MH836612), Tenebrionidae sp. (MH836613 and MH751303), Paramarygmus sp. (JX412808; Partial mitochondrial genome), Cteniopus sp. (KX087267; Partial mitochondrial genome), Zophobasatratus (NC_041101), Uloma sp. (KT876915), Ulomoides dermestoides (NC_025332), Nalassus laevioctostriatus (KT876905), Platydema sp. (JX412842), Tenebrio molitor (NC_024633), Tenebrio obscurus (NC_037196), Tribolium confusum (NC_026702), Tribolium audax (NC_024600), Tribolium castaneum (NC_003081, KM009121, and KM244661), Adelium sp. (NC_013554), Asbolus verrucosus (NC_027256), and Leiochrinini sp. (MH836599 and MH908183). Phylogenetic tree was drawn based on maximum-likelihood tree. The numbers above branches indicate bootstrap support values of maximum-likelihood and neighbor-joining phylogenetic trees and posterior probability value of Bayesian inference tree, respectively. Tribe names were displayed as light gray color. Bolded supportive values indicate nodes that all three phylogenetic trees show different topologies.

Figure 1. Bayesian inference (1,000,000 generations), maximum-likelihood (1000 bootstrap repeats), and neighbor-joining (10,000 bootstrap repeats) phylogenetic trees of 24 Tenebrionidae mitochondrial genomes: Alphitobius diaperinus (MT165524), Amarygmini sp. (MH789725; Partial mitochondrial genome; MH836607, and MH836612), Tenebrionidae sp. (MH836613 and MH751303), Paramarygmus sp. (JX412808; Partial mitochondrial genome), Cteniopus sp. (KX087267; Partial mitochondrial genome), Zophobasatratus (NC_041101), Uloma sp. (KT876915), Ulomoides dermestoides (NC_025332), Nalassus laevioctostriatus (KT876905), Platydema sp. (JX412842), Tenebrio molitor (NC_024633), Tenebrio obscurus (NC_037196), Tribolium confusum (NC_026702), Tribolium audax (NC_024600), Tribolium castaneum (NC_003081, KM009121, and KM244661), Adelium sp. (NC_013554), Asbolus verrucosus (NC_027256), and Leiochrinini sp. (MH836599 and MH908183). Phylogenetic tree was drawn based on maximum-likelihood tree. The numbers above branches indicate bootstrap support values of maximum-likelihood and neighbor-joining phylogenetic trees and posterior probability value of Bayesian inference tree, respectively. Tribe names were displayed as light gray color. Bolded supportive values indicate nodes that all three phylogenetic trees show different topologies.

Disclosure statement

The authors declare that they have no competing interests.

Data availability statement

The data that support the findings of this study are openly available in NCBI (National Center for Biotechnology Information) at https://www.ncbi.nlm.nih.gov/nuccore/MT165524.

Additional information

Funding

This study was supported by the R&D project ‘Study on infestation status and control measures of darkling beetle in broiler house [project number: Z-1543084-2018-19-01]’.

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