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Mitogenome Announcement

The first mitochondrial genome of Sepsis monostigma (Diptera: Sepsidae)

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Pages 2517-2518 | Received 20 Jan 2021, Accepted 18 Jul 2021, Published online: 29 Jul 2021

Abstract

The sepsid fly Sepsis monostigma belongs to the genus Sepsis of Sepsidae. We sequenced and annotated the mitogenome of S. monostigma which as the first representative of genus Sepsis with nearly complete mitochondrial data. This mitogenome is 14,887bp long, which contains of 22 transfer RNA genes, 13 protein coding genes (PCGs) and 2 ribosomal RNA genes and a part of the AT control region. ML phylogenetic outcome strongly supported the monophyly of Sepsidae, and the family Sepsidae is more close to the family Heleomyzidae. It also indicated that the genus Sepsis is the sister group to Nemopoda, and the genus Archisepsis is the sister group to Microsepsis.

Sepsidae is a global distributed fly family with more than 320 described species (Ozerov Citation2005), and it is a relatively small, morphologically and ecologically uniform family of the Sciomyzoiedea in the acalyptrate series of Diptera (Pont and Meier Citation2002). Sepsis monostigma (Thmpson,1869) is a rather important model-organisms insect and a sanitary fly of biological significance, which can perify the ecosystem (Li et al. Citation2015). The mitochondrial genome was often used for the research of species identification and phylogenetic relationships (Fu et al. Citation2016). Due to their tiny size, usually 2–12 mm, it is very difficult to extract enough genomic DNA. Hence, we sequenced the mitochondrial genome of S. monostigma, which is the first been reported in the Genus Sepsis. This study develop mitochondrial genome data of Sepsidae species, contributes to discussion on the evolutionary relationshios and provides theoretical basis for sexual seletion research.

S. monostigma (Voucher: Sepsidae001) was collected on 19 September 2020 at Bayi Park (latitude: 123.5236 N and longitude: 41.5243 E), Shenyang City, Liaoning Province, China. Each specimen was identified by entomologist according to taxonomic keys (Ang and Meier Citation2010). The voucher specimens and their DNA were deposited in the Natural History Museum of Shenyang University (JianfengWang, [email protected]) under the voucher number Sepsidae001.

The genomic DNA was extracted from the adult’s muscle tissues of the leg using the TIANamp Genomic DNA Kit (TIANGEN, Beijing, China), and sequenced under the next generation sequence technology with 22 primer pairs (Simon et al. Citation1994; Zhang et al. Citation2013; Zhao et al. Citation2013; Li et al. Citation2015). DNA fragments were sequenced on both strands by Applied Biosystems 3730 DNA Analyzer (Sangon Biotech Co. Ltd., Shanghai, China). Genome sequence was assembled by DNAman Version 6 software and was annotated by MITOS2 online software (http://mitos2.bioinf.uni-leipzig.de). Meanwhile, High-throughput sequencing was performed using Illumina Hiseq PE 150 Platform, using NOVOPlasty in de novo assembling. Almost the entire mitochondrial genome has been accurately obtained by two methods, except for the absence of the AT control region. This mitogenome of S. monostigma is 14,887 bp long, which contains of 22 transfer RNA genes, 13 protein coding genes (PCGs), 2 ribosomal RNA genes and a part of the AT control region, it was similar with related species reported before (Simon et al. Citation1994; Zhang et al. Citation2013; Zhao et al. Citation2013; Li et al. Citation2015; Chen et al. Citation2018; She et al. Citation2020).

The nucleotide composition of S. monostigma mitochondrial genome was 37.9% of A, 9.9% of G, 13.9% of C and 38.3% of T. The A + T content was 76.2% which conforms to the characteristics of AT preference like other flies. The codon ATG was the most popular start codon shared with the COII, ATP6, COIII, NAD4, NAD4L, CytB, and start codon ATT was shared with NAD2, ATP8, NAD3, NAD5, NAD6. Particularly, the COI begins with codon TCG, and the NAD1 begins with codon TTG. The conservative stop codon TAA was shared with NAD2, COI, COII, ATP8, ATP6, COIII, NAD4L, NAD6, NAD1. Another common stop codon TAG was shared with NAD3 and CytB. Particularly, the NAD5 and NAD4 stop with codon T. To make sure the authenticity of gene boundaries, all PCGs were compared with other muscid mitochondrial sequences under performed in MEGA 7.0 (Kumar et al. Citation2016).

Maximum Likelihood (ML) Phylogenetic analysis of four Sepsidae species, two Heleomyzidae species, three Drosophilidae speceis and four Muscidae species as the outgroup based on 13 PCGs by MEGA 7.0 software with 1000 bootstrap replicates (Kumar et al. Citation2016), and the topology is shown in . According to the phylogenetic outcome, the outgroups four Muscidae species form a clade. Our results strongly supported the monophyly of Sepsidae, and the family Sepsidae is more close to the family Heleomyzidae. It also indicated that the genus Sepsis is the sister group to the genus Nemopoda, and the genus Archisepsis is the sister group to the genus Microsepsis. In addition, the mitochondrial genome sequences could also be useful in identifying Sepsidae species.

Figure 1. ML phylogenetic tree of thirteen species which consist of four Sepsidae species, two Heleomyzidae species, three Drosophilidae speceis and four Muscidae species as the outgroup using MEGA 7.0 software. The numbers in the nodes indicated the support values with 1000 bootstrap replicates. *indicates this study.

Figure 1. ML phylogenetic tree of thirteen species which consist of four Sepsidae species, two Heleomyzidae species, three Drosophilidae speceis and four Muscidae species as the outgroup using MEGA 7.0 software. The numbers in the nodes indicated the support values with 1000 bootstrap replicates. *indicates this study.

Disclosure statement

The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.

Data availability statement

The genome sequence data that support the findings of this study are openly available in GenBank of NCBI at (https://www.ncbi.nlm.nih.gov/) under the accession no. MW438294.

Additional information

Funding

The research was supported by the Natural Science Foundation of Liaoning Province [2019-ZD-0539] and the Fund of National Natural Science Foundation of China [31672332].

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